diff --git a/data/_ontologies/Diseases.csv b/data/_ontologies/Diseases.csv index b4512a97ac..6a530f7a2d 100644 --- a/data/_ontologies/Diseases.csv +++ b/data/_ontologies/Diseases.csv @@ -4,18 +4,18 @@ I Certain infectious and parasitic diseases,2,I,,,,ICD-10 A00-A09 Intestinal infectious diseases,3,A00-A09,I Certain infectious and parasitic diseases,,,ICD-10 A00 Cholera,4,A00,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A00,,ICD-10 "A00.0 Cholera due to Vibrio cholerae 01, biovar cholerae",5,A00.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A00.0,,ICD-10 -"A00.1 Cholera due to Vibrio cholerae 01, biovar eltor",6,A00.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A00.1,ORPHAcode: 173 Cholera +"A00.1 Cholera due to Vibrio cholerae 01, biovar eltor",6,A00.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A00.1,ORPHAcode: 173 Cholera,ICD-10 "A00.9 Cholera, unspecified",7,A00.9,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A00.9,,ICD-10 A01 Typhoid and paratyphoid fevers,8,A01,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01,,ICD-10 -A01.0 Typhoid fever,9,A01.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01.0,ORPHAcode: 99745 Typhoid -A01.1 Paratyphoid fever A,10,A01.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01.1,ORPHAcode: 443227 Paratyphoid fever +A01.0 Typhoid fever,9,A01.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01.0,ORPHAcode: 99745 Typhoid,ICD-10 +A01.1 Paratyphoid fever A,10,A01.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01.1,ORPHAcode: 443227 Paratyphoid fever,ICD-10 A01.2 Paratyphoid fever B,11,A01.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01.2,,ICD-10 A01.3 Paratyphoid fever C,12,A01.3,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01.3,,ICD-10 "A01.4 Paratyphoid fever, unspecified",13,A01.4,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A01.4,,ICD-10 A02 Other salmonella infections,14,A02,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A02,,ICD-10 A02.0 Salmonella enteritis,15,A02.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A02.0,,ICD-10 A02.1 Salmonella sepsis,16,A02.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A02.1,,ICD-10 -A02.2 Localized salmonella infections,17,A02.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A02.2,ORPHAcode: 324648 Invasive non-typhoidal salmonellosis +A02.2 Localized salmonella infections,17,A02.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A02.2,ORPHAcode: 324648 Invasive non-typhoidal salmonellosis,ICD-10 A02.8 Other specified salmonella infections,18,A02.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A02.8,,ICD-10 "A02.9 Salmonella infection, unspecified",19,A02.9,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A02.9,,ICD-10 A03 Shigellosis,20,A03,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A03,,ICD-10 @@ -23,7 +23,7 @@ A03.0 Shigellosis due to Shigella dysenteriae,21,A03.0,A00-A09 Intestinal infect A03.1 Shigellosis due to Shigella flexneri,22,A03.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A03.1,,ICD-10 A03.2 Shigellosis due to Shigella boydii,23,A03.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A03.2,,ICD-10 A03.3 Shigellosis due to Shigella sonnei,24,A03.3,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A03.3,,ICD-10 -A03.8 Other shigellosis,25,A03.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A03.8,ORPHAcode: 810 Shigellosis +A03.8 Other shigellosis,25,A03.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A03.8,ORPHAcode: 810 Shigellosis,ICD-10 "A03.9 Shigellosis, unspecified",26,A03.9,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A03.9,,ICD-10 A04 Other bacterial intestinal infections,27,A04,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04,,ICD-10 A04.0 Other bacterial intestinal infections - Enteropathogenic Escherichia coli infection,28,A04.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04.0,,ICD-10 @@ -34,18 +34,18 @@ A04.4 Other intestinal Escherichia coli infections,32,A04.4,A00-A09 Intestinal i A04.5 Other bacterial intestinal infections - Campylobacter enteritis,33,A04.5,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04.5,,ICD-10 A04.6 Other bacterial intestinal infections - Enteritis due to Yersinia enterocolitica,34,A04.6,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04.6,,ICD-10 A04.7 Other bacterial intestinal infections - Enterocolitis due to Clostridium difficile,35,A04.7,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04.7,,ICD-10 -A04.8 Other specified bacterial intestinal infections,36,A04.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04.8,ORPHAcode: 90078 Invasive infections due to vancomycin-resistant enterococci +A04.8 Other specified bacterial intestinal infections,36,A04.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04.8,ORPHAcode: 90078 Invasive infections due to vancomycin-resistant enterococci,ICD-10 "A04.9 Bacterial intestinal infection, unspecified",37,A04.9,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A04.9,,ICD-10 "A05 Other bacterial foodborne intoxications, not elsewhere classified",38,A05,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05,,ICD-10 A05.0 Foodborne staphylococcal intoxication,39,A05.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.0,,ICD-10 -"A05.1 Other bacterial foodborne intoxications, not elsewhere classified - Botulism",40,A05.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.1,ORPHAcode: 1267 Botulism +"A05.1 Other bacterial foodborne intoxications, not elsewhere classified - Botulism",40,A05.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.1,ORPHAcode: 1267 Botulism,ICD-10 A05.2 Foodborne Clostridium perfringens [Clostridium welchii] intoxication,41,A05.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.2,,ICD-10 A05.3 Foodborne Vibrio parahaemolyticus intoxication,42,A05.3,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.3,,ICD-10 A05.4 Foodborne Bacillus cereus intoxication,43,A05.4,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.4,,ICD-10 A05.8 Other specified bacterial foodborne intoxications,44,A05.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.8,,ICD-10 "A05.9 Bacterial foodborne intoxication, unspecified",45,A05.9,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A05.9,,ICD-10 A06 Amoebiasis,46,A06,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06,,ICD-10 -A06.0 Amoebiasis - Acute amoebic dysentery,47,A06.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06.0,ORPHAcode: 67 Amoebiasis due to Entamoeba histolytica +A06.0 Amoebiasis - Acute amoebic dysentery,47,A06.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06.0,ORPHAcode: 67 Amoebiasis due to Entamoeba histolytica,ICD-10 A06.1 Chronic intestinal amoebiasis,48,A06.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06.1,,ICD-10 A06.2 Amoebiasis - Amoebic nondysenteric colitis,49,A06.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06.2,,ICD-10 A06.3 Amoebiasis - Amoeboma of intestine,50,A06.3,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06.3,,ICD-10 @@ -56,12 +56,12 @@ A06.7 Cutaneous amoebiasis,54,A06.7,A00-A09 Intestinal infectious diseases,http: A06.8 Amoebiasis - Amoebic infection of other sites,55,A06.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06.8,,ICD-10 "A06.9 Amoebiasis, unspecified",56,A06.9,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A06.9,,ICD-10 A07 Other protozoal intestinal diseases,57,A07,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07,,ICD-10 -A07.0 Other protozoal intestinal diseases - Balantidiasis,58,A07.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.0,ORPHAcode: 1223 Balantidiasis +A07.0 Other protozoal intestinal diseases - Balantidiasis,58,A07.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.0,ORPHAcode: 1223 Balantidiasis,ICD-10 A07.1 Other protozoal intestinal diseases - Giardiasis [lambliasis],59,A07.1,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.1,,ICD-10 "A15.3 Tuberculosis of lung, confirmed by unspecified means",60,A15.3,A15-A19 Tuberculosis,http://identifiers.org/icd/A15.3,,ICD-10 -A07.2 Other protozoal intestinal diseases - Cryptosporidiosis,61,A07.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.2,ORPHAcode: 1549 Cryptosporidiosis -A07.3 Other protozoal intestinal diseases - Isosporiasis,62,A07.3,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.3,ORPHAcode: 210 Cyclosporosis -A07.8 Other specified protozoal intestinal diseases,63,A07.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.8,ORPHAcode: 54368 Sarcocystosis +A07.2 Other protozoal intestinal diseases - Cryptosporidiosis,61,A07.2,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.2,ORPHAcode: 1549 Cryptosporidiosis,ICD-10 +A07.3 Other protozoal intestinal diseases - Isosporiasis,62,A07.3,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.3,ORPHAcode: 210 Cyclosporosis,ICD-10 +A07.8 Other specified protozoal intestinal diseases,63,A07.8,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.8,ORPHAcode: 54368 Sarcocystosis,ICD-10 "A07.9 Protozoal intestinal disease, unspecified",64,A07.9,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A07.9,,ICD-10 A08 Viral and other specified intestinal infections,65,A08,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A08,,ICD-10 A08.0 Rotaviral enteritis,66,A08.0,A00-A09 Intestinal infectious diseases,http://identifiers.org/icd/A08.0,,ICD-10 @@ -95,8 +95,8 @@ B74 Filariasis,80,B74,B65-B83 Helminthiases,http://identifiers.org/icd/B74,,ICD- A16.7 Primary respiratory tuberculosis without mention of bacteriological or histological confirmation,94,A16.7,A15-A19 Tuberculosis,http://identifiers.org/icd/A16.7,,ICD-10 "A16.8 Other respiratory tuberculosis, without mention of bacteriological or histological confirmation",95,A16.8,A15-A19 Tuberculosis,http://identifiers.org/icd/A16.8,,ICD-10 "A16.9 Respiratory tuberculosis unspecified, without mention of bacteriological or histological confirmation",96,A16.9,A15-A19 Tuberculosis,http://identifiers.org/icd/A16.9,,ICD-10 -A17 Tuberculosis of nervous system,97,A17,A15-A19 Tuberculosis,http://identifiers.org/icd/A17,ORPHAcode: 3389 Tuberculosis -A17.0 Tuberculosis of nervous system - Tuberculous meningitis,98,A17.0,A15-A19 Tuberculosis,http://identifiers.org/icd/A17.0,ORPHAcode: 499004 Tuberculous meningitis +A17 Tuberculosis of nervous system,97,A17,A15-A19 Tuberculosis,http://identifiers.org/icd/A17,ORPHAcode: 3389 Tuberculosis,ICD-10 +A17.0 Tuberculosis of nervous system - Tuberculous meningitis,98,A17.0,A15-A19 Tuberculosis,http://identifiers.org/icd/A17.0,ORPHAcode: 499004 Tuberculous meningitis,ICD-10 A17.1 Tuberculosis of nervous system - Meningeal tuberculoma,99,A17.1,A15-A19 Tuberculosis,http://identifiers.org/icd/A17.1,,ICD-10 A17.8 Other tuberculosis of nervous system,100,A17.8,A15-A19 Tuberculosis,http://identifiers.org/icd/A17.8,,ICD-10 "A17.9 Tuberculosis of nervous system, unspecified",101,A17.9,A15-A19 Tuberculosis,http://identifiers.org/icd/A17.9,,ICD-10 @@ -118,7 +118,7 @@ A19.8 Other miliary tuberculosis,116,A19.8,A15-A19 Tuberculosis,http://identifie "A19.9 Miliary tuberculosis, unspecified",117,A19.9,A15-A19 Tuberculosis,http://identifiers.org/icd/A19.9,,ICD-10 A20-A28 Certain zoonotic bacterial diseases,118,,I Certain infectious and parasitic diseases,,,ICD-10 A20 Plague,119,A20,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20,,ICD-10 -A20.0 Bubonic plague,120,A20.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20.0,ORPHAcode: 707 Plague +A20.0 Bubonic plague,120,A20.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20.0,ORPHAcode: 707 Plague,ICD-10 A20.1 Cellulocutaneous plague,121,A20.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20.1,,ICD-10 A20.2 Pneumonic plague,122,A20.2,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20.2,,ICD-10 A20.3 Plague meningitis,123,A20.3,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20.3,,ICD-10 @@ -126,7 +126,7 @@ A20.7 Septicaemic plague,124,A20.7,A20-A28 Certain zoonotic bacterial diseases,h A20.8 Other forms of plague,125,A20.8,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20.8,,ICD-10 "A20.9 Plague, unspecified",126,A20.9,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A20.9,,ICD-10 A21 Tularaemia,127,A21,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A21,,ICD-10 -A21.0 Ulceroglandular tularaemia,128,A21.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A21.0,ORPHAcode: 3392 Tularemia +A21.0 Ulceroglandular tularaemia,128,A21.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A21.0,ORPHAcode: 3392 Tularemia,ICD-10 A21.1 Oculoglandular tularaemia,129,A21.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A21.1,,ICD-10 A21.2 Pulmonary tularaemia,130,A21.2,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A21.2,,ICD-10 A21.3 Gastrointestinal tularaemia,131,A21.3,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A21.3,,ICD-10 @@ -135,7 +135,7 @@ A21.8 Other forms of tularaemia,133,A21.8,A20-A28 Certain zoonotic bacterial dis "A21.9 Tularaemia, unspecified",134,A21.9,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A21.9,,ICD-10 A22 Anthrax,135,A22,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A22,,ICD-10 A22.0 Cutaneous anthrax,136,A22.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A22.0,,ICD-10 -A22.1 Pulmonary anthrax,137,A22.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A22.1,ORPHAcode: 247257 Inhalational anthrax +A22.1 Pulmonary anthrax,137,A22.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A22.1,ORPHAcode: 247257 Inhalational anthrax,ICD-10 A22.2 Gastrointestinal anthrax,138,A22.2,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A22.2,,ICD-10 A22.7 Anthrax sepsis,139,A22.7,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A22.7,,ICD-10 A22.8 Other forms of anthrax,140,A22.8,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A22.8,,ICD-10 @@ -144,17 +144,17 @@ A23 Brucellosis,142,A23,A20-A28 Certain zoonotic bacterial diseases,http://ident A23.0 Brucellosis due to Brucella melitensis,143,A23.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A23.0,,ICD-10 A23.1 Brucellosis due to Brucella abortus,144,A23.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A23.1,,ICD-10 A23.2 Brucellosis due to Brucella suis,145,A23.2,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A23.2,,ICD-10 -A23.3 Brucellosis due to Brucella canis,146,A23.3,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A23.3,ORPHAcode: 1304 Brucellosis +A23.3 Brucellosis due to Brucella canis,146,A23.3,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A23.3,ORPHAcode: 1304 Brucellosis,ICD-10 A23.8 Other brucellosis,147,A23.8,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A23.8,,ICD-10 "A23.9 Brucellosis, unspecified",148,A23.9,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A23.9,,ICD-10 A24 Glanders and melioidosis,149,A24,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A24,,ICD-10 A24.0 Glanders,150,A24.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A24.0,,ICD-10 -A24.1 Acute and fulminating melioidosis,151,A24.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A24.1,ORPHAcode: 31202 Melioidosis +A24.1 Acute and fulminating melioidosis,151,A24.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A24.1,ORPHAcode: 31202 Melioidosis,ICD-10 A24.2 Subacute and chronic melioidosis,152,A24.2,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A24.2,,ICD-10 A24.3 Other melioidosis,153,A24.3,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A24.3,,ICD-10 "A24.4 Melioidosis, unspecified",154,A24.4,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A24.4,,ICD-10 A25 Rat-bite fevers,155,A25,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A25,,ICD-10 -A25.0 Rat-bite fevers - Spirillosis,156,A25.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A25.0,ORPHAcode: 31205 Rat-bite fever +A25.0 Rat-bite fevers - Spirillosis,156,A25.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A25.0,ORPHAcode: 31205 Rat-bite fever,ICD-10 A25.1 Rat-bite fevers - Streptobacillosis,157,A25.1,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A25.1,,ICD-10 "A25.9 Rat-bite fevers - Rat-bite fever, unspecified",158,A25.9,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A25.9,,ICD-10 A26 Erysipeloid,159,A26,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A26,,ICD-10 @@ -164,13 +164,13 @@ A26.8 Other forms of erysipeloid,162,A26.8,A20-A28 Certain zoonotic bacterial di "A26.9 Erysipeloid, unspecified",163,A26.9,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A26.9,,ICD-10 A27 Leptospirosis,164,A27,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A27,,ICD-10 A27.0 Leptospirosis icterohaemorrhagica,165,A27.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A27.0,,ICD-10 -A27.8 Other forms of leptospirosis,166,A27.8,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A27.8,ORPHAcode: 509 Leptospirosis +A27.8 Other forms of leptospirosis,166,A27.8,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A27.8,ORPHAcode: 509 Leptospirosis,ICD-10 "A27.9 Leptospirosis, unspecified",167,A27.9,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A27.9,,ICD-10 "A28 Other zoonotic bacterial diseases, not elsewhere classified",168,A28,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A28,,ICD-10 "A28.0 Other zoonotic bacterial diseases, not elsewhere classified - Pasteurellosis",169,A28.0,A20-A28 Certain zoonotic bacterial diseases,http://identifiers.org/icd/A28.0,,ICD-10 A30-A49 Other bacterial diseases,170,,I Certain infectious and parasitic diseases,,,ICD-10 A30 Leprosy [Hansen disease],171,A30,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30,,ICD-10 -A30.0 Indeterminate leprosy,172,A30.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30.0,ORPHAcode: 548 Leprosy +A30.0 Indeterminate leprosy,172,A30.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30.0,ORPHAcode: 548 Leprosy,ICD-10 A30.1 Tuberculoid leprosy,173,A30.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30.1,,ICD-10 A30.2 Borderline tuberculoid leprosy,174,A30.2,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30.2,,ICD-10 A30.3 Borderline leprosy,175,A30.3,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30.3,,ICD-10 @@ -179,32 +179,32 @@ A30.5 Lepromatous leprosy,177,A30.5,A30-A49 Other bacterial diseases,http://iden A30.8 Other forms of leprosy,178,A30.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30.8,,ICD-10 "A30.9 Leprosy, unspecified",179,A30.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A30.9,,ICD-10 A31 Infection due to other mycobacteria,180,A31,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A31,,ICD-10 -A31.0 Pulmonary mycobacterial infection,181,A31.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A31.0,ORPHAcode: 411703 Pulmonary non-tuberculous mycobacterial infection +A31.0 Pulmonary mycobacterial infection,181,A31.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A31.0,ORPHAcode: 411703 Pulmonary non-tuberculous mycobacterial infection,ICD-10 A31.1 Cutaneous mycobacterial infection,182,A31.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A31.1,,ICD-10 A31.8 Other mycobacterial infections,183,A31.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A31.8,,ICD-10 "A31.9 Mycobacterial infection, unspecified",184,A31.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A31.9,,ICD-10 A32 Listeriosis,185,A32,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A32,,ICD-10 -A32.0 Cutaneous listeriosis,186,A32.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A32.0,ORPHAcode: 533 Listeriosis +A32.0 Cutaneous listeriosis,186,A32.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A32.0,ORPHAcode: 533 Listeriosis,ICD-10 A32.1 Listeriosis - Listerial meningitis and meningoencephalitis,187,A32.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A32.1,,ICD-10 A32.7 Listeriosis - Listerial sepsis,188,A32.7,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A32.7,,ICD-10 A32.8 Other forms of listeriosis,189,A32.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A32.8,,ICD-10 "A32.9 Listeriosis, unspecified",190,A32.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A32.9,,ICD-10 -A33 Tetanus neonatorum,191,A33,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A33,ORPHAcode: 3299 Tetanus +A33 Tetanus neonatorum,191,A33,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A33,ORPHAcode: 3299 Tetanus,ICD-10 A34 Obstetrical tetanus,192,A34,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A34,,ICD-10 A35 Other tetanus,193,A35,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A35,,ICD-10 A36 Diphtheria,194,A36,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36,,ICD-10 A36.0 Pharyngeal diphtheria,195,A36.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36.0,,ICD-10 -A36.1 Nasopharyngeal diphtheria,196,A36.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36.1,ORPHAcode: 1679 Diphtheria +A36.1 Nasopharyngeal diphtheria,196,A36.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36.1,ORPHAcode: 1679 Diphtheria,ICD-10 A36.2 Laryngeal diphtheria,197,A36.2,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36.2,,ICD-10 A36.3 Cutaneous diphtheria,198,A36.3,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36.3,,ICD-10 A36.8 Other diphtheria,199,A36.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36.8,,ICD-10 "A36.9 Diphtheria, unspecified",200,A36.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A36.9,,ICD-10 A37 Whooping cough,201,A37,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A37,,ICD-10 -A37.0 Whooping cough due to Bordetella pertussis,202,A37.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A37.0,ORPHAcode: 1489 Whooping cough +A37.0 Whooping cough due to Bordetella pertussis,202,A37.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A37.0,ORPHAcode: 1489 Whooping cough,ICD-10 A37.1 Whooping cough due to Bordetella parapertussis,203,A37.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A37.1,,ICD-10 A37.8 Whooping cough due to other Bordetella species,204,A37.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A37.8,,ICD-10 "A37.9 Whooping cough, unspecified",205,A37.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A37.9,,ICD-10 -A38 Scarlet fever,206,A38,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A38,ORPHAcode: 36235 Staphylococcal scarlet fever +A38 Scarlet fever,206,A38,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A38,ORPHAcode: 36235 Staphylococcal scarlet fever,ICD-10 A39 Meningococcal infection,207,A39,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A39,,ICD-10 A39.0 Meningococcal meningitis,208,A39.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A39.0,,ICD-10 A39.1 Meningococcal infection - Waterhouse-Friderichsen syndrome,209,A39.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A39.1,,ICD-10 @@ -235,26 +235,26 @@ A42.0 Pulmonary actinomycosis,233,A42.0,A30-A49 Other bacterial diseases,http:// A42.1 Abdominal actinomycosis,234,A42.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A42.1,,ICD-10 A42.2 Cervicofacial actinomycosis,235,A42.2,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A42.2,,ICD-10 A42.7 Actinomycosis - Actinomycotic sepsis,236,A42.7,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A42.7,,ICD-10 -A42.8 Other forms of actinomycosis,237,A42.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A42.8,ORPHAcode: 457095 Actinomycosis +A42.8 Other forms of actinomycosis,237,A42.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A42.8,ORPHAcode: 457095 Actinomycosis,ICD-10 "A42.9 Actinomycosis, unspecified",238,A42.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A42.9,,ICD-10 A43 Nocardiosis,239,A43,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A43,,ICD-10 -A43.0 Pulmonary nocardiosis,240,A43.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A43.0,ORPHAcode: 31204 Nocardiosis +A43.0 Pulmonary nocardiosis,240,A43.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A43.0,ORPHAcode: 31204 Nocardiosis,ICD-10 A43.1 Cutaneous nocardiosis,241,A43.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A43.1,,ICD-10 A43.8 Other forms of nocardiosis,242,A43.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A43.8,,ICD-10 "A43.9 Nocardiosis, unspecified",243,A43.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A43.9,,ICD-10 A44 Bartonellosis,244,A44,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A44,,ICD-10 -A44.0 Systemic bartonellosis,245,A44.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A44.0,ORPHAcode: 64692 Oroya fever +A44.0 Systemic bartonellosis,245,A44.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A44.0,ORPHAcode: 64692 Oroya fever,ICD-10 A44.1 Cutaneous and mucocutaneous bartonellosis,246,A44.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A44.1,,ICD-10 A44.8 Other forms of bartonellosis,247,A44.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A44.8,,ICD-10 "A44.9 Bartonellosis, unspecified",248,A44.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A44.9,,ICD-10 A46 Erysipelas,249,A46,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A46,,ICD-10 "A48 Other bacterial diseases, not elsewhere classified",250,A48,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48,,ICD-10 "A48.0 Other bacterial diseases, not elsewhere classified - Gas gangrene",251,A48.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.0,,ICD-10 -"A48.1 Other bacterial diseases, not elsewhere classified - Legionnaires disease",252,A48.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.1,ORPHAcode: 549 Legionnaires disease -"A48.2 Other bacterial diseases, not elsewhere classified - Nonpneumonic Legionnaires disease [Pontiac fever]",253,A48.2,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.2,ORPHAcode: 99748 Pontiac fever -"A48.3 Other bacterial diseases, not elsewhere classified - Toxic shock syndrome",254,A48.3,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.3,ORPHAcode: 36234 Bacterial toxic-shock syndrome +"A48.1 Other bacterial diseases, not elsewhere classified - Legionnaires disease",252,A48.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.1,ORPHAcode: 549 Legionnaires disease,ICD-10 +"A48.2 Other bacterial diseases, not elsewhere classified - Nonpneumonic Legionnaires disease [Pontiac fever]",253,A48.2,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.2,ORPHAcode: 99748 Pontiac fever,ICD-10 +"A48.3 Other bacterial diseases, not elsewhere classified - Toxic shock syndrome",254,A48.3,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.3,ORPHAcode: 36234 Bacterial toxic-shock syndrome,ICD-10 "A48.4 Other bacterial diseases, not elsewhere classified - Brazilian purpuric fever",255,A48.4,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.4,,ICD-10 -A48.8 Other specified bacterial diseases,256,A48.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.8,ORPHAcode: 1902 Ehrlichiosis +A48.8 Other specified bacterial diseases,256,A48.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A48.8,ORPHAcode: 1902 Ehrlichiosis,ICD-10 A49 Bacterial infection of unspecified site,257,A49,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A49,,ICD-10 "A49.0 Staphylococcal infection, unspecified site",258,A49.0,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A49.0,,ICD-10 "A49.1 Streptococcal and enterococcal infection, unspecified site",259,A49.1,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A49.1,,ICD-10 @@ -263,7 +263,7 @@ A49 Bacterial infection of unspecified site,257,A49,A30-A49 Other bacterial dise A49.8 Other bacterial infections of unspecified site,262,A49.8,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A49.8,,ICD-10 "A49.9 Bacterial infection, unspecified",263,A49.9,A30-A49 Other bacterial diseases,http://identifiers.org/icd/A49.9,,ICD-10 A50-A64 Infections with a predominantly sexual mode of transmission,264,,I Certain infectious and parasitic diseases,,,ICD-10 -A50 Congenital syphilis,265,A50,A50-A64 Infections with a predominantly sexual mode of transmission,http://identifiers.org/icd/A50,ORPHAcode: 499009 Congenital syphilis +A50 Congenital syphilis,265,A50,A50-A64 Infections with a predominantly sexual mode of transmission,http://identifiers.org/icd/A50,ORPHAcode: 499009 Congenital syphilis,ICD-10 "A50.0 Early congenital syphilis, symptomatic",266,A50.0,A50-A64 Infections with a predominantly sexual mode of transmission,http://identifiers.org/icd/A50.0,,ICD-10 A67.0 Primary lesions of pinta,267,A67.0,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A67.0,,ICD-10 "A50.1 Early congenital syphilis, latent",268,A50.1,A50-A64 Infections with a predominantly sexual mode of transmission,http://identifiers.org/icd/A50.1,,ICD-10 @@ -344,13 +344,13 @@ A67.2 Late lesions of pinta,342,A67.2,A65-A69 Other spirochaetal diseases,http:/ A67.3 Mixed lesions of pinta,343,A67.3,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A67.3,,ICD-10 "A67.9 Pinta, unspecified",344,A67.9,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A67.9,,ICD-10 A68 Relapsing fevers,345,A68,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A68,,ICD-10 -A68.0 Louse-borne relapsing fever,346,A68.0,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A68.0,ORPHAcode: 91547 Relapsing fever +A68.0 Louse-borne relapsing fever,346,A68.0,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A68.0,ORPHAcode: 91547 Relapsing fever,ICD-10 A68.1 Tick-borne relapsing fever,347,A68.1,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A68.1,,ICD-10 "A68.9 Relapsing fever, unspecified",348,A68.9,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A68.9,,ICD-10 A69 Other spirochaetal infections,349,A69,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69,,ICD-10 -A69.0 Other spirochaetal infections - Necrotizing ulcerative stomatitis,350,A69.0,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69.0,ORPHAcode: 2700 Noma +A69.0 Other spirochaetal infections - Necrotizing ulcerative stomatitis,350,A69.0,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69.0,ORPHAcode: 2700 Noma,ICD-10 A69.1 Other Vincent infections,351,A69.1,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69.1,,ICD-10 -A69.2 Other spirochaetal infections - Lyme disease,352,A69.2,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69.2,ORPHAcode: 91546 Lyme disease +A69.2 Other spirochaetal infections - Lyme disease,352,A69.2,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69.2,ORPHAcode: 91546 Lyme disease,ICD-10 A69.8 Other specified spirochaetal infections,353,A69.8,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69.8,,ICD-10 "A69.9 Spirochaetal infection, unspecified",354,A69.9,A65-A69 Other spirochaetal diseases,http://identifiers.org/icd/A69.9,,ICD-10 A70-A74 Other diseases caused by chlamydiae,355,,I Certain infectious and parasitic diseases,,,ICD-10 @@ -365,23 +365,23 @@ A74.8 Other chlamydial diseases,363,A74.8,A70-A74 Other diseases caused by chlam "A74.9 Other diseases caused by chlamydiae - Chlamydial infection, unspecified",364,A74.9,A70-A74 Other diseases caused by chlamydiae,http://identifiers.org/icd/A74.9,,ICD-10 A75-A79 Rickettsioses,365,,I Certain infectious and parasitic diseases,,,ICD-10 A75 Typhus fever,366,A75,A75-A79 Rickettsioses,http://identifiers.org/icd/A75,,ICD-10 -A75.0 Epidemic louse-borne typhus fever due to Rickettsia prowazekii,367,A75.0,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.0,ORPHAcode: 83314 Epidemic typhus +A75.0 Epidemic louse-borne typhus fever due to Rickettsia prowazekii,367,A75.0,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.0,ORPHAcode: 83314 Epidemic typhus,ICD-10 A75.1 Recrudescent typhus [Brill disease],368,A75.1,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.1,,ICD-10 -A75.2 Typhus fever due to Rickettsia typhi,369,A75.2,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.2,ORPHAcode: 83315 Murine typhus -A75.3 Typhus fever due to Rickettsia tsutsugamushi,370,A75.3,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.3,ORPHAcode: 83317 Scrub typhus +A75.2 Typhus fever due to Rickettsia typhi,369,A75.2,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.2,ORPHAcode: 83315 Murine typhus,ICD-10 +A75.3 Typhus fever due to Rickettsia tsutsugamushi,370,A75.3,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.3,ORPHAcode: 83317 Scrub typhus,ICD-10 "A75.9 Typhus fever, unspecified",371,A75.9,A75-A79 Rickettsioses,http://identifiers.org/icd/A75.9,,ICD-10 A77 Spotted fever [tick-borne rickettsioses],372,A77,A75-A79 Rickettsioses,http://identifiers.org/icd/A77,,ICD-10 -A77.0 Spotted fever due to Rickettsia rickettsii,373,A77.0,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.0,ORPHAcode: 83311 Rocky Mountain spotted fever -A77.1 Spotted fever due to Rickettsia conorii,374,A77.1,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.1,ORPHAcode: 83313 Boutonneuse fever +A77.0 Spotted fever due to Rickettsia rickettsii,373,A77.0,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.0,ORPHAcode: 83311 Rocky Mountain spotted fever,ICD-10 +A77.1 Spotted fever due to Rickettsia conorii,374,A77.1,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.1,ORPHAcode: 83313 Boutonneuse fever,ICD-10 A77.2 Spotted fever due to Rickettsia sibirica,375,A77.2,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.2,,ICD-10 A77.3 Spotted fever due to Rickettsia australis,376,A77.3,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.3,,ICD-10 A77.8 Other spotted fevers,377,A77.8,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.8,,ICD-10 "A77.9 Spotted fever, unspecified",378,A77.9,A75-A79 Rickettsioses,http://identifiers.org/icd/A77.9,,ICD-10 -A78 Q fever,379,A78,A75-A79 Rickettsioses,http://identifiers.org/icd/A78,ORPHAcode: 781 Q fever +A78 Q fever,379,A78,A75-A79 Rickettsioses,http://identifiers.org/icd/A78,ORPHAcode: 781 Q fever,ICD-10 A79 Other rickettsioses,380,A79,A75-A79 Rickettsioses,http://identifiers.org/icd/A79,,ICD-10 -A79.0 Other rickettsioses - Trench fever,381,A79.0,A75-A79 Rickettsioses,http://identifiers.org/icd/A79.0,ORPHAcode: 64694 Trench fever -A79.1 Other rickettsioses - Rickettsialpox due to Rickettsia akari,382,A79.1,A75-A79 Rickettsioses,http://identifiers.org/icd/A79.1,ORPHAcode: 83312 Rickettsialpox -A79.8 Other specified rickettsioses,383,A79.8,A75-A79 Rickettsioses,http://identifiers.org/icd/A79.8,ORPHAcode: 83316 Pseudotyphus of California +A79.0 Other rickettsioses - Trench fever,381,A79.0,A75-A79 Rickettsioses,http://identifiers.org/icd/A79.0,ORPHAcode: 64694 Trench fever,ICD-10 +A79.1 Other rickettsioses - Rickettsialpox due to Rickettsia akari,382,A79.1,A75-A79 Rickettsioses,http://identifiers.org/icd/A79.1,ORPHAcode: 83312 Rickettsialpox,ICD-10 +A79.8 Other specified rickettsioses,383,A79.8,A75-A79 Rickettsioses,http://identifiers.org/icd/A79.8,ORPHAcode: 83316 Pseudotyphus of California,ICD-10 "A79.9 Other rickettsioses - Rickettsiosis, unspecified",384,A79.9,A75-A79 Rickettsioses,http://identifiers.org/icd/A79.9,,ICD-10 A80-A89 Viral infections of the central nervous system,385,,I Certain infectious and parasitic diseases,,,ICD-10 A80 Acute poliomyelitis,386,A80,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A80,,ICD-10 @@ -389,30 +389,30 @@ A80 Acute poliomyelitis,386,A80,A80-A89 Viral infections of the central nervous "A80.1 Acute paralytic poliomyelitis, wild virus, imported",388,A80.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A80.1,,ICD-10 "A80.2 Acute paralytic poliomyelitis, wild virus, indigenous",389,A80.2,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A80.2,,ICD-10 "A80.3 Acute paralytic poliomyelitis, other and unspecified",390,A80.3,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A80.3,,ICD-10 -A80.4 Acute nonparalytic poliomyelitis,391,A80.4,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A80.4,ORPHAcode: 2912 Poliomyelitis +A80.4 Acute nonparalytic poliomyelitis,391,A80.4,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A80.4,ORPHAcode: 2912 Poliomyelitis,ICD-10 "A80.9 Acute poliomyelitis, unspecified",392,A80.9,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A80.9,,ICD-10 A81 Atypical virus infections of central nervous system,393,A81,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81,,ICD-10 -A81.0 Atypical virus infections of central nervous system - Creutzfeldt-Jakob disease,394,A81.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.0,ORPHAcode: 204 Sporadic Creutzfeldt-Jakob disease -A81.1 Atypical virus infections of central nervous system - Subacute sclerosing panencephalitis,395,A81.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.1,ORPHAcode: 2806 Subacute sclerosing leukoencephalitis -A81.2 Atypical virus infections of central nervous system - Progressive multifocal leukoencephalopathy,396,A81.2,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.2,ORPHAcode: 217260 Progressive multifocal leukoencephalopathy -A81.8 Other atypical virus infections of central nervous system,397,A81.8,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.8,ORPHAcode: 356 Gerstmann-Straussler-Scheinker syndrome -"A81.9 Atypical virus infection of central nervous system, unspecified",398,A81.9,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.9,ORPHAcode: 586130 Sporadic fatal insomnia +A81.0 Atypical virus infections of central nervous system - Creutzfeldt-Jakob disease,394,A81.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.0,ORPHAcode: 204 Sporadic Creutzfeldt-Jakob disease,ICD-10 +A81.1 Atypical virus infections of central nervous system - Subacute sclerosing panencephalitis,395,A81.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.1,ORPHAcode: 2806 Subacute sclerosing leukoencephalitis,ICD-10 +A81.2 Atypical virus infections of central nervous system - Progressive multifocal leukoencephalopathy,396,A81.2,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.2,ORPHAcode: 217260 Progressive multifocal leukoencephalopathy,ICD-10 +A81.8 Other atypical virus infections of central nervous system,397,A81.8,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.8,ORPHAcode: 356 Gerstmann-Straussler-Scheinker syndrome,ICD-10 +"A81.9 Atypical virus infection of central nervous system, unspecified",398,A81.9,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A81.9,ORPHAcode: 586130 Sporadic fatal insomnia,ICD-10 A82 Rabies,399,A82,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A82,,ICD-10 -A82.0 Sylvatic rabies,400,A82.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A82.0,ORPHAcode: 770 Rabies +A82.0 Sylvatic rabies,400,A82.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A82.0,ORPHAcode: 770 Rabies,ICD-10 A82.1 Urban rabies,401,A82.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A82.1,,ICD-10 "A82.9 Rabies, unspecified",402,A82.9,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A82.9,,ICD-10 A83 Mosquito-borne viral encephalitis,403,A83,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83,,ICD-10 -A83.0 Japanese encephalitis,404,A83.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.0,ORPHAcode: 79139 Japanese encephalitis -A83.1 Western equine encephalitis,405,A83.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.1,ORPHAcode: 83593 Western equine encephalitis -A83.2 Eastern equine encephalitis,406,A83.2,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.2,ORPHAcode: 83594 Eastern equine encephalitis -A83.3 St Louis encephalitis,407,A83.3,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.3,ORPHAcode: 83484 St. Louis encephalitis +A83.0 Japanese encephalitis,404,A83.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.0,ORPHAcode: 79139 Japanese encephalitis,ICD-10 +A83.1 Western equine encephalitis,405,A83.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.1,ORPHAcode: 83593 Western equine encephalitis,ICD-10 +A83.2 Eastern equine encephalitis,406,A83.2,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.2,ORPHAcode: 83594 Eastern equine encephalitis,ICD-10 +A83.3 St Louis encephalitis,407,A83.3,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.3,ORPHAcode: 83484 St. Louis encephalitis,ICD-10 A83.4 Australian encephalitis,408,A83.4,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.4,,ICD-10 -A83.5 California encephalitis,409,A83.5,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.5,ORPHAcode: 83483 La Crosse encephalitis +A83.5 California encephalitis,409,A83.5,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.5,ORPHAcode: 83483 La Crosse encephalitis,ICD-10 A83.6 Mosquito-borne viral encephalitis - Rocio virus disease,410,A83.6,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.6,,ICD-10 A83.8 Other mosquito-borne viral encephalitis,411,A83.8,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.8,,ICD-10 "A83.9 Mosquito-borne viral encephalitis, unspecified",412,A83.9,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A83.9,,ICD-10 A84 Tick-borne viral encephalitis,413,A84,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A84,,ICD-10 -A84.0 Far Eastern tick-borne encephalitis [Russian spring-summer encephalitis],414,A84.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A84.0,ORPHAcode: 297 Tick-borne encephalitis +A84.0 Far Eastern tick-borne encephalitis [Russian spring-summer encephalitis],414,A84.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A84.0,ORPHAcode: 297 Tick-borne encephalitis,ICD-10 A84.1 Central European tick-borne encephalitis,415,A84.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A84.1,,ICD-10 A84.8 Other tick-borne viral encephalitis,416,A84.8,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A84.8,,ICD-10 "A84.9 Tick-borne viral encephalitis, unspecified",417,A84.9,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A84.9,,ICD-10 @@ -420,7 +420,7 @@ A84.8 Other tick-borne viral encephalitis,416,A84.8,A80-A89 Viral infections of A85.0 Enteroviral encephalitis,419,A85.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A85.0,,ICD-10 A85.1 Adenoviral encephalitis,420,A85.1,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A85.1,,ICD-10 "A85.2 Arthropod-borne viral encephalitis, unspecified",421,A85.2,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A85.2,,ICD-10 -A85.8 Other specified viral encephalitis,422,A85.8,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A85.8,ORPHAcode: 83600 Encephalitis lethargica +A85.8 Other specified viral encephalitis,422,A85.8,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A85.8,ORPHAcode: 83600 Encephalitis lethargica,ICD-10 A86 Unspecified viral encephalitis,423,A86,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A86,,ICD-10 A87 Viral meningitis,424,A87,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A87,,ICD-10 A87.0 Enteroviral meningitis,425,A87.0,A80-A89 Viral infections of the central nervous system,http://identifiers.org/icd/A87.0,,ICD-10 @@ -436,43 +436,43 @@ A89 Unspecified viral infection of central nervous system,434,A89,A80-A89 Viral A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,435,,I Certain infectious and parasitic diseases,,,ICD-10 A92 Other mosquito-borne viral fevers,436,A92,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92,,ICD-10 B21.0 HIV disease resulting in Kaposi sarcoma,437,B21.0,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B21.0,,ICD-10 -A92.0 Other mosquito-borne viral fevers - Chikungunya virus disease,438,A92.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.0,ORPHAcode: 324625 Chikungunya +A92.0 Other mosquito-borne viral fevers - Chikungunya virus disease,438,A92.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.0,ORPHAcode: 324625 Chikungunya,ICD-10 A92.1 Other mosquito-borne viral fevers - O'nyong-nyong fever,439,A92.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.1,,ICD-10 A92.2 Other mosquito-borne viral fevers - Venezuelan equine fever,440,A92.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.2,,ICD-10 -A92.3 Other mosquito-borne viral fevers - West Nile virus infection,441,A92.3,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.3,ORPHAcode: 83476 West-Nile encephalitis -A92.4 Other mosquito-borne viral fevers - Rift Valley fever,442,A92.4,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.4,ORPHAcode: 319251 Rift valley fever +A92.3 Other mosquito-borne viral fevers - West Nile virus infection,441,A92.3,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.3,ORPHAcode: 83476 West-Nile encephalitis,ICD-10 +A92.4 Other mosquito-borne viral fevers - Rift Valley fever,442,A92.4,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.4,ORPHAcode: 319251 Rift valley fever,ICD-10 A92.8 Other specified mosquito-borne viral fevers,443,A92.8,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.8,,ICD-10 "A92.9 Mosquito-borne viral fever, unspecified",444,A92.9,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A92.9,,ICD-10 "A93 Other arthropod-borne viral fevers, not elsewhere classified",445,A93,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A93,,ICD-10 "A93.0 Other arthropod-borne viral fevers, not elsewhere classified - Oropouche virus disease",446,A93.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A93.0,,ICD-10 "A93.1 Other arthropod-borne viral fevers, not elsewhere classified - Sandfly fever",447,A93.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A93.1,,ICD-10 -"A93.2 Other arthropod-borne viral fevers, not elsewhere classified - Colorado tick fever",448,A93.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A93.2,ORPHAcode: 83595 Colorado tick fever +"A93.2 Other arthropod-borne viral fevers, not elsewhere classified - Colorado tick fever",448,A93.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A93.2,ORPHAcode: 83595 Colorado tick fever,ICD-10 A93.8 Other specified arthropod-borne viral fevers,449,A93.8,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A93.8,,ICD-10 A94 Unspecified arthropod-borne viral fever,450,A94,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A94,,ICD-10 A95 Yellow fever,451,A95,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A95,,ICD-10 -A95.0 Sylvatic yellow fever,452,A95.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A95.0,ORPHAcode: 99829 Yellow fever +A95.0 Sylvatic yellow fever,452,A95.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A95.0,ORPHAcode: 99829 Yellow fever,ICD-10 A95.1 Urban yellow fever,453,A95.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A95.1,,ICD-10 "A95.9 Yellow fever, unspecified",454,A95.9,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A95.9,,ICD-10 A96 Arenaviral haemorrhagic fever,455,A96,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96,,ICD-10 -A96.0 Junin haemorrhagic fever,456,A96.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.0,ORPHAcode: 319223 Argentine hemorrhagic fever -A96.1 Machupo haemorrhagic fever,457,A96.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.1,ORPHAcode: 319229 Bolivian hemorrhagic fever -A96.2 Lassa fever,458,A96.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.2,ORPHAcode: 99824 Lassa fever -A96.8 Other arenaviral haemorrhagic fevers,459,A96.8,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.8,ORPHAcode: 319213 Lujo hemorrhagic fever +A96.0 Junin haemorrhagic fever,456,A96.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.0,ORPHAcode: 319223 Argentine hemorrhagic fever,ICD-10 +A96.1 Machupo haemorrhagic fever,457,A96.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.1,ORPHAcode: 319229 Bolivian hemorrhagic fever,ICD-10 +A96.2 Lassa fever,458,A96.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.2,ORPHAcode: 99824 Lassa fever,ICD-10 +A96.8 Other arenaviral haemorrhagic fevers,459,A96.8,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.8,ORPHAcode: 319213 Lujo hemorrhagic fever,ICD-10 "A96.9 Arenaviral haemorrhagic fever, unspecified",460,A96.9,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A96.9,,ICD-10 A97 Dengue,461,A97,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A97,,ICD-10 A97.0 Dengue without warning signs,462,A97.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A97.0,,ICD-10 A97.1 Dengue with warning signs,463,A97.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A97.1,,ICD-10 -A97.2 Severe Dengue,464,A97.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A97.2,ORPHAcode: 99828 Dengue fever +A97.2 Severe Dengue,464,A97.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A97.2,ORPHAcode: 99828 Dengue fever,ICD-10 "A97.9 Dengue, unspecified",465,A97.9,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A97.9,,ICD-10 "A98 Other viral haemorrhagic fevers, not elsewhere classified",466,A98,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98,,ICD-10 -A98.0 Crimean-Congo haemorrhagic fever,467,A98.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.0,ORPHAcode: 99827 Crimean-Congo hemorrhagic fever -A98.1 Omsk haemorrhagic fever,468,A98.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.1,ORPHAcode: 319266 Omsk hemorrhagic fever -"A98.2 Other viral haemorrhagic fevers, not elsewhere classified - Kyasanur Forest disease",469,A98.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.2,ORPHAcode: 319254 Kyasanur forest disease +A98.0 Crimean-Congo haemorrhagic fever,467,A98.0,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.0,ORPHAcode: 99827 Crimean-Congo hemorrhagic fever,ICD-10 +A98.1 Omsk haemorrhagic fever,468,A98.1,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.1,ORPHAcode: 319266 Omsk hemorrhagic fever,ICD-10 +"A98.2 Other viral haemorrhagic fevers, not elsewhere classified - Kyasanur Forest disease",469,A98.2,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.2,ORPHAcode: 319254 Kyasanur forest disease,ICD-10 B01.0 Varicella meningitis,470,B01.0,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B01.0,,ICD-10 -"A98.3 Other viral haemorrhagic fevers, not elsewhere classified - Marburg virus disease",471,A98.3,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.3,ORPHAcode: 99826 Marburg hemorrhagic fever -"A98.4 Other viral haemorrhagic fevers, not elsewhere classified - Ebola virus disease",472,A98.4,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.4,ORPHAcode: 319218 Ebola hemorrhagic fever +"A98.3 Other viral haemorrhagic fevers, not elsewhere classified - Marburg virus disease",471,A98.3,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.3,ORPHAcode: 99826 Marburg hemorrhagic fever,ICD-10 +"A98.4 Other viral haemorrhagic fevers, not elsewhere classified - Ebola virus disease",472,A98.4,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.4,ORPHAcode: 319218 Ebola hemorrhagic fever,ICD-10 A98.5 Haemorrhagic fever with renal syndrome,473,A98.5,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.5,,ICD-10 -A98.8 Other specified viral haemorrhagic fevers,474,A98.8,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.8,ORPHAcode: 99825 Nipah virus disease +A98.8 Other specified viral haemorrhagic fevers,474,A98.8,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A98.8,ORPHAcode: 99825 Nipah virus disease,ICD-10 A99 Unspecified viral haemorrhagic fever,475,A99,A92-A99 Arthropod-borne viral fevers and viral haemorrhagic fevers,http://identifiers.org/icd/A99,,ICD-10 B00-B09 Viral infections characterized by skin and mucous membrane lesions,476,,I Certain infectious and parasitic diseases,,,ICD-10 B00 Herpesviral [herpes simplex] infections,477,B00,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B00,,ICD-10 @@ -512,9 +512,9 @@ B06 Rubella [German measles],510,B06,B00-B09 Viral infections characterized by s B06.0 Rubella with neurological complications,511,B06.0,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B06.0,,ICD-10 B06.8 Rubella with other complications,512,B06.8,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B06.8,,ICD-10 B06.9 Rubella without complication,513,B06.9,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B06.9,,ICD-10 -B07 Viral warts,514,B07,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B07,ORPHAcode: 302 Epidermodysplasia verruciformis +B07 Viral warts,514,B07,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B07,ORPHAcode: 302 Epidermodysplasia verruciformis,ICD-10 "B08 Other viral infections characterized by skin and mucous membrane lesions, not elsewhere classified",515,B08,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B08,,ICD-10 -B08.0 Other orthopoxvirus infections,516,B08.0,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B08.0,ORPHAcode: 438279 Human infection by orthopoxvirus +B08.0 Other orthopoxvirus infections,516,B08.0,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B08.0,ORPHAcode: 438279 Human infection by orthopoxvirus,ICD-10 "B08.1 Other viral infections characterized by skin and mucous membrane lesions, not elsewhere classified - Molluscum contagiosum",517,B08.1,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B08.1,,ICD-10 "B08.2 Other viral infections characterized by skin and mucous membrane lesions, not elsewhere classified - Exanthema subitum [sixth disease]",518,B08.2,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B08.2,,ICD-10 "B08.3 Other viral infections characterized by skin and mucous membrane lesions, not elsewhere classified - Erythema infectiosum [fifth disease]",519,B08.3,B00-B09 Viral infections characterized by skin and mucous membrane lesions,http://identifiers.org/icd/B08.3,,ICD-10 @@ -533,14 +533,14 @@ B16.1 Acute hepatitis B with delta-agent (coinfection) without hepatic coma,531, B16.2 Acute hepatitis B without delta-agent with hepatic coma,532,B16.2,B15-B19 Viral hepatitis,http://identifiers.org/icd/B16.2,,ICD-10 B16.9 Acute hepatitis B without delta-agent and without hepatic coma,533,B16.9,B15-B19 Viral hepatitis,http://identifiers.org/icd/B16.9,,ICD-10 B17 Other acute viral hepatitis,534,B17,B15-B19 Viral hepatitis,http://identifiers.org/icd/B17,,ICD-10 -B17.0 Acute delta-(super)infection of hepatitis B carrier,535,B17.0,B15-B19 Viral hepatitis,http://identifiers.org/icd/B17.0,ORPHAcode: 402823 Hepatitis delta +B17.0 Acute delta-(super)infection of hepatitis B carrier,535,B17.0,B15-B19 Viral hepatitis,http://identifiers.org/icd/B17.0,ORPHAcode: 402823 Hepatitis delta,ICD-10 B17.1 Acute hepatitis C,536,B17.1,B15-B19 Viral hepatitis,http://identifiers.org/icd/B17.1,,ICD-10 B17.2 Acute hepatitis E,537,B17.2,B15-B19 Viral hepatitis,http://identifiers.org/icd/B17.2,,ICD-10 B17.8 Other specified acute viral hepatitis,538,B17.8,B15-B19 Viral hepatitis,http://identifiers.org/icd/B17.8,,ICD-10 "B17.9 Acute viral hepatitis, unspecified",539,B17.9,B15-B19 Viral hepatitis,http://identifiers.org/icd/B17.9,,ICD-10 B18 Chronic viral hepatitis,540,B18,B15-B19 Viral hepatitis,http://identifiers.org/icd/B18,,ICD-10 -B18.0 Chronic viral hepatitis B with delta-agent,541,B18.0,B15-B19 Viral hepatitis,http://identifiers.org/icd/B18.0,ORPHAcode: 90073 Hepatitis B reinfection following liver transplantation -B18.2 Chronic viral hepatitis C,542,B18.2,B15-B19 Viral hepatitis,http://identifiers.org/icd/B18.2,ORPHAcode: 90052 Recurrent hepatitis C virus induced liver disease in liver transplant recipients +B18.0 Chronic viral hepatitis B with delta-agent,541,B18.0,B15-B19 Viral hepatitis,http://identifiers.org/icd/B18.0,ORPHAcode: 90073 Hepatitis B reinfection following liver transplantation,ICD-10 +B18.2 Chronic viral hepatitis C,542,B18.2,B15-B19 Viral hepatitis,http://identifiers.org/icd/B18.2,ORPHAcode: 90052 Recurrent hepatitis C virus induced liver disease in liver transplant recipients,ICD-10 B18.8 Other chronic viral hepatitis,543,B18.8,B15-B19 Viral hepatitis,http://identifiers.org/icd/B18.8,,ICD-10 "B18.9 Chronic viral hepatitis, unspecified",544,B18.9,B15-B19 Viral hepatitis,http://identifiers.org/icd/B18.9,,ICD-10 B19 Unspecified viral hepatitis,545,B19,B15-B19 Viral hepatitis,http://identifiers.org/icd/B19,,ICD-10 @@ -563,12 +563,12 @@ B21.1 HIV disease resulting in Burkitt lymphoma,561,B21.1,B20-B24 Human immunode B21.2 HIV disease resulting in other types of non-Hodgkin lymphoma,562,B21.2,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B21.2,,ICD-10 "B21.3 HIV disease resulting in other malignant neoplasms of lymphoid, haematopoietic and related tissue",563,B21.3,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B21.3,,ICD-10 B21.7 HIV disease resulting in multiple malignant neoplasms,564,B21.7,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B21.7,,ICD-10 -B21.8 HIV disease resulting in other malignant neoplasms,565,B21.8,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B21.8,ORPHAcode: 443291 HIV-associated cancer +B21.8 HIV disease resulting in other malignant neoplasms,565,B21.8,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B21.8,ORPHAcode: 443291 HIV-associated cancer,ICD-10 B21.9 HIV disease resulting in unspecified malignant neoplasm,566,B21.9,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B21.9,,ICD-10 B22 Human immunodeficiency virus [HIV] disease resulting in other specified diseases,567,B22,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B22,,ICD-10 B22.0 HIV disease resulting in encephalopathy,568,B22.0,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B22.0,,ICD-10 B22.1 HIV disease resulting in lymphoid interstitial pneumonitis,569,B22.1,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B22.1,,ICD-10 -B22.2 HIV disease resulting in wasting syndrome,570,B22.2,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B22.2,ORPHAcode: 90081 AIDS wasting syndrome +B22.2 HIV disease resulting in wasting syndrome,570,B22.2,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B22.2,ORPHAcode: 90081 AIDS wasting syndrome,ICD-10 B22.7 HIV disease resulting in multiple diseases classified elsewhere,571,B22.7,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B22.7,,ICD-10 B23 Human immunodeficiency virus [HIV] disease resulting in other conditions,572,B23,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B23,,ICD-10 B23.0 Acute HIV infection syndrome,573,B23.0,B20-B24 Human immunodeficiency virus [HIV] disease,http://identifiers.org/icd/B23.0,,ICD-10 @@ -581,7 +581,7 @@ B25 Cytomegaloviral disease,579,B25,B25-B34 Other viral diseases,http://identifi B25.0 Cytomegaloviral pneumonitis,580,B25.0,B25-B34 Other viral diseases,http://identifiers.org/icd/B25.0,,ICD-10 B25.1 Cytomegaloviral hepatitis,581,B25.1,B25-B34 Other viral diseases,http://identifiers.org/icd/B25.1,,ICD-10 B25.2 Cytomegaloviral pancreatitis,582,B25.2,B25-B34 Other viral diseases,http://identifiers.org/icd/B25.2,,ICD-10 -B25.8 Other cytomegaloviral diseases,583,B25.8,B25-B34 Other viral diseases,http://identifiers.org/icd/B25.8,ORPHAcode: 35062 Idiopathic disseminated cytomegalovirus infection +B25.8 Other cytomegaloviral diseases,583,B25.8,B25-B34 Other viral diseases,http://identifiers.org/icd/B25.8,ORPHAcode: 35062 Idiopathic disseminated cytomegalovirus infection,ICD-10 "B25.9 Cytomegaloviral disease, unspecified",584,B25.9,B25-B34 Other viral diseases,http://identifiers.org/icd/B25.9,,ICD-10 B26 Mumps,585,B26,B25-B34 Other viral diseases,http://identifiers.org/icd/B26,,ICD-10 B26.0 Mumps orchitis,586,B26.0,B25-B34 Other viral diseases,http://identifiers.org/icd/B26.0,,ICD-10 @@ -591,7 +591,7 @@ B26.3 Mumps pancreatitis,589,B26.3,B25-B34 Other viral diseases,http://identifie B26.8 Mumps with other complications,590,B26.8,B25-B34 Other viral diseases,http://identifiers.org/icd/B26.8,,ICD-10 B26.9 Mumps without complication,591,B26.9,B25-B34 Other viral diseases,http://identifiers.org/icd/B26.9,,ICD-10 B27 Infectious mononucleosis,592,B27,B25-B34 Other viral diseases,http://identifiers.org/icd/B27,,ICD-10 -B27.0 Gammaherpesviral mononucleosis,593,B27.0,B25-B34 Other viral diseases,http://identifiers.org/icd/B27.0,ORPHAcode: 2566 Chronic Epstein-Barr virus infection syndrome +B27.0 Gammaherpesviral mononucleosis,593,B27.0,B25-B34 Other viral diseases,http://identifiers.org/icd/B27.0,ORPHAcode: 2566 Chronic Epstein-Barr virus infection syndrome,ICD-10 B27.1 Cytomegaloviral mononucleosis,594,B27.1,B25-B34 Other viral diseases,http://identifiers.org/icd/B27.1,,ICD-10 B27.8 Other infectious mononucleosis,595,B27.8,B25-B34 Other viral diseases,http://identifiers.org/icd/B27.8,,ICD-10 "B27.9 Infectious mononucleosis, unspecified",596,B27.9,B25-B34 Other viral diseases,http://identifiers.org/icd/B27.9,,ICD-10 @@ -608,9 +608,9 @@ B30.8 Other viral conjunctivitis,602,B30.8,B25-B34 Other viral diseases,http://i B33.2 Viral carditis,607,B33.2,B25-B34 Other viral diseases,http://identifiers.org/icd/B33.2,,ICD-10 "B33.3 Retrovirus infections, not elsewhere classified",608,B33.3,B25-B34 Other viral diseases,http://identifiers.org/icd/B33.3,,ICD-10 "B33.4 Other viral diseases, not elsewhere classified - Hantavirus",609,B33.4,B25-B34 Other viral diseases,http://identifiers.org/icd/B33.4,,ICD-10 -B33.8 Other specified viral diseases,610,B33.8,B25-B34 Other viral diseases,http://identifiers.org/icd/B33.8,ORPHAcode: 324632 Hendra virus infection +B33.8 Other specified viral diseases,610,B33.8,B25-B34 Other viral diseases,http://identifiers.org/icd/B33.8,ORPHAcode: 324632 Hendra virus infection,ICD-10 B34 Viral infection of unspecified site,611,B34,B25-B34 Other viral diseases,http://identifiers.org/icd/B34,,ICD-10 -"B34.0 Adenovirus infection, unspecified site",612,B34.0,B25-B34 Other viral diseases,http://identifiers.org/icd/B34.0,ORPHAcode: 91127 Adenovirus infection in immunocompromised patients +"B34.0 Adenovirus infection, unspecified site",612,B34.0,B25-B34 Other viral diseases,http://identifiers.org/icd/B34.0,ORPHAcode: 91127 Adenovirus infection in immunocompromised patients,ICD-10 "B34.1 Enterovirus infection, unspecified site",613,B34.1,B25-B34 Other viral diseases,http://identifiers.org/icd/B34.1,,ICD-10 "B34.2 Coronavirus infection, unspecified site",614,B34.2,B25-B34 Other viral diseases,http://identifiers.org/icd/B34.2,,ICD-10 "B34.3 Parvovirus infection, unspecified site",615,B34.3,B25-B34 Other viral diseases,http://identifiers.org/icd/B34.3,,ICD-10 @@ -619,14 +619,14 @@ B34.8 Other viral infections of unspecified site,617,B34.8,B25-B34 Other viral d "B34.9 Viral infection, unspecified",618,B34.9,B25-B34 Other viral diseases,http://identifiers.org/icd/B34.9,,ICD-10 B35-B49 Mycoses,619,,I Certain infectious and parasitic diseases,,,ICD-10 B35 Dermatophytosis,620,B35,B35-B49 Mycoses,http://identifiers.org/icd/B35,,ICD-10 -B35.0 Dermatophytosis - Tinea barbae and tinea capitis,621,B35.0,B35-B49 Mycoses,http://identifiers.org/icd/B35.0,ORPHAcode: 499 Kerion celsi +B35.0 Dermatophytosis - Tinea barbae and tinea capitis,621,B35.0,B35-B49 Mycoses,http://identifiers.org/icd/B35.0,ORPHAcode: 499 Kerion celsi,ICD-10 B35.1 Dermatophytosis - Tinea unguium,622,B35.1,B35-B49 Mycoses,http://identifiers.org/icd/B35.1,,ICD-10 B35.2 Dermatophytosis - Tinea manuum,623,B35.2,B35-B49 Mycoses,http://identifiers.org/icd/B35.2,,ICD-10 B35.3 Dermatophytosis - Tinea pedis,624,B35.3,B35-B49 Mycoses,http://identifiers.org/icd/B35.3,,ICD-10 B35.4 Dermatophytosis - Tinea corporis,625,B35.4,B35-B49 Mycoses,http://identifiers.org/icd/B35.4,,ICD-10 B35.5 Dermatophytosis - Tinea imbricata,626,B35.5,B35-B49 Mycoses,http://identifiers.org/icd/B35.5,,ICD-10 B35.6 Dermatophytosis - Tinea inguinalis [Tinea cruris],627,B35.6,B35-B49 Mycoses,http://identifiers.org/icd/B35.6,,ICD-10 -B35.8 Dermatophytosis - Other dermatophytoses,628,B35.8,B35-B49 Mycoses,http://identifiers.org/icd/B35.8,ORPHAcode: 397587 Deep dermatophytosis +B35.8 Dermatophytosis - Other dermatophytoses,628,B35.8,B35-B49 Mycoses,http://identifiers.org/icd/B35.8,ORPHAcode: 397587 Deep dermatophytosis,ICD-10 "B35.9 Dermatophytosis, unspecified",629,B35.9,B35-B49 Mycoses,http://identifiers.org/icd/B35.9,,ICD-10 B36 Other superficial mycoses,630,B36,B35-B49 Mycoses,http://identifiers.org/icd/B36,,ICD-10 B36.0 Other superficial mycoses - Pityriasis versicolor,631,B36.0,B35-B49 Mycoses,http://identifiers.org/icd/B36.0,,ICD-10 @@ -638,7 +638,7 @@ B36.8 Other specified superficial mycoses,635,B36.8,B35-B49 Mycoses,http://ident B37 Candidiasis,637,B37,B35-B49 Mycoses,http://identifiers.org/icd/B37,,ICD-10 B37.0 Candidiasis - Candidal stomatitis,638,B37.0,B35-B49 Mycoses,http://identifiers.org/icd/B37.0,,ICD-10 B37.1 Pulmonary candidiasis,639,B37.1,B35-B49 Mycoses,http://identifiers.org/icd/B37.1,,ICD-10 -B37.2 Candidiasis of skin and nail,640,B37.2,B35-B49 Mycoses,http://identifiers.org/icd/B37.2,ORPHAcode: 1334 Chronic mucocutaneous candidiasis +B37.2 Candidiasis of skin and nail,640,B37.2,B35-B49 Mycoses,http://identifiers.org/icd/B37.2,ORPHAcode: 1334 Chronic mucocutaneous candidiasis,ICD-10 B37.3 Candidiasis of vulva and vagina,641,B37.3,B35-B49 Mycoses,http://identifiers.org/icd/B37.3,,ICD-10 B37.4 Candidiasis of other urogenital sites,642,B37.4,B35-B49 Mycoses,http://identifiers.org/icd/B37.4,,ICD-10 B37.5 Candidiasis - Candidal meningitis,643,B37.5,B35-B49 Mycoses,http://identifiers.org/icd/B37.5,,ICD-10 @@ -647,7 +647,7 @@ B37.7 Candidiasis - Candidal sepsis,645,B37.7,B35-B49 Mycoses,http://identifiers B37.8 Candidiasis of other sites,646,B37.8,B35-B49 Mycoses,http://identifiers.org/icd/B37.8,,ICD-10 "B37.9 Candidiasis, unspecified",647,B37.9,B35-B49 Mycoses,http://identifiers.org/icd/B37.9,,ICD-10 B38 Coccidioidomycosis,648,B38,B35-B49 Mycoses,http://identifiers.org/icd/B38,,ICD-10 -B38.0 Acute pulmonary coccidioidomycosis,649,B38.0,B35-B49 Mycoses,http://identifiers.org/icd/B38.0,ORPHAcode: 228123 Coccidioidomycosis +B38.0 Acute pulmonary coccidioidomycosis,649,B38.0,B35-B49 Mycoses,http://identifiers.org/icd/B38.0,ORPHAcode: 228123 Coccidioidomycosis,ICD-10 B38.1 Chronic pulmonary coccidioidomycosis,650,B38.1,B35-B49 Mycoses,http://identifiers.org/icd/B38.1,,ICD-10 "B38.2 Pulmonary coccidioidomycosis, unspecified",651,B38.2,B35-B49 Mycoses,http://identifiers.org/icd/B38.2,,ICD-10 B38.3 Cutaneous coccidioidomycosis,652,B38.3,B35-B49 Mycoses,http://identifiers.org/icd/B38.3,,ICD-10 @@ -656,7 +656,7 @@ B38.7 Disseminated coccidioidomycosis,654,B38.7,B35-B49 Mycoses,http://identifie B38.8 Other forms of coccidioidomycosis,655,B38.8,B35-B49 Mycoses,http://identifiers.org/icd/B38.8,,ICD-10 "B38.9 Coccidioidomycosis, unspecified",656,B38.9,B35-B49 Mycoses,http://identifiers.org/icd/B38.9,,ICD-10 B39 Histoplasmosis,657,B39,B35-B49 Mycoses,http://identifiers.org/icd/B39,,ICD-10 -B39.0 Acute pulmonary histoplasmosis capsulati,658,B39.0,B35-B49 Mycoses,http://identifiers.org/icd/B39.0,ORPHAcode: 390 Histoplasmosis +B39.0 Acute pulmonary histoplasmosis capsulati,658,B39.0,B35-B49 Mycoses,http://identifiers.org/icd/B39.0,ORPHAcode: 390 Histoplasmosis,ICD-10 B39.1 Chronic pulmonary histoplasmosis capsulati,659,B39.1,B35-B49 Mycoses,http://identifiers.org/icd/B39.1,,ICD-10 "B39.2 Pulmonary histoplasmosis capsulati, unspecified",660,B39.2,B35-B49 Mycoses,http://identifiers.org/icd/B39.2,,ICD-10 B39.3 Disseminated histoplasmosis capsulati,661,B39.3,B35-B49 Mycoses,http://identifiers.org/icd/B39.3,,ICD-10 @@ -675,22 +675,22 @@ B40.8 Other forms of blastomycosis,672,B40.8,B35-B49 Mycoses,http://identifiers. B41 Paracoccidioidomycosis,674,B41,B35-B49 Mycoses,http://identifiers.org/icd/B41,,ICD-10 B41.0 Pulmonary paracoccidioidomycosis,675,B41.0,B35-B49 Mycoses,http://identifiers.org/icd/B41.0,,ICD-10 B41.7 Disseminated paracoccidioidomycosis,676,B41.7,B35-B49 Mycoses,http://identifiers.org/icd/B41.7,,ICD-10 -B41.8 Other forms of paracoccidioidomycosis,677,B41.8,B35-B49 Mycoses,http://identifiers.org/icd/B41.8,ORPHAcode: 73260 Paracoccidioidomycosis +B41.8 Other forms of paracoccidioidomycosis,677,B41.8,B35-B49 Mycoses,http://identifiers.org/icd/B41.8,ORPHAcode: 73260 Paracoccidioidomycosis,ICD-10 "B41.9 Paracoccidioidomycosis, unspecified",678,B41.9,B35-B49 Mycoses,http://identifiers.org/icd/B41.9,,ICD-10 B42 Sporotrichosis,679,B42,B35-B49 Mycoses,http://identifiers.org/icd/B42,,ICD-10 -B42.0 Pulmonary sporotrichosis,680,B42.0,B35-B49 Mycoses,http://identifiers.org/icd/B42.0,ORPHAcode: 826 Sporotrichosis +B42.0 Pulmonary sporotrichosis,680,B42.0,B35-B49 Mycoses,http://identifiers.org/icd/B42.0,ORPHAcode: 826 Sporotrichosis,ICD-10 B42.1 Lymphocutaneous sporotrichosis,681,B42.1,B35-B49 Mycoses,http://identifiers.org/icd/B42.1,,ICD-10 B42.7 Disseminated sporotrichosis,682,B42.7,B35-B49 Mycoses,http://identifiers.org/icd/B42.7,,ICD-10 B42.8 Other forms of sporotrichosis,683,B42.8,B35-B49 Mycoses,http://identifiers.org/icd/B42.8,,ICD-10 "B42.9 Sporotrichosis, unspecified",684,B42.9,B35-B49 Mycoses,http://identifiers.org/icd/B42.9,,ICD-10 B43 Chromomycosis and phaeomycotic abscess,685,B43,B35-B49 Mycoses,http://identifiers.org/icd/B43,,ICD-10 B43.0 Cutaneous chromomycosis,686,B43.0,B35-B49 Mycoses,http://identifiers.org/icd/B43.0,,ICD-10 -B43.1 Phaeomycotic brain abscess,687,B43.1,B35-B49 Mycoses,http://identifiers.org/icd/B43.1,ORPHAcode: 182 Chromomycosis +B43.1 Phaeomycotic brain abscess,687,B43.1,B35-B49 Mycoses,http://identifiers.org/icd/B43.1,ORPHAcode: 182 Chromomycosis,ICD-10 B43.2 Subcutaneous phaeomycotic abscess and cyst,688,B43.2,B35-B49 Mycoses,http://identifiers.org/icd/B43.2,,ICD-10 B43.8 Other forms of chromomycosis,689,B43.8,B35-B49 Mycoses,http://identifiers.org/icd/B43.8,,ICD-10 "B43.9 Chromomycosis, unspecified",690,B43.9,B35-B49 Mycoses,http://identifiers.org/icd/B43.9,,ICD-10 B44 Aspergillosis,691,B44,B35-B49 Mycoses,http://identifiers.org/icd/B44,,ICD-10 -B44.0 Invasive pulmonary aspergillosis,692,B44.0,B35-B49 Mycoses,http://identifiers.org/icd/B44.0,ORPHAcode: 1163 Aspergillosis +B44.0 Invasive pulmonary aspergillosis,692,B44.0,B35-B49 Mycoses,http://identifiers.org/icd/B44.0,ORPHAcode: 1163 Aspergillosis,ICD-10 B44.1 Other pulmonary aspergillosis,693,B44.1,B35-B49 Mycoses,http://identifiers.org/icd/B44.1,,ICD-10 B44.2 Tonsillar aspergillosis,694,B44.2,B35-B49 Mycoses,http://identifiers.org/icd/B44.2,,ICD-10 B44.7 Disseminated aspergillosis,695,B44.7,B35-B49 Mycoses,http://identifiers.org/icd/B44.7,,ICD-10 @@ -698,14 +698,14 @@ B44.8 Other forms of aspergillosis,696,B44.8,B35-B49 Mycoses,http://identifiers. "B44.9 Aspergillosis, unspecified",697,B44.9,B35-B49 Mycoses,http://identifiers.org/icd/B44.9,,ICD-10 B45 Cryptococcosis,698,B45,B35-B49 Mycoses,http://identifiers.org/icd/B45,,ICD-10 B45.0 Pulmonary cryptococcosis,699,B45.0,B35-B49 Mycoses,http://identifiers.org/icd/B45.0,,ICD-10 -B45.1 Cerebral cryptococcosis,700,B45.1,B35-B49 Mycoses,http://identifiers.org/icd/B45.1,ORPHAcode: 1546 Cryptococcosis +B45.1 Cerebral cryptococcosis,700,B45.1,B35-B49 Mycoses,http://identifiers.org/icd/B45.1,ORPHAcode: 1546 Cryptococcosis,ICD-10 B45.2 Cutaneous cryptococcosis,701,B45.2,B35-B49 Mycoses,http://identifiers.org/icd/B45.2,,ICD-10 B45.3 Osseous cryptococcosis,702,B45.3,B35-B49 Mycoses,http://identifiers.org/icd/B45.3,,ICD-10 B45.7 Disseminated cryptococcosis,703,B45.7,B35-B49 Mycoses,http://identifiers.org/icd/B45.7,,ICD-10 B45.8 Other forms of cryptococcosis,704,B45.8,B35-B49 Mycoses,http://identifiers.org/icd/B45.8,,ICD-10 "B45.9 Cryptococcosis, unspecified",705,B45.9,B35-B49 Mycoses,http://identifiers.org/icd/B45.9,,ICD-10 B46 Zygomycosis,706,B46,B35-B49 Mycoses,http://identifiers.org/icd/B46,,ICD-10 -B46.0 Zygomycosis - Pulmonary mucormycosis,707,B46.0,B35-B49 Mycoses,http://identifiers.org/icd/B46.0,ORPHAcode: 73263 Zygomycosis +B46.0 Zygomycosis - Pulmonary mucormycosis,707,B46.0,B35-B49 Mycoses,http://identifiers.org/icd/B46.0,ORPHAcode: 73263 Zygomycosis,ICD-10 B46.1 Zygomycosis - Rhinocerebral mucormycosis,708,B46.1,B35-B49 Mycoses,http://identifiers.org/icd/B46.1,,ICD-10 B46.2 Zygomycosis - Gastrointestinal mucormycosis,709,B46.2,B35-B49 Mycoses,http://identifiers.org/icd/B46.2,,ICD-10 B46.3 Zygomycosis - Cutaneous mucormycosis,710,B46.3,B35-B49 Mycoses,http://identifiers.org/icd/B46.3,,ICD-10 @@ -714,7 +714,7 @@ B46.4 Zygomycosis - Disseminated mucormycosis,711,B46.4,B35-B49 Mycoses,http://i B46.8 Zygomycosis - Other zygomycoses,713,B46.8,B35-B49 Mycoses,http://identifiers.org/icd/B46.8,,ICD-10 "B46.9 Zygomycosis, unspecified",714,B46.9,B35-B49 Mycoses,http://identifiers.org/icd/B46.9,,ICD-10 B47 Mycetoma,715,B47,B35-B49 Mycoses,http://identifiers.org/icd/B47,,ICD-10 -B47.0 Eumycetoma,716,B47.0,B35-B49 Mycoses,http://identifiers.org/icd/B47.0,ORPHAcode: 2583 Mycetoma +B47.0 Eumycetoma,716,B47.0,B35-B49 Mycoses,http://identifiers.org/icd/B47.0,ORPHAcode: 2583 Mycetoma,ICD-10 B47.1 Actinomycetoma,717,B47.1,B35-B49 Mycoses,http://identifiers.org/icd/B47.1,,ICD-10 "B47.9 Mycetoma, unspecified",718,B47.9,B35-B49 Mycoses,http://identifiers.org/icd/B47.9,,ICD-10 "B48 Other mycoses, not elsewhere classified",719,B48,B35-B49 Mycoses,http://identifiers.org/icd/B48,,ICD-10 @@ -723,7 +723,7 @@ B47.1 Actinomycetoma,717,B47.1,B35-B49 Mycoses,http://identifiers.org/icd/B47.1, "B48.2 Other mycoses, not elsewhere classified - Allescheriasis",722,B48.2,B35-B49 Mycoses,http://identifiers.org/icd/B48.2,,ICD-10 "B48.3 Other mycoses, not elsewhere classified - Geotrichosis",723,B48.3,B35-B49 Mycoses,http://identifiers.org/icd/B48.3,,ICD-10 "B48.4 Other mycoses, not elsewhere classified - Penicillosis",724,B48.4,B35-B49 Mycoses,http://identifiers.org/icd/B48.4,,ICD-10 -B48.7 Opportunistic mycoses,725,B48.7,B35-B49 Mycoses,http://identifiers.org/icd/B48.7,ORPHAcode: 228119 Fusariosis +B48.7 Opportunistic mycoses,725,B48.7,B35-B49 Mycoses,http://identifiers.org/icd/B48.7,ORPHAcode: 228119 Fusariosis,ICD-10 B48.8 Other specified mycoses,726,B48.8,B35-B49 Mycoses,http://identifiers.org/icd/B48.8,,ICD-10 B49 Unspecified mycosis,727,B49,B35-B49 Mycoses,http://identifiers.org/icd/B49,,ICD-10 B50-B64 Protozoal diseases,728,,I Certain infectious and parasitic diseases,,,ICD-10 @@ -743,18 +743,18 @@ B53 Other parasitologically confirmed malaria,741,B53,B50-B64 Protozoal diseases B53.0 Plasmodium ovale malaria,742,B53.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B53.0,,ICD-10 B53.1 Malaria due to simian plasmodia,743,B53.1,B50-B64 Protozoal diseases,http://identifiers.org/icd/B53.1,,ICD-10 "B53.8 Other parasitologically confirmed malaria, not elsewhere classified",744,B53.8,B50-B64 Protozoal diseases,http://identifiers.org/icd/B53.8,,ICD-10 -B54 Unspecified malaria,745,B54,B50-B64 Protozoal diseases,http://identifiers.org/icd/B54,ORPHAcode: 673 Malaria +B54 Unspecified malaria,745,B54,B50-B64 Protozoal diseases,http://identifiers.org/icd/B54,ORPHAcode: 673 Malaria,ICD-10 B55 Leishmaniasis,746,B55,B50-B64 Protozoal diseases,http://identifiers.org/icd/B55,,ICD-10 -B55.0 Visceral leishmaniasis,747,B55.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B55.0,ORPHAcode: 507 Leishmaniasis +B55.0 Visceral leishmaniasis,747,B55.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B55.0,ORPHAcode: 507 Leishmaniasis,ICD-10 B55.1 Cutaneous leishmaniasis,748,B55.1,B50-B64 Protozoal diseases,http://identifiers.org/icd/B55.1,,ICD-10 B55.2 Mucocutaneous leishmaniasis,749,B55.2,B50-B64 Protozoal diseases,http://identifiers.org/icd/B55.2,,ICD-10 "B55.9 Leishmaniasis, unspecified",750,B55.9,B50-B64 Protozoal diseases,http://identifiers.org/icd/B55.9,,ICD-10 B56 African trypanosomiasis,751,B56,B50-B64 Protozoal diseases,http://identifiers.org/icd/B56,,ICD-10 -B56.0 Gambiense trypanosomiasis,752,B56.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B56.0,ORPHAcode: 3385 African trypanosomiasis +B56.0 Gambiense trypanosomiasis,752,B56.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B56.0,ORPHAcode: 3385 African trypanosomiasis,ICD-10 B56.1 Rhodesiense trypanosomiasis,753,B56.1,B50-B64 Protozoal diseases,http://identifiers.org/icd/B56.1,,ICD-10 "B56.9 African trypanosomiasis, unspecified",754,B56.9,B50-B64 Protozoal diseases,http://identifiers.org/icd/B56.9,,ICD-10 B57 Chagas disease,755,B57,B50-B64 Protozoal diseases,http://identifiers.org/icd/B57,,ICD-10 -B57.0 Acute Chagas disease with heart involvement,756,B57.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B57.0,ORPHAcode: 3386 American trypanosomiasis +B57.0 Acute Chagas disease with heart involvement,756,B57.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B57.0,ORPHAcode: 3386 American trypanosomiasis,ICD-10 B57.1 Acute Chagas disease without heart involvement,757,B57.1,B50-B64 Protozoal diseases,http://identifiers.org/icd/B57.1,,ICD-10 B57.2 Chagas disease (chronic) with heart involvement,758,B57.2,B50-B64 Protozoal diseases,http://identifiers.org/icd/B57.2,,ICD-10 B80 Enterobiasis,759,B80,B65-B83 Helminthiases,http://identifiers.org/icd/B80,,ICD-10 @@ -770,22 +770,22 @@ B58.8 Toxoplasmosis with other organ involvement,768,B58.8,B50-B64 Protozoal dis "B58.9 Toxoplasmosis, unspecified",769,B58.9,B50-B64 Protozoal diseases,http://identifiers.org/icd/B58.9,,ICD-10 B59 Pneumocystosis,770,B59,B50-B64 Protozoal diseases,http://identifiers.org/icd/B59,,ICD-10 "B60 Other protozoal diseases, not elsewhere classified",771,B60,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60,,ICD-10 -"B60.0 Other protozoal diseases, not elsewhere classified - Babesiosis",772,B60.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60.0,ORPHAcode: 108 Babesiosis -"B60.1 Other protozoal diseases, not elsewhere classified - Acanthamoebiasis",773,B60.1,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60.1,ORPHAcode: 68 Amoebiasis due to free-living amoebae +"B60.0 Other protozoal diseases, not elsewhere classified - Babesiosis",772,B60.0,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60.0,ORPHAcode: 108 Babesiosis,ICD-10 +"B60.1 Other protozoal diseases, not elsewhere classified - Acanthamoebiasis",773,B60.1,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60.1,ORPHAcode: 68 Amoebiasis due to free-living amoebae,ICD-10 "B60.2 Other protozoal diseases, not elsewhere classified - Naegleriasis",774,B60.2,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60.2,,ICD-10 -B60.8 Other specified protozoal diseases,775,B60.8,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60.8,ORPHAcode: 2552 Microsporidiosis +B60.8 Other specified protozoal diseases,775,B60.8,B50-B64 Protozoal diseases,http://identifiers.org/icd/B60.8,ORPHAcode: 2552 Microsporidiosis,ICD-10 B64 Unspecified protozoal disease,776,B64,B50-B64 Protozoal diseases,http://identifiers.org/icd/B64,,ICD-10 B65-B83 Helminthiases,777,,I Certain infectious and parasitic diseases,,,ICD-10 B65 Schistosomiasis [bilharziasis],778,B65,B65-B83 Helminthiases,http://identifiers.org/icd/B65,,ICD-10 -B65.0 Schistosomiasis due to Schistosoma haematobium [urinary schistosomiasis],779,B65.0,B65-B83 Helminthiases,http://identifiers.org/icd/B65.0,ORPHAcode: 1247 Schistosomiasis -B73 Onchocerciasis,780,B73,B65-B83 Helminthiases,http://identifiers.org/icd/B73,ORPHAcode: 2737 Onchocerciasis +B65.0 Schistosomiasis due to Schistosoma haematobium [urinary schistosomiasis],779,B65.0,B65-B83 Helminthiases,http://identifiers.org/icd/B65.0,ORPHAcode: 1247 Schistosomiasis,ICD-10 +B73 Onchocerciasis,780,B73,B65-B83 Helminthiases,http://identifiers.org/icd/B73,ORPHAcode: 2737 Onchocerciasis,ICD-10 B65.1 Schistosomiasis due to Schistosoma mansoni [intestinal schistosomiasis],781,B65.1,B65-B83 Helminthiases,http://identifiers.org/icd/B65.1,,ICD-10 B65.2 Schistosomiasis due to Schistosoma japonicum,782,B65.2,B65-B83 Helminthiases,http://identifiers.org/icd/B65.2,,ICD-10 B65.3 Schistosomiasis [bilharziasis] - Cercarial dermatitis,783,B65.3,B65-B83 Helminthiases,http://identifiers.org/icd/B65.3,,ICD-10 B65.8 Schistosomiasis [bilharziasis] - Other schistosomiases,784,B65.8,B65-B83 Helminthiases,http://identifiers.org/icd/B65.8,,ICD-10 "B65.9 Schistosomiasis, unspecified",785,B65.9,B65-B83 Helminthiases,http://identifiers.org/icd/B65.9,,ICD-10 B66 Other fluke infections,786,B66,B65-B83 Helminthiases,http://identifiers.org/icd/B66,,ICD-10 -B66.0 Other fluke infections - Opisthorchiasis,787,B66.0,B65-B83 Helminthiases,http://identifiers.org/icd/B66.0,ORPHAcode: 1685 Distomatosis +B66.0 Other fluke infections - Opisthorchiasis,787,B66.0,B65-B83 Helminthiases,http://identifiers.org/icd/B66.0,ORPHAcode: 1685 Distomatosis,ICD-10 B66.1 Other fluke infections - Clonorchiasis,788,B66.1,B65-B83 Helminthiases,http://identifiers.org/icd/B66.1,,ICD-10 B66.2 Other fluke infections - Dicrocoeliasis,789,B66.2,B65-B83 Helminthiases,http://identifiers.org/icd/B66.2,,ICD-10 B66.3 Other fluke infections - Fascioliasis,790,B66.3,B65-B83 Helminthiases,http://identifiers.org/icd/B66.3,,ICD-10 @@ -794,13 +794,13 @@ B66.5 Other fluke infections - Fasciolopsiasis,792,B66.5,B65-B83 Helminthiases,h B66.8 Other specified fluke infections,793,B66.8,B65-B83 Helminthiases,http://identifiers.org/icd/B66.8,,ICD-10 "B66.9 Fluke infection, unspecified",794,B66.9,B65-B83 Helminthiases,http://identifiers.org/icd/B66.9,,ICD-10 B67 Echinococcosis,795,B67,B65-B83 Helminthiases,http://identifiers.org/icd/B67,,ICD-10 -B67.0 Echinococcosis - Echinococcus granulosus infection of liver,796,B67.0,B65-B83 Helminthiases,http://identifiers.org/icd/B67.0,ORPHAcode: 400 Cystic echinococcosis +B67.0 Echinococcosis - Echinococcus granulosus infection of liver,796,B67.0,B65-B83 Helminthiases,http://identifiers.org/icd/B67.0,ORPHAcode: 400 Cystic echinococcosis,ICD-10 B67.1 Echinococcosis - Echinococcus granulosus infection of lung,797,B67.1,B65-B83 Helminthiases,http://identifiers.org/icd/B67.1,,ICD-10 B67.2 Echinococcosis - Echinococcus granulosus infection of bone,798,B67.2,B65-B83 Helminthiases,http://identifiers.org/icd/B67.2,,ICD-10 "B67.3 Echinococcosis - Echinococcus granulosus infection, other and multiple sites",799,B67.3,B65-B83 Helminthiases,http://identifiers.org/icd/B67.3,,ICD-10 "B67.4 Echinococcosis - Echinococcus granulosus infection, unspecified",800,B67.4,B65-B83 Helminthiases,http://identifiers.org/icd/B67.4,,ICD-10 B67.5 Echinococcosis - Echinococcus multilocularis infection of liver,801,B67.5,B65-B83 Helminthiases,http://identifiers.org/icd/B67.5,,ICD-10 -"B67.6 Echinococcosis - Echinococcus multilocularis infection, other and multiple sites",802,B67.6,B65-B83 Helminthiases,http://identifiers.org/icd/B67.6,ORPHAcode: 284 Alveolar echinococcosis +"B67.6 Echinococcosis - Echinococcus multilocularis infection, other and multiple sites",802,B67.6,B65-B83 Helminthiases,http://identifiers.org/icd/B67.6,ORPHAcode: 284 Alveolar echinococcosis,ICD-10 "B67.7 Echinococcosis - Echinococcus multilocularis infection, unspecified",803,B67.7,B65-B83 Helminthiases,http://identifiers.org/icd/B67.7,,ICD-10 "B67.8 Echinococcosis, unspecified, of liver",804,B67.8,B65-B83 Helminthiases,http://identifiers.org/icd/B67.8,,ICD-10 "B67.9 Echinococcosis, other and unspecified",805,B67.9,B65-B83 Helminthiases,http://identifiers.org/icd/B67.9,,ICD-10 @@ -809,53 +809,53 @@ B68.0 Taenia solium taeniasis,807,B68.0,B65-B83 Helminthiases,http://identifiers B68.1 Taenia saginata taeniasis,808,B68.1,B65-B83 Helminthiases,http://identifiers.org/icd/B68.1,,ICD-10 "B68.9 Taeniasis, unspecified",809,B68.9,B65-B83 Helminthiases,http://identifiers.org/icd/B68.9,,ICD-10 B69 Cysticercosis,810,B69,B65-B83 Helminthiases,http://identifiers.org/icd/B69,,ICD-10 -B69.0 Cysticercosis of central nervous system,811,B69.0,B65-B83 Helminthiases,http://identifiers.org/icd/B69.0,ORPHAcode: 1560 Cysticercosis +B69.0 Cysticercosis of central nervous system,811,B69.0,B65-B83 Helminthiases,http://identifiers.org/icd/B69.0,ORPHAcode: 1560 Cysticercosis,ICD-10 B69.1 Cysticercosis of eye,812,B69.1,B65-B83 Helminthiases,http://identifiers.org/icd/B69.1,,ICD-10 B69.8 Cysticercosis of other sites,813,B69.8,B65-B83 Helminthiases,http://identifiers.org/icd/B69.8,,ICD-10 "B69.9 Cysticercosis, unspecified",814,B69.9,B65-B83 Helminthiases,http://identifiers.org/icd/B69.9,,ICD-10 B70 Diphyllobothriasis and sparganosis,815,B70,B65-B83 Helminthiases,http://identifiers.org/icd/B70,,ICD-10 -B70.0 Diphyllobothriasis,816,B70.0,B65-B83 Helminthiases,http://identifiers.org/icd/B70.0,ORPHAcode: 128 Diphyllobothriasis +B70.0 Diphyllobothriasis,816,B70.0,B65-B83 Helminthiases,http://identifiers.org/icd/B70.0,ORPHAcode: 128 Diphyllobothriasis,ICD-10 B70.1 Sparganosis,817,B70.1,B65-B83 Helminthiases,http://identifiers.org/icd/B70.1,,ICD-10 B71 Other cestode infections,818,B71,B65-B83 Helminthiases,http://identifiers.org/icd/B71,,ICD-10 -B71.0 Other cestode infections - Hymenolepiasis,819,B71.0,B65-B83 Helminthiases,http://identifiers.org/icd/B71.0,ORPHAcode: 401 Hymenolepiasis +B71.0 Other cestode infections - Hymenolepiasis,819,B71.0,B65-B83 Helminthiases,http://identifiers.org/icd/B71.0,ORPHAcode: 401 Hymenolepiasis,ICD-10 B71.1 Other cestode infections - Dipylidiasis,820,B71.1,B65-B83 Helminthiases,http://identifiers.org/icd/B71.1,,ICD-10 B71.8 Other specified cestode infections,821,B71.8,B65-B83 Helminthiases,http://identifiers.org/icd/B71.8,,ICD-10 "B71.9 Cestode infection, unspecified",822,B71.9,B65-B83 Helminthiases,http://identifiers.org/icd/B71.9,,ICD-10 -B72 Dracunculiasis,823,B72,B65-B83 Helminthiases,http://identifiers.org/icd/B72,ORPHAcode: 231 Dracunculiasis -B74.0 Filariasis due to Wuchereria bancrofti,824,B74.0,B65-B83 Helminthiases,http://identifiers.org/icd/B74.0,ORPHAcode: 2035 Lymphatic filariasis +B72 Dracunculiasis,823,B72,B65-B83 Helminthiases,http://identifiers.org/icd/B72,ORPHAcode: 231 Dracunculiasis,ICD-10 +B74.0 Filariasis due to Wuchereria bancrofti,824,B74.0,B65-B83 Helminthiases,http://identifiers.org/icd/B74.0,ORPHAcode: 2035 Lymphatic filariasis,ICD-10 B74.1 Filariasis due to Brugia malayi,825,B74.1,B65-B83 Helminthiases,http://identifiers.org/icd/B74.1,,ICD-10 B74.2 Filariasis due to Brugia timori,826,B74.2,B65-B83 Helminthiases,http://identifiers.org/icd/B74.2,,ICD-10 -B74.3 Filariasis - Loiasis,827,B74.3,B65-B83 Helminthiases,http://identifiers.org/icd/B74.3,ORPHAcode: 2404 Loiasis -B74.4 Filariasis - Mansonelliasis,828,B74.4,B65-B83 Helminthiases,http://identifiers.org/icd/B74.4,ORPHAcode: 2459 Mansonelliasis -B74.8 Filariasis - Other filariases,829,B74.8,B65-B83 Helminthiases,http://identifiers.org/icd/B74.8,ORPHAcode: 166291 Dirofilariasis +B74.3 Filariasis - Loiasis,827,B74.3,B65-B83 Helminthiases,http://identifiers.org/icd/B74.3,ORPHAcode: 2404 Loiasis,ICD-10 +B74.4 Filariasis - Mansonelliasis,828,B74.4,B65-B83 Helminthiases,http://identifiers.org/icd/B74.4,ORPHAcode: 2459 Mansonelliasis,ICD-10 +B74.8 Filariasis - Other filariases,829,B74.8,B65-B83 Helminthiases,http://identifiers.org/icd/B74.8,ORPHAcode: 166291 Dirofilariasis,ICD-10 "B74.9 Filariasis, unspecified",830,B74.9,B65-B83 Helminthiases,http://identifiers.org/icd/B74.9,,ICD-10 -B75 Trichinellosis,831,B75,B65-B83 Helminthiases,http://identifiers.org/icd/B75,ORPHAcode: 863 Trichinellosis +B75 Trichinellosis,831,B75,B65-B83 Helminthiases,http://identifiers.org/icd/B75,ORPHAcode: 863 Trichinellosis,ICD-10 B76 Hookworm diseases,832,B76,B65-B83 Helminthiases,http://identifiers.org/icd/B76,,ICD-10 B76.0 Hookworm diseases - Ancylostomiasis,833,B76.0,B65-B83 Helminthiases,http://identifiers.org/icd/B76.0,,ICD-10 -B76.1 Hookworm diseases - Necatoriasis,834,B76.1,B65-B83 Helminthiases,http://identifiers.org/icd/B76.1,ORPHAcode: 78 Ankylostomiasis +B76.1 Hookworm diseases - Necatoriasis,834,B76.1,B65-B83 Helminthiases,http://identifiers.org/icd/B76.1,ORPHAcode: 78 Ankylostomiasis,ICD-10 B76.8 Other hookworm diseases,835,B76.8,B65-B83 Helminthiases,http://identifiers.org/icd/B76.8,,ICD-10 -"B76.9 Hookworm disease, unspecified",836,B76.9,B65-B83 Helminthiases,http://identifiers.org/icd/B76.9,ORPHAcode: 423717 Cutaneous larva migrans +"B76.9 Hookworm disease, unspecified",836,B76.9,B65-B83 Helminthiases,http://identifiers.org/icd/B76.9,ORPHAcode: 423717 Cutaneous larva migrans,ICD-10 B77 Ascariasis,837,B77,B65-B83 Helminthiases,http://identifiers.org/icd/B77,,ICD-10 B77.0 Ascariasis with intestinal complications,838,B77.0,B65-B83 Helminthiases,http://identifiers.org/icd/B77.0,,ICD-10 B77.8 Ascariasis with other complications,839,B77.8,B65-B83 Helminthiases,http://identifiers.org/icd/B77.8,,ICD-10 "B77.9 Ascariasis, unspecified",840,B77.9,B65-B83 Helminthiases,http://identifiers.org/icd/B77.9,,ICD-10 B78 Strongyloidiasis,841,B78,B65-B83 Helminthiases,http://identifiers.org/icd/B78,,ICD-10 -B78.0 Intestinal strongyloidiasis,842,B78.0,B65-B83 Helminthiases,http://identifiers.org/icd/B78.0,ORPHAcode: 76 Strongyloidiasis +B78.0 Intestinal strongyloidiasis,842,B78.0,B65-B83 Helminthiases,http://identifiers.org/icd/B78.0,ORPHAcode: 76 Strongyloidiasis,ICD-10 B78.1 Cutaneous strongyloidiasis,843,B78.1,B65-B83 Helminthiases,http://identifiers.org/icd/B78.1,,ICD-10 B78.7 Disseminated strongyloidiasis,844,B78.7,B65-B83 Helminthiases,http://identifiers.org/icd/B78.7,,ICD-10 "B78.9 Strongyloidiasis, unspecified",845,B78.9,B65-B83 Helminthiases,http://identifiers.org/icd/B78.9,,ICD-10 "B81 Other intestinal helminthiases, not elsewhere classified",846,B81,B65-B83 Helminthiases,http://identifiers.org/icd/B81,,ICD-10 -"B81.0 Other intestinal helminthiases, not elsewhere classified - Anisakiasis",847,B81.0,B65-B83 Helminthiases,http://identifiers.org/icd/B81.0,ORPHAcode: 1070 Anisakiasis +"B81.0 Other intestinal helminthiases, not elsewhere classified - Anisakiasis",847,B81.0,B65-B83 Helminthiases,http://identifiers.org/icd/B81.0,ORPHAcode: 1070 Anisakiasis,ICD-10 B81.1 Intestinal capillariasis,848,B81.1,B65-B83 Helminthiases,http://identifiers.org/icd/B81.1,,ICD-10 "B81.2 Other intestinal helminthiases, not elsewhere classified - Trichostrongyliasis",849,B81.2,B65-B83 Helminthiases,http://identifiers.org/icd/B81.2,,ICD-10 -B81.3 Intestinal angiostrongyliasis,850,B81.3,B65-B83 Helminthiases,http://identifiers.org/icd/B81.3,ORPHAcode: 74 Angiostrongyliasis +B81.3 Intestinal angiostrongyliasis,850,B81.3,B65-B83 Helminthiases,http://identifiers.org/icd/B81.3,ORPHAcode: 74 Angiostrongyliasis,ICD-10 B81.4 Mixed intestinal helminthiases,851,B81.4,B65-B83 Helminthiases,http://identifiers.org/icd/B81.4,,ICD-10 B81.8 Other specified intestinal helminthiases,852,B81.8,B65-B83 Helminthiases,http://identifiers.org/icd/B81.8,,ICD-10 B82 Unspecified intestinal parasitism,853,B82,B65-B83 Helminthiases,http://identifiers.org/icd/B82,,ICD-10 "B82.0 Intestinal helminthiasis, unspecified",854,B82.0,B65-B83 Helminthiases,http://identifiers.org/icd/B82.0,,ICD-10 "B82.9 Intestinal parasitism, unspecified",855,B82.9,B65-B83 Helminthiases,http://identifiers.org/icd/B82.9,,ICD-10 B83 Other helminthiases,856,B83,B65-B83 Helminthiases,http://identifiers.org/icd/B83,,ICD-10 -B83.0 Other helminthiases - Visceral larva migrans,857,B83.0,B65-B83 Helminthiases,http://identifiers.org/icd/B83.0,ORPHAcode: 3343 Toxocariasis +B83.0 Other helminthiases - Visceral larva migrans,857,B83.0,B65-B83 Helminthiases,http://identifiers.org/icd/B83.0,ORPHAcode: 3343 Toxocariasis,ICD-10 B83.1 Other helminthiases - Gnathostomiasis,858,B83.1,B65-B83 Helminthiases,http://identifiers.org/icd/B83.1,,ICD-10 B83.2 Other helminthiases - Angiostrongyliasis due to Parastrongylus cantonensis,859,B83.2,B65-B83 Helminthiases,http://identifiers.org/icd/B83.2,,ICD-10 B83.3 Other helminthiases - Syngamiasis,860,B83.3,B65-B83 Helminthiases,http://identifiers.org/icd/B83.3,,ICD-10 @@ -871,16 +871,16 @@ B85.3 Phthiriasis,869,B85.3,"B85-B89 Pediculosis, acariasis and other infestatio B85.4 Mixed pediculosis and phthiriasis,870,B85.4,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B85.4,,ICD-10 B86 Scabies,871,B86,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B86,,ICD-10 B87 Myiasis,872,B87,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87,,ICD-10 -B87.0 Cutaneous myiasis,873,B87.0,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.0,ORPHAcode: 504 Creeping myiasis -B87.1 Wound myiasis,874,B87.1,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.1,ORPHAcode: 165955 Wound myiasis +B87.0 Cutaneous myiasis,873,B87.0,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.0,ORPHAcode: 504 Creeping myiasis,ICD-10 +B87.1 Wound myiasis,874,B87.1,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.1,ORPHAcode: 165955 Wound myiasis,ICD-10 B87.2 Ocular myiasis,875,B87.2,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.2,,ICD-10 B87.3 Nasopharyngeal myiasis,876,B87.3,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.3,,ICD-10 B87.4 Aural myiasis,877,B87.4,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.4,,ICD-10 -B87.8 Myiasis of other sites,878,B87.8,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.8,ORPHAcode: 165958 Cavitary myiasis +B87.8 Myiasis of other sites,878,B87.8,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.8,ORPHAcode: 165958 Cavitary myiasis,ICD-10 "B87.9 Myiasis, unspecified",879,B87.9,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B87.9,,ICD-10 B88 Other infestations,880,B88,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88,,ICD-10 -B88.0 Other acariasis,881,B88.0,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88.0,ORPHAcode: 283 Demodicidosis -B88.1 Other infestations - Tungiasis [sandflea infestation],882,B88.1,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88.1,ORPHAcode: 879 Tungiasis +B88.0 Other acariasis,881,B88.0,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88.0,ORPHAcode: 283 Demodicidosis,ICD-10 +B88.1 Other infestations - Tungiasis [sandflea infestation],882,B88.1,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88.1,ORPHAcode: 879 Tungiasis,ICD-10 B88.2 Other arthropod infestations,883,B88.2,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88.2,,ICD-10 B88.3 Other infestations - External hirudiniasis,884,B88.3,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88.3,,ICD-10 B88.8 Other specified infestations,885,B88.8,"B85-B89 Pediculosis, acariasis and other infestations",http://identifiers.org/icd/B88.8,,ICD-10 @@ -914,7 +914,7 @@ B95.6 Staphylococcus aureus as the cause of diseases classified to other chapter B95.7 Other staphylococcus as the cause of diseases classified to other chapters,913,B95.7,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B95.7,,ICD-10 B95.8 Unspecified staphylococcus as the cause of diseases classified to other chapters,914,B95.8,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B95.8,,ICD-10 B96 Other specified bacterial agents as the cause of diseases classified to other chapters,915,B96,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B96,,ICD-10 -B96.0 Mycoplasma pneumoniae [M. pneumoniae] as the cause of diseases classified to other chapters,916,B96.0,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B96.0,ORPHAcode: 83482 Mycoplasma encephalitis +B96.0 Mycoplasma pneumoniae [M. pneumoniae] as the cause of diseases classified to other chapters,916,B96.0,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B96.0,ORPHAcode: 83482 Mycoplasma encephalitis,ICD-10 B96.1 Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified to other chapters,917,B96.1,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B96.1,,ICD-10 B96.2 Escherichia coli [E. coli] as the cause of diseases classified to other chapters,918,B96.2,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B96.2,,ICD-10 B96.3 Haemophilus influenzae [H. influenzae] as the cause of diseases classified to other chapters,919,B96.3,"B95-B98 Bacterial, viral and other infectious agents",http://identifiers.org/icd/B96.3,,ICD-10 @@ -945,7 +945,7 @@ C00-C97 Malignant neoplasms,942,,II Neoplasms,,,ICD-10 "C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",944,C00-C14,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 C00 Malignant neoplasm of lip,945,C00,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C00,,ICD-10 C00.0 Malignant neoplasm of lip - External upper lip,946,C00.0,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C00.0,,ICD-10 -C00.1 Malignant neoplasm of lip - External lower lip,947,C00.1,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C00.1,ORPHAcode: 502366 Squamous cell carcinoma of the lip +C00.1 Malignant neoplasm of lip - External lower lip,947,C00.1,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C00.1,ORPHAcode: 502366 Squamous cell carcinoma of the lip,ICD-10 "C00.2 Malignant neoplasm of lip - External lip, unspecified",948,C00.2,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C00.2,,ICD-10 "C00.3 Malignant neoplasm of lip - Upper lip, inner aspect",949,C00.3,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C00.3,,ICD-10 "C00.4 Malignant neoplasm of lip - Lower lip, inner aspect",950,C00.4,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C00.4,,ICD-10 @@ -983,8 +983,8 @@ C06.0 Malignant neoplasm of other and unspecified parts of mouth - Cheek mucosa, C06.1 Malignant neoplasm of other and unspecified parts of mouth - Vestibule of mouth,982,C06.1,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C06.1,,ICD-10 C06.2 Malignant neoplasm of other and unspecified parts of mouth - Retromolar area,983,C06.2,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C06.2,,ICD-10 C06.8 Malignant neoplasm of other and unspecified parts of mouth - Overlapping lesion of other and unspecified parts of mouth,984,C06.8,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C06.8,,ICD-10 -"C06.9 Malignant neoplasm of other and unspecified parts of mouth - Mouth, unspecified",985,C06.9,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C06.9,ORPHAcode: 502363 Squamous cell carcinoma of the oral cavity -C07 Malignant neoplasm of parotid gland,986,C07,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C07,ORPHAcode: 276145 Malignant epithelial tumor of salivary glands +"C06.9 Malignant neoplasm of other and unspecified parts of mouth - Mouth, unspecified",985,C06.9,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C06.9,ORPHAcode: 502363 Squamous cell carcinoma of the oral cavity,ICD-10 +C07 Malignant neoplasm of parotid gland,986,C07,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C07,ORPHAcode: 276145 Malignant epithelial tumor of salivary glands,ICD-10 C08 Malignant neoplasm of other and unspecified major salivary glands,987,C08,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C08,,ICD-10 C08.0 Malignant neoplasm of other and unspecified major salivary glands - Submandibular gland,988,C08.0,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C08.0,,ICD-10 C08.1 Malignant neoplasm of other and unspecified major salivary glands - Sublingual gland,989,C08.1,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C08.1,,ICD-10 @@ -1001,16 +1001,16 @@ C10.1 Malignant neoplasm of oropharynx - Anterior surface of epiglottis,999,C10. C10.2 Malignant neoplasm of oropharynx - Lateral wall of oropharynx,1000,C10.2,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C10.2,,ICD-10 C10.3 Malignant neoplasm of oropharynx - Posterior wall of oropharynx,1001,C10.3,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C10.3,,ICD-10 C10.4 Malignant neoplasm of oropharynx - Branchial cleft,1002,C10.4,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C10.4,,ICD-10 -C10.8 Malignant neoplasm of oropharynx - Overlapping lesion of oropharynx,1003,C10.8,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C10.8,ORPHAcode: 500478 Squamous cell carcinoma of the oropharynx +C10.8 Malignant neoplasm of oropharynx - Overlapping lesion of oropharynx,1003,C10.8,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C10.8,ORPHAcode: 500478 Squamous cell carcinoma of the oropharynx,ICD-10 "C10.9 Malignant neoplasm of oropharynx - Oropharynx, unspecified",1004,C10.9,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C10.9,,ICD-10 C11 Malignant neoplasm of nasopharynx,1005,C11,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11,,ICD-10 -C11.0 Malignant neoplasm of nasopharynx - Superior wall of nasopharynx,1006,C11.0,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11.0,ORPHAcode: 150 Nasopharyngeal carcinoma +C11.0 Malignant neoplasm of nasopharynx - Superior wall of nasopharynx,1006,C11.0,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11.0,ORPHAcode: 150 Nasopharyngeal carcinoma,ICD-10 C11.1 Malignant neoplasm of nasopharynx - Posterior wall of nasopharynx,1007,C11.1,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11.1,,ICD-10 C11.2 Malignant neoplasm of nasopharynx - Lateral wall of nasopharynx,1008,C11.2,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11.2,,ICD-10 C11.3 Malignant neoplasm of nasopharynx - Anterior wall of nasopharynx,1009,C11.3,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11.3,,ICD-10 C11.8 Malignant neoplasm of nasopharynx - Overlapping lesion of nasopharynx,1010,C11.8,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11.8,,ICD-10 "C11.9 Malignant neoplasm of nasopharynx - Nasopharynx, unspecified",1011,C11.9,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C11.9,,ICD-10 -C12 Malignant neoplasm of piriform sinus,1012,C12,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C12,ORPHAcode: 494547 Squamous cell carcinoma of the hypopharynx +C12 Malignant neoplasm of piriform sinus,1012,C12,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C12,ORPHAcode: 494547 Squamous cell carcinoma of the hypopharynx,ICD-10 C13 Malignant neoplasm of hypopharynx,1013,C13,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C13,,ICD-10 C13.0 Malignant neoplasm of hypopharynx - Postcricoid region,1014,C13.0,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C13.0,,ICD-10 "C13.1 Malignant neoplasm of hypopharynx - Aryepiglottic fold, hypopharyngeal aspect",1015,C13.1,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C13.1,,ICD-10 @@ -1023,84 +1023,84 @@ C13.8 Malignant neoplasm of hypopharynx - Overlapping lesion of hypopharynx,1017 "C14.8 Malignant neoplasm of other and ill-defined sites in the lip, oral cavity and pharynx - Overlapping lesion of lip, oral cavity and pharynx",1022,C14.8,"C00-C14 Malignant neoplasms of lip, oral cavity and pharynx",http://identifiers.org/icd/C14.8,,ICD-10 C15-C26 Malignant neoplasms of digestive organs,1023,C15-C26,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 C15 Malignant neoplasm of oesophagus,1024,C15,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15,,ICD-10 -C15.0 Malignant neoplasm of oesophagus - Cervical part of oesophagus,1025,C15.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.0,ORPHAcode: 418951 Undifferentiated carcinoma of esophagus -C15.1 Malignant neoplasm of oesophagus - Thoracic part of oesophagus,1026,C15.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.1,"ORPHAcode: 418945 Carcinoma of esophagus, salivary gland type" -C15.2 Malignant neoplasm of oesophagus - Abdominal part of oesophagus,1027,C15.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.2,ORPHAcode: 99976 Adenocarcinoma of the esophagus -C15.3 Malignant neoplasm of oesophagus - Upper third of oesophagus,1028,C15.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.3,ORPHAcode: 99977 Squamous cell carcinoma of the esophagus +C15.0 Malignant neoplasm of oesophagus - Cervical part of oesophagus,1025,C15.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.0,ORPHAcode: 418951 Undifferentiated carcinoma of esophagus,ICD-10 +C15.1 Malignant neoplasm of oesophagus - Thoracic part of oesophagus,1026,C15.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.1,"ORPHAcode: 418945 Carcinoma of esophagus, salivary gland type",ICD-10 +C15.2 Malignant neoplasm of oesophagus - Abdominal part of oesophagus,1027,C15.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.2,ORPHAcode: 99976 Adenocarcinoma of the esophagus,ICD-10 +C15.3 Malignant neoplasm of oesophagus - Upper third of oesophagus,1028,C15.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.3,ORPHAcode: 99977 Squamous cell carcinoma of the esophagus,ICD-10 C15.4 Malignant neoplasm of oesophagus - Middle third of oesophagus,1029,C15.4,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.4,,ICD-10 C15.5 Malignant neoplasm of oesophagus - Lower third of oesophagus,1030,C15.5,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.5,,ICD-10 -C15.8 Malignant neoplasm of oesophagus - Overlapping lesion of oesophagus,1031,C15.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.8,ORPHAcode: 506136 Neuroendocrine neoplasm of esophagus +C15.8 Malignant neoplasm of oesophagus - Overlapping lesion of oesophagus,1031,C15.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.8,ORPHAcode: 506136 Neuroendocrine neoplasm of esophagus,ICD-10 "C15.9 Malignant neoplasm of oesophagus - Oesophagus, unspecified",1032,C15.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C15.9,,ICD-10 C16 Malignant neoplasm of stomach,1033,C16,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16,,ICD-10 -C16.0 Malignant neoplasm of stomach - Cardia,1034,C16.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.0,ORPHAcode: 418959 Squamous cell carcinoma of the stomach +C16.0 Malignant neoplasm of stomach - Cardia,1034,C16.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.0,ORPHAcode: 418959 Squamous cell carcinoma of the stomach,ICD-10 C16.1 Malignant neoplasm of stomach - Fundus of stomach,1035,C16.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.1,,ICD-10 "D04.9 Skin, unspecified",1036,D04.9,D00-D09 In situ neoplasms,http://identifiers.org/icd/D04.9,,ICD-10 -C16.2 Malignant neoplasm of stomach - Body of stomach,1037,C16.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.2,ORPHAcode: 313920 Epstein-Barr virus-associated gastric carcinoma +C16.2 Malignant neoplasm of stomach - Body of stomach,1037,C16.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.2,ORPHAcode: 313920 Epstein-Barr virus-associated gastric carcinoma,ICD-10 C16.3 Malignant neoplasm of stomach - Pyloric antrum,1038,C16.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.3,,ICD-10 C16.4 Malignant neoplasm of stomach - Pylorus,1039,C16.4,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.4,,ICD-10 "C16.5 Malignant neoplasm of stomach - Lesser curvature of stomach, unspecified",1040,C16.5,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.5,,ICD-10 "C16.6 Malignant neoplasm of stomach - Greater curvature of stomach, unspecified",1041,C16.6,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.6,,ICD-10 C16.8 Malignant neoplasm of stomach - Overlapping lesion of stomach,1042,C16.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.8,,ICD-10 -"C16.9 Malignant neoplasm of stomach - Stomach, unspecified",1043,C16.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.9,ORPHAcode: 26106 Hereditary diffuse gastric cancer +"C16.9 Malignant neoplasm of stomach - Stomach, unspecified",1043,C16.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C16.9,ORPHAcode: 26106 Hereditary diffuse gastric cancer,ICD-10 C17 Malignant neoplasm of small intestine,1044,C17,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17,,ICD-10 -C17.0 Malignant neoplasm of small intestine - Duodenum,1045,C17.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.0,ORPHAcode: 423968 Squamous cell carcinoma of the small intestine -C17.1 Malignant neoplasm of small intestine - Jejunum,1046,C17.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.1,ORPHAcode: 104076 Leiomyosarcoma of small intestine -C17.2 Malignant neoplasm of small intestine - Ileum,1047,C17.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.2,ORPHAcode: 100078 Ileal neuroendocrine tumor +C17.0 Malignant neoplasm of small intestine - Duodenum,1045,C17.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.0,ORPHAcode: 423968 Squamous cell carcinoma of the small intestine,ICD-10 +C17.1 Malignant neoplasm of small intestine - Jejunum,1046,C17.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.1,ORPHAcode: 104076 Leiomyosarcoma of small intestine,ICD-10 +C17.2 Malignant neoplasm of small intestine - Ileum,1047,C17.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.2,ORPHAcode: 100078 Ileal neuroendocrine tumor,ICD-10 C17.3 Malignant neoplasm of small intestine - Meckel diverticulum,1048,C17.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.3,,ICD-10 C17.8 Malignant neoplasm of small intestine - Overlapping lesion of small intestine,1049,C17.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.8,,ICD-10 -"C17.9 Malignant neoplasm of small intestine - Small intestine, unspecified",1050,C17.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.9,ORPHAcode: 456333 Hereditary neuroendocrine tumor of small intestine +"C17.9 Malignant neoplasm of small intestine - Small intestine, unspecified",1050,C17.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C17.9,ORPHAcode: 456333 Hereditary neuroendocrine tumor of small intestine,ICD-10 C18 Malignant neoplasm of colon,1051,C18,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18,,ICD-10 -C18.0 Malignant neoplasm of colon - Caecum,1052,C18.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.0,ORPHAcode: 440437 Familial colorectal cancer Type X -C18.1 Malignant neoplasm of colon - Appendix,1053,C18.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.1,ORPHAcode: 100079 Neuroendocrine neoplasm of appendix +C18.0 Malignant neoplasm of colon - Caecum,1052,C18.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.0,ORPHAcode: 440437 Familial colorectal cancer Type X,ICD-10 +C18.1 Malignant neoplasm of colon - Appendix,1053,C18.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.1,ORPHAcode: 100079 Neuroendocrine neoplasm of appendix,ICD-10 C18.2 Malignant neoplasm of colon - Ascending colon,1054,C18.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.2,,ICD-10 -C18.3 Malignant neoplasm of colon - Hepatic flexure,1055,C18.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.3,ORPHAcode: 423994 Squamous cell carcinoma of the colon +C18.3 Malignant neoplasm of colon - Hepatic flexure,1055,C18.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.3,ORPHAcode: 423994 Squamous cell carcinoma of the colon,ICD-10 C18.4 Malignant neoplasm of colon - Transverse colon,1056,C18.4,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.4,,ICD-10 C18.5 Malignant neoplasm of colon - Splenic flexure,1057,C18.5,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.5,,ICD-10 C18.6 Malignant neoplasm of colon - Descending colon,1058,C18.6,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.6,,ICD-10 C18.7 Malignant neoplasm of colon - Sigmoid colon,1059,C18.7,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.7,,ICD-10 -C18.8 Malignant neoplasm of colon - Overlapping lesion of colon,1060,C18.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.8,ORPHAcode: 100080 Neuroendocrine tumor of the colon +C18.8 Malignant neoplasm of colon - Overlapping lesion of colon,1060,C18.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.8,ORPHAcode: 100080 Neuroendocrine tumor of the colon,ICD-10 "C18.9 Malignant neoplasm of colon - Colon, unspecified",1061,C18.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C18.9,,ICD-10 -C19 Malignant neoplasm of rectosigmoid junction,1062,C19,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C19,ORPHAcode: 300576 Oligodontia-cancer predisposition syndrome -C20 Malignant neoplasm of rectum,1063,C20,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C20,ORPHAcode: 100081 Neuroendocrine tumor of the rectum +C19 Malignant neoplasm of rectosigmoid junction,1062,C19,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C19,ORPHAcode: 300576 Oligodontia-cancer predisposition syndrome,ICD-10 +C20 Malignant neoplasm of rectum,1063,C20,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C20,ORPHAcode: 100081 Neuroendocrine tumor of the rectum,ICD-10 C21 Malignant neoplasm of anus and anal canal,1064,C21,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C21,,ICD-10 "C21.0 Malignant neoplasm of anus and anal canal - Anus, unspecified",1065,C21.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C21.0,,ICD-10 -C21.1 Malignant neoplasm of anus and anal canal - Anal canal,1066,C21.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C21.1,ORPHAcode: 100082 Neuroendocrine tumor of anal canal +C21.1 Malignant neoplasm of anus and anal canal - Anal canal,1066,C21.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C21.1,ORPHAcode: 100082 Neuroendocrine tumor of anal canal,ICD-10 C21.2 Malignant neoplasm of anus and anal canal - Cloacogenic zone,1067,C21.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C21.2,,ICD-10 "C21.8 Malignant neoplasm of anus and anal canal - Overlapping lesion of rectum, anus and anal canal",1068,C21.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C21.8,,ICD-10 C22 Malignant neoplasm of liver and intrahepatic bile ducts,1069,C22,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22,,ICD-10 -C22.0 Malignant neoplasm of liver and intrahepatic bile ducts - Liver cell carcinoma,1070,C22.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.0,ORPHAcode: 33402 Pediatric hepatocellular carcinoma -C22.1 Malignant neoplasm of liver and intrahepatic bile ducts - Intrahepatic bile duct carcinoma,1071,C22.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.1,ORPHAcode: 424975 Squamous cell carcinoma of liver and intrahepatic biliary tract -C22.2 Malignant neoplasm of liver and intrahepatic bile ducts - Hepatoblastoma,1072,C22.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.2,ORPHAcode: 449 Hepatoblastoma +C22.0 Malignant neoplasm of liver and intrahepatic bile ducts - Liver cell carcinoma,1070,C22.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.0,ORPHAcode: 33402 Pediatric hepatocellular carcinoma,ICD-10 +C22.1 Malignant neoplasm of liver and intrahepatic bile ducts - Intrahepatic bile duct carcinoma,1071,C22.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.1,ORPHAcode: 424975 Squamous cell carcinoma of liver and intrahepatic biliary tract,ICD-10 +C22.2 Malignant neoplasm of liver and intrahepatic bile ducts - Hepatoblastoma,1072,C22.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.2,ORPHAcode: 449 Hepatoblastoma,ICD-10 C22.3 Malignant neoplasm of liver and intrahepatic bile ducts - Angiosarcoma of liver,1073,C22.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.3,,ICD-10 C22.4 Malignant neoplasm of liver and intrahepatic bile ducts - Other sarcomas of liver,1074,C22.4,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.4,,ICD-10 -C22.7 Malignant neoplasm of liver and intrahepatic bile ducts - Other specified carcinomas of liver,1075,C22.7,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.7,ORPHAcode: 100085 Primary hepatic neuroendocrine carcinoma +C22.7 Malignant neoplasm of liver and intrahepatic bile ducts - Other specified carcinomas of liver,1075,C22.7,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.7,ORPHAcode: 100085 Primary hepatic neuroendocrine carcinoma,ICD-10 "C22.9 Malignant neoplasm of liver and intrahepatic bile ducts - Liver, unspecified",1076,C22.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C22.9,,ICD-10 -C23 Malignant neoplasm of gallbladder,1077,C23,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C23,ORPHAcode: 100086 Gallbladder neuroendocrine tumor +C23 Malignant neoplasm of gallbladder,1077,C23,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C23,ORPHAcode: 100086 Gallbladder neuroendocrine tumor,ICD-10 C24 Malignant neoplasm of other and unspecified parts of biliary tract,1078,C24,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24,,ICD-10 -C24.0 Malignant neoplasm of other and unspecified parts of biliary tract - Extrahepatic bile duct,1079,C24.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24.0,ORPHAcode: 99978 Klatskin tumor -C24.1 Malignant neoplasm of other and unspecified parts of biliary tract - Ampulla of Vater,1080,C24.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24.1,ORPHAcode: 300557 Carcinoma of the ampulla of Vater -C24.8 Malignant neoplasm of other and unspecified parts of biliary tract - Overlapping lesion of biliary tract,1081,C24.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24.8,ORPHAcode: 70567 Cholangiocarcinoma +C24.0 Malignant neoplasm of other and unspecified parts of biliary tract - Extrahepatic bile duct,1079,C24.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24.0,ORPHAcode: 99978 Klatskin tumor,ICD-10 +C24.1 Malignant neoplasm of other and unspecified parts of biliary tract - Ampulla of Vater,1080,C24.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24.1,ORPHAcode: 300557 Carcinoma of the ampulla of Vater,ICD-10 +C24.8 Malignant neoplasm of other and unspecified parts of biliary tract - Overlapping lesion of biliary tract,1081,C24.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24.8,ORPHAcode: 70567 Cholangiocarcinoma,ICD-10 "C24.9 Malignant neoplasm of other and unspecified parts of biliary tract - Biliary tract, unspecified",1082,C24.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C24.9,,ICD-10 -C25 Malignant neoplasm of pancreas,1083,C25,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25,ORPHAcode: 1333 Familial pancreatic carcinoma +C25 Malignant neoplasm of pancreas,1083,C25,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25,ORPHAcode: 1333 Familial pancreatic carcinoma,ICD-10 D05 Carcinoma in situ of breast,1084,D05,D00-D09 In situ neoplasms,http://identifiers.org/icd/D05,,ICD-10 -C25.0 Malignant neoplasm of pancreas - Head of pancreas,1085,C25.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.0,ORPHAcode: 424039 Squamous cell carcinoma of pancreas -C25.1 Malignant neoplasm of pancreas - Body of pancreas,1086,C25.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.1,ORPHAcode: 677 Pancreatoblastoma +C25.0 Malignant neoplasm of pancreas - Head of pancreas,1085,C25.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.0,ORPHAcode: 424039 Squamous cell carcinoma of pancreas,ICD-10 +C25.1 Malignant neoplasm of pancreas - Body of pancreas,1086,C25.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.1,ORPHAcode: 677 Pancreatoblastoma,ICD-10 C25.2 Malignant neoplasm of pancreas - Tail of pancreas,1087,C25.2,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.2,,ICD-10 -C25.3 Malignant neoplasm of pancreas - Pancreatic duct,1088,C25.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.3,ORPHAcode: 424058 Intraductal papillary mucinous carcinoma of pancreas +C25.3 Malignant neoplasm of pancreas - Pancreatic duct,1088,C25.3,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.3,ORPHAcode: 424058 Intraductal papillary mucinous carcinoma of pancreas,ICD-10 C25.4 Malignant neoplasm of pancreas - Endocrine pancreas,1089,C25.4,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.4,,ICD-10 C25.7 Malignant neoplasm of pancreas - Other parts of pancreas,1090,C25.7,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.7,,ICD-10 -C25.8 Malignant neoplasm of pancreas - Overlapping lesion of pancreas,1091,C25.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.8,ORPHAcode: 424053 Mucinous cystadenocarcinoma of the pancreas -"C25.9 Malignant neoplasm of pancreas - Pancreas, unspecified",1092,C25.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.9,ORPHAcode: 506075 Non-functioning neuroendocrine tumor of pancreas +C25.8 Malignant neoplasm of pancreas - Overlapping lesion of pancreas,1091,C25.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.8,ORPHAcode: 424053 Mucinous cystadenocarcinoma of the pancreas,ICD-10 +"C25.9 Malignant neoplasm of pancreas - Pancreas, unspecified",1092,C25.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C25.9,ORPHAcode: 506075 Non-functioning neuroendocrine tumor of pancreas,ICD-10 C26 Malignant neoplasm of other and ill-defined digestive organs,1093,C26,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C26,,ICD-10 "C26.0 Malignant neoplasm of other and ill-defined digestive organs - Intestinal tract, part unspecified",1094,C26.0,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C26.0,,ICD-10 C26.1 Malignant neoplasm of other and ill-defined digestive organs - Spleen,1095,C26.1,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C26.1,,ICD-10 C26.8 Malignant neoplasm of other and ill-defined digestive organs - Overlapping lesion of digestive system,1096,C26.8,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C26.8,,ICD-10 -C26.9 Malignant neoplasm of other and ill-defined digestive organs - Ill-defined sites within the digestive system,1097,C26.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C26.9,ORPHAcode: 44890 Gastrointestinal stromal tumor +C26.9 Malignant neoplasm of other and ill-defined digestive organs - Ill-defined sites within the digestive system,1097,C26.9,C15-C26 Malignant neoplasms of digestive organs,http://identifiers.org/icd/C26.9,ORPHAcode: 44890 Gastrointestinal stromal tumor,ICD-10 C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,1098,C30-C39,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 C30 Malignant neoplasm of nasal cavity and middle ear,1099,C30,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C30,,ICD-10 J93 Pneumothorax,1100,J93,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J93,,ICD-10 -C30.0 Malignant neoplasm of nasal cavity and middle ear - Nasal cavity,1101,C30.0,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C30.0,ORPHAcode: 1957 Esthesioneuroblastoma -C30.1 Malignant neoplasm of nasal cavity and middle ear - Middle ear,1102,C30.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C30.1,ORPHAcode: 100084 Middle ear neuroendocrine tumor +C30.0 Malignant neoplasm of nasal cavity and middle ear - Nasal cavity,1101,C30.0,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C30.0,ORPHAcode: 1957 Esthesioneuroblastoma,ICD-10 +C30.1 Malignant neoplasm of nasal cavity and middle ear - Middle ear,1102,C30.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C30.1,ORPHAcode: 100084 Middle ear neuroendocrine tumor,ICD-10 C31 Malignant neoplasm of accessory sinuses,1103,C31,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C31,,ICD-10 C31.0 Malignant neoplasm of accessory sinuses - Maxillary sinus,1104,C31.0,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C31.0,,ICD-10 C31.1 Malignant neoplasm of accessory sinuses - Ethmoidal sinus,1105,C31.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C31.1,,ICD-10 @@ -1110,25 +1110,25 @@ C31.8 Malignant neoplasm of accessory sinuses - Overlapping lesion of accessory "C31.9 Malignant neoplasm of accessory sinuses - Accessory sinus, unspecified",1109,C31.9,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C31.9,,ICD-10 C32 Malignant neoplasm of larynx,1110,C32,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32,,ICD-10 C32.0 Malignant neoplasm of larynx - Glottis,1111,C32.0,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.0,,ICD-10 -C32.1 Malignant neoplasm of larynx - Supraglottis,1112,C32.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.1,ORPHAcode: 100083 Laryngeal neuroendocrine tumor +C32.1 Malignant neoplasm of larynx - Supraglottis,1112,C32.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.1,ORPHAcode: 100083 Laryngeal neuroendocrine tumor,ICD-10 C32.2 Malignant neoplasm of larynx - Subglottis,1113,C32.2,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.2,,ICD-10 C32.3 Malignant neoplasm of larynx - Laryngeal cartilage,1114,C32.3,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.3,,ICD-10 -C32.8 Malignant neoplasm of larynx - Overlapping lesion of larynx,1115,C32.8,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.8,ORPHAcode: 494550 Squamous cell carcinoma of the larynx +C32.8 Malignant neoplasm of larynx - Overlapping lesion of larynx,1115,C32.8,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.8,ORPHAcode: 494550 Squamous cell carcinoma of the larynx,ICD-10 "C32.9 Malignant neoplasm of larynx - Larynx, unspecified",1116,C32.9,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C32.9,,ICD-10 C33 Malignant neoplasm of trachea,1117,C33,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C33,,ICD-10 C34 Malignant neoplasm of bronchus and lung,1118,C34,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34,,ICD-10 C34.0 Malignant neoplasm of bronchus and lung - Main bronchus,1119,C34.0,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.0,,ICD-10 -"C34.1 Malignant neoplasm of bronchus and lung - Upper lobe, bronchus or lung",1120,C34.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.1,ORPHAcode: 284395 Well-differentiated fetal adenocarcinoma of the lung -"C34.2 Malignant neoplasm of bronchus and lung - Middle lobe, bronchus or lung",1121,C34.2,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.2,ORPHAcode: 64741 Pulmonary blastoma -"C34.3 Malignant neoplasm of bronchus and lung - Lower lobe, bronchus or lung",1122,C34.3,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.3,ORPHAcode: 64742 Pleuropulmonary blastoma +"C34.1 Malignant neoplasm of bronchus and lung - Upper lobe, bronchus or lung",1120,C34.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.1,ORPHAcode: 284395 Well-differentiated fetal adenocarcinoma of the lung,ICD-10 +"C34.2 Malignant neoplasm of bronchus and lung - Middle lobe, bronchus or lung",1121,C34.2,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.2,ORPHAcode: 64741 Pulmonary blastoma,ICD-10 +"C34.3 Malignant neoplasm of bronchus and lung - Lower lobe, bronchus or lung",1122,C34.3,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.3,ORPHAcode: 64742 Pleuropulmonary blastoma,ICD-10 C34.8 Malignant neoplasm of bronchus and lung - Overlapping lesion of bronchus and lung,1123,C34.8,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.8,,ICD-10 -"C34.9 Malignant neoplasm of bronchus and lung - Bronchus or lung, unspecified",1124,C34.9,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.9,ORPHAcode: 70573 Small cell lung cancer -C37 Malignant neoplasm of thymus,1125,C37,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C37,ORPHAcode: 97289 Thymic neuroendocrine tumor +"C34.9 Malignant neoplasm of bronchus and lung - Bronchus or lung, unspecified",1124,C34.9,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C34.9,ORPHAcode: 70573 Small cell lung cancer,ICD-10 +C37 Malignant neoplasm of thymus,1125,C37,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C37,ORPHAcode: 97289 Thymic neuroendocrine tumor,ICD-10 "C38 Malignant neoplasm of heart, mediastinum and pleura",1126,C38,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38,,ICD-10 -"C38.0 Malignant neoplasm of heart, mediastinum and pleura - Heart",1127,C38.0,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.0,ORPHAcode: 874 Primary adult heart tumor +"C38.0 Malignant neoplasm of heart, mediastinum and pleura - Heart",1127,C38.0,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.0,ORPHAcode: 874 Primary adult heart tumor,ICD-10 "C38.1 Malignant neoplasm of heart, mediastinum and pleura - Anterior mediastinum",1128,C38.1,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.1,,ICD-10 "C38.2 Malignant neoplasm of heart, mediastinum and pleura - Posterior mediastinum",1129,C38.2,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.2,,ICD-10 -"C38.3 Malignant neoplasm of heart, mediastinum and pleura - Mediastinum, part unspecified",1130,C38.3,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.3,ORPHAcode: 182127 Extragonadal germinoma +"C38.3 Malignant neoplasm of heart, mediastinum and pleura - Mediastinum, part unspecified",1130,C38.3,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.3,ORPHAcode: 182127 Extragonadal germinoma,ICD-10 "C38.4 Malignant neoplasm of heart, mediastinum and pleura - Pleura",1131,C38.4,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.4,,ICD-10 "C38.8 Malignant neoplasm of heart, mediastinum and pleura - Overlapping lesion of heart, mediastinum and pleura",1132,C38.8,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C38.8,,ICD-10 C39 Malignant neoplasm of other and ill-defined sites in the respiratory system and intrathoracic organs,1133,C39,C30-C39 Malignant neoplasms of respiratory and intrathoracic organs,http://identifiers.org/icd/C39,,ICD-10 @@ -1139,19 +1139,19 @@ C40-C41 Malignant neoplasms of bone and articular cartilage,1137,C40-C41,"C00-C7 C40 Malignant neoplasm of bone and articular cartilage of limbs,1138,C40,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40,,ICD-10 C40.0 Malignant neoplasm of bone and articular cartilage of limbs - Scapula and long bones of upper limb,1139,C40.0,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40.0,,ICD-10 C40.1 Malignant neoplasm of bone and articular cartilage of limbs - Short bones of upper limb,1140,C40.1,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40.1,,ICD-10 -C40.2 Malignant neoplasm of bone and articular cartilage of limbs - Long bones of lower limb,1141,C40.2,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40.2,ORPHAcode: 55881 Adamantinoma +C40.2 Malignant neoplasm of bone and articular cartilage of limbs - Long bones of lower limb,1141,C40.2,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40.2,ORPHAcode: 55881 Adamantinoma,ICD-10 C40.3 Malignant neoplasm of bone and articular cartilage of limbs - Short bones of lower limb,1142,C40.3,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40.3,,ICD-10 C40.8 Malignant neoplasm of bone and articular cartilage of limbs - Overlapping lesion of bone and articular cartilage of limbs,1143,C40.8,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40.8,,ICD-10 "C40.9 Malignant neoplasm of bone and articular cartilage of limbs - Bone and articular cartilage of limb, unspecified",1144,C40.9,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C40.9,,ICD-10 C50.6 Malignant neoplasm of breast - Axillary tail of breast,1145,C50.6,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.6,,ICD-10 C41 Malignant neoplasm of bone and articular cartilage of other and unspecified sites,1146,C41,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41,,ICD-10 C41.0 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Bones of skull and face,1147,C41.0,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.0,,ICD-10 -C41.1 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Mandible,1148,C41.1,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.1,ORPHAcode: 314422 Ameloblastic carcinoma +C41.1 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Mandible,1148,C41.1,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.1,ORPHAcode: 314422 Ameloblastic carcinoma,ICD-10 C41.2 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Vertebral column,1149,C41.2,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.2,,ICD-10 "C41.3 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Ribs, sternum and clavicle",1150,C41.3,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.3,,ICD-10 -"C41.4 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Pelvic bones, sacrum and coccyx",1151,C41.4,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.4,ORPHAcode: 319 Skeletal Ewing sarcoma +"C41.4 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Pelvic bones, sacrum and coccyx",1151,C41.4,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.4,ORPHAcode: 319 Skeletal Ewing sarcoma,ICD-10 C41.8 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Overlapping lesion of bone and articular cartilage,1152,C41.8,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.8,,ICD-10 -"C41.9 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Bone and articular cartilage, unspecified",1153,C41.9,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.9,ORPHAcode: 668 Osteosarcoma +"C41.9 Malignant neoplasm of bone and articular cartilage of other and unspecified sites - Bone and articular cartilage, unspecified",1153,C41.9,C40-C41 Malignant neoplasms of bone and articular cartilage,http://identifiers.org/icd/C41.9,ORPHAcode: 668 Osteosarcoma,ICD-10 C43-C44 Melanoma and other malignant neoplasms of skin,1154,C43-C44,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 C43 Malignant melanoma of skin,1155,C43,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43,,ICD-10 C43.0 Malignant melanoma of lip,1156,C43.0,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.0,,ICD-10 @@ -1159,31 +1159,31 @@ C43.0 Malignant melanoma of lip,1156,C43.0,C43-C44 Melanoma and other malignant C43.2 Malignant melanoma of ear and external auricular canal,1158,C43.2,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.2,,ICD-10 C43.3 Malignant melanoma of other and unspecified parts of face,1159,C43.3,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.3,,ICD-10 C43.4 Malignant melanoma of scalp and neck,1160,C43.4,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.4,,ICD-10 -C43.5 Malignant melanoma of trunk,1161,C43.5,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.5,ORPHAcode: 618 Familial melanoma +C43.5 Malignant melanoma of trunk,1161,C43.5,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.5,ORPHAcode: 618 Familial melanoma,ICD-10 "C43.6 Malignant melanoma of upper limb, including shoulder",1162,C43.6,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.6,,ICD-10 "C43.7 Malignant melanoma of lower limb, including hip",1163,C43.7,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.7,,ICD-10 C43.8 Overlapping malignant melanoma of skin,1164,C43.8,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.8,,ICD-10 -"C43.9 Malignant melanoma of skin, unspecified",1165,C43.9,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.9,ORPHAcode: 97338 Melanoma of soft tissue +"C43.9 Malignant melanoma of skin, unspecified",1165,C43.9,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C43.9,ORPHAcode: 97338 Melanoma of soft tissue,ICD-10 C44 Other malignant neoplasms of skin,1166,C44,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44,,ICD-10 C44.0 Skin of lip,1167,C44.0,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.0,,ICD-10 "C44.1 Skin of eyelid, including canthus",1168,C44.1,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.1,,ICD-10 C44.2 Skin of ear and external auricular canal,1169,C44.2,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.2,,ICD-10 -C44.3 Skin of other and unspecified parts of face,1170,C44.3,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.3,ORPHAcode: 499182 Pilomatrix carcinoma +C44.3 Skin of other and unspecified parts of face,1170,C44.3,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.3,ORPHAcode: 499182 Pilomatrix carcinoma,ICD-10 C44.4 Skin of scalp and neck,1171,C44.4,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.4,,ICD-10 -C44.5 Skin of trunk,1172,C44.5,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.5,ORPHAcode: 2800 Extramammary Paget disease -"C44.6 Skin of upper limb, including shoulder",1173,C44.6,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.6,ORPHAcode: 65748 Multiple self-healing squamous epithelioma +C44.5 Skin of trunk,1172,C44.5,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.5,ORPHAcode: 2800 Extramammary Paget disease,ICD-10 +"C44.6 Skin of upper limb, including shoulder",1173,C44.6,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.6,ORPHAcode: 65748 Multiple self-healing squamous epithelioma,ICD-10 "C44.7 Skin of lower limb, including hip",1174,C44.7,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.7,,ICD-10 C44.8 Overlapping lesion of skin,1175,C44.8,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.8,,ICD-10 -"C44.9 Malignant neoplasm of skin, unspecified",1176,C44.9,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.9,ORPHAcode: 377 Gorlin syndrome +"C44.9 Malignant neoplasm of skin, unspecified",1176,C44.9,C43-C44 Melanoma and other malignant neoplasms of skin,http://identifiers.org/icd/C44.9,ORPHAcode: 377 Gorlin syndrome,ICD-10 C45-C49 Malignant neoplasms of mesothelial and soft tissue,1177,C45-C49,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 C45 Mesothelioma,1178,C45,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45,,ICD-10 -C45.0 Mesothelioma of pleura,1179,C45.0,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45.0,ORPHAcode: 50251 Pleural mesothelioma -C45.1 Mesothelioma of peritoneum,1180,C45.1,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45.1,ORPHAcode: 168811 Malignant peritoneal mesothelioma +C45.0 Mesothelioma of pleura,1179,C45.0,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45.0,ORPHAcode: 50251 Pleural mesothelioma,ICD-10 +C45.1 Mesothelioma of peritoneum,1180,C45.1,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45.1,ORPHAcode: 168811 Malignant peritoneal mesothelioma,ICD-10 C45.2 Mesothelioma of pericardium,1181,C45.2,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45.2,,ICD-10 C45.7 Mesothelioma of other sites,1182,C45.7,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45.7,,ICD-10 "C45.9 Mesothelioma, unspecified",1183,C45.9,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C45.9,,ICD-10 C46 Kaposi sarcoma,1184,C46,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C46,,ICD-10 -C46.0 Kaposi sarcoma of skin,1185,C46.0,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C46.0,ORPHAcode: 33276 Kaposi sarcoma +C46.0 Kaposi sarcoma of skin,1185,C46.0,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C46.0,ORPHAcode: 33276 Kaposi sarcoma,ICD-10 C46.1 Kaposi sarcoma of soft tissue,1186,C46.1,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C46.1,,ICD-10 C46.2 Kaposi sarcoma of palate,1187,C46.2,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C46.2,,ICD-10 C46.3 Kaposi sarcoma of lymph nodes,1188,C46.3,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C46.3,,ICD-10 @@ -1199,26 +1199,26 @@ C47.4 Malignant neoplasm of peripheral nerves and autonomic nervous system - Per C47.5 Malignant neoplasm of peripheral nerves and autonomic nervous system - Peripheral nerves of pelvis,1198,C47.5,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C47.5,,ICD-10 "C47.6 Malignant neoplasm of peripheral nerves and autonomic nervous system - Peripheral nerves of trunk, unspecified",1199,C47.6,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C47.6,,ICD-10 C47.8 Malignant neoplasm of peripheral nerves and autonomic nervous system - Overlapping lesion of peripheral nerves and autonomic nervous system,1200,C47.8,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C47.8,,ICD-10 -"C47.9 Malignant neoplasm of peripheral nerves and autonomic nervous system - Peripheral nerves and autonomic nervous system, unspecified",1201,C47.9,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C47.9,ORPHAcode: 3148 Malignant peripheral nerve sheath tumor +"C47.9 Malignant neoplasm of peripheral nerves and autonomic nervous system - Peripheral nerves and autonomic nervous system, unspecified",1201,C47.9,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C47.9,ORPHAcode: 3148 Malignant peripheral nerve sheath tumor,ICD-10 C48 Malignant neoplasm of retroperitoneum and peritoneum,1202,C48,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C48,,ICD-10 -C48.0 Malignant neoplasm of retroperitoneum and peritoneum - Retroperitoneum,1203,C48.0,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C48.0,ORPHAcode: 398980 Primary peritoneal serous/papillary carcinoma +C48.0 Malignant neoplasm of retroperitoneum and peritoneum - Retroperitoneum,1203,C48.0,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C48.0,ORPHAcode: 398980 Primary peritoneal serous/papillary carcinoma,ICD-10 C48.1 Malignant neoplasm of retroperitoneum and peritoneum - Specified parts of peritoneum,1204,C48.1,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C48.1,,ICD-10 -"C48.2 Malignant neoplasm of retroperitoneum and peritoneum - Peritoneum, unspecified",1205,C48.2,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C48.2,ORPHAcode: 83469 Desmoplastic small round cell tumor +"C48.2 Malignant neoplasm of retroperitoneum and peritoneum - Peritoneum, unspecified",1205,C48.2,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C48.2,ORPHAcode: 83469 Desmoplastic small round cell tumor,ICD-10 C48.8 Malignant neoplasm of retroperitoneum and peritoneum - Overlapping lesion of retroperitoneum and peritoneum,1206,C48.8,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C48.8,,ICD-10 C49 Malignant neoplasm of other connective and soft tissue,1207,C49,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49,,ICD-10 "C49.0 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of head, face and neck",1208,C49.0,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.0,,ICD-10 "C49.1 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of upper limb, including shoulder",1209,C49.1,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.1,,ICD-10 "C49.2 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of lower limb, including hip",1210,C49.2,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.2,,ICD-10 -C49.3 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of thorax,1211,C49.3,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.3,ORPHAcode: 466962 SMARCA4-deficient sarcoma of thorax +C49.3 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of thorax,1211,C49.3,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.3,ORPHAcode: 466962 SMARCA4-deficient sarcoma of thorax,ICD-10 C49.4 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of abdomen,1212,C49.4,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.4,,ICD-10 C49.5 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of pelvis,1213,C49.5,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.5,,ICD-10 "C49.6 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue of trunk, unspecified",1214,C49.6,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.6,,ICD-10 C49.8 Malignant neoplasm of other connective and soft tissue - Overlapping lesion of connective and soft tissue,1215,C49.8,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.8,,ICD-10 -"C49.9 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue, unspecified",1216,C49.9,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.9,ORPHAcode: 780 Rhabdomyosarcoma +"C49.9 Malignant neoplasm of other connective and soft tissue - Connective and soft tissue, unspecified",1216,C49.9,C45-C49 Malignant neoplasms of mesothelial and soft tissue,http://identifiers.org/icd/C49.9,ORPHAcode: 780 Rhabdomyosarcoma,ICD-10 C50-C50 Malignant neoplasm of breast,1217,C50-C50,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 -C50 Malignant neoplasm of breast,1218,C50,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50,ORPHAcode: 145 Hereditary breast and ovarian cancer syndrome -C50.0 Malignant neoplasm of breast - Nipple and areola,1219,C50.0,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.0,ORPHAcode: 180275 Paget disease of the nipple -C50.1 Malignant neoplasm of breast - Central portion of breast,1220,C50.1,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.1,ORPHAcode: 227535 Hereditary breast cancer +C50 Malignant neoplasm of breast,1218,C50,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50,ORPHAcode: 145 Hereditary breast and ovarian cancer syndrome,ICD-10 +C50.0 Malignant neoplasm of breast - Nipple and areola,1219,C50.0,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.0,ORPHAcode: 180275 Paget disease of the nipple,ICD-10 +C50.1 Malignant neoplasm of breast - Central portion of breast,1220,C50.1,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.1,ORPHAcode: 227535 Hereditary breast cancer,ICD-10 C50.2 Malignant neoplasm of breast - Upper-inner quadrant of breast,1221,C50.2,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.2,,ICD-10 C50.3 Malignant neoplasm of breast - Lower-inner quadrant of breast,1222,C50.3,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.3,,ICD-10 C50.4 Malignant neoplasm of breast - Upper-outer quadrant of breast,1223,C50.4,C50-C50 Malignant neoplasm of breast,http://identifiers.org/icd/C50.4,,ICD-10 @@ -1232,23 +1232,23 @@ C51.1 Malignant neoplasm of vulva - Labium minus,1230,C51.1,C51-C58 Malignant ne C51.2 Malignant neoplasm of vulva - Clitoris,1231,C51.2,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C51.2,,ICD-10 C51.8 Malignant neoplasm of vulva - Overlapping lesion of vulva,1232,C51.8,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C51.8,,ICD-10 "C51.9 Malignant neoplasm of vulva - Vulva, unspecified",1233,C51.9,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C51.9,,ICD-10 -C52 Malignant neoplasm of vagina,1234,C52,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C52,ORPHAcode: 180247 Vaginal carcinoma -C53 Malignant neoplasm of cervix uteri,1235,C53,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C53,ORPHAcode: 213787 Carcinosarcoma of the cervix uteri -C53.0 Malignant neoplasm of cervix uteri - Endocervix,1236,C53.0,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C53.0,ORPHAcode: 213767 Squamous cell carcinoma of the cervix uteri +C52 Malignant neoplasm of vagina,1234,C52,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C52,ORPHAcode: 180247 Vaginal carcinoma,ICD-10 +C53 Malignant neoplasm of cervix uteri,1235,C53,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C53,ORPHAcode: 213787 Carcinosarcoma of the cervix uteri,ICD-10 +C53.0 Malignant neoplasm of cervix uteri - Endocervix,1236,C53.0,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C53.0,ORPHAcode: 213767 Squamous cell carcinoma of the cervix uteri,ICD-10 C53.1 Malignant neoplasm of cervix uteri - Exocervix,1237,C53.1,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C53.1,,ICD-10 C53.8 Malignant neoplasm of cervix uteri - Overlapping lesion of cervix uteri,1238,C53.8,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C53.8,,ICD-10 "C53.9 Malignant neoplasm of cervix uteri - Cervix uteri, unspecified",1239,C53.9,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C53.9,,ICD-10 C54 Malignant neoplasm of corpus uteri,1240,C54,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54,,ICD-10 -C54.0 Malignant neoplasm of corpus uteri - Isthmus uteri,1241,C54.0,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.0,ORPHAcode: 213605 Carcinofibroma of the corpus uteri -C54.1 Malignant neoplasm of corpus uteri - Endometrium,1242,C54.1,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.1,ORPHAcode: 213574 Rare variants of adenocarcinoma of the corpus uteri -C54.2 Malignant neoplasm of corpus uteri - Myometrium,1243,C54.2,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.2,ORPHAcode: 213600 Adenosarcoma of the corpus uteri +C54.0 Malignant neoplasm of corpus uteri - Isthmus uteri,1241,C54.0,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.0,ORPHAcode: 213605 Carcinofibroma of the corpus uteri,ICD-10 +C54.1 Malignant neoplasm of corpus uteri - Endometrium,1242,C54.1,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.1,ORPHAcode: 213574 Rare variants of adenocarcinoma of the corpus uteri,ICD-10 +C54.2 Malignant neoplasm of corpus uteri - Myometrium,1243,C54.2,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.2,ORPHAcode: 213600 Adenosarcoma of the corpus uteri,ICD-10 C54.3 Malignant neoplasm of corpus uteri - Fundus uteri,1244,C54.3,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.3,,ICD-10 C54.8 Malignant neoplasm of corpus uteri - Overlapping lesion of corpus uteri,1245,C54.8,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.8,,ICD-10 -"C54.9 Malignant neoplasm of corpus uteri - Corpus uteri, unspecified",1246,C54.9,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.9,ORPHAcode: 213610 Carcinosarcoma of the corpus uteri +"C54.9 Malignant neoplasm of corpus uteri - Corpus uteri, unspecified",1246,C54.9,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C54.9,ORPHAcode: 213610 Carcinosarcoma of the corpus uteri,ICD-10 "C55 Malignant neoplasm of uterus, part unspecified",1247,C55,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C55,,ICD-10 -C56 Malignant neoplasm of ovary,1248,C56,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C56,ORPHAcode: 876 Yolk sac tumor +C56 Malignant neoplasm of ovary,1248,C56,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C56,ORPHAcode: 876 Yolk sac tumor,ICD-10 C57 Malignant neoplasm of other and unspecified female genital organs,1249,C57,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57,,ICD-10 -C57.0 Malignant neoplasm of other and unspecified female genital organs - Fallopian tube,1250,C57.0,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57.0,ORPHAcode: 180242 Malignant tumor of fallopian tubes +C57.0 Malignant neoplasm of other and unspecified female genital organs - Fallopian tube,1250,C57.0,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57.0,ORPHAcode: 180242 Malignant tumor of fallopian tubes,ICD-10 C57.1 Malignant neoplasm of other and unspecified female genital organs - Broad ligament,1251,C57.1,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57.1,,ICD-10 C57.2 Malignant neoplasm of other and unspecified female genital organs - Round ligament,1252,C57.2,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57.2,,ICD-10 C57.3 Malignant neoplasm of other and unspecified female genital organs - Parametrium,1253,C57.3,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57.3,,ICD-10 @@ -1257,35 +1257,35 @@ C57.7 Malignant neoplasm of other and unspecified female genital organs - Other C57.8 Malignant neoplasm of other and unspecified female genital organs - Overlapping lesion of female genital organs,1256,C57.8,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57.8,,ICD-10 K71 Toxic liver disease,1257,K71,K70-K77 Diseases of liver,http://identifiers.org/icd/K71,,ICD-10 "C57.9 Malignant neoplasm of other and unspecified female genital organs - Female genital organ, unspecified",1258,C57.9,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C57.9,,ICD-10 -C58 Malignant neoplasm of placenta,1259,C58,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C58,ORPHAcode: 99926 Gestational choriocarcinoma +C58 Malignant neoplasm of placenta,1259,C58,C51-C58 Malignant neoplasms of female genital organs,http://identifiers.org/icd/C58,ORPHAcode: 99926 Gestational choriocarcinoma,ICD-10 C60-C63 Malignant neoplasms of male genital organs,1260,C60-C63,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 C60 Malignant neoplasm of penis,1261,C60,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60,,ICD-10 C60.0 Malignant neoplasm of penis - Prepuce,1262,C60.0,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60.0,,ICD-10 -C60.1 Malignant neoplasm of penis - Glans penis,1263,C60.1,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60.1,ORPHAcode: 398053 Adenocarcinoma of the penis -C60.2 Malignant neoplasm of penis - Body of penis,1264,C60.2,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60.2,ORPHAcode: 398058 Squamous cell carcinoma of the penis +C60.1 Malignant neoplasm of penis - Glans penis,1263,C60.1,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60.1,ORPHAcode: 398053 Adenocarcinoma of the penis,ICD-10 +C60.2 Malignant neoplasm of penis - Body of penis,1264,C60.2,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60.2,ORPHAcode: 398058 Squamous cell carcinoma of the penis,ICD-10 C60.8 Malignant neoplasm of penis - Overlapping lesion of penis,1265,C60.8,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60.8,,ICD-10 "C60.9 Malignant neoplasm of penis - Penis, unspecified",1266,C60.9,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C60.9,,ICD-10 -C61 Malignant neoplasm of prostate,1267,C61,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C61,ORPHAcode: 1331 Familial prostate cancer +C61 Malignant neoplasm of prostate,1267,C61,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C61,ORPHAcode: 1331 Familial prostate cancer,ICD-10 C62 Malignant neoplasm of testis,1268,C62,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C62,,ICD-10 C62.0 Malignant neoplasm of testis - Undescended testis,1269,C62.0,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C62.0,,ICD-10 -C62.1 Malignant neoplasm of testis - Descended testis,1270,C62.1,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C62.1,ORPHAcode: 363489 Sex cord-stromal tumor of testis -"C62.9 Malignant neoplasm of testis - Testis, unspecified",1271,C62.9,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C62.9,ORPHAcode: 842 Testicular seminomatous germ cell tumor +C62.1 Malignant neoplasm of testis - Descended testis,1270,C62.1,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C62.1,ORPHAcode: 363489 Sex cord-stromal tumor of testis,ICD-10 +"C62.9 Malignant neoplasm of testis - Testis, unspecified",1271,C62.9,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C62.9,ORPHAcode: 842 Testicular seminomatous germ cell tumor,ICD-10 C63 Malignant neoplasm of other and unspecified male genital organs,1272,C63,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63,,ICD-10 C63.0 Malignant neoplasm of other and unspecified male genital organs - Epididymis,1273,C63.0,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63.0,,ICD-10 D05.0 Lobular carcinoma in situ,1274,D05.0,D00-D09 In situ neoplasms,http://identifiers.org/icd/D05.0,,ICD-10 -C63.1 Malignant neoplasm of other and unspecified male genital organs - Spermatic cord,1275,C63.1,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63.1,ORPHAcode: 363478 Paratesticular adenocarcinoma +C63.1 Malignant neoplasm of other and unspecified male genital organs - Spermatic cord,1275,C63.1,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63.1,ORPHAcode: 363478 Paratesticular adenocarcinoma,ICD-10 C63.2 Malignant neoplasm of other and unspecified male genital organs - Scrotum,1276,C63.2,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63.2,,ICD-10 C63.7 Malignant neoplasm of other and unspecified male genital organs - Other specified male genital organs,1277,C63.7,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63.7,,ICD-10 C63.8 Malignant neoplasm of other and unspecified male genital organs - Overlapping lesion of male genital organs,1278,C63.8,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63.8,,ICD-10 "C63.9 Malignant neoplasm of other and unspecified male genital organs - Male genital organ, unspecified",1279,C63.9,C60-C63 Malignant neoplasms of male genital organs,http://identifiers.org/icd/C63.9,,ICD-10 C64-C68 Malignant neoplasms of urinary tract,1280,C64-C68,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 -"C64 Malignant neoplasm of kidney, except renal pelvis",1281,C64,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C64,ORPHAcode: 523 Hereditary leiomyomatosis and renal cell cancer +"C64 Malignant neoplasm of kidney, except renal pelvis",1281,C64,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C64,ORPHAcode: 523 Hereditary leiomyomatosis and renal cell cancer,ICD-10 C65 Malignant neoplasm of renal pelvis,1282,C65,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C65,,ICD-10 C66 Malignant neoplasm of ureter,1283,C66,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C66,,ICD-10 C67 Malignant neoplasm of bladder,1284,C67,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67,,ICD-10 C67.0 Malignant neoplasm of bladder - Trigone of bladder,1285,C67.0,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.0,,ICD-10 -C67.1 Malignant neoplasm of bladder - Dome of bladder,1286,C67.1,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.1,ORPHAcode: 284400 Small cell carcinoma of the bladder -C67.2 Malignant neoplasm of bladder - Lateral wall of bladder,1287,C67.2,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.2,ORPHAcode: 209989 Non-papillary transitional cell carcinoma of the bladder +C67.1 Malignant neoplasm of bladder - Dome of bladder,1286,C67.1,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.1,ORPHAcode: 284400 Small cell carcinoma of the bladder,ICD-10 +C67.2 Malignant neoplasm of bladder - Lateral wall of bladder,1287,C67.2,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.2,ORPHAcode: 209989 Non-papillary transitional cell carcinoma of the bladder,ICD-10 C67.3 Malignant neoplasm of bladder - Anterior wall of bladder,1288,C67.3,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.3,,ICD-10 C67.4 Malignant neoplasm of bladder - Posterior wall of bladder,1289,C67.4,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.4,,ICD-10 C67.5 Malignant neoplasm of bladder - Bladder neck,1290,C67.5,C64-C68 Malignant neoplasms of urinary tract,http://identifiers.org/icd/C67.5,,ICD-10 @@ -1302,8 +1302,8 @@ C68.8 Malignant neoplasm of other and unspecified urinary organs - Overlapping l C69 Malignant neoplasm of eye and adnexa,1301,C69,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69,,ICD-10 C69.0 Malignant neoplasm of eye and adnexa - Conjunctiva,1302,C69.0,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.0,,ICD-10 C69.1 Malignant neoplasm of eye and adnexa - Cornea,1303,C69.1,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.1,,ICD-10 -C69.2 Malignant neoplasm of eye and adnexa - Retina,1304,C69.2,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.2,ORPHAcode: 790 Retinoblastoma -C69.3 Malignant neoplasm of eye and adnexa - Choroid,1305,C69.3,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.3,ORPHAcode: 39044 Uveal melanoma +C69.2 Malignant neoplasm of eye and adnexa - Retina,1304,C69.2,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.2,ORPHAcode: 790 Retinoblastoma,ICD-10 +C69.3 Malignant neoplasm of eye and adnexa - Choroid,1305,C69.3,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.3,ORPHAcode: 39044 Uveal melanoma,ICD-10 C69.4 Malignant neoplasm of eye and adnexa - Ciliary body,1306,C69.4,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.4,,ICD-10 C69.5 Malignant neoplasm of eye and adnexa - Lacrimal gland and duct,1307,C69.5,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.5,,ICD-10 C69.6 Malignant neoplasm of eye and adnexa - Orbit,1308,C69.6,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C69.6,,ICD-10 @@ -1312,18 +1312,18 @@ C69.8 Malignant neoplasm of eye and adnexa - Overlapping lesion of eye and adnex C70 Malignant neoplasm of meninges,1311,C70,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C70,,ICD-10 C70.0 Malignant neoplasm of meninges - Cerebral meninges,1312,C70.0,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C70.0,,ICD-10 C70.1 Malignant neoplasm of meninges - Spinal meninges,1313,C70.1,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C70.1,,ICD-10 -"C70.9 Malignant neoplasm of meninges - Meninges, unspecified",1314,C70.9,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C70.9,ORPHAcode: 252031 Diffuse leptomeningeal melanocytosis +"C70.9 Malignant neoplasm of meninges - Meninges, unspecified",1314,C70.9,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C70.9,ORPHAcode: 252031 Diffuse leptomeningeal melanocytosis,ICD-10 C71 Malignant neoplasm of brain,1315,C71,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71,,ICD-10 -"C71.0 Malignant neoplasm of brain - Cerebrum, except lobes and ventricles",1316,C71.0,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.0,ORPHAcode: 251582 Gliomatosis cerebri +"C71.0 Malignant neoplasm of brain - Cerebrum, except lobes and ventricles",1316,C71.0,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.0,ORPHAcode: 251582 Gliomatosis cerebri,ICD-10 C71.1 Malignant neoplasm of brain - Frontal lobe,1317,C71.1,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.1,,ICD-10 -C71.2 Malignant neoplasm of brain - Temporal lobe,1318,C71.2,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.2,ORPHAcode: 252015 Choriocarcinoma of the central nervous system +C71.2 Malignant neoplasm of brain - Temporal lobe,1318,C71.2,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.2,ORPHAcode: 252015 Choriocarcinoma of the central nervous system,ICD-10 C71.3 Malignant neoplasm of brain - Parietal lobe,1319,C71.3,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.3,,ICD-10 C71.4 Malignant neoplasm of brain - Occipital lobe,1320,C71.4,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.4,,ICD-10 -C71.5 Malignant neoplasm of brain - Cerebral ventricle,1321,C71.5,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.5,ORPHAcode: 251902 Atypical papilloma of choroid plexus -C71.6 Malignant neoplasm of brain - Cerebellum,1322,C71.6,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.6,ORPHAcode: 616 Medulloblastoma -C71.7 Malignant neoplasm of brain - Brain stem,1323,C71.7,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.7,ORPHAcode: 251899 Choroid plexus carcinoma +C71.5 Malignant neoplasm of brain - Cerebral ventricle,1321,C71.5,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.5,ORPHAcode: 251902 Atypical papilloma of choroid plexus,ICD-10 +C71.6 Malignant neoplasm of brain - Cerebellum,1322,C71.6,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.6,ORPHAcode: 616 Medulloblastoma,ICD-10 +C71.7 Malignant neoplasm of brain - Brain stem,1323,C71.7,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.7,ORPHAcode: 251899 Choroid plexus carcinoma,ICD-10 C71.8 Malignant neoplasm of brain - Overlapping lesion of brain,1324,C71.8,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.8,,ICD-10 -"C71.9 Malignant neoplasm of brain - Brain, unspecified",1325,C71.9,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.9,ORPHAcode: 360 Glioblastoma +"C71.9 Malignant neoplasm of brain - Brain, unspecified",1325,C71.9,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C71.9,ORPHAcode: 360 Glioblastoma,ICD-10 "C72 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system",1326,C72,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72,,ICD-10 "C72.0 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Spinal cord",1327,C72.0,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.0,,ICD-10 "C72.1 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Cauda equina",1328,C72.1,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.1,,ICD-10 @@ -1331,20 +1331,20 @@ C71.8 Malignant neoplasm of brain - Overlapping lesion of brain,1324,C71.8,"C69- "C72.3 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Optic nerve",1330,C72.3,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.3,,ICD-10 "C72.4 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Acoustic nerve",1331,C72.4,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.4,,ICD-10 "C72.5 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Other and unspecified cranial nerves",1332,C72.5,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.5,,ICD-10 -"C72.8 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Overlapping lesion of brain and other parts of central nervous system",1333,C72.8,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.8,ORPHAcode: 1672 Diencephalic syndrome +"C72.8 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Overlapping lesion of brain and other parts of central nervous system",1333,C72.8,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.8,ORPHAcode: 1672 Diencephalic syndrome,ICD-10 "C75.8 Malignant neoplasm of other endocrine glands and related structures - Pluriglandular involvement, unspecified",1334,C75.8,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.8,,ICD-10 -"C72.9 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Central nervous system, unspecified",1335,C72.9,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.9,ORPHAcode: 251883 Medulloepithelioma of the central nervous system +"C72.9 Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system - Central nervous system, unspecified",1335,C72.9,"C69-C72 Malignant neoplasms of eye, brain and other parts of central nervous system",http://identifiers.org/icd/C72.9,ORPHAcode: 251883 Medulloepithelioma of the central nervous system,ICD-10 C73-C75 Malignant neoplasms of thyroid and other endocrine glands,1336,C73-C75,"C00-C75 Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic and related tissue",,,ICD-10 -C73 Malignant neoplasm of thyroid gland,1337,C73,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C73,ORPHAcode: 142 Anaplastic thyroid carcinoma +C73 Malignant neoplasm of thyroid gland,1337,C73,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C73,ORPHAcode: 142 Anaplastic thyroid carcinoma,ICD-10 C74 Malignant neoplasm of adrenal gland,1338,C74,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C74,,ICD-10 -C74.0 Malignant neoplasm of adrenal gland - Cortex of adrenal gland,1339,C74.0,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C74.0,ORPHAcode: 1501 Adrenocortical carcinoma -C74.1 Malignant neoplasm of adrenal gland - Medulla of adrenal gland,1340,C74.1,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C74.1,ORPHAcode: 29072 Hereditary pheochromocytoma-paraganglioma -"C74.9 Malignant neoplasm of adrenal gland - Adrenal gland, unspecified",1341,C74.9,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C74.9,ORPHAcode: 635 Neuroblastoma +C74.0 Malignant neoplasm of adrenal gland - Cortex of adrenal gland,1339,C74.0,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C74.0,ORPHAcode: 1501 Adrenocortical carcinoma,ICD-10 +C74.1 Malignant neoplasm of adrenal gland - Medulla of adrenal gland,1340,C74.1,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C74.1,ORPHAcode: 29072 Hereditary pheochromocytoma-paraganglioma,ICD-10 +"C74.9 Malignant neoplasm of adrenal gland - Adrenal gland, unspecified",1341,C74.9,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C74.9,ORPHAcode: 635 Neuroblastoma,ICD-10 C75 Malignant neoplasm of other endocrine glands and related structures,1342,C75,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75,,ICD-10 -C75.0 Malignant neoplasm of other endocrine glands and related structures - Parathyroid gland,1343,C75.0,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.0,ORPHAcode: 143 Parathyroid carcinoma -C75.1 Malignant neoplasm of other endocrine glands and related structures - Pituitary gland,1344,C75.1,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.1,ORPHAcode: 300385 Pituitary carcinoma +C75.0 Malignant neoplasm of other endocrine glands and related structures - Parathyroid gland,1343,C75.0,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.0,ORPHAcode: 143 Parathyroid carcinoma,ICD-10 +C75.1 Malignant neoplasm of other endocrine glands and related structures - Pituitary gland,1344,C75.1,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.1,ORPHAcode: 300385 Pituitary carcinoma,ICD-10 C75.2 Malignant neoplasm of other endocrine glands and related structures - Craniopharyngeal duct,1345,C75.2,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.2,,ICD-10 -C75.3 Malignant neoplasm of other endocrine glands and related structures - Pineal gland,1346,C75.3,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.3,ORPHAcode: 251909 Pineoblastoma +C75.3 Malignant neoplasm of other endocrine glands and related structures - Pineal gland,1346,C75.3,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.3,ORPHAcode: 251909 Pineoblastoma,ICD-10 C75.4 Malignant neoplasm of other endocrine glands and related structures - Carotid body,1347,C75.4,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.4,,ICD-10 C75.5 Malignant neoplasm of other endocrine glands and related structures - Aortic body and other paraganglia,1348,C75.5,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.5,,ICD-10 "C75.9 Malignant neoplasm of other endocrine glands and related structures - Endocrine gland, unspecified",1349,C75.9,C73-C75 Malignant neoplasms of thyroid and other endocrine glands,http://identifiers.org/icd/C75.9,,ICD-10 @@ -1356,7 +1356,7 @@ C76.2 Malignant neoplasm of other and ill-defined sites - Abdomen,1354,C76.2,"C7 C76.3 Malignant neoplasm of other and ill-defined sites - Pelvis,1355,C76.3,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C76.3,,ICD-10 C76.4 Malignant neoplasm of other and ill-defined sites - Upper limb,1356,C76.4,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C76.4,,ICD-10 C76.5 Malignant neoplasm of other and ill-defined sites - Lower limb,1357,C76.5,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C76.5,,ICD-10 -C76.7 Malignant neoplasm of other and ill-defined sites - Other ill-defined sites,1358,C76.7,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C76.7,ORPHAcode: 178 Chordoma +C76.7 Malignant neoplasm of other and ill-defined sites - Other ill-defined sites,1358,C76.7,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C76.7,ORPHAcode: 178 Chordoma,ICD-10 C76.8 Malignant neoplasm of other and ill-defined sites - Overlapping lesion of other and ill-defined sites,1359,C76.8,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C76.8,,ICD-10 C77 Secondary and unspecified malignant neoplasm of lymph nodes,1360,C77,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C77,,ICD-10 "C77.0 Secondary and unspecified malignant neoplasm of lymph nodes - Lymph nodes of head, face and neck",1361,C77.0,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C77.0,,ICD-10 @@ -1375,7 +1375,7 @@ C78.2 Secondary malignant neoplasm of pleura,1373,C78.2,"C76-C80 Malignant neopl C78.3 Secondary malignant neoplasm of other and unspecified respiratory organs,1374,C78.3,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C78.3,,ICD-10 C78.4 Secondary malignant neoplasm of small intestine,1375,C78.4,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C78.4,,ICD-10 C78.5 Secondary malignant neoplasm of large intestine and rectum,1376,C78.5,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C78.5,,ICD-10 -C78.6 Secondary malignant neoplasm of retroperitoneum and peritoneum,1377,C78.6,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C78.6,ORPHAcode: 26790 Pseudomyxoma peritonei +C78.6 Secondary malignant neoplasm of retroperitoneum and peritoneum,1377,C78.6,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C78.6,ORPHAcode: 26790 Pseudomyxoma peritonei,ICD-10 C78.7 Secondary malignant neoplasm of liver and intrahepatic bile duct,1378,C78.7,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C78.7,,ICD-10 C78.8 Secondary malignant neoplasm of other and unspecified digestive organs,1379,C78.8,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C78.8,,ICD-10 C79 Secondary malignant neoplasm of other and unspecified sites,1380,C79,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C79,,ICD-10 @@ -1391,121 +1391,121 @@ C79.8 Secondary malignant neoplasm of other specified sites,1389,C79.8,"C76-C80 "C79.9 Secondary malignant neoplasm, unspecified site",1390,C79.9,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C79.9,,ICD-10 "C80 Malignant neoplasm, without specification of site",1391,C80,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C80,,ICD-10 "C80.0 Malignant neoplasm, primary site unknown, so stated",1392,C80.0,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C80.0,,ICD-10 -"C80.9 Malignant neoplasm, primary site unspecified",1393,C80.9,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C80.9,ORPHAcode: 180229 Polyembryoma +"C80.9 Malignant neoplasm, primary site unspecified",1393,C80.9,"C76-C80 Malignant neoplasms of ill-defined, secondary and unspecified sites",http://identifiers.org/icd/C80.9,ORPHAcode: 180229 Polyembryoma,ICD-10 "C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",1394,C81-C96,C00-C97 Malignant neoplasms,,,ICD-10 -C81.0 Nodular lymphocyte predominant Hodgkin lymphoma,1395,C81.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.0,ORPHAcode: 86893 Nodular lymphocyte predominant Hodgkin lymphoma +C81.0 Nodular lymphocyte predominant Hodgkin lymphoma,1395,C81.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.0,ORPHAcode: 86893 Nodular lymphocyte predominant Hodgkin lymphoma,ICD-10 C81.1 Nodular sclerosis (classical) Hodgkin lymphoma,1396,C81.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.1,,ICD-10 C81.2 Mixed cellularity (classical) Hodgkin lymphoma,1397,C81.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.2,,ICD-10 C81.3 Lymphocyte depleted (classical) Hodgkin lymphoma,1398,C81.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.3,,ICD-10 C81.4 Lymphocyte-rich (classical) Hodgkin lymphoma,1399,C81.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.4,,ICD-10 -C81.7 Other (classical) Hodgkin lymphoma,1400,C81.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.7,ORPHAcode: 391 Classic Hodgkin lymphoma +C81.7 Other (classical) Hodgkin lymphoma,1400,C81.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.7,ORPHAcode: 391 Classic Hodgkin lymphoma,ICD-10 "C81.9 Hodgkin lymphoma, unspecified",1401,C81.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C81.9,,ICD-10 C82 Follicular lymphoma,1402,C82,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82,,ICD-10 C82.0 Follicular lymphoma grade I,1403,C82.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.0,,ICD-10 -C82.1 Follicular lymphoma grade II,1404,C82.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.1,ORPHAcode: 545 Follicular lymphoma +C82.1 Follicular lymphoma grade II,1404,C82.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.1,ORPHAcode: 545 Follicular lymphoma,ICD-10 "C82.2 Follicular lymphoma grade III, unspecified",1405,C82.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.2,,ICD-10 C82.3 Follicular lymphoma grade IIIa,1406,C82.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.3,,ICD-10 C82.4 Follicular lymphoma grade IIIb,1407,C82.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.4,,ICD-10 C82.5 Diffuse follicle centre lymphoma,1408,C82.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.5,,ICD-10 D05.1 Intraductal carcinoma in situ,1409,D05.1,D00-D09 In situ neoplasms,http://identifiers.org/icd/D05.1,,ICD-10 -C82.6 Cutaneous follicle centre lymphoma,1410,C82.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.6,ORPHAcode: 178540 Primary cutaneous follicle center lymphoma +C82.6 Cutaneous follicle centre lymphoma,1410,C82.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.6,ORPHAcode: 178540 Primary cutaneous follicle center lymphoma,ICD-10 C82.7 Other types of follicular lymphoma,1411,C82.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.7,,ICD-10 "C82.9 Follicular lymphoma, unspecified",1412,C82.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C82.9,,ICD-10 C83 Non-follicular lymphoma,1413,C83,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83,,ICD-10 -C83.0 Small cell B-cell lymphoma,1414,C83.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.0,ORPHAcode: 86854 Splenic marginal zone lymphoma -C83.1 Mantle cell lymphoma,1415,C83.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.1,ORPHAcode: 52416 Mantle cell lymphoma -C83.3 Diffuse large B-cell lymphoma,1416,C83.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.3,ORPHAcode: 46135 Primary central nervous system lymphoma +C83.0 Small cell B-cell lymphoma,1414,C83.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.0,ORPHAcode: 86854 Splenic marginal zone lymphoma,ICD-10 +C83.1 Mantle cell lymphoma,1415,C83.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.1,ORPHAcode: 52416 Mantle cell lymphoma,ICD-10 +C83.3 Diffuse large B-cell lymphoma,1416,C83.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.3,ORPHAcode: 46135 Primary central nervous system lymphoma,ICD-10 C83.5 Lymphoblastic (diffuse) lymphoma,1417,C83.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.5,,ICD-10 -C83.7 Burkitt lymphoma,1418,C83.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.7,ORPHAcode: 543 Burkitt lymphoma -C83.8 Other non-follicular lymphoma,1419,C83.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.8,ORPHAcode: 48686 Primary effusion lymphoma +C83.7 Burkitt lymphoma,1418,C83.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.7,ORPHAcode: 543 Burkitt lymphoma,ICD-10 +C83.8 Other non-follicular lymphoma,1419,C83.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.8,ORPHAcode: 48686 Primary effusion lymphoma,ICD-10 "C83.9 Non-follicular (diffuse) lymphoma, unspecified",1420,C83.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C83.9,,ICD-10 C84 Mature T/NK-cell lymphomas,1421,C84,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84,,ICD-10 -C84.0 Mature T/NK-cell lymphomas - Mycosis fungoides,1422,C84.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.0,ORPHAcode: 2584 Classic mycosis fungoides -C84.1 Sézary diseas,1423,C84.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.1,ORPHAcode: 3162 S zary sy -"C84.4 Mature T/NK-cell lymphomas - Peripheral T-cell lymphoma, not elsewhere classified",1424,C84.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.4,ORPHAcode: 86885 Primary cutaneous peripheral T-cell lymphoma not otherwise specified -C84.5 Other mature T/NK-cell lymphomas,1425,C84.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.5,ORPHAcode: 178528 Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma -"C84.6 Mature T/NK-cell lymphomas - Anaplastic large cell lymphoma, ALK-positive",1426,C84.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.6,ORPHAcode: 98841 Anaplastic large cell lymphoma +C84.0 Mature T/NK-cell lymphomas - Mycosis fungoides,1422,C84.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.0,ORPHAcode: 2584 Classic mycosis fungoides,ICD-10 +C84.1 Sézary diseas,1423,C84.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.1,ORPHAcode: 3162 S zary sy,ICD-10 +"C84.4 Mature T/NK-cell lymphomas - Peripheral T-cell lymphoma, not elsewhere classified",1424,C84.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.4,ORPHAcode: 86885 Primary cutaneous peripheral T-cell lymphoma not otherwise specified,ICD-10 +C84.5 Other mature T/NK-cell lymphomas,1425,C84.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.5,ORPHAcode: 178528 Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma,ICD-10 +"C84.6 Mature T/NK-cell lymphomas - Anaplastic large cell lymphoma, ALK-positive",1426,C84.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.6,ORPHAcode: 98841 Anaplastic large cell lymphoma,ICD-10 "C84.7 Mature T/NK-cell lymphomas - Anaplastic large cell lymphoma, ALK-negative",1427,C84.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.7,,ICD-10 "C84.8 Mature T/NK-cell lymphomas - Cutaneous T-cell lymphoma, unspecified",1428,C84.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.8,,ICD-10 "C84.9 Mature T/NK-cell lymphoma, unspecified",1429,C84.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C84.9,,ICD-10 C85 Other and unspecified types of non-Hodgkin lymphoma,1430,C85,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C85,,ICD-10 "C85.1 B-cell lymphoma, unspecified",1431,C85.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C85.1,,ICD-10 C85.2 Mediastinal (thymic) large B-cell lymphoma,1432,C85.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C85.2,,ICD-10 -C85.7 Other specified types of non-Hodgkin lymphoma,1433,C85.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C85.7,ORPHAcode: 2420 Primary pulmonary lymphoma +C85.7 Other specified types of non-Hodgkin lymphoma,1433,C85.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C85.7,ORPHAcode: 2420 Primary pulmonary lymphoma,ICD-10 "C85.9 Non-Hodgkin lymphoma, unspecified",1434,C85.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C85.9,,ICD-10 C86 Other specified types of T/NK-cell lymphoma,1435,C86,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86,,ICD-10 -"C86.0 Extranodal NK/T-cell lymphoma, nasal type",1436,C86.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.0,ORPHAcode: 86879 Extranodal nasal NK/T cell lymphoma -C86.1 Hepatosplenic T-cell lymphoma,1437,C86.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.1,ORPHAcode: 86882 Hepatosplenic T-cell lymphoma -C86.2 Enteropathy-type (intestinal) T-cell lymphoma,1438,C86.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.2,ORPHAcode: 86880 Enteropathy-associated T-cell lymphoma +"C86.0 Extranodal NK/T-cell lymphoma, nasal type",1436,C86.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.0,ORPHAcode: 86879 Extranodal nasal NK/T cell lymphoma,ICD-10 +C86.1 Hepatosplenic T-cell lymphoma,1437,C86.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.1,ORPHAcode: 86882 Hepatosplenic T-cell lymphoma,ICD-10 +C86.2 Enteropathy-type (intestinal) T-cell lymphoma,1438,C86.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.2,ORPHAcode: 86880 Enteropathy-associated T-cell lymphoma,ICD-10 C86.3 Subcutaneous panniculitis-like T-cell lymphoma,1439,C86.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.3,,ICD-10 -C86.4 Blastic NK-cell lymphoma,1440,C86.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.4,ORPHAcode: 86870 CD4+/CD56+ hematodermic neoplasm -C86.5 Angioimmunoblastic T-cell lymphoma,1441,C86.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.5,ORPHAcode: 86886 Angioimmunoblastic T-cell lymphoma -C86.6 Other specified types of T/NK-cell lymphoma - Primary cutaneous CD30-positive T-cell proliferations,1442,C86.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.6,ORPHAcode: 98842 Lymphomatoid papulosis +C86.4 Blastic NK-cell lymphoma,1440,C86.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.4,ORPHAcode: 86870 CD4+/CD56+ hematodermic neoplasm,ICD-10 +C86.5 Angioimmunoblastic T-cell lymphoma,1441,C86.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.5,ORPHAcode: 86886 Angioimmunoblastic T-cell lymphoma,ICD-10 +C86.6 Other specified types of T/NK-cell lymphoma - Primary cutaneous CD30-positive T-cell proliferations,1442,C86.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C86.6,ORPHAcode: 98842 Lymphomatoid papulosis,ICD-10 C88 Malignant immunoproliferative diseases,1443,C88,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88,,ICD-10 -C88.0 Waldenström macroglobulinaemi,1444,C88.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.0,ORPHAcode: 33226 Waldenstr m macroglobul -C88.2 Malignant immunoproliferative diseases - Other heavy chain disease,1445,C88.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.2,ORPHAcode: 86864 Heavy chain disease +C88.0 Waldenström macroglobulinaemi,1444,C88.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.0,ORPHAcode: 33226 Waldenstr m macroglobul,ICD-10 +C88.2 Malignant immunoproliferative diseases - Other heavy chain disease,1445,C88.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.2,ORPHAcode: 86864 Heavy chain disease,ICD-10 C88.3 Immunoproliferative small intestinal disease,1446,C88.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.3,,ICD-10 -C88.4 Malignant immunoproliferative diseases - Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue [MALT-lyphoma],1447,C88.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.4,ORPHAcode: 52417 MALT lymphoma +C88.4 Malignant immunoproliferative diseases - Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue [MALT-lyphoma],1447,C88.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.4,ORPHAcode: 52417 MALT lymphoma,ICD-10 C88.7 Other malignant immunoproliferative diseases,1448,C88.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.7,,ICD-10 D02.0 Carcinoma in situ of middle ear and respiratory system - Larynx,1449,D02.0,D00-D09 In situ neoplasms,http://identifiers.org/icd/D02.0,,ICD-10 "C88.9 Malignant immunoproliferative disease, unspecified",1450,C88.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C88.9,,ICD-10 C90 Multiple myeloma and malignant plasma cell neoplasms,1451,C90,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90,,ICD-10 -C90.0 Multiple myeloma,1452,C90.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90.0,ORPHAcode: 29073 Multiple myeloma -C90.1 Plasma cell leukaemia,1453,C90.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90.1,ORPHAcode: 454714 Plasma cell leukemia -C90.2 Extramedullary plasmacytoma,1454,C90.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90.2,ORPHAcode: 86855 Plasmacytoma +C90.0 Multiple myeloma,1452,C90.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90.0,ORPHAcode: 29073 Multiple myeloma,ICD-10 +C90.1 Plasma cell leukaemia,1453,C90.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90.1,ORPHAcode: 454714 Plasma cell leukemia,ICD-10 +C90.2 Extramedullary plasmacytoma,1454,C90.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90.2,ORPHAcode: 86855 Plasmacytoma,ICD-10 C90.3 Solitary plasmacytoma,1455,C90.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C90.3,,ICD-10 C91 Lymphoid leukaemia,1456,C91,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91,,ICD-10 -C91.0 Acute lymphoblastic leukaemia [ALL],1457,C91.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.0,ORPHAcode: 99860 Precursor B-cell acute lymphoblastic leukemia -C91.1 Chronic lymphocytic leukaemia of B-cell type,1458,C91.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.1,ORPHAcode: 67038 B-cell chronic lymphocytic leukemia -C91.3 Prolymphocytic leukaemia of B-cell type,1459,C91.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.3,ORPHAcode: 86852 B-cell prolymphocytic leukemia -C91.4 Hairy-cell leukaemia,1460,C91.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.4,ORPHAcode: 58017 Classic hairy cell leukemia -C91.5 Adult T-cell lymphoma/leukaemia [HTLV-1-associated],1461,C91.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.5,ORPHAcode: 86875 Adult T-cell leukemia/lymphoma -C91.6 Prolymphocytic leukaemia of T-cell type,1462,C91.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.6,ORPHAcode: 86871 T-cell prolymphocytic leukemia +C91.0 Acute lymphoblastic leukaemia [ALL],1457,C91.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.0,ORPHAcode: 99860 Precursor B-cell acute lymphoblastic leukemia,ICD-10 +C91.1 Chronic lymphocytic leukaemia of B-cell type,1458,C91.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.1,ORPHAcode: 67038 B-cell chronic lymphocytic leukemia,ICD-10 +C91.3 Prolymphocytic leukaemia of B-cell type,1459,C91.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.3,ORPHAcode: 86852 B-cell prolymphocytic leukemia,ICD-10 +C91.4 Hairy-cell leukaemia,1460,C91.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.4,ORPHAcode: 58017 Classic hairy cell leukemia,ICD-10 +C91.5 Adult T-cell lymphoma/leukaemia [HTLV-1-associated],1461,C91.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.5,ORPHAcode: 86875 Adult T-cell leukemia/lymphoma,ICD-10 +C91.6 Prolymphocytic leukaemia of T-cell type,1462,C91.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.6,ORPHAcode: 86871 T-cell prolymphocytic leukemia,ICD-10 D02.1 Carcinoma in situ of middle ear and respiratory system - Trachea,1463,D02.1,D00-D09 In situ neoplasms,http://identifiers.org/icd/D02.1,,ICD-10 -C91.7 Other lymphoid leukaemia,1464,C91.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.7,ORPHAcode: 86872 T-cell large granular lymphocyte leukemia +C91.7 Other lymphoid leukaemia,1464,C91.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.7,ORPHAcode: 86872 T-cell large granular lymphocyte leukemia,ICD-10 C91.8 Mature B-cell leukaemia Burkitt-type,1465,C91.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.8,,ICD-10 "C91.9 Lymphoid leukaemia, unspecified",1466,C91.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C91.9,,ICD-10 C92 Myeloid leukaemia,1467,C92,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92,,ICD-10 -C92.0 Acute myeloblastic leukaemia [AML],1468,C92.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.0,ORPHAcode: 98832 Acute myeloid leukemia with minimal differentiation -"C92.1 Chronic myeloid leukaemia [CML], BCR/ABL-positive",1469,C92.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.1,ORPHAcode: 521 Chronic myeloid leukemia -"C92.2 Atypical chronic myeloid leukaemia, BCR/ABL- negative",1470,C92.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.2,ORPHAcode: 98824 Atypical chronic myeloid leukemia -C92.3 Myeloid sarcoma,1471,C92.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.3,ORPHAcode: 86850 Myeloid sarcoma -C92.4 Acute promyelocytic leukaemia [PML],1472,C92.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.4,ORPHAcode: 520 Acute promyelocytic leukemia -C92.5 Acute myelomonocytic leukaemia,1473,C92.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.5,ORPHAcode: 517 Acute myelomonocytic leukemia -C92.6 Acute myeloid leukaemia with 11q23-abnormality,1474,C92.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.6,ORPHAcode: 98831 Acute myeloid leukemia with 11q23 abnormalities -C92.7 Other myeloid leukaemia,1475,C92.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.7,ORPHAcode: 514 Acute monoblastic/monocytic leukemia -C92.8 Acute myeloid leukaemia with multilineage dysplasia,1476,C92.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.8,ORPHAcode: 86845 Acute myeloid leukaemia with myelodysplasia-related features +C92.0 Acute myeloblastic leukaemia [AML],1468,C92.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.0,ORPHAcode: 98832 Acute myeloid leukemia with minimal differentiation,ICD-10 +"C92.1 Chronic myeloid leukaemia [CML], BCR/ABL-positive",1469,C92.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.1,ORPHAcode: 521 Chronic myeloid leukemia,ICD-10 +"C92.2 Atypical chronic myeloid leukaemia, BCR/ABL- negative",1470,C92.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.2,ORPHAcode: 98824 Atypical chronic myeloid leukemia,ICD-10 +C92.3 Myeloid sarcoma,1471,C92.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.3,ORPHAcode: 86850 Myeloid sarcoma,ICD-10 +C92.4 Acute promyelocytic leukaemia [PML],1472,C92.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.4,ORPHAcode: 520 Acute promyelocytic leukemia,ICD-10 +C92.5 Acute myelomonocytic leukaemia,1473,C92.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.5,ORPHAcode: 517 Acute myelomonocytic leukemia,ICD-10 +C92.6 Acute myeloid leukaemia with 11q23-abnormality,1474,C92.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.6,ORPHAcode: 98831 Acute myeloid leukemia with 11q23 abnormalities,ICD-10 +C92.7 Other myeloid leukaemia,1475,C92.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.7,ORPHAcode: 514 Acute monoblastic/monocytic leukemia,ICD-10 +C92.8 Acute myeloid leukaemia with multilineage dysplasia,1476,C92.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.8,ORPHAcode: 86845 Acute myeloid leukaemia with myelodysplasia-related features,ICD-10 "C92.9 Myeloid leukaemia, unspecified",1477,C92.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C92.9,,ICD-10 C93 Monocytic leukaemia,1478,C93,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93,,ICD-10 C93.0 Acute monoblastic/monocytic leukaemia,1479,C93.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93.0,,ICD-10 -C93.1 Chronic myelomonocytic leukaemia,1480,C93.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93.1,ORPHAcode: 98823 Chronic myelomonocytic leukemia -C93.3 Juvenile myelomonocytic leukaemia,1481,C93.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93.3,ORPHAcode: 86834 Juvenile myelomonocytic leukemia +C93.1 Chronic myelomonocytic leukaemia,1480,C93.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93.1,ORPHAcode: 98823 Chronic myelomonocytic leukemia,ICD-10 +C93.3 Juvenile myelomonocytic leukaemia,1481,C93.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93.3,ORPHAcode: 86834 Juvenile myelomonocytic leukemia,ICD-10 C93.7 Other monocytic leukaemia,1482,C93.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93.7,,ICD-10 "C93.9 Monocytic leukaemia, unspecified",1483,C93.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C93.9,,ICD-10 C94 Other leukaemias of specified cell type,1484,C94,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94,,ICD-10 -C94.0 Other leukaemias of specified cell type - Acute erythroid leukaemia,1485,C94.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.0,ORPHAcode: 318 Acute erythroid leukemia -C94.2 Other leukaemias of specified cell type - Acute megakaryoblastic leukaemia,1486,C94.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.2,ORPHAcode: 518 Acute megakaryoblastic leukemia -C94.3 Mast cell leukaemia,1487,C94.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.3,ORPHAcode: 98851 Mast cell leukemia -C94.4 Acute panmyelosis with myelofibrosis,1488,C94.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.4,ORPHAcode: 86843 Acute panmyelosis with myelofibrosis -"C94.6 Other leukaemias of specified cell type - Myelodysplastic and myeloproliferative disease, not elsewhere classified",1489,C94.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.6,ORPHAcode: 98825 Unclassified myelodysplastic/myeloproliferative disease +C94.0 Other leukaemias of specified cell type - Acute erythroid leukaemia,1485,C94.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.0,ORPHAcode: 318 Acute erythroid leukemia,ICD-10 +C94.2 Other leukaemias of specified cell type - Acute megakaryoblastic leukaemia,1486,C94.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.2,ORPHAcode: 518 Acute megakaryoblastic leukemia,ICD-10 +C94.3 Mast cell leukaemia,1487,C94.3,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.3,ORPHAcode: 98851 Mast cell leukemia,ICD-10 +C94.4 Acute panmyelosis with myelofibrosis,1488,C94.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.4,ORPHAcode: 86843 Acute panmyelosis with myelofibrosis,ICD-10 +"C94.6 Other leukaemias of specified cell type - Myelodysplastic and myeloproliferative disease, not elsewhere classified",1489,C94.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.6,ORPHAcode: 98825 Unclassified myelodysplastic/myeloproliferative disease,ICD-10 L50-L54 Urticaria and erythema,1490,,XII Diseases of the skin and subcutaneous tissue,,,ICD-10 -C94.7 Other specified leukaemias,1491,C94.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.7,ORPHAcode: 86849 Acute basophilic leukemia +C94.7 Other specified leukaemias,1491,C94.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C94.7,ORPHAcode: 86849 Acute basophilic leukemia,ICD-10 C95 Leukaemia of unspecified cell type,1492,C95,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C95,,ICD-10 -C95.0 Acute leukaemia of unspecified cell type,1493,C95.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C95.0,ORPHAcode: 98835 Acute undifferentiated leukemia +C95.0 Acute leukaemia of unspecified cell type,1493,C95.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C95.0,ORPHAcode: 98835 Acute undifferentiated leukemia,ICD-10 C95.1 Chronic leukaemia of unspecified cell type,1494,C95.1,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C95.1,,ICD-10 C95.7 Other leukaemia of unspecified cell type,1495,C95.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C95.7,,ICD-10 "C95.9 Leukaemia, unspecified",1496,C95.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C95.9,,ICD-10 "C96 Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue",1497,C96,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96,,ICD-10 -C96.0 Multifocal and multisystemic (disseminated) Langerhans-cell histiocytosis [Letterer-Siwe disease],1498,C96.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.0,ORPHAcode: 389 Langerhans cell histiocytosis -C96.2 Malignant mast cell tumour,1499,C96.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.2,ORPHAcode: 66661 Mast cell sarcoma -C96.4 Sarcoma of dendritic cells (accessory cells),1500,C96.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.4,ORPHAcode: 86897 Langerhans cell sarcoma +C96.0 Multifocal and multisystemic (disseminated) Langerhans-cell histiocytosis [Letterer-Siwe disease],1498,C96.0,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.0,ORPHAcode: 389 Langerhans cell histiocytosis,ICD-10 +C96.2 Malignant mast cell tumour,1499,C96.2,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.2,ORPHAcode: 66661 Mast cell sarcoma,ICD-10 +C96.4 Sarcoma of dendritic cells (accessory cells),1500,C96.4,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.4,ORPHAcode: 86897 Langerhans cell sarcoma,ICD-10 C96.5 Multifocal and unisystemic Langerhans-cell histiocytosis,1501,C96.5,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.5,,ICD-10 "C96.6 Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue - Unifocal Langerhans-cell histiocytosis",1502,C96.6,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.6,,ICD-10 -"C96.7 Other specified malignant neoplasms of lymphoid, haematopoietic and related tissue",1503,C96.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.7,ORPHAcode: 488647 DDX41-related hematologic malignancy predisposition syndrome -"C96.8 Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue - Histiocytic sarcoma",1504,C96.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.8,ORPHAcode: 86896 Histiocytic sarcoma +"C96.7 Other specified malignant neoplasms of lymphoid, haematopoietic and related tissue",1503,C96.7,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.7,ORPHAcode: 488647 DDX41-related hematologic malignancy predisposition syndrome,ICD-10 +"C96.8 Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue - Histiocytic sarcoma",1504,C96.8,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.8,ORPHAcode: 86896 Histiocytic sarcoma,ICD-10 "C96.9 Malignant neoplasm of lymphoid, haematopoietic and related tissue, unspecified",1505,C96.9,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",http://identifiers.org/icd/C96.9,,ICD-10 C97-C97 Malignant neoplasms of independent (primary) multiple sites,1506,C97-C97,"C81-C96 Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue",,,ICD-10 -C97 Malignant neoplasms of independent (primary) multiple sites,1507,C97,C97-C97 Malignant neoplasms of independent (primary) multiple sites,http://identifiers.org/icd/C97,ORPHAcode: 524 Li-Fraumeni syndrome +C97 Malignant neoplasms of independent (primary) multiple sites,1507,C97,C97-C97 Malignant neoplasms of independent (primary) multiple sites,http://identifiers.org/icd/C97,ORPHAcode: 524 Li-Fraumeni syndrome,ICD-10 D00-D09 In situ neoplasms,1508,,II Neoplasms,,,ICD-10 "D00 Carcinoma in situ of oral cavity, oesophagus and stomach",1509,D00,D00-D09 In situ neoplasms,http://identifiers.org/icd/D00,,ICD-10 "D00.0 Lip, oral cavity and pharynx",1510,D00.0,D00-D09 In situ neoplasms,http://identifiers.org/icd/D00.0,,ICD-10 @@ -1516,12 +1516,12 @@ D01.0 Carcinoma in situ of other and unspecified digestive organs - Colon,1514,D D01.1 Carcinoma in situ of other and unspecified digestive organs - Rectosigmoid junction,1515,D01.1,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.1,,ICD-10 D01.2 Carcinoma in situ of other and unspecified digestive organs - Rectum,1516,D01.2,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.2,,ICD-10 D01.3 Anus and anal canal,1517,D01.3,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.3,,ICD-10 -D01.4 Other and unspecified parts of intestine,1518,D01.4,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.4,ORPHAcode: 104075 Adenocarcinoma of the small intestine +D01.4 Other and unspecified parts of intestine,1518,D01.4,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.4,ORPHAcode: 104075 Adenocarcinoma of the small intestine,ICD-10 "D01.5 Liver, gallbladder and bile ducts",1519,D01.5,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.5,,ICD-10 D01.7 Other specified digestive organs,1520,D01.7,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.7,,ICD-10 "D01.9 Digestive organ, unspecified",1521,D01.9,D00-D09 In situ neoplasms,http://identifiers.org/icd/D01.9,,ICD-10 D02 Carcinoma in situ of middle ear and respiratory system,1522,D02,D00-D09 In situ neoplasms,http://identifiers.org/icd/D02,,ICD-10 -D02.3 Other parts of respiratory system,1523,D02.3,D00-D09 In situ neoplasms,http://identifiers.org/icd/D02.3,ORPHAcode: 500464 Squamous cell carcinoma of the nasal cavity and paranasal sinuses +D02.3 Other parts of respiratory system,1523,D02.3,D00-D09 In situ neoplasms,http://identifiers.org/icd/D02.3,ORPHAcode: 500464 Squamous cell carcinoma of the nasal cavity and paranasal sinuses,ICD-10 "D02.4 Respiratory system, unspecified",1524,D02.4,D00-D09 In situ neoplasms,http://identifiers.org/icd/D02.4,,ICD-10 D03 Melanoma in situ,1525,D03,D00-D09 In situ neoplasms,http://identifiers.org/icd/D03,,ICD-10 D03.0 Melanoma in situ of lip,1526,D03.0,D00-D09 In situ neoplasms,http://identifiers.org/icd/D03.0,,ICD-10 @@ -1533,7 +1533,7 @@ D03.5 Melanoma in situ of trunk,1531,D03.5,D00-D09 In situ neoplasms,http://iden "D03.6 Melanoma in situ of upper limb, including shoulder",1532,D03.6,D00-D09 In situ neoplasms,http://identifiers.org/icd/D03.6,,ICD-10 "D03.7 Melanoma in situ of lower limb, including hip",1533,D03.7,D00-D09 In situ neoplasms,http://identifiers.org/icd/D03.7,,ICD-10 D03.8 Melanoma in situ of other sites,1534,D03.8,D00-D09 In situ neoplasms,http://identifiers.org/icd/D03.8,,ICD-10 -"D03.9 Melanoma in situ, unspecified",1535,D03.9,D00-D09 In situ neoplasms,http://identifiers.org/icd/D03.9,ORPHAcode: 168999 Malignant melanoma of the mucosa +"D03.9 Melanoma in situ, unspecified",1535,D03.9,D00-D09 In situ neoplasms,http://identifiers.org/icd/D03.9,ORPHAcode: 168999 Malignant melanoma of the mucosa,ICD-10 D04 Carcinoma in situ of skin,1536,D04,D00-D09 In situ neoplasms,http://identifiers.org/icd/D04,,ICD-10 D04.0 Skin of lip,1537,D04.0,D00-D09 In situ neoplasms,http://identifiers.org/icd/D04.0,,ICD-10 "D04.1 Skin of eyelid, including canthus",1538,D04.1,D00-D09 In situ neoplasms,http://identifiers.org/icd/D04.1,,ICD-10 @@ -1551,7 +1551,7 @@ D06.7 Other parts of cervix,1549,D06.7,D00-D09 In situ neoplasms,http://identifi "D06.9 Cervix, unspecified",1550,D06.9,D00-D09 In situ neoplasms,http://identifiers.org/icd/D06.9,,ICD-10 D07 Carcinoma in situ of other and unspecified genital organs,1551,D07,D00-D09 In situ neoplasms,http://identifiers.org/icd/D07,,ICD-10 D07.0 Carcinoma in situ of other and unspecified genital organs - Endometrium,1552,D07.0,D00-D09 In situ neoplasms,http://identifiers.org/icd/D07.0,,ICD-10 -D07.1 Carcinoma in situ of other and unspecified genital organs - Vulva,1553,D07.1,D00-D09 In situ neoplasms,http://identifiers.org/icd/D07.1,ORPHAcode: 137583 Vulvar intraepithelial neoplasia +D07.1 Carcinoma in situ of other and unspecified genital organs - Vulva,1553,D07.1,D00-D09 In situ neoplasms,http://identifiers.org/icd/D07.1,ORPHAcode: 137583 Vulvar intraepithelial neoplasia,ICD-10 D07.2 Vagina,1554,D07.2,D00-D09 In situ neoplasms,http://identifiers.org/icd/D07.2,,ICD-10 D07.3 Other and unspecified female genital organs,1555,D07.3,D00-D09 In situ neoplasms,http://identifiers.org/icd/D07.3,,ICD-10 D07.4 Carcinoma in situ of other and unspecified genital organs - Penis,1556,D07.4,D00-D09 In situ neoplasms,http://identifiers.org/icd/D07.4,,ICD-10 @@ -1572,11 +1572,11 @@ D10.2 Benign neoplasm of mouth and pharynx - Floor of mouth,1570,D10.2,D10-D36 B D10.3 Benign neoplasm of mouth and pharynx - Other and unspecified parts of mouth,1571,D10.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D10.3,,ICD-10 D10.4 Benign neoplasm of mouth and pharynx - Tonsil,1572,D10.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D10.4,,ICD-10 D10.5 Benign neoplasm of mouth and pharynx - Other parts of oropharynx,1573,D10.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D10.5,,ICD-10 -D10.6 Benign neoplasm of mouth and pharynx - Nasopharynx,1574,D10.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D10.6,ORPHAcode: 289596 Juvenile nasopharyngeal angiofibroma +D10.6 Benign neoplasm of mouth and pharynx - Nasopharynx,1574,D10.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D10.6,ORPHAcode: 289596 Juvenile nasopharyngeal angiofibroma,ICD-10 D10.7 Benign neoplasm of mouth and pharynx - Hypopharynx,1575,D10.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D10.7,,ICD-10 "D10.9 Benign neoplasm of mouth and pharynx - Pharynx, unspecified",1576,D10.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D10.9,,ICD-10 D11 Benign neoplasm of major salivary glands,1577,D11,D10-D36 Benign neoplasms,http://identifiers.org/icd/D11,,ICD-10 -D11.0 Benign neoplasm of major salivary glands - Parotid gland,1578,D11.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D11.0,ORPHAcode: 276148 Benign epithelial tumor of salivary glands +D11.0 Benign neoplasm of major salivary glands - Parotid gland,1578,D11.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D11.0,ORPHAcode: 276148 Benign epithelial tumor of salivary glands,ICD-10 D11.7 Benign neoplasm of major salivary glands - Other major salivary glands,1579,D11.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D11.7,,ICD-10 "D11.9 Benign neoplasm of major salivary glands - Major salivary gland, unspecified",1580,D11.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D11.9,,ICD-10 "D12 Benign neoplasm of colon, rectum, anus and anal canal",1581,D12,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12,,ICD-10 @@ -1586,7 +1586,7 @@ D11.7 Benign neoplasm of major salivary glands - Other major salivary glands,157 "D12.3 Benign neoplasm of colon, rectum, anus and anal canal - Transverse colon",1585,D12.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.3,,ICD-10 "D12.4 Benign neoplasm of colon, rectum, anus and anal canal - Descending colon",1586,D12.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.4,,ICD-10 "D12.5 Benign neoplasm of colon, rectum, anus and anal canal - Sigmoid colon",1587,D12.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.5,,ICD-10 -"D12.6 Benign neoplasm of colon, rectum, anus and anal canal - Colon, unspecified",1588,D12.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.6,ORPHAcode: 733 Familial adenomatous polyposis +"D12.6 Benign neoplasm of colon, rectum, anus and anal canal - Colon, unspecified",1588,D12.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.6,ORPHAcode: 733 Familial adenomatous polyposis,ICD-10 "D12.7 Benign neoplasm of colon, rectum, anus and anal canal - Rectosigmoid junction",1589,D12.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.7,,ICD-10 "D12.8 Benign neoplasm of colon, rectum, anus and anal canal - Rectum",1590,D12.8,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.8,,ICD-10 "D12.9 Benign neoplasm of colon, rectum, anus and anal canal - Anus and anal canal",1591,D12.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D12.9,,ICD-10 @@ -1595,9 +1595,9 @@ D13.0 Benign neoplasm of other and ill-defined parts of digestive system - Oesop D13.1 Benign neoplasm of other and ill-defined parts of digestive system - Stomach,1594,D13.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.1,,ICD-10 D13.2 Benign neoplasm of other and ill-defined parts of digestive system - Duodenum,1595,D13.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.2,,ICD-10 D13.3 Benign neoplasm of other and ill-defined parts of digestive system - Other and unspecified parts of small intestine,1596,D13.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.3,,ICD-10 -D13.4 Benign neoplasm of other and ill-defined parts of digestive system - Liver,1597,D13.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.4,ORPHAcode: 386 Hepatic cystic hamartoma +D13.4 Benign neoplasm of other and ill-defined parts of digestive system - Liver,1597,D13.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.4,ORPHAcode: 386 Hepatic cystic hamartoma,ICD-10 D13.5 Benign neoplasm of other and ill-defined parts of digestive system - Extrahepatic bile ducts,1598,D13.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.5,,ICD-10 -D13.6 Benign neoplasm of other and ill-defined parts of digestive system - Pancreas,1599,D13.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.6,ORPHAcode: 93292 Adenoma of pancreas +D13.6 Benign neoplasm of other and ill-defined parts of digestive system - Pancreas,1599,D13.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.6,ORPHAcode: 93292 Adenoma of pancreas,ICD-10 D13.7 Benign neoplasm of other and ill-defined parts of digestive system - Endocrine pancreas,1600,D13.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.7,,ICD-10 D13.9 Benign neoplasm of other and ill-defined parts of digestive system - Ill-defined sites within the digestive system,1601,D13.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D13.9,,ICD-10 D14 Benign neoplasm of middle ear and respiratory system,1602,D14,D10-D36 Benign neoplasms,http://identifiers.org/icd/D14,,ICD-10 @@ -1608,22 +1608,22 @@ D14.3 Benign neoplasm of middle ear and respiratory system - Bronchus and lung,1 "D14.4 Benign neoplasm of middle ear and respiratory system - Respiratory system, unspecified",1607,D14.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D14.4,,ICD-10 D15 Benign neoplasm of other and unspecified intrathoracic organs,1608,D15,D10-D36 Benign neoplasms,http://identifiers.org/icd/D15,,ICD-10 D15.0 Benign neoplasm of other and unspecified intrathoracic organs - Thymus,1609,D15.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D15.0,,ICD-10 -D15.1 Benign neoplasm of other and unspecified intrathoracic organs - Heart,1610,D15.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D15.1,ORPHAcode: 615 Familial atrial myxoma +D15.1 Benign neoplasm of other and unspecified intrathoracic organs - Heart,1610,D15.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D15.1,ORPHAcode: 615 Familial atrial myxoma,ICD-10 D15.2 Benign neoplasm of other and unspecified intrathoracic organs - Mediastinum,1611,D15.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D15.2,,ICD-10 D15.7 Benign neoplasm of other and unspecified intrathoracic organs - Other specified intrathoracic organs,1612,D15.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D15.7,,ICD-10 "D15.9 Benign neoplasm of other and unspecified intrathoracic organs - Intrathoracic organ, unspecified",1613,D15.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D15.9,,ICD-10 D16 Benign neoplasm of bone and articular cartilage,1614,D16,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16,,ICD-10 D16.0 Benign neoplasm of bone and articular cartilage - Scapula and long bones of upper limb,1615,D16.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.0,,ICD-10 -D16.1 Benign neoplasm of bone and articular cartilage - Short bones of upper limb,1616,D16.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.1,ORPHAcode: 58040 Osteoblastoma +D16.1 Benign neoplasm of bone and articular cartilage - Short bones of upper limb,1616,D16.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.1,ORPHAcode: 58040 Osteoblastoma,ICD-10 D16.2 Benign neoplasm of bone and articular cartilage - Long bones of lower limb,1617,D16.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.2,,ICD-10 D16.3 Benign neoplasm of bone and articular cartilage - Short bones of lower limb,1618,D16.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.3,,ICD-10 -"D18.1 Lymphangioma, any site",1619,D18.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D18.1,ORPHAcode: 79489 Macrocystic lymphatic malformation -D16.4 Benign neoplasm of bone and articular cartilage - Bones of skull and face,1620,D16.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.4,ORPHAcode: 83451 Florid cemento-osseous dysplasia -D16.5 Benign neoplasm of bone and articular cartilage - Lower jaw bone,1621,D16.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.5,ORPHAcode: 314419 Ameloblastoma +"D18.1 Lymphangioma, any site",1619,D18.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D18.1,ORPHAcode: 79489 Macrocystic lymphatic malformation,ICD-10 +D16.4 Benign neoplasm of bone and articular cartilage - Bones of skull and face,1620,D16.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.4,ORPHAcode: 83451 Florid cemento-osseous dysplasia,ICD-10 +D16.5 Benign neoplasm of bone and articular cartilage - Lower jaw bone,1621,D16.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.5,ORPHAcode: 314419 Ameloblastoma,ICD-10 D16.6 Benign neoplasm of bone and articular cartilage - Vertebral column,1622,D16.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.6,,ICD-10 "D16.7 Benign neoplasm of bone and articular cartilage - Ribs, sternum and clavicle",1623,D16.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.7,,ICD-10 "D16.8 Benign neoplasm of bone and articular cartilage - Pelvic bones, sacrum and coccyx",1624,D16.8,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.8,,ICD-10 -"D16.9 Benign neoplasm of bone and articular cartilage - Bone and articular cartilage, unspecified",1625,D16.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.9,ORPHAcode: 2767 Carpotarsal osteochondromatosis +"D16.9 Benign neoplasm of bone and articular cartilage - Bone and articular cartilage, unspecified",1625,D16.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D16.9,ORPHAcode: 2767 Carpotarsal osteochondromatosis,ICD-10 D17 Benign lipomatous neoplasm,1626,D17,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17,,ICD-10 "D17.0 Benign lipomatous neoplasm of skin and subcutaneous tissue of head, face and neck",1627,D17.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17.0,,ICD-10 D17.1 Benign lipomatous neoplasm of skin and subcutaneous tissue of trunk,1628,D17.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17.1,,ICD-10 @@ -1633,9 +1633,9 @@ D17.4 Benign lipomatous neoplasm of intrathoracic organs,1631,D17.4,D10-D36 Beni D17.5 Benign lipomatous neoplasm of intra-abdominal organs,1632,D17.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17.5,,ICD-10 D17.6 Benign lipomatous neoplasm of spermatic cord,1633,D17.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17.6,,ICD-10 D17.7 Benign lipomatous neoplasm of other sites,1634,D17.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17.7,,ICD-10 -"D17.9 Benign lipomatous neoplasm, unspecified",1635,D17.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17.9,ORPHAcode: 199279 Familial angiolipomatosis +"D17.9 Benign lipomatous neoplasm, unspecified",1635,D17.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D17.9,ORPHAcode: 199279 Familial angiolipomatosis,ICD-10 "D18 Haemangioma and lymphangioma, any site",1636,D18,D10-D36 Benign neoplasms,http://identifiers.org/icd/D18,,ICD-10 -"D18.0 Haemangioma, any site",1637,D18.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D18.0,ORPHAcode: 1062 Hereditary neurocutaneous malformation +"D18.0 Haemangioma, any site",1637,D18.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D18.0,ORPHAcode: 1062 Hereditary neurocutaneous malformation,ICD-10 D19 Benign neoplasm of mesothelial tissue,1638,D19,D10-D36 Benign neoplasms,http://identifiers.org/icd/D19,,ICD-10 D19.0 Benign neoplasm of mesothelial tissue - Mesothelial tissue of pleura,1639,D19.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D19.0,,ICD-10 D19.1 Benign neoplasm of mesothelial tissue - Mesothelial tissue of peritoneum,1640,D19.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D19.1,,ICD-10 @@ -1643,7 +1643,7 @@ D19.7 Benign neoplasm of mesothelial tissue - Mesothelial tissue of other sites, "D19.9 Benign neoplasm of mesothelial tissue - Mesothelial tissue, unspecified",1642,D19.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D19.9,,ICD-10 D20 Benign neoplasm of soft tissue of retroperitoneum and peritoneum,1643,D20,D10-D36 Benign neoplasms,http://identifiers.org/icd/D20,,ICD-10 D20.0 Benign neoplasm of soft tissue of retroperitoneum and peritoneum - Retroperitoneum,1644,D20.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D20.0,,ICD-10 -D20.1 Benign neoplasm of soft tissue of retroperitoneum and peritoneum - Peritoneum,1645,D20.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D20.1,ORPHAcode: 71274 Disseminated peritoneal leiomyomatosis +D20.1 Benign neoplasm of soft tissue of retroperitoneum and peritoneum - Peritoneum,1645,D20.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D20.1,ORPHAcode: 71274 Disseminated peritoneal leiomyomatosis,ICD-10 D21 Other benign neoplasms of connective and other soft tissue,1646,D21,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21,,ICD-10 "D21.0 Connective and other soft tissue of head, face and neck",1647,D21.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21.0,,ICD-10 "D21.1 Connective and other soft tissue of upper limb, including shoulder",1648,D21.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21.1,,ICD-10 @@ -1652,28 +1652,28 @@ D21.3 Connective and other soft tissue of thorax,1650,D21.3,D10-D36 Benign neopl D21.4 Connective and other soft tissue of abdomen,1651,D21.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21.4,,ICD-10 D21.5 Connective and other soft tissue of pelvis,1652,D21.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21.5,,ICD-10 "D21.6 Connective and other soft tissue of trunk, unspecified",1653,D21.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21.6,,ICD-10 -"D21.9 Connective and other soft tissue, unspecified",1654,D21.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21.9,ORPHAcode: 2126 Solitary fibrous tumor/hemangiopericytoma +"D21.9 Connective and other soft tissue, unspecified",1654,D21.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D21.9,ORPHAcode: 2126 Solitary fibrous tumor/hemangiopericytoma,ICD-10 D22 Melanocytic naevi,1655,D22,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22,,ICD-10 D22.0 Melanocytic naevi of lip,1656,D22.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.0,,ICD-10 "D22.1 Melanocytic naevi of eyelid, including canthus",1657,D22.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.1,,ICD-10 D22.2 Melanocytic naevi of ear and external auricular canal,1658,D22.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.2,,ICD-10 -D22.3 Melanocytic naevi of other and unspecified parts of face,1659,D22.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.3,ORPHAcode: 263425 Nevus of Ota -D22.4 Melanocytic naevi of scalp and neck,1660,D22.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.4,ORPHAcode: 2481 Neurocutaneous melanocytosis -D22.5 Melanocytic naevi of trunk,1661,D22.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.5,ORPHAcode: 64755 Becker nevus syndrome -"D22.6 Melanocytic naevi of upper limb, including shoulder",1662,D22.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.6,ORPHAcode: 263432 Nevus of Ito +D22.3 Melanocytic naevi of other and unspecified parts of face,1659,D22.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.3,ORPHAcode: 263425 Nevus of Ota,ICD-10 +D22.4 Melanocytic naevi of scalp and neck,1660,D22.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.4,ORPHAcode: 2481 Neurocutaneous melanocytosis,ICD-10 +D22.5 Melanocytic naevi of trunk,1661,D22.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.5,ORPHAcode: 64755 Becker nevus syndrome,ICD-10 +"D22.6 Melanocytic naevi of upper limb, including shoulder",1662,D22.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.6,ORPHAcode: 263432 Nevus of Ito,ICD-10 "D22.7 Melanocytic naevi of lower limb, including hip",1663,D22.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.7,,ICD-10 "D22.9 Melanocytic naevi, unspecified",1664,D22.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D22.9,,ICD-10 D23 Other benign neoplasms of skin,1665,D23,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23,,ICD-10 D23.0 Skin of lip,1666,D23.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.0,,ICD-10 "D23.1 Skin of eyelid, including canthus",1667,D23.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.1,,ICD-10 D23.2 Skin of ear and external auricular canal,1668,D23.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.2,,ICD-10 -D23.3 Skin of other and unspecified parts of face,1669,D23.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.3,ORPHAcode: 91414 Pilomatrixoma -D23.4 Skin of scalp and neck,1670,D23.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.4,ORPHAcode: 79414 Woolly hair nevus +D23.3 Skin of other and unspecified parts of face,1669,D23.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.3,ORPHAcode: 91414 Pilomatrixoma,ICD-10 +D23.4 Skin of scalp and neck,1670,D23.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.4,ORPHAcode: 79414 Woolly hair nevus,ICD-10 D23.5 Skin of trunk,1671,D23.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.5,,ICD-10 "D23.6 Skin of upper limb, including shoulder",1672,D23.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.6,,ICD-10 "D23.7 Skin of lower limb, including hip",1673,D23.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.7,,ICD-10 -"D23.9 Skin, unspecified",1674,D23.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.9,ORPHAcode: 122 Birt-Hogg-Dub sy -D24 Benign neoplasm of breast,1675,D24,D10-D36 Benign neoplasms,http://identifiers.org/icd/D24,ORPHAcode: 180267 Giant adenofibroma of the breast +"D23.9 Skin, unspecified",1674,D23.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D23.9,ORPHAcode: 122 Birt-Hogg-Dub sy,ICD-10 +D24 Benign neoplasm of breast,1675,D24,D10-D36 Benign neoplasms,http://identifiers.org/icd/D24,ORPHAcode: 180267 Giant adenofibroma of the breast,ICD-10 D25 Leiomyoma of uterus,1676,D25,D10-D36 Benign neoplasms,http://identifiers.org/icd/D25,,ICD-10 D25.0 Submucous leiomyoma of uterus,1677,D25.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D25.0,,ICD-10 D25.1 Intramural leiomyoma of uterus,1678,D25.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D25.1,,ICD-10 @@ -1684,11 +1684,11 @@ D26.0 Other benign neoplasms of uterus - Cervix uteri,1682,D26.0,D10-D36 Benign D26.1 Other benign neoplasms of uterus - Corpus uteri,1683,D26.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D26.1,,ICD-10 D26.7 Other parts of uterus,1684,D26.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D26.7,,ICD-10 "D26.9 Uterus, unspecified",1685,D26.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D26.9,,ICD-10 -D27 Benign neoplasm of ovary,1686,D27,D10-D36 Benign neoplasms,http://identifiers.org/icd/D27,ORPHAcode: 206470 Cystadenoma of childhood +D27 Benign neoplasm of ovary,1686,D27,D10-D36 Benign neoplasms,http://identifiers.org/icd/D27,ORPHAcode: 206470 Cystadenoma of childhood,ICD-10 D28 Benign neoplasm of other and unspecified female genital organs,1687,D28,D10-D36 Benign neoplasms,http://identifiers.org/icd/D28,,ICD-10 D28.0 Benign neoplasm of other and unspecified female genital organs - Vulva,1688,D28.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D28.0,,ICD-10 D28.1 Benign neoplasm of other and unspecified female genital organs - Vagina,1689,D28.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D28.1,,ICD-10 -D28.2 Benign neoplasm of other and unspecified female genital organs - Uterine tubes and ligaments,1690,D28.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D28.2,ORPHAcode: 180237 Benign tumor of fallopian tubes +D28.2 Benign neoplasm of other and unspecified female genital organs - Uterine tubes and ligaments,1690,D28.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D28.2,ORPHAcode: 180237 Benign tumor of fallopian tubes,ICD-10 D28.7 Benign neoplasm of other and unspecified female genital organs - Other specified female genital organs,1691,D28.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D28.7,,ICD-10 "D28.9 Benign neoplasm of other and unspecified female genital organs - Female genital organ, unspecified",1692,D28.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D28.9,,ICD-10 D29 Benign neoplasm of male genital organs,1693,D29,D10-D36 Benign neoplasms,http://identifiers.org/icd/D29,,ICD-10 @@ -1700,7 +1700,7 @@ D29.4 Benign neoplasm of male genital organs - Scrotum,1698,D29.4,D10-D36 Benign D29.7 Benign neoplasm of male genital organs - Other male genital organs,1699,D29.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D29.7,,ICD-10 "D29.9 Benign neoplasm of male genital organs - Male genital organ, unspecified",1700,D29.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D29.9,,ICD-10 D30 Benign neoplasm of urinary organs,1701,D30,D10-D36 Benign neoplasms,http://identifiers.org/icd/D30,,ICD-10 -D30.0 Benign neoplasm of urinary organs - Kidney,1702,D30.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D30.0,ORPHAcode: 464359 Benign metanephric tumor +D30.0 Benign neoplasm of urinary organs - Kidney,1702,D30.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D30.0,ORPHAcode: 464359 Benign metanephric tumor,ICD-10 D30.1 Benign neoplasm of urinary organs - Renal pelvis,1703,D30.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D30.1,,ICD-10 D30.2 Benign neoplasm of urinary organs - Ureter,1704,D30.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D30.2,,ICD-10 D30.3 Benign neoplasm of urinary organs - Bladder,1705,D30.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D30.3,,ICD-10 @@ -1709,32 +1709,32 @@ D30.7 Benign neoplasm of urinary organs - Other urinary organs,1707,D30.7,D10-D3 "D30.9 Benign neoplasm of urinary organs - Urinary organ, unspecified",1708,D30.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D30.9,,ICD-10 D31 Benign neoplasm of eye and adnexa,1709,D31,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31,,ICD-10 D31.0 Benign neoplasm of eye and adnexa - Conjunctiva,1710,D31.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.0,,ICD-10 -D31.1 Benign neoplasm of eye and adnexa - Cornea,1711,D31.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.1,ORPHAcode: 91481 Ring dermoid of cornea -D31.2 Benign neoplasm of eye and adnexa - Retina,1712,D31.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.2,ORPHAcode: 353356 Vasoproliferative tumor of the retina +D31.1 Benign neoplasm of eye and adnexa - Cornea,1711,D31.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.1,ORPHAcode: 91481 Ring dermoid of cornea,ICD-10 +D31.2 Benign neoplasm of eye and adnexa - Retina,1712,D31.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.2,ORPHAcode: 353356 Vasoproliferative tumor of the retina,ICD-10 D31.3 Benign neoplasm of eye and adnexa - Choroid,1713,D31.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.3,,ICD-10 -D31.4 Benign neoplasm of eye and adnexa - Ciliary body,1714,D31.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.4,ORPHAcode: 268139 Intraocular medulloepithelioma +D31.4 Benign neoplasm of eye and adnexa - Ciliary body,1714,D31.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.4,ORPHAcode: 268139 Intraocular medulloepithelioma,ICD-10 D31.5 Benign neoplasm of eye and adnexa - Lacrimal gland and duct,1715,D31.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.5,,ICD-10 -"D31.6 Benign neoplasm of eye and adnexa - Orbit, unspecified",1716,D31.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.6,ORPHAcode: 52994 Orbital leiomyoma +"D31.6 Benign neoplasm of eye and adnexa - Orbit, unspecified",1716,D31.6,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.6,ORPHAcode: 52994 Orbital leiomyoma,ICD-10 L50 Urticaria,1717,L50,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50,,ICD-10 "D31.9 Benign neoplasm of eye and adnexa - Eye, unspecified",1718,D31.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D31.9,,ICD-10 D32 Benign neoplasm of meninges,1719,D32,D10-D36 Benign neoplasms,http://identifiers.org/icd/D32,,ICD-10 D32.0 Benign neoplasm of meninges - Cerebral meninges,1720,D32.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D32.0,,ICD-10 D32.1 Benign neoplasm of meninges - Spinal meninges,1721,D32.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D32.1,,ICD-10 -"D32.9 Benign neoplasm of meninges - Meninges, unspecified",1722,D32.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D32.9,ORPHAcode: 2495 Meningioma +"D32.9 Benign neoplasm of meninges - Meninges, unspecified",1722,D32.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D32.9,ORPHAcode: 2495 Meningioma,ICD-10 D33 Benign neoplasm of brain and other parts of central nervous system,1723,D33,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33,,ICD-10 -"D33.0 Benign neoplasm of brain and other parts of central nervous system - Brain, supratentorial",1724,D33.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.0,ORPHAcode: 2807 Papilloma of choroid plexus -"D33.1 Benign neoplasm of brain and other parts of central nervous system - Brain, infratentorial",1725,D33.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.1,ORPHAcode: 251931 Cerebellar liponeurocytoma +"D33.0 Benign neoplasm of brain and other parts of central nervous system - Brain, supratentorial",1724,D33.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.0,ORPHAcode: 2807 Papilloma of choroid plexus,ICD-10 +"D33.1 Benign neoplasm of brain and other parts of central nervous system - Brain, infratentorial",1725,D33.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.1,ORPHAcode: 251931 Cerebellar liponeurocytoma,ICD-10 "D33.2 Benign neoplasm of brain and other parts of central nervous system - Brain, unspecified",1726,D33.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.2,,ICD-10 -D33.3 Benign neoplasm of brain and other parts of central nervous system - Cranial nerves,1727,D33.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.3,ORPHAcode: 2086 Optic pathway glioma -D33.4 Benign neoplasm of brain and other parts of central nervous system - Spinal cord,1728,D33.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.4,ORPHAcode: 252054 Hemangioblastoma +D33.3 Benign neoplasm of brain and other parts of central nervous system - Cranial nerves,1727,D33.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.3,ORPHAcode: 2086 Optic pathway glioma,ICD-10 +D33.4 Benign neoplasm of brain and other parts of central nervous system - Spinal cord,1728,D33.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.4,ORPHAcode: 252054 Hemangioblastoma,ICD-10 D33.7 Benign neoplasm of brain and other parts of central nervous system - Other specified parts of central nervous system,1729,D33.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.7,,ICD-10 "D33.9 Benign neoplasm of brain and other parts of central nervous system - Central nervous system, unspecified",1730,D33.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D33.9,,ICD-10 D34 Benign neoplasm of thyroid gland,1731,D34,D10-D36 Benign neoplasms,http://identifiers.org/icd/D34,,ICD-10 D35 Benign neoplasm of other and unspecified endocrine glands,1732,D35,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35,,ICD-10 -D35.0 Benign neoplasm of other and unspecified endocrine glands - Adrenal gland,1733,D35.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.0,ORPHAcode: 276621 Sporadic pheochromocytoma/secreting paraganglioma +D35.0 Benign neoplasm of other and unspecified endocrine glands - Adrenal gland,1733,D35.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.0,ORPHAcode: 276621 Sporadic pheochromocytoma/secreting paraganglioma,ICD-10 D35.1 Benign neoplasm of other and unspecified endocrine glands - Parathyroid gland,1734,D35.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.1,,ICD-10 M60 Myositis,1735,M60,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60,,ICD-10 -D35.2 Benign neoplasm of other and unspecified endocrine glands - Pituitary gland,1736,D35.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.2,ORPHAcode: 2965 Prolactinoma +D35.2 Benign neoplasm of other and unspecified endocrine glands - Pituitary gland,1736,D35.2,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.2,ORPHAcode: 2965 Prolactinoma,ICD-10 D35.3 Benign neoplasm of other and unspecified endocrine glands - Craniopharyngeal duct,1737,D35.3,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.3,,ICD-10 D35.4 Benign neoplasm of other and unspecified endocrine glands - Pineal gland,1738,D35.4,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.4,,ICD-10 D35.5 Benign neoplasm of other and unspecified endocrine glands - Carotid body,1739,D35.5,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.5,,ICD-10 @@ -1744,7 +1744,7 @@ D35.8 Benign neoplasm of other and unspecified endocrine glands - Pluriglandular "D35.9 Benign neoplasm of other and unspecified endocrine glands - Endocrine gland, unspecified",1743,D35.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D35.9,,ICD-10 D36 Benign neoplasm of other and unspecified sites,1744,D36,D10-D36 Benign neoplasms,http://identifiers.org/icd/D36,,ICD-10 D36.0 Benign neoplasm of other and unspecified sites - Lymph nodes,1745,D36.0,D10-D36 Benign neoplasms,http://identifiers.org/icd/D36.0,,ICD-10 -D36.1 Benign neoplasm of other and unspecified sites - Peripheral nerves and autonomic nervous system,1746,D36.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D36.1,ORPHAcode: 100002 Extraneural perineurioma +D36.1 Benign neoplasm of other and unspecified sites - Peripheral nerves and autonomic nervous system,1746,D36.1,D10-D36 Benign neoplasms,http://identifiers.org/icd/D36.1,ORPHAcode: 100002 Extraneural perineurioma,ICD-10 D36.7 Benign neoplasm of other and unspecified sites - Other specified sites,1747,D36.7,D10-D36 Benign neoplasms,http://identifiers.org/icd/D36.7,,ICD-10 D36.9 Benign neoplasm of unspecified site,1748,D36.9,D10-D36 Benign neoplasms,http://identifiers.org/icd/D36.9,,ICD-10 D37-D48 Neoplasms of uncertain or unknown behaviour,1749,,II Neoplasms,,,ICD-10 @@ -1761,16 +1761,16 @@ D37.7 Neoplasm of uncertain or unknown behaviour of oral cavity and digestive or "D37.9 Neoplasm of uncertain or unknown behaviour of oral cavity and digestive organs - Digestive organ, unspecified",1760,D37.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D37.9,,ICD-10 D38 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs,1761,D38,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38,,ICD-10 D38.0 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Larynx,1762,D38.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.0,,ICD-10 -"D38.1 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Trachea, bronchus and lung",1763,D38.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.1,ORPHAcode: 97287 Bronchial neuroendocrine tumor +"D38.1 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Trachea, bronchus and lung",1763,D38.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.1,ORPHAcode: 97287 Bronchial neuroendocrine tumor,ICD-10 D38.2 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Pleura,1764,D38.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.2,,ICD-10 D38.3 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Mediastinum,1765,D38.3,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.3,,ICD-10 -D38.4 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Thymus,1766,D38.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.4,ORPHAcode: 99867 Thymoma +D38.4 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Thymus,1766,D38.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.4,ORPHAcode: 99867 Thymoma,ICD-10 D38.5 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Other respiratory organs,1767,D38.5,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.5,,ICD-10 "D38.6 Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs - Respiratory organ, unspecified",1768,D38.6,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D38.6,,ICD-10 D39 Neoplasm of uncertain or unknown behaviour of female genital organs,1769,D39,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39,,ICD-10 D39.0 Neoplasm of uncertain or unknown behaviour of female genital organs - Uterus,1770,D39.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39.0,,ICD-10 -D39.1 Neoplasm of uncertain or unknown behaviour of female genital organs - Ovary,1771,D39.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39.1,ORPHAcode: 99914 Gynandroblastoma -D39.2 Neoplasm of uncertain or unknown behaviour of female genital organs - Placenta,1772,D39.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39.2,ORPHAcode: 99925 Invasive mole +D39.1 Neoplasm of uncertain or unknown behaviour of female genital organs - Ovary,1771,D39.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39.1,ORPHAcode: 99914 Gynandroblastoma,ICD-10 +D39.2 Neoplasm of uncertain or unknown behaviour of female genital organs - Placenta,1772,D39.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39.2,ORPHAcode: 99925 Invasive mole,ICD-10 D39.7 Neoplasm of uncertain or unknown behaviour of female genital organs - Other female genital organs,1773,D39.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39.7,,ICD-10 "D39.9 Neoplasm of uncertain or unknown behaviour of female genital organs - Female genital organ, unspecified",1774,D39.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D39.9,,ICD-10 D40 Neoplasm of uncertain or unknown behaviour of male genital organs,1775,D40,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D40,,ICD-10 @@ -1779,7 +1779,7 @@ D40.1 Neoplasm of uncertain or unknown behaviour of male genital organs - Testis D40.7 Neoplasm of uncertain or unknown behaviour of male genital organs - Other male genital organs,1778,D40.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D40.7,,ICD-10 "D40.9 Neoplasm of uncertain or unknown behaviour of male genital organs - Male genital organ, unspecified",1779,D40.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D40.9,,ICD-10 D41 Neoplasm of uncertain or unknown behaviour of urinary organs,1780,D41,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D41,,ICD-10 -D41.0 Neoplasm of uncertain or unknown behaviour of urinary organs - Kidney,1781,D41.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D41.0,ORPHAcode: 2665 Congenital mesoblastic nephroma +D41.0 Neoplasm of uncertain or unknown behaviour of urinary organs - Kidney,1781,D41.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D41.0,ORPHAcode: 2665 Congenital mesoblastic nephroma,ICD-10 D41.1 Neoplasm of uncertain or unknown behaviour of urinary organs - Renal pelvis,1782,D41.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D41.1,,ICD-10 D41.2 Neoplasm of uncertain or unknown behaviour of urinary organs - Ureter,1783,D41.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D41.2,,ICD-10 D41.3 Neoplasm of uncertain or unknown behaviour of urinary organs - Urethra,1784,D41.3,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D41.3,,ICD-10 @@ -1790,10 +1790,10 @@ D42 Neoplasm of uncertain or unknown behaviour of meninges,1788,D42,D37-D48 Neop D42.0 Neoplasm of uncertain or unknown behaviour of meninges - Cerebral meninges,1789,D42.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D42.0,,ICD-10 D42.1 Neoplasm of uncertain or unknown behaviour of meninges - Spinal meninges,1790,D42.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D42.1,,ICD-10 "D42.9 Neoplasm of uncertain or unknown behaviour of meninges - Meninges, unspecified",1791,D42.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D42.9,,ICD-10 -D43 Neoplasm of uncertain or unknown behaviour of brain and central nervous system,1792,D43,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43,ORPHAcode: 252206 Melanoma and neural system tumor syndrome -"D43.0 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Brain, supratentorial",1793,D43.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.0,ORPHAcode: 251957 Anaplastic ganglioglioma +D43 Neoplasm of uncertain or unknown behaviour of brain and central nervous system,1792,D43,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43,ORPHAcode: 252206 Melanoma and neural system tumor syndrome,ICD-10 +"D43.0 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Brain, supratentorial",1793,D43.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.0,ORPHAcode: 251957 Anaplastic ganglioglioma,ICD-10 "D43.1 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Brain, infratentorial",1794,D43.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.1,,ICD-10 -"D43.2 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Brain, unspecified",1795,D43.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.2,ORPHAcode: 251618 Subependymal giant cell astrocytoma +"D43.2 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Brain, unspecified",1795,D43.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.2,ORPHAcode: 251618 Subependymal giant cell astrocytoma,ICD-10 D43.3 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Cranial nerves,1796,D43.3,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.3,,ICD-10 D43.4 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Spinal cord,1797,D43.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.4,,ICD-10 D43.7 Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Other parts of central nervous system,1798,D43.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D43.7,,ICD-10 @@ -1803,58 +1803,58 @@ D44.0 Neoplasm of uncertain or unknown behaviour of endocrine glands - Thyroid g D44.1 Neoplasm of uncertain or unknown behaviour of endocrine glands - Adrenal gland,1802,D44.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.1,,ICD-10 D44.2 Neoplasm of uncertain or unknown behaviour of endocrine glands - Parathyroid gland,1803,D44.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.2,,ICD-10 D44.3 Neoplasm of uncertain or unknown behaviour of endocrine glands - Pituitary gland,1804,D44.3,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.3,,ICD-10 -D44.4 Neoplasm of uncertain or unknown behaviour of endocrine glands - Craniopharyngeal duct,1805,D44.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.4,ORPHAcode: 54595 Craniopharyngioma -D44.5 Neoplasm of uncertain or unknown behaviour of endocrine glands - Pineal gland,1806,D44.5,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.5,ORPHAcode: 251912 Pineocytoma +D44.4 Neoplasm of uncertain or unknown behaviour of endocrine glands - Craniopharyngeal duct,1805,D44.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.4,ORPHAcode: 54595 Craniopharyngioma,ICD-10 +D44.5 Neoplasm of uncertain or unknown behaviour of endocrine glands - Pineal gland,1806,D44.5,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.5,ORPHAcode: 251912 Pineocytoma,ICD-10 D44.6 Neoplasm of uncertain or unknown behaviour of endocrine glands - Carotid body,1807,D44.6,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.6,,ICD-10 -D44.7 Neoplasm of uncertain or unknown behaviour of endocrine glands - Aortic body and other paraganglia,1808,D44.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.7,ORPHAcode: 94080 Non-functioning paraganglioma -D44.8 Neoplasm of uncertain or unknown behaviour of endocrine glands - Pluriglandular involvement,1809,D44.8,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.8,ORPHAcode: 652 Multiple endocrine neoplasia type 1 +D44.7 Neoplasm of uncertain or unknown behaviour of endocrine glands - Aortic body and other paraganglia,1808,D44.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.7,ORPHAcode: 94080 Non-functioning paraganglioma,ICD-10 +D44.8 Neoplasm of uncertain or unknown behaviour of endocrine glands - Pluriglandular involvement,1809,D44.8,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.8,ORPHAcode: 652 Multiple endocrine neoplasia type 1,ICD-10 "D44.9 Neoplasm of uncertain or unknown behaviour of endocrine glands - Endocrine gland, unspecified",1810,D44.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D44.9,,ICD-10 -D45 Polycythaemia vera,1811,D45,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D45,ORPHAcode: 729 Polycythemia vera -D46 Myelodysplastic syndromes,1812,D46,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46,ORPHAcode: 164726 Acute myeloid leukemia and myelodysplastic syndromes related to radiation +D45 Polycythaemia vera,1811,D45,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D45,ORPHAcode: 729 Polycythemia vera,ICD-10 +D46 Myelodysplastic syndromes,1812,D46,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46,ORPHAcode: 164726 Acute myeloid leukemia and myelodysplastic syndromes related to radiation,ICD-10 "D46.0 Myelodysplastic syndromes - Refractory anaemia without ring sideroblasts, so stated",1813,D46.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.0,,ICD-10 D46.1 Myelodysplastic syndromes - Refractory anaemia with ring sideroblasts,1814,D46.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.1,,ICD-10 -D46.2 Myelodysplastic syndromes - Refractory anaemia with excess of blasts [RAEB],1815,D46.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.2,ORPHAcode: 86839 Refractory anemia with excess blasts +D46.2 Myelodysplastic syndromes - Refractory anaemia with excess of blasts [RAEB],1815,D46.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.2,ORPHAcode: 86839 Refractory anemia with excess blasts,ICD-10 "D46.4 Myelodysplastic syndromes - Refractory anaemia, unspecified",1816,D46.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.4,,ICD-10 D46.5 Myelodysplastic syndromes - Refractory anaemia with multi-lineage dysplasia,1817,D46.5,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.5,,ICD-10 D46.6 Myelodysplastic syndrome with isolated del(5q) chromosomal abnormality,1818,D46.6,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.6,,ICD-10 -D46.7 Other myelodysplastic syndromes,1819,D46.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.7,ORPHAcode: 3226 Deafness-lymphedema-leukemia syndrome +D46.7 Other myelodysplastic syndromes,1819,D46.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.7,ORPHAcode: 3226 Deafness-lymphedema-leukemia syndrome,ICD-10 "D46.9 Myelodysplastic syndrome, unspecified",1820,D46.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D46.9,,ICD-10 "D47 Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue",1821,D47,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47,,ICD-10 -D47.0 Histiocytic and mast cell tumours of uncertain and unknown behaviour,1822,D47.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.0,ORPHAcode: 98848 Indolent systemic mastocytosis -"D47.1 Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue - Chronic myeloproliferative disease",1823,D47.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.1,ORPHAcode: 86829 Chronic neutrophilic leukemia +D47.0 Histiocytic and mast cell tumours of uncertain and unknown behaviour,1822,D47.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.0,ORPHAcode: 98848 Indolent systemic mastocytosis,ICD-10 +"D47.1 Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue - Chronic myeloproliferative disease",1823,D47.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.1,ORPHAcode: 86829 Chronic neutrophilic leukemia,ICD-10 D47.2 Monoclonal gammopathy of undetermined significance (MGUS),1824,D47.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.2,,ICD-10 -D47.3 Essential (haemorrhagic) thrombocythaemia,1825,D47.3,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.3,ORPHAcode: 3318 Essential thrombocythemia -D47.4 Osteomyelofibrosis,1826,D47.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.4,ORPHAcode: 824 Primary myelofibrosis -"D47.5 Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue - Chronic eosinophilic leukaemia [hypereosinophilic syndrome]",1827,D47.5,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.5,ORPHAcode: 3260 Idiopathic hypereosinophilic syndrome -"D47.7 Other specified neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue",1828,D47.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.7,ORPHAcode: 160 Castleman disease -"D47.9 Neoplasm of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue, unspecified",1829,D47.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.9,ORPHAcode: 3261 Autoimmune lymphoproliferative syndrome +D47.3 Essential (haemorrhagic) thrombocythaemia,1825,D47.3,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.3,ORPHAcode: 3318 Essential thrombocythemia,ICD-10 +D47.4 Osteomyelofibrosis,1826,D47.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.4,ORPHAcode: 824 Primary myelofibrosis,ICD-10 +"D47.5 Other neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue - Chronic eosinophilic leukaemia [hypereosinophilic syndrome]",1827,D47.5,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.5,ORPHAcode: 3260 Idiopathic hypereosinophilic syndrome,ICD-10 +"D47.7 Other specified neoplasms of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue",1828,D47.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.7,ORPHAcode: 160 Castleman disease,ICD-10 +"D47.9 Neoplasm of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue, unspecified",1829,D47.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D47.9,ORPHAcode: 3261 Autoimmune lymphoproliferative syndrome,ICD-10 D48 Neoplasm of uncertain or unknown behaviour of other and unspecified sites,1830,D48,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48,,ICD-10 -D48.0 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Bone and articular cartilage,1831,D48.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.0,ORPHAcode: 363976 Giant cell tumor of bone -D48.1 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Connective and other soft tissue,1832,D48.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.1,ORPHAcode: 873 Desmoid tumor +D48.0 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Bone and articular cartilage,1831,D48.0,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.0,ORPHAcode: 363976 Giant cell tumor of bone,ICD-10 +D48.1 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Connective and other soft tissue,1832,D48.1,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.1,ORPHAcode: 873 Desmoid tumor,ICD-10 D48.2 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Peripheral nerves and autonomic nervous system,1833,D48.2,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.2,,ICD-10 D48.3 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Retroperitoneum,1834,D48.3,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.3,,ICD-10 D48.4 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Peritoneum,1835,D48.4,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.4,,ICD-10 D48.5 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Skin,1836,D48.5,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.5,,ICD-10 -D48.6 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Breast,1837,D48.6,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.6,ORPHAcode: 180261 Phyllodes tumor of the breast -D48.7 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Other specified sites,1838,D48.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.7,ORPHAcode: 538 Lymphangioleiomyomatosis -"D48.9 Neoplasm of uncertain or unknown behaviour, unspecified",1839,D48.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.9,ORPHAcode: 144 Lynch syndrome +D48.6 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Breast,1837,D48.6,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.6,ORPHAcode: 180261 Phyllodes tumor of the breast,ICD-10 +D48.7 Neoplasm of uncertain or unknown behaviour of other and unspecified sites - Other specified sites,1838,D48.7,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.7,ORPHAcode: 538 Lymphangioleiomyomatosis,ICD-10 +"D48.9 Neoplasm of uncertain or unknown behaviour, unspecified",1839,D48.9,D37-D48 Neoplasms of uncertain or unknown behaviour,http://identifiers.org/icd/D48.9,ORPHAcode: 144 Lynch syndrome,ICD-10 III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism,1840,,,,,ICD-10 D50-D53 Nutritional anaemias,1841,,III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism,,,ICD-10 D50 Iron deficiency anaemia,1842,D50,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D50,,ICD-10 -D50.1 Iron deficiency anaemia - Sideropenic dysphagia,1843,D50.1,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D50.1,ORPHAcode: 54028 Plummer-Vinson syndrome -D50.8 Other iron deficiency anaemias,1844,D50.8,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D50.8,ORPHAcode: 83642 Microcytic anemia with liver iron overload +D50.1 Iron deficiency anaemia - Sideropenic dysphagia,1843,D50.1,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D50.1,ORPHAcode: 54028 Plummer-Vinson syndrome,ICD-10 +D50.8 Other iron deficiency anaemias,1844,D50.8,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D50.8,ORPHAcode: 83642 Microcytic anemia with liver iron overload,ICD-10 "D50.9 Iron deficiency anaemia, unspecified",1845,D50.9,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D50.9,,ICD-10 D51 deficiency anaemia,1846,D51,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51,,ICD-10 -D51.0 deficiency anaemia due to intrinsic factor deficiency,1847,D51.0,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.0,ORPHAcode: 332 Congenital intrinsic factor deficiency -D51.1 deficiency anaemia - malabsorption with proteinuria,1848,D51.1,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.1,ORPHAcode: 35858 Imerslund-Gr sbeck sy -D51.2 Transcobalamin II deficiency,1849,D51.2,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.2,ORPHAcode: 859 Transcobalamin deficiency +D51.0 deficiency anaemia due to intrinsic factor deficiency,1847,D51.0,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.0,ORPHAcode: 332 Congenital intrinsic factor deficiency,ICD-10 +D51.1 deficiency anaemia - malabsorption with proteinuria,1848,D51.1,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.1,ORPHAcode: 35858 Imerslund-Gr sbeck sy,ICD-10 +D51.2 Transcobalamin II deficiency,1849,D51.2,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.2,ORPHAcode: 859 Transcobalamin deficiency,ICD-10 D51.3 deficiency anaemia,1850,D51.3,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.3,,ICD-10 D51.8 deficiency anaemias,1851,D51.8,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.8,,ICD-10 "D51.9 deficiency anaemia, unspecified",1852,D51.9,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D51.9,,ICD-10 D52 Folate deficiency anaemia,1853,D52,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D52,,ICD-10 D52.0 Dietary folate deficiency anaemia,1854,D52.0,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D52.0,,ICD-10 D52.1 Drug-induced folate deficiency anaemia,1855,D52.1,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D52.1,,ICD-10 -D52.8 Other folate deficiency anaemias,1856,D52.8,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D52.8,ORPHAcode: 90045 Hereditary folate malabsorption +D52.8 Other folate deficiency anaemias,1856,D52.8,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D52.8,ORPHAcode: 90045 Hereditary folate malabsorption,ICD-10 "D52.9 Folate deficiency anaemia, unspecified",1857,D52.9,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D52.9,,ICD-10 D53 Other nutritional anaemias,1858,D53,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D53,,ICD-10 D53.0 Other nutritional anaemias - Protein deficiency anaemia,1859,D53.0,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D53.0,,ICD-10 @@ -1864,52 +1864,52 @@ D53.8 Other specified nutritional anaemias,1862,D53.8,D50-D53 Nutritional anaemi "D53.9 Nutritional anaemia, unspecified",1863,D53.9,D50-D53 Nutritional anaemias,http://identifiers.org/icd/D53.9,,ICD-10 D55-D59 Haemolytic anaemias,1864,,III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism,,,ICD-10 D55 Anaemia due to enzyme disorders,1865,D55,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55,,ICD-10 -D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency,1866,D55.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.0,ORPHAcode: 466026 Class I glucose-6-phosphate dehydrogenase deficiency -D55.1 Anaemia due to other disorders of glutathione metabolism,1867,D55.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.1,ORPHAcode: 32 Glutathione synthetase deficiency -D55.2 Anaemia due to disorders of glycolytic enzymes,1868,D55.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.2,ORPHAcode: 712 Hemolytic anemia due to glucophosphate isomerase deficiency -D55.3 Anaemia due to disorders of nucleotide metabolism,1869,D55.3,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.3,ORPHAcode: 35120 Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency +D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency,1866,D55.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.0,ORPHAcode: 466026 Class I glucose-6-phosphate dehydrogenase deficiency,ICD-10 +D55.1 Anaemia due to other disorders of glutathione metabolism,1867,D55.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.1,ORPHAcode: 32 Glutathione synthetase deficiency,ICD-10 +D55.2 Anaemia due to disorders of glycolytic enzymes,1868,D55.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.2,ORPHAcode: 712 Hemolytic anemia due to glucophosphate isomerase deficiency,ICD-10 +D55.3 Anaemia due to disorders of nucleotide metabolism,1869,D55.3,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.3,ORPHAcode: 35120 Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency,ICD-10 D55.8 Other anaemias due to enzyme disorders,1870,D55.8,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.8,,ICD-10 "D55.9 Anaemia due to enzyme disorder, unspecified",1871,D55.9,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D55.9,,ICD-10 D56 Thalassaemia,1872,D56,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56,,ICD-10 -D56.0 Alpha thalassaemia,1873,D56.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.0,ORPHAcode: 846 Alpha-thalassemia -D56.1 Beta thalassaemia,1874,D56.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.1,ORPHAcode: 848 Beta-thalassemia -D56.2 Delta-beta thalassaemia,1875,D56.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.2,ORPHAcode: 231237 Delta-beta-thalassemia +D56.0 Alpha thalassaemia,1873,D56.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.0,ORPHAcode: 846 Alpha-thalassemia,ICD-10 +D56.1 Beta thalassaemia,1874,D56.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.1,ORPHAcode: 848 Beta-thalassemia,ICD-10 +D56.2 Delta-beta thalassaemia,1875,D56.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.2,ORPHAcode: 231237 Delta-beta-thalassemia,ICD-10 D56.3 Thalassaemia trait,1876,D56.3,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.3,,ICD-10 -D56.4 Thalassaemia - Hereditary persistence of fetal haemoglobin [HPFH],1877,D56.4,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.4,ORPHAcode: 46532 Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome -D56.8 Other thalassaemias,1878,D56.8,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.8,ORPHAcode: 330032 Hemoglobin Lepore-beta-thalassemia syndrome +D56.4 Thalassaemia - Hereditary persistence of fetal haemoglobin [HPFH],1877,D56.4,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.4,ORPHAcode: 46532 Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome,ICD-10 +D56.8 Other thalassaemias,1878,D56.8,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.8,ORPHAcode: 330032 Hemoglobin Lepore-beta-thalassemia syndrome,ICD-10 "D56.9 Thalassaemia, unspecified",1879,D56.9,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D56.9,,ICD-10 D57 Sickle-cell disorders,1880,D57,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57,,ICD-10 D63.8 Anaemia in other chronic diseases classified elsewhere,1881,D63.8,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D63.8,,ICD-10 -D57.0 Sickle-cell disorders - Sickle-cell anaemia with crisis,1882,D57.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57.0,ORPHAcode: 232 Sickle cell anemia +D57.0 Sickle-cell disorders - Sickle-cell anaemia with crisis,1882,D57.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57.0,ORPHAcode: 232 Sickle cell anemia,ICD-10 D57.1 Sickle-cell disorders - Sickle-cell anaemia without crisis,1883,D57.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57.1,,ICD-10 -D57.2 Double heterozygous sickling disorders,1884,D57.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57.2,ORPHAcode: 251359 Sickle cell-beta-thalassemia disease syndrome +D57.2 Double heterozygous sickling disorders,1884,D57.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57.2,ORPHAcode: 251359 Sickle cell-beta-thalassemia disease syndrome,ICD-10 D57.3 Sickle-cell disorders - Sickle-cell trait,1885,D57.3,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57.3,,ICD-10 D57.8 Other sickle-cell disorders,1886,D57.8,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D57.8,,ICD-10 D58 Other hereditary haemolytic anaemias,1887,D58,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58,,ICD-10 -D58.0 Hereditary spherocytosis,1888,D58.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.0,ORPHAcode: 822 Hereditary spherocytosis -D58.1 Hereditary elliptocytosis,1889,D58.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.1,ORPHAcode: 288 Hereditary elliptocytosis -D58.2 Other haemoglobinopathies,1890,D58.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.2,ORPHAcode: 2132 Hemoglobin C disease -D58.8 Other specified hereditary haemolytic anaemias,1891,D58.8,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.8,ORPHAcode: 1046 Lethal hemolytic anemia-genital anomalies syndrome +D58.0 Hereditary spherocytosis,1888,D58.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.0,ORPHAcode: 822 Hereditary spherocytosis,ICD-10 +D58.1 Hereditary elliptocytosis,1889,D58.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.1,ORPHAcode: 288 Hereditary elliptocytosis,ICD-10 +D58.2 Other haemoglobinopathies,1890,D58.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.2,ORPHAcode: 2132 Hemoglobin C disease,ICD-10 +D58.8 Other specified hereditary haemolytic anaemias,1891,D58.8,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.8,ORPHAcode: 1046 Lethal hemolytic anemia-genital anomalies syndrome,ICD-10 "D58.9 Hereditary haemolytic anaemia, unspecified",1892,D58.9,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D58.9,,ICD-10 D59 Acquired haemolytic anaemia,1893,D59,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59,,ICD-10 -D59.0 Drug-induced autoimmune haemolytic anaemia,1894,D59.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.0,ORPHAcode: 90037 Drug-induced autoimmune hemolytic anemia -D59.1 Other autoimmune haemolytic anaemias,1895,D59.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.1,ORPHAcode: 56425 Cold agglutinin disease +D59.0 Drug-induced autoimmune haemolytic anaemia,1894,D59.0,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.0,ORPHAcode: 90037 Drug-induced autoimmune hemolytic anemia,ICD-10 +D59.1 Other autoimmune haemolytic anaemias,1895,D59.1,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.1,ORPHAcode: 56425 Cold agglutinin disease,ICD-10 D59.2 Drug-induced nonautoimmune haemolytic anaemia,1896,D59.2,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.2,,ICD-10 D59.3 Haemolytic-uraemic syndrome,1897,D59.3,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.3,,ICD-10 D59.4 Other nonautoimmune haemolytic anaemias,1898,D59.4,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.4,,ICD-10 -D59.5 Acquired haemolytic anaemia - Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli],1899,D59.5,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.5,ORPHAcode: 447 Paroxysmal nocturnal hemoglobinuria +D59.5 Acquired haemolytic anaemia - Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli],1899,D59.5,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.5,ORPHAcode: 447 Paroxysmal nocturnal hemoglobinuria,ICD-10 D64 Other anaemias,1900,D64,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64,,ICD-10 -D59.6 Acquired haemolytic anaemia - Haemoglobinuria due to haemolysis from other external causes,1901,D59.6,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.6,ORPHAcode: 90035 Paroxysmal cold hemoglobinuria +D59.6 Acquired haemolytic anaemia - Haemoglobinuria due to haemolysis from other external causes,1901,D59.6,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.6,ORPHAcode: 90035 Paroxysmal cold hemoglobinuria,ICD-10 D59.8 Other acquired haemolytic anaemias,1902,D59.8,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.8,,ICD-10 "D59.9 Acquired haemolytic anaemia, unspecified",1903,D59.9,D55-D59 Haemolytic anaemias,http://identifiers.org/icd/D59.9,,ICD-10 D60-D64 Aplastic and other anaemias,1904,,III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism,,,ICD-10 D60 Acquired pure red cell aplasia [erythroblastopenia],1905,D60,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D60,,ICD-10 -D60.0 Chronic acquired pure red cell aplasia,1906,D60.0,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D60.0,ORPHAcode: 98872 Primary acquired pure red cell aplasia -D60.1 Transient acquired pure red cell aplasia,1907,D60.1,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D60.1,ORPHAcode: 98871 Transient erythroblastopenia of childhood +D60.0 Chronic acquired pure red cell aplasia,1906,D60.0,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D60.0,ORPHAcode: 98872 Primary acquired pure red cell aplasia,ICD-10 +D60.1 Transient acquired pure red cell aplasia,1907,D60.1,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D60.1,ORPHAcode: 98871 Transient erythroblastopenia of childhood,ICD-10 D60.8 Other acquired pure red cell aplasias,1908,D60.8,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D60.8,,ICD-10 "D60.9 Acquired pure red cell aplasia, unspecified",1909,D60.9,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D60.9,,ICD-10 D61 Other aplastic anaemias,1910,D61,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D61,,ICD-10 -D61.0 Constitutional aplastic anaemia,1911,D61.0,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D61.0,ORPHAcode: 84 Fanconi anemia +D61.0 Constitutional aplastic anaemia,1911,D61.0,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D61.0,ORPHAcode: 84 Fanconi anemia,ICD-10 D61.1 Drug-induced aplastic anaemia,1912,D61.1,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D61.1,,ICD-10 D61.2 Aplastic anaemia due to other external agents,1913,D61.2,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D61.2,,ICD-10 D61.3 Idiopathic aplastic anaemia,1914,D61.3,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D61.3,,ICD-10 @@ -1919,44 +1919,44 @@ D62 Acute posthaemorrhagic anaemia,1917,D62,D60-D64 Aplastic and other anaemias, D63 Anaemia in chronic diseases classified elsewhere,1918,D63,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D63,,ICD-10 D63.0 Anaemia in neoplastic disease,1919,D63.0,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D63.0,,ICD-10 "F00-F09 Organic, including symptomatic, mental disorders",1920,,V Mental and behavioural disorders,,,ICD-10 -D64.0 Other anaemias - Hereditary sideroblastic anaemia,1921,D64.0,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.0,ORPHAcode: 699 Pearson syndrome +D64.0 Other anaemias - Hereditary sideroblastic anaemia,1921,D64.0,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.0,ORPHAcode: 699 Pearson syndrome,ICD-10 D64.1 Other anaemias - Secondary sideroblastic anaemia due to disease,1922,D64.1,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.1,,ICD-10 D64.2 Other anaemias - Secondary sideroblastic anaemia due to drugs and toxins,1923,D64.2,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.2,,ICD-10 -D64.3 Other sideroblastic anaemias,1924,D64.3,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.3,ORPHAcode: 75564 Acquired idiopathic sideroblastic anemia -D64.4 Other anaemias - Congenital dyserythropoietic anaemia,1925,D64.4,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.4,ORPHAcode: 98869 Congenital dyserythropoietic anemia type I +D64.3 Other sideroblastic anaemias,1924,D64.3,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.3,ORPHAcode: 75564 Acquired idiopathic sideroblastic anemia,ICD-10 +D64.4 Other anaemias - Congenital dyserythropoietic anaemia,1925,D64.4,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.4,ORPHAcode: 98869 Congenital dyserythropoietic anemia type I,ICD-10 D64.8 Other specified anaemias,1926,D64.8,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.8,,ICD-10 "D64.9 Other anaemias - Anaemia, unspecified",1927,D64.9,D60-D64 Aplastic and other anaemias,http://identifiers.org/icd/D64.9,,ICD-10 "D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",1928,,III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism,,,ICD-10 -D65 Disseminated intravascular coagulation [defibrination syndrome],1929,D65,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D65,ORPHAcode: 49566 Acquired purpura fulminans -D66 Hereditary factor VIII deficiency,1930,D66,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D66,ORPHAcode: 98878 Hemophilia A -D67 Hereditary factor IX deficiency,1931,D67,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D67,ORPHAcode: 98879 Hemophilia B +D65 Disseminated intravascular coagulation [defibrination syndrome],1929,D65,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D65,ORPHAcode: 49566 Acquired purpura fulminans,ICD-10 +D66 Hereditary factor VIII deficiency,1930,D66,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D66,ORPHAcode: 98878 Hemophilia A,ICD-10 +D67 Hereditary factor IX deficiency,1931,D67,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D67,ORPHAcode: 98879 Hemophilia B,ICD-10 D68 Other coagulation defects,1932,D68,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68,,ICD-10 -D68.0 Other coagulation defects - Von Willebrand disease,1933,D68.0,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.0,ORPHAcode: 903 Von Willebrand disease -D68.1 Other coagulation defects - Hereditary factor XI deficiency,1934,D68.1,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.1,ORPHAcode: 329 Congenital factor XI deficiency -D68.2 Hereditary deficiency of other clotting factors,1935,D68.2,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.2,ORPHAcode: 325 Congenital factor II deficiency -D68.3 Other coagulation defects - Haemorrhagic disorder due to circulating anticoagulants,1936,D68.3,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.3,ORPHAcode: 436169 Thrombomodulin-related bleeding disorder -D68.4 Acquired coagulation factor deficiency,1937,D68.4,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.4,ORPHAcode: 26348 Acquired prothrombin deficiency -D68.5 Other coagulation defects - Primary thrombophilia,1938,D68.5,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.5,ORPHAcode: 82 Hereditary thrombophilia due to congenital antithrombin deficiency -D68.6 Other thrombophilia,1939,D68.6,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.6,ORPHAcode: 398097 Neonatal antiphospholipid syndrome -D68.8 Other specified coagulation defects,1940,D68.8,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.8,ORPHAcode: 79 Congenital alpha2-antiplasmin deficiency +D68.0 Other coagulation defects - Von Willebrand disease,1933,D68.0,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.0,ORPHAcode: 903 Von Willebrand disease,ICD-10 +D68.1 Other coagulation defects - Hereditary factor XI deficiency,1934,D68.1,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.1,ORPHAcode: 329 Congenital factor XI deficiency,ICD-10 +D68.2 Hereditary deficiency of other clotting factors,1935,D68.2,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.2,ORPHAcode: 325 Congenital factor II deficiency,ICD-10 +D68.3 Other coagulation defects - Haemorrhagic disorder due to circulating anticoagulants,1936,D68.3,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.3,ORPHAcode: 436169 Thrombomodulin-related bleeding disorder,ICD-10 +D68.4 Acquired coagulation factor deficiency,1937,D68.4,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.4,ORPHAcode: 26348 Acquired prothrombin deficiency,ICD-10 +D68.5 Other coagulation defects - Primary thrombophilia,1938,D68.5,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.5,ORPHAcode: 82 Hereditary thrombophilia due to congenital antithrombin deficiency,ICD-10 +D68.6 Other thrombophilia,1939,D68.6,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.6,ORPHAcode: 398097 Neonatal antiphospholipid syndrome,ICD-10 +D68.8 Other specified coagulation defects,1940,D68.8,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.8,ORPHAcode: 79 Congenital alpha2-antiplasmin deficiency,ICD-10 "D68.9 Coagulation defect, unspecified",1941,D68.9,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D68.9,,ICD-10 D69 Purpura and other haemorrhagic conditions,1942,D69,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69,,ICD-10 -D69.0 Allergic purpura,1943,D69.0,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.0,ORPHAcode: 761 Immunoglobulin A vasculitis -D69.1 Purpura and other haemorrhagic conditions - Qualitative platelet defects,1944,D69.1,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.1,ORPHAcode: 274 Bernard-Soulier syndrome -D69.2 Other nonthrombocytopenic purpura,1945,D69.2,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.2,ORPHAcode: 324636 Autoerythrocyte sensitization syndrome -D69.3 Idiopathic thrombocytopenic purpura,1946,D69.3,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.3,ORPHAcode: 1959 Evans syndrome -D69.4 Other primary thrombocytopenia,1947,D69.4,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.4,ORPHAcode: 851 Paris-Trousseau thrombocytopenia -D69.5 Purpura and other haemorrhagic conditions - Secondary thrombocytopenia,1948,D69.5,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.5,ORPHAcode: 3325 Heparin-induced thrombocytopenia +D69.0 Allergic purpura,1943,D69.0,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.0,ORPHAcode: 761 Immunoglobulin A vasculitis,ICD-10 +D69.1 Purpura and other haemorrhagic conditions - Qualitative platelet defects,1944,D69.1,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.1,ORPHAcode: 274 Bernard-Soulier syndrome,ICD-10 +D69.2 Other nonthrombocytopenic purpura,1945,D69.2,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.2,ORPHAcode: 324636 Autoerythrocyte sensitization syndrome,ICD-10 +D69.3 Idiopathic thrombocytopenic purpura,1946,D69.3,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.3,ORPHAcode: 1959 Evans syndrome,ICD-10 +D69.4 Other primary thrombocytopenia,1947,D69.4,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.4,ORPHAcode: 851 Paris-Trousseau thrombocytopenia,ICD-10 +D69.5 Purpura and other haemorrhagic conditions - Secondary thrombocytopenia,1948,D69.5,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.5,ORPHAcode: 3325 Heparin-induced thrombocytopenia,ICD-10 "D69.6 Purpura and other haemorrhagic conditions - Thrombocytopenia, unspecified",1949,D69.6,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.6,,ICD-10 -D69.8 Other specified haemorrhagic conditions,1950,D69.8,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.8,ORPHAcode: 806 Scott syndrome +D69.8 Other specified haemorrhagic conditions,1950,D69.8,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.8,ORPHAcode: 806 Scott syndrome,ICD-10 "D69.9 Haemorrhagic condition, unspecified",1951,D69.9,"D65-D69 Coagulation defects, purpura and other haemorrhagic conditions",http://identifiers.org/icd/D69.9,,ICD-10 D70-D77 Other diseases of blood and blood-forming organs,1952,,III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism,,,ICD-10 -D70 Agranulocytosis,1953,D70,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D70,ORPHAcode: 486 Autosomal dominant severe congenital neutropenia -D71 Functional disorders of polymorphonuclear neutrophils,1954,D71,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D71,ORPHAcode: 379 Chronic granulomatous disease +D70 Agranulocytosis,1953,D70,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D70,ORPHAcode: 486 Autosomal dominant severe congenital neutropenia,ICD-10 +D71 Functional disorders of polymorphonuclear neutrophils,1954,D71,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D71,ORPHAcode: 379 Chronic granulomatous disease,ICD-10 D72 Other disorders of white blood cells,1955,D72,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D72,,ICD-10 D72.0 Genetic anomalies of leukocytes,1956,D72.0,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D72.0,,ICD-10 D72.1 Other disorders of white blood cells - Eosinophilia,1957,D72.1,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D72.1,,ICD-10 -D72.8 Other specified disorders of white blood cells,1958,D72.8,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D72.8,ORPHAcode: 228000 Idiopathic CD4 lymphocytopenia +D72.8 Other specified disorders of white blood cells,1958,D72.8,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D72.8,ORPHAcode: 228000 Idiopathic CD4 lymphocytopenia,ICD-10 "D72.9 Disorder of white blood cells, unspecified",1959,D72.9,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D72.9,,ICD-10 D73 Diseases of spleen,1960,D73,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D73,,ICD-10 D73.0 Diseases of spleen - Hyposplenism,1961,D73.0,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D73.0,,ICD-10 @@ -1968,18 +1968,18 @@ D73.5 Infarction of spleen,1966,D73.5,D70-D77 Other diseases of blood and blood- D73.8 Other diseases of spleen,1967,D73.8,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D73.8,,ICD-10 "D73.9 Disease of spleen, unspecified",1968,D73.9,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D73.9,,ICD-10 D74 Methaemoglobinaemia,1969,D74,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D74,,ICD-10 -D74.0 Congenital methaemoglobinaemia,1970,D74.0,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D74.0,ORPHAcode: 621 Hereditary methemoglobinemia -D74.8 Other methaemoglobinaemias,1971,D74.8,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D74.8,ORPHAcode: 464453 Acquired methemoglobinemia +D74.0 Congenital methaemoglobinaemia,1970,D74.0,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D74.0,ORPHAcode: 621 Hereditary methemoglobinemia,ICD-10 +D74.8 Other methaemoglobinaemias,1971,D74.8,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D74.8,ORPHAcode: 464453 Acquired methemoglobinemia,ICD-10 "D74.9 Methaemoglobinaemia, unspecified",1972,D74.9,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D74.9,,ICD-10 D75 Other diseases of blood and blood-forming organs,1973,D75,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D75,,ICD-10 -D75.0 Other diseases of blood and blood-forming organs - Familial erythrocytosis,1974,D75.0,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D75.0,ORPHAcode: 90042 Primary familial polycythemia -D75.1 Other diseases of blood and blood-forming organs - Secondary polycythaemia,1975,D75.1,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D75.1,ORPHAcode: 90041 Gaisb ck sy +D75.0 Other diseases of blood and blood-forming organs - Familial erythrocytosis,1974,D75.0,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D75.0,ORPHAcode: 90042 Primary familial polycythemia,ICD-10 +D75.1 Other diseases of blood and blood-forming organs - Secondary polycythaemia,1975,D75.1,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D75.1,ORPHAcode: 90041 Gaisb ck sy,ICD-10 D75.8 Other specified diseases of blood and blood-forming organs,1976,D75.8,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D75.8,,ICD-10 "D75.9 Disease of blood and blood-forming organs, unspecified",1977,D75.9,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D75.9,,ICD-10 D76 Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue,1978,D76,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D76,,ICD-10 -D76.1 Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue - Haemophagocytic lymphohistiocytosis,1979,D76.1,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D76.1,ORPHAcode: 540 Familial hemophagocytic lymphohistiocytosis -"D76.2 Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue - Haemophagocytic syndrome, infection-associated",1980,D76.2,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D76.2,ORPHAcode: 158048 Hemophagocytic syndrome associated with an infection -D76.3 Other histiocytosis syndromes,1981,D76.3,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D76.3,ORPHAcode: 35687 Erdheim-Chester disease +D76.1 Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue - Haemophagocytic lymphohistiocytosis,1979,D76.1,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D76.1,ORPHAcode: 540 Familial hemophagocytic lymphohistiocytosis,ICD-10 +"D76.2 Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue - Haemophagocytic syndrome, infection-associated",1980,D76.2,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D76.2,ORPHAcode: 158048 Hemophagocytic syndrome associated with an infection,ICD-10 +D76.3 Other histiocytosis syndromes,1981,D76.3,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D76.3,ORPHAcode: 35687 Erdheim-Chester disease,ICD-10 D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere,1982,D77,D70-D77 Other diseases of blood and blood-forming organs,http://identifiers.org/icd/D77,,ICD-10 D80-D89 Certain disorders involving the immune mechanism,1983,,III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism,,,ICD-10 D80 Immunodeficiency with predominantly antibody defects,1984,D80,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80,,ICD-10 @@ -1987,55 +1987,55 @@ D80.0 Immunodeficiency with predominantly antibody defects - Hereditary hypogamm D80.1 Immunodeficiency with predominantly antibody defects - Nonfamilial hypogammaglobulinaemia,1986,D80.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.1,,ICD-10 D80.2 Immunodeficiency with predominantly antibody defects - Selective deficiency of immunoglobulin A [IgA],1987,D80.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.2,,ICD-10 D80.3 Immunodeficiency with predominantly antibody defects - Selective deficiency of immunoglobulin G [IgG] subclasses,1988,D80.3,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.3,,ICD-10 -D80.4 Immunodeficiency with predominantly antibody defects - Selective deficiency of immunoglobulin M [IgM],1989,D80.4,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.4,ORPHAcode: 331235 Selective IgM deficiency -D80.5 Immunodeficiency with increased immunoglobulin M [IgM],1990,D80.5,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.5,ORPHAcode: 183663 Hyper-IgM syndrome with susceptibility to opportunistic infections +D80.4 Immunodeficiency with predominantly antibody defects - Selective deficiency of immunoglobulin M [IgM],1989,D80.4,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.4,ORPHAcode: 331235 Selective IgM deficiency,ICD-10 +D80.5 Immunodeficiency with increased immunoglobulin M [IgM],1990,D80.5,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.5,ORPHAcode: 183663 Hyper-IgM syndrome with susceptibility to opportunistic infections,ICD-10 D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia,1991,D80.6,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.6,,ICD-10 -D80.7 Immunodeficiency with predominantly antibody defects - Transient hypogammaglobulinaemia of infancy,1992,D80.7,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.7,ORPHAcode: 169139 Transient hypogammaglobulinemia of infancy -D80.8 Other immunodeficiencies with predominantly antibody defects,1993,D80.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.8,ORPHAcode: 70593 Immunodeficiency due to selective anti-polysaccharide antibody deficiency +D80.7 Immunodeficiency with predominantly antibody defects - Transient hypogammaglobulinaemia of infancy,1992,D80.7,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.7,ORPHAcode: 169139 Transient hypogammaglobulinemia of infancy,ICD-10 +D80.8 Other immunodeficiencies with predominantly antibody defects,1993,D80.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.8,ORPHAcode: 70593 Immunodeficiency due to selective anti-polysaccharide antibody deficiency,ICD-10 "D80.9 Immunodeficiency with predominantly antibody defects, unspecified",1994,D80.9,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D80.9,,ICD-10 D81 Combined immunodeficiencies,1995,D81,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81,,ICD-10 -D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis,1996,D81.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.0,ORPHAcode: 33355 Reticular dysgenesis -D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers,1997,D81.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.1,ORPHAcode: 275 Severe combined immunodeficiency due to DCLRE1C deficiency -D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers,1998,D81.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.2,ORPHAcode: 276 T-B+ severe combined immunodeficiency due to gamma chain deficiency -D81.3 Combined immunodeficiencies - Adenosine deaminase [ADA] deficiency,1999,D81.3,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.3,ORPHAcode: 277 Severe combined immunodeficiency due to adenosine deaminase deficiency -D81.4 Combined immunodeficiencies - Nezelof syndrome,2000,D81.4,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.4,ORPHAcode: 83471 Thymic aplasia -D81.5 Combined immunodeficiencies - Purine nucleoside phosphorylase [PNP] deficiency,2001,D81.5,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.5,ORPHAcode: 760 Purine nucleoside phosphorylase deficiency -D81.6 Combined immunodeficiencies - Major histocompatibility complex class I deficiency,2002,D81.6,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.6,ORPHAcode: 34592 Immunodeficiency by defective expression of MHC class I -D81.7 Combined immunodeficiencies - Major histocompatibility complex class II deficiency,2003,D81.7,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.7,ORPHAcode: 572 Immunodeficiency by defective expression of MHC class II -D81.8 Other combined immunodeficiencies,2004,D81.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.8,ORPHAcode: 911 Combined immunodeficiency due to ZAP70 deficiency +D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis,1996,D81.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.0,ORPHAcode: 33355 Reticular dysgenesis,ICD-10 +D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers,1997,D81.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.1,ORPHAcode: 275 Severe combined immunodeficiency due to DCLRE1C deficiency,ICD-10 +D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers,1998,D81.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.2,ORPHAcode: 276 T-B+ severe combined immunodeficiency due to gamma chain deficiency,ICD-10 +D81.3 Combined immunodeficiencies - Adenosine deaminase [ADA] deficiency,1999,D81.3,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.3,ORPHAcode: 277 Severe combined immunodeficiency due to adenosine deaminase deficiency,ICD-10 +D81.4 Combined immunodeficiencies - Nezelof syndrome,2000,D81.4,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.4,ORPHAcode: 83471 Thymic aplasia,ICD-10 +D81.5 Combined immunodeficiencies - Purine nucleoside phosphorylase [PNP] deficiency,2001,D81.5,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.5,ORPHAcode: 760 Purine nucleoside phosphorylase deficiency,ICD-10 +D81.6 Combined immunodeficiencies - Major histocompatibility complex class I deficiency,2002,D81.6,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.6,ORPHAcode: 34592 Immunodeficiency by defective expression of MHC class I,ICD-10 +D81.7 Combined immunodeficiencies - Major histocompatibility complex class II deficiency,2003,D81.7,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.7,ORPHAcode: 572 Immunodeficiency by defective expression of MHC class II,ICD-10 +D81.8 Other combined immunodeficiencies,2004,D81.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.8,ORPHAcode: 911 Combined immunodeficiency due to ZAP70 deficiency,ICD-10 "D81.9 Combined immunodeficiency, unspecified",2005,D81.9,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D81.9,,ICD-10 D82 Immunodeficiency associated with other major defects,2006,D82,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82,,ICD-10 -D82.0 Immunodeficiency associated with other major defects - Wiskott-Aldrich syndrome,2007,D82.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.0,ORPHAcode: 906 Wiskott-Aldrich syndrome -D82.1 Immunodeficiency associated with other major defects - Di George syndrome,2008,D82.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.1,ORPHAcode: 567 22q11.2 deletion syndrome -D82.2 Immunodeficiency with short-limbed stature,2009,D82.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.2,ORPHAcode: 935 Short-limb skeletal dysplasia with severe combined immunodeficiency -D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus,2010,D82.3,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.3,ORPHAcode: 538931 X-linked lymphoproliferative disease due to SH2D1A deficiency -D82.4 Immunodeficiency associated with other major defects - Hyperimmunoglobulin E [IgE] syndrome,2011,D82.4,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.4,ORPHAcode: 2314 Autosomal dominant hyper-IgE syndrome +D82.0 Immunodeficiency associated with other major defects - Wiskott-Aldrich syndrome,2007,D82.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.0,ORPHAcode: 906 Wiskott-Aldrich syndrome,ICD-10 +D82.1 Immunodeficiency associated with other major defects - Di George syndrome,2008,D82.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.1,ORPHAcode: 567 22q11.2 deletion syndrome,ICD-10 +D82.2 Immunodeficiency with short-limbed stature,2009,D82.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.2,ORPHAcode: 935 Short-limb skeletal dysplasia with severe combined immunodeficiency,ICD-10 +D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus,2010,D82.3,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.3,ORPHAcode: 538931 X-linked lymphoproliferative disease due to SH2D1A deficiency,ICD-10 +D82.4 Immunodeficiency associated with other major defects - Hyperimmunoglobulin E [IgE] syndrome,2011,D82.4,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.4,ORPHAcode: 2314 Autosomal dominant hyper-IgE syndrome,ICD-10 D86.3 Sarcoidosis of skin,2012,D86.3,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86.3,,ICD-10 -D82.8 Immunodeficiency associated with other specified major defects,2013,D82.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.8,ORPHAcode: 2571 X-linked immunoneurologic disorder +D82.8 Immunodeficiency associated with other specified major defects,2013,D82.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.8,ORPHAcode: 2571 X-linked immunoneurologic disorder,ICD-10 "D82.9 Immunodeficiency associated with major defect, unspecified",2014,D82.9,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D82.9,,ICD-10 D83 Common variable immunodeficiency,2015,D83,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D83,,ICD-10 -D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function,2016,D83.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D83.0,ORPHAcode: 1572 Common variable immunodeficiency +D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function,2016,D83.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D83.0,ORPHAcode: 1572 Common variable immunodeficiency,ICD-10 D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders,2017,D83.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D83.1,,ICD-10 D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells,2018,D83.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D83.2,,ICD-10 D83.8 Other common variable immunodeficiencies,2019,D83.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D83.8,,ICD-10 "D83.9 Common variable immunodeficiency, unspecified",2020,D83.9,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D83.9,,ICD-10 D84 Other immunodeficiencies,2021,D84,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D84,,ICD-10 D84.0 Other immunodeficiencies - Lymphocyte function antigen-1 [LFA-1] defect,2022,D84.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D84.0,,ICD-10 -D84.1 Other immunodeficiencies - Defects in the complement system,2023,D84.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D84.1,ORPHAcode: 2966 Properdin deficiency -D84.8 Other specified immunodeficiencies,2024,D84.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D84.8,ORPHAcode: 2268 ICF syndrome +D84.1 Other immunodeficiencies - Defects in the complement system,2023,D84.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D84.1,ORPHAcode: 2966 Properdin deficiency,ICD-10 +D84.8 Other specified immunodeficiencies,2024,D84.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D84.8,ORPHAcode: 2268 ICF syndrome,ICD-10 "D84.9 Other immunodeficiencies - Immunodeficiency, unspecified",2025,D84.9,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D84.9,,ICD-10 D86 Sarcoidosis,2026,D86,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86,,ICD-10 -D86.0 Sarcoidosis of lung,2027,D86.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86.0,ORPHAcode: 797 Sarcoidosis +D86.0 Sarcoidosis of lung,2027,D86.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86.0,ORPHAcode: 797 Sarcoidosis,ICD-10 D86.1 Sarcoidosis of lymph nodes,2028,D86.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86.1,,ICD-10 D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes,2029,D86.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86.2,,ICD-10 D86.8 Sarcoidosis of other and combined sites,2030,D86.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86.8,,ICD-10 "D86.9 Sarcoidosis, unspecified",2031,D86.9,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D86.9,,ICD-10 "D89 Other disorders involving the immune mechanism, not elsewhere classified",2032,D89,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89,,ICD-10 -"D89.0 Other disorders involving the immune mechanism, not elsewhere classified - Polyclonal hypergammaglobulinaemia",2033,D89.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.0,ORPHAcode: 450322 Polyclonal hyperviscosity syndrome -"D89.1 Other disorders involving the immune mechanism, not elsewhere classified - Cryoglobulinaemia",2034,D89.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.1,ORPHAcode: 91138 Cryoglobulinemic vasculitis +"D89.0 Other disorders involving the immune mechanism, not elsewhere classified - Polyclonal hypergammaglobulinaemia",2033,D89.0,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.0,ORPHAcode: 450322 Polyclonal hyperviscosity syndrome,ICD-10 +"D89.1 Other disorders involving the immune mechanism, not elsewhere classified - Cryoglobulinaemia",2034,D89.1,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.1,ORPHAcode: 91138 Cryoglobulinemic vasculitis,ICD-10 "D89.2 Other disorders involving the immune mechanism, not elsewhere classified - Hypergammaglobulinaemia, unspecified",2035,D89.2,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.2,,ICD-10 D89.3 Immune reconstitution syndrome,2036,D89.3,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.3,,ICD-10 -"D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified",2037,D89.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.8,ORPHAcode: 54251 Corticosteroid-sensitive aseptic abscess syndrome +"D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified",2037,D89.8,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.8,ORPHAcode: 54251 Corticosteroid-sensitive aseptic abscess syndrome,ICD-10 "D89.9 Disorder involving the immune mechanism, unspecified",2038,D89.9,D80-D89 Certain disorders involving the immune mechanism,http://identifiers.org/icd/D89.9,,ICD-10 "IV Endocrine, nutritional and metabolic diseases",2039,,,,,ICD-10 E00-E07 Disorders of thyroid gland,2040,,"IV Endocrine, nutritional and metabolic diseases",,,ICD-10 @@ -2052,28 +2052,28 @@ E01.1 Iodine-deficiency-related thyroid disorders and allied conditions - Iodine E01.8 Other iodine-deficiency-related thyroid disorders and allied conditions,2051,E01.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E01.8,,ICD-10 E02 Subclinical iodine-deficiency hypothyroidism,2052,E02,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E02,,ICD-10 E03 Other hypothyroidism,2053,E03,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03,,ICD-10 -E03.0 Congenital hypothyroidism with diffuse goitre,2054,E03.0,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.0,ORPHAcode: 95716 Familial thyroid dyshormonogenesis -E03.1 Congenital hypothyroidism without goitre,2055,E03.1,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.1,ORPHAcode: 1226 Bamforth-Lazarus syndrome +E03.0 Congenital hypothyroidism with diffuse goitre,2054,E03.0,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.0,ORPHAcode: 95716 Familial thyroid dyshormonogenesis,ICD-10 +E03.1 Congenital hypothyroidism without goitre,2055,E03.1,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.1,ORPHAcode: 1226 Bamforth-Lazarus syndrome,ICD-10 E03.2 Hypothyroidism due to medicaments and other exogenous substances,2056,E03.2,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.2,,ICD-10 E03.3 Postinfectious hypothyroidism,2057,E03.3,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.3,,ICD-10 E03.4 Other hypothyroidism - Atrophy of thyroid (acquired),2058,E03.4,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.4,,ICD-10 E03.5 Other hypothyroidism - Myxoedema coma,2059,E03.5,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.5,,ICD-10 -E03.8 Other specified hypothyroidism,2060,E03.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.8,ORPHAcode: 88643 Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome +E03.8 Other specified hypothyroidism,2060,E03.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.8,ORPHAcode: 88643 Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome,ICD-10 "E03.9 Hypothyroidism, unspecified",2061,E03.9,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E03.9,,ICD-10 E04 Other nontoxic goitre,2062,E04,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E04,,ICD-10 E04.0 Nontoxic diffuse goitre,2063,E04.0,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E04.0,,ICD-10 E04.1 Nontoxic single thyroid nodule,2064,E04.1,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E04.1,,ICD-10 -E04.2 Nontoxic multinodular goitre,2065,E04.2,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E04.2,ORPHAcode: 276399 Familial multinodular goiter +E04.2 Nontoxic multinodular goitre,2065,E04.2,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E04.2,ORPHAcode: 276399 Familial multinodular goiter,ICD-10 E04.8 Other specified nontoxic goitre,2066,E04.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E04.8,,ICD-10 "E04.9 Nontoxic goitre, unspecified",2067,E04.9,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E04.9,,ICD-10 E05 Thyrotoxicosis [hyperthyroidism],2068,E05,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05,,ICD-10 -E05.0 Thyrotoxicosis with diffuse goitre,2069,E05.0,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.0,ORPHAcode: 525731 Pediatric-onset Graves disease +E05.0 Thyrotoxicosis with diffuse goitre,2069,E05.0,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.0,ORPHAcode: 525731 Pediatric-onset Graves disease,ICD-10 E05.1 Thyrotoxicosis with toxic single thyroid nodule,2070,E05.1,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.1,,ICD-10 E05.2 Thyrotoxicosis with toxic multinodular goitre,2071,E05.2,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.2,,ICD-10 E05.3 Thyrotoxicosis from ectopic thyroid tissue,2072,E05.3,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.3,,ICD-10 E05.4 Thyrotoxicosis factitia,2073,E05.4,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.4,,ICD-10 E05.5 Thyrotoxicosis [hyperthyroidism] - Thyroid crisis or storm,2074,E05.5,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.5,,ICD-10 -E05.8 Other thyrotoxicosis,2075,E05.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.8,ORPHAcode: 424 Familial hyperthyroidism due to mutations in TSH receptor +E05.8 Other thyrotoxicosis,2075,E05.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.8,ORPHAcode: 424 Familial hyperthyroidism due to mutations in TSH receptor,ICD-10 "E05.9 Thyrotoxicosis, unspecified",2076,E05.9,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E05.9,,ICD-10 E06 Thyroiditis,2077,E06,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E06,,ICD-10 E06.0 Acute thyroiditis,2078,E06.0,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E06.0,,ICD-10 @@ -2085,8 +2085,8 @@ E06.5 Other chronic thyroiditis,2083,E06.5,E00-E07 Disorders of thyroid gland,ht "E06.9 Thyroiditis, unspecified",2084,E06.9,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E06.9,,ICD-10 E07 Other disorders of thyroid,2085,E07,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E07,,ICD-10 E07.0 Hypersecretion of calcitonin,2086,E07.0,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E07.0,,ICD-10 -E07.1 Other disorders of thyroid - Dyshormogenetic goitre,2087,E07.1,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E07.1,ORPHAcode: 705 Pendred syndrome -E07.8 Other specified disorders of thyroid,2088,E07.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E07.8,ORPHAcode: 566231 Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha +E07.1 Other disorders of thyroid - Dyshormogenetic goitre,2087,E07.1,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E07.1,ORPHAcode: 705 Pendred syndrome,ICD-10 +E07.8 Other specified disorders of thyroid,2088,E07.8,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E07.8,ORPHAcode: 566231 Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha,ICD-10 "E07.9 Disorder of thyroid, unspecified",2089,E07.9,E00-E07 Disorders of thyroid gland,http://identifiers.org/icd/E07.9,,ICD-10 E10-E14 Diabetes mellitus,2090,,"IV Endocrine, nutritional and metabolic diseases",,,ICD-10 E10 Type 1 diabetes mellitus,2091,E10,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E10,,ICD-10 @@ -2122,7 +2122,7 @@ E12.6 Malnutrition-related diabetes mellitus with other specified complications, E12.7 Malnutrition-related diabetes mellitus with multiple complications,2121,E12.7,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E12,,ICD-10 E12.8 Malnutrition-related diabetes mellitus with with unspecified complications,2122,E12.8,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E12,,ICD-10 E12.9 Malnutrition-related diabetes mellitus without complications,2123,E12.9,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E12,,ICD-10 -E13 Other specified diabetes mellitus,2124,E13,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,ORPHAcode: 552 MODY +E13 Other specified diabetes mellitus,2124,E13,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,ORPHAcode: 552 MODY,ICD-10 E13.0 Other specified diabetes mellitus with coma,2125,E13.0,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,,ICD-10 H11.3 Conjunctival haemorrhage,2126,H11.3,H10-H13 Disorders of conjunctiva,http://identifiers.org/icd/H11.3,,ICD-10 E13.1 Other specified diabetes mellitus with ketoacidosis,2127,E13.1,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,,ICD-10 @@ -2132,7 +2132,7 @@ E13.4 Other specified diabetes mellitus with neurological complications,2130,E13 E13.5 Other specified diabetes mellitus with peripheral circulatory complications,2131,E13.5,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,,ICD-10 E13.6 Other specified diabetes mellitus with other specified complications,2132,E13.6,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,,ICD-10 E13.7 Other specified diabetes mellitus with multiple complications,2133,E13.7,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,,ICD-10 -E13.8 Other specified diabetes mellitus with unspecified complications,2134,E13.8,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,ORPHAcode: 225 Maternally-inherited diabetes and deafness +E13.8 Other specified diabetes mellitus with unspecified complications,2134,E13.8,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,ORPHAcode: 225 Maternally-inherited diabetes and deafness,ICD-10 E13.9 Other specified diabetes mellitus without complications,2135,E13.9,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E13,,ICD-10 E14 Unspecified diabetes mellitus,2136,E14,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E14,,ICD-10 E14.0 Unspecified diabetes mellitus with coma,2137,E14.0,E10-E14 Diabetes mellitus,http://identifiers.org/icd/E14,,ICD-10 @@ -2149,99 +2149,99 @@ E15-E16 Other disorders of glucose regulation and pancreatic internal secretion, E15 Nondiabetic hypoglycaemic coma,2148,E15,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E15,,ICD-10 E16 Other disorders of pancreatic internal secretion,2149,E16,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16,,ICD-10 E16.0 Other disorders of pancreatic internal secretion - Drug-induced hypoglycaemia without coma,2150,E16.0,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.0,,ICD-10 -E16.1 Other hypoglycaemia,2151,E16.1,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.1,ORPHAcode: 79299 Hyperinsulinism due to glucokinase deficiency +E16.1 Other hypoglycaemia,2151,E16.1,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.1,ORPHAcode: 79299 Hyperinsulinism due to glucokinase deficiency,ICD-10 "E16.2 Other disorders of pancreatic internal secretion - Hypoglycaemia, unspecified",2152,E16.2,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.2,,ICD-10 -E16.3 Increased secretion of glucagon,2153,E16.3,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.3,ORPHAcode: 438274 GCGR-related hyperglucagonemia -E16.4 Abnormal secretion of gastrin,2154,E16.4,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.4,ORPHAcode: 913 Zollinger-Ellison syndrome -E16.8 Other specified disorders of pancreatic internal secretion,2155,E16.8,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.8,ORPHAcode: 97261 GRFoma +E16.3 Increased secretion of glucagon,2153,E16.3,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.3,ORPHAcode: 438274 GCGR-related hyperglucagonemia,ICD-10 +E16.4 Abnormal secretion of gastrin,2154,E16.4,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.4,ORPHAcode: 913 Zollinger-Ellison syndrome,ICD-10 +E16.8 Other specified disorders of pancreatic internal secretion,2155,E16.8,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.8,ORPHAcode: 97261 GRFoma,ICD-10 "E16.9 Disorder of pancreatic internal secretion, unspecified",2156,E16.9,E15-E16 Other disorders of glucose regulation and pancreatic internal secretion,http://identifiers.org/icd/E16.9,,ICD-10 E20-E35 Disorders of other endocrine glands,2157,,"IV Endocrine, nutritional and metabolic diseases",,,ICD-10 E20 Hypoparathyroidism,2158,E20,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E20,,ICD-10 E20.0 Idiopathic hypoparathyroidism,2159,E20.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E20.0,,ICD-10 -E20.1 Pseudohypoparathyroidism,2160,E20.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E20.1,ORPHAcode: 79443 Pseudohypoparathyroidism type 1A -E20.8 Other hypoparathyroidism,2161,E20.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E20.8,ORPHAcode: 2238 Familial isolated hypoparathyroidism +E20.1 Pseudohypoparathyroidism,2160,E20.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E20.1,ORPHAcode: 79443 Pseudohypoparathyroidism type 1A,ICD-10 +E20.8 Other hypoparathyroidism,2161,E20.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E20.8,ORPHAcode: 2238 Familial isolated hypoparathyroidism,ICD-10 "E20.9 Hypoparathyroidism, unspecified",2162,E20.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E20.9,,ICD-10 E21 Hyperparathyroidism and other disorders of parathyroid gland,2163,E21,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21,,ICD-10 -E21.0 Primary hyperparathyroidism,2164,E21.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21.0,ORPHAcode: 417 Neonatal severe primary hyperparathyroidism +E21.0 Primary hyperparathyroidism,2164,E21.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21.0,ORPHAcode: 417 Neonatal severe primary hyperparathyroidism,ICD-10 "E21.1 Secondary hyperparathyroidism, not elsewhere classified",2165,E21.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21.1,,ICD-10 E21.2 Other hyperparathyroidism,2166,E21.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21.2,,ICD-10 "E21.3 Hyperparathyroidism, unspecified",2167,E21.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21.3,,ICD-10 E21.4 Other specified disorders of parathyroid gland,2168,E21.4,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21.4,,ICD-10 "E21.5 Disorder of parathyroid gland, unspecified",2169,E21.5,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E21.5,,ICD-10 E22 Hyperfunction of pituitary gland,2170,E22,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22,,ICD-10 -E22.0 Acromegaly and pituitary gigantism,2171,E22.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.0,ORPHAcode: 963 Acromegaly -E22.1 Hyperfunction of pituitary gland - Hyperprolactinaemia,2172,E22.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.1,ORPHAcode: 397685 Familial hyperprolactinemia -E22.2 Syndrome of inappropriate secretion of antidiuretic hormone,2173,E22.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.2,ORPHAcode: 93606 Nephrogenic syndrome of inappropriate antidiuresis -E22.8 Other hyperfunction of pituitary gland,2174,E22.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.8,ORPHAcode: 759 Central precocious puberty +E22.0 Acromegaly and pituitary gigantism,2171,E22.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.0,ORPHAcode: 963 Acromegaly,ICD-10 +E22.1 Hyperfunction of pituitary gland - Hyperprolactinaemia,2172,E22.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.1,ORPHAcode: 397685 Familial hyperprolactinemia,ICD-10 +E22.2 Syndrome of inappropriate secretion of antidiuretic hormone,2173,E22.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.2,ORPHAcode: 93606 Nephrogenic syndrome of inappropriate antidiuresis,ICD-10 +E22.8 Other hyperfunction of pituitary gland,2174,E22.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.8,ORPHAcode: 759 Central precocious puberty,ICD-10 "E22.9 Hyperfunction of pituitary gland, unspecified",2175,E22.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E22.9,,ICD-10 E23 Hypofunction and other disorders of pituitary gland,2176,E23,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23,,ICD-10 -E23.0 Hypofunction and other disorders of pituitary gland - Hypopituitarism,2177,E23.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.0,ORPHAcode: 631 Non-acquired isolated growth hormone deficiency -E23.1 Hypofunction and other disorders of pituitary gland - Drug-induced hypopituitarism,2178,E23.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.1,ORPHAcode: 95619 Post-traumatic pituitary deficiency -E23.2 Hypofunction and other disorders of pituitary gland - Diabetes insipidus,2179,E23.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.2,ORPHAcode: 178029 Central diabetes insipidus -"E23.3 Hypofunction and other disorders of pituitary gland - Hypothalamic dysfunction, not elsewhere classified",2180,E23.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.3,ORPHAcode: 443101 Hypothalamic adipsic hypernatraemia syndrome -E23.6 Other disorders of pituitary gland,2181,E23.6,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.6,ORPHAcode: 52901 Isolated follicle stimulating hormone deficiency +E23.0 Hypofunction and other disorders of pituitary gland - Hypopituitarism,2177,E23.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.0,ORPHAcode: 631 Non-acquired isolated growth hormone deficiency,ICD-10 +E23.1 Hypofunction and other disorders of pituitary gland - Drug-induced hypopituitarism,2178,E23.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.1,ORPHAcode: 95619 Post-traumatic pituitary deficiency,ICD-10 +E23.2 Hypofunction and other disorders of pituitary gland - Diabetes insipidus,2179,E23.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.2,ORPHAcode: 178029 Central diabetes insipidus,ICD-10 +"E23.3 Hypofunction and other disorders of pituitary gland - Hypothalamic dysfunction, not elsewhere classified",2180,E23.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.3,ORPHAcode: 443101 Hypothalamic adipsic hypernatraemia syndrome,ICD-10 +E23.6 Other disorders of pituitary gland,2181,E23.6,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.6,ORPHAcode: 52901 Isolated follicle stimulating hormone deficiency,ICD-10 "E23.7 Disorder of pituitary gland, unspecified",2182,E23.7,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E23.7,,ICD-10 E24 Cushing syndrome,2183,E24,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24,,ICD-10 -E24.0 Pituitary-dependent Cushing disease,2184,E24.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.0,ORPHAcode: 96253 Cushing disease -E24.1 Nelson syndrome,2185,E24.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.1,ORPHAcode: 199244 Nelson syndrome +E24.0 Pituitary-dependent Cushing disease,2184,E24.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.0,ORPHAcode: 96253 Cushing disease,ICD-10 +E24.1 Nelson syndrome,2185,E24.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.1,ORPHAcode: 199244 Nelson syndrome,ICD-10 E24.2 Drug-induced Cushing syndrome,2186,E24.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.2,,ICD-10 -E24.3 Ectopic ACTH syndrome,2187,E24.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.3,ORPHAcode: 99889 Cushing syndrome due to ectopic ACTH secretion +E24.3 Ectopic ACTH syndrome,2187,E24.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.3,ORPHAcode: 99889 Cushing syndrome due to ectopic ACTH secretion,ICD-10 E24.4 Alcohol-induced pseudo-Cushing syndrome,2188,E24.4,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.4,,ICD-10 -E24.8 Other Cushing syndrome,2189,E24.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.8,ORPHAcode: 189427 Cushing syndrome due to macronodular adrenal hyperplasia +E24.8 Other Cushing syndrome,2189,E24.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.8,ORPHAcode: 189427 Cushing syndrome due to macronodular adrenal hyperplasia,ICD-10 "E24.9 Cushing syndrome, unspecified",2190,E24.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E24.9,,ICD-10 E25 Adrenogenital disorders,2191,E25,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E25,,ICD-10 -E25.0 Congenital adrenogenital disorders associated with enzyme deficiency,2192,E25.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E25.0,ORPHAcode: 90790 Congenital lipoid adrenal hyperplasia due to STAR deficency -E25.8 Other adrenogenital disorders,2193,E25.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E25.8,ORPHAcode: 91 Aromatase deficiency +E25.0 Congenital adrenogenital disorders associated with enzyme deficiency,2192,E25.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E25.0,ORPHAcode: 90790 Congenital lipoid adrenal hyperplasia due to STAR deficency,ICD-10 +E25.8 Other adrenogenital disorders,2193,E25.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E25.8,ORPHAcode: 91 Aromatase deficiency,ICD-10 "E25.9 Adrenogenital disorder, unspecified",2194,E25.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E25.9,,ICD-10 E26 Hyperaldosteronism,2195,E26,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26,,ICD-10 -E26.0 Primary hyperaldosteronism,2196,E26.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26.0,ORPHAcode: 403 Familial hyperaldosteronism type I +E26.0 Primary hyperaldosteronism,2196,E26.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26.0,ORPHAcode: 403 Familial hyperaldosteronism type I,ICD-10 E32.8 Other diseases of thymus,2197,E32.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E32.8,,ICD-10 -E26.1 Secondary hyperaldosteronism,2198,E26.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26.1,ORPHAcode: 320 Apparent mineralocorticoid excess -E26.8 Other hyperaldosteronism,2199,E26.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26.8,ORPHAcode: 112 Bartter syndrome +E26.1 Secondary hyperaldosteronism,2198,E26.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26.1,ORPHAcode: 320 Apparent mineralocorticoid excess,ICD-10 +E26.8 Other hyperaldosteronism,2199,E26.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26.8,ORPHAcode: 112 Bartter syndrome,ICD-10 "E26.9 Hyperaldosteronism, unspecified",2200,E26.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E26.9,,ICD-10 E27 Other disorders of adrenal gland,2201,E27,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27,,ICD-10 E27.0 Other adrenocortical overactivity,2202,E27.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.0,,ICD-10 -E27.1 Other disorders of adrenal gland - Primary adrenocortical insufficiency,2203,E27.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.1,ORPHAcode: 361 Familial glucocorticoid deficiency -E27.2 Other disorders of adrenal gland - Addisonian crisis,2204,E27.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.2,ORPHAcode: 95409 Acute adrenal insufficiency +E27.1 Other disorders of adrenal gland - Primary adrenocortical insufficiency,2203,E27.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.1,ORPHAcode: 361 Familial glucocorticoid deficiency,ICD-10 +E27.2 Other disorders of adrenal gland - Addisonian crisis,2204,E27.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.2,ORPHAcode: 95409 Acute adrenal insufficiency,ICD-10 E27.3 Other disorders of adrenal gland - Drug-induced adrenocortical insufficiency,2205,E27.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.3,,ICD-10 -E27.4 Other and unspecified adrenocortical insufficiency,2206,E27.4,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.4,ORPHAcode: 427 Familial hypoaldosteronism +E27.4 Other and unspecified adrenocortical insufficiency,2206,E27.4,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.4,ORPHAcode: 427 Familial hypoaldosteronism,ICD-10 E27.5 Other disorders of adrenal gland - Adrenomedullary hyperfunction,2207,E27.5,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.5,,ICD-10 -E27.8 Other specified disorders of adrenal gland,2208,E27.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.8,ORPHAcode: 199247 Corticosteroid-binding globulin deficiency +E27.8 Other specified disorders of adrenal gland,2208,E27.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.8,ORPHAcode: 199247 Corticosteroid-binding globulin deficiency,ICD-10 "E27.9 Disorder of adrenal gland, unspecified",2209,E27.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E27.9,,ICD-10 E28 Ovarian dysfunction,2210,E28,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28,,ICD-10 E28.0 Ovarian dysfunction - Estrogen excess,2211,E28.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28.0,,ICD-10 E28.1 Ovarian dysfunction - Androgen excess,2212,E28.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28.1,,ICD-10 E28.2 Polycystic ovarian syndrome,2213,E28.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28.2,,ICD-10 -E28.3 Primary ovarian failure,2214,E28.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28.3,ORPHAcode: 2232 Primary hypergonadotropic hypogonadism-partial alopecia syndrome +E28.3 Primary ovarian failure,2214,E28.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28.3,ORPHAcode: 2232 Primary hypergonadotropic hypogonadism-partial alopecia syndrome,ICD-10 E28.8 Other ovarian dysfunction,2215,E28.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28.8,,ICD-10 "E28.9 Ovarian dysfunction, unspecified",2216,E28.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E28.9,,ICD-10 E29 Testicular dysfunction,2217,E29,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E29,,ICD-10 E29.0 Testicular hyperfunction,2218,E29.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E29.0,,ICD-10 -E29.1 Testicular hypofunction,2219,E29.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E29.1,"ORPHAcode: 752 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency" +E29.1 Testicular hypofunction,2219,E29.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E29.1,"ORPHAcode: 752 46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency",ICD-10 E29.8 Other testicular dysfunction,2220,E29.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E29.8,,ICD-10 "E29.9 Testicular dysfunction, unspecified",2221,E29.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E29.9,,ICD-10 -"E30 Disorders of puberty, not elsewhere classified",2222,E30,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E30,ORPHAcode: 785 Estrogen resistance syndrome +"E30 Disorders of puberty, not elsewhere classified",2222,E30,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E30,ORPHAcode: 785 Estrogen resistance syndrome,ICD-10 E30.0 Delayed puberty,2223,E30.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E30.0,,ICD-10 -E30.1 Precocious puberty,2224,E30.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E30.1,ORPHAcode: 3000 Familial male-limited precocious puberty +E30.1 Precocious puberty,2224,E30.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E30.1,ORPHAcode: 3000 Familial male-limited precocious puberty,ICD-10 E30.8 Other disorders of puberty,2225,E30.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E30.8,,ICD-10 "E30.9 Disorder of puberty, unspecified",2226,E30.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E30.9,,ICD-10 E31 Polyglandular dysfunction,2227,E31,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E31,,ICD-10 -E31.0 Autoimmune polyglandular failure,2228,E31.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E31.0,ORPHAcode: 3143 Autoimmune polyendocrinopathy type 2 +E31.0 Autoimmune polyglandular failure,2228,E31.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E31.0,ORPHAcode: 3143 Autoimmune polyendocrinopathy type 2,ICD-10 E31.1 Polyglandular hyperfunction,2229,E31.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E31.1,,ICD-10 -E31.8 Other polyglandular dysfunction,2230,E31.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E31.8,ORPHAcode: 1227 Bangstad syndrome +E31.8 Other polyglandular dysfunction,2230,E31.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E31.8,ORPHAcode: 1227 Bangstad syndrome,ICD-10 "E31.9 Polyglandular dysfunction, unspecified",2231,E31.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E31.9,,ICD-10 E32 Diseases of thymus,2232,E32,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E32,,ICD-10 E32.0 Persistent hyperplasia of thymus,2233,E32.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E32.0,,ICD-10 E32.1 Abscess of thymus,2234,E32.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E32.1,,ICD-10 "E32.9 Disease of thymus, unspecified",2235,E32.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E32.9,,ICD-10 E34 Other endocrine disorders,2236,E34,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34,,ICD-10 -E34.0 Other endocrine disorders - Carcinoid syndrome,2237,E34.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.0,ORPHAcode: 100093 Carcinoid syndrome +E34.0 Other endocrine disorders - Carcinoid syndrome,2237,E34.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.0,ORPHAcode: 100093 Carcinoid syndrome,ICD-10 E34.1 Other hypersecretion of intestinal hormones,2238,E34.1,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.1,,ICD-10 "E34.2 Other endocrine disorders - Ectopic hormone secretion, not elsewhere classified",2239,E34.2,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.2,,ICD-10 -"E34.3 Other endocrine disorders - Short stature, not elsewhere classified",2240,E34.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.3,ORPHAcode: 633 Laron syndrome +"E34.3 Other endocrine disorders - Short stature, not elsewhere classified",2240,E34.3,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.3,ORPHAcode: 633 Laron syndrome,ICD-10 E34.4 Other endocrine disorders - Constitutional tall stature,2241,E34.4,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.4,,ICD-10 -E34.5 Other endocrine disorders - Androgen resistance syndrome,2242,E34.5,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.5,ORPHAcode: 90797 Partial androgen insensitivity syndrome -E34.8 Other specified endocrine disorders,2243,E34.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.8,ORPHAcode: 64 Alstr m sy +E34.5 Other endocrine disorders - Androgen resistance syndrome,2242,E34.5,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.5,ORPHAcode: 90797 Partial androgen insensitivity syndrome,ICD-10 +E34.8 Other specified endocrine disorders,2243,E34.8,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.8,ORPHAcode: 64 Alstr m sy,ICD-10 "E34.9 Endocrine disorder, unspecified",2244,E34.9,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E34.9,,ICD-10 E35 Disorders of endocrine glands in diseases classified elsewhere,2245,E35,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E35,,ICD-10 E35.0 Disorders of thyroid gland in diseases classified elsewhere,2246,E35.0,E20-E35 Disorders of other endocrine glands,http://identifiers.org/icd/E35.0,,ICD-10 @@ -2267,22 +2267,22 @@ E50.4 Vitamin A deficiency with keratomalacia,2265,E50.4,E50-E64 Other nutrition E50.5 Vitamin A deficiency with night blindness,2266,E50.5,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E50.5,,ICD-10 E50.6 Vitamin A deficiency with xerophthalmic scars of cornea,2267,E50.6,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E50.6,,ICD-10 E50.7 Other ocular manifestations of vitamin A deficiency,2268,E50.7,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E50.7,,ICD-10 -E50.8 Other manifestations of vitamin A deficiency,2269,E50.8,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E50.8,ORPHAcode: 199285 Hereditary hypercarotenemia and vitamin A deficiency +E50.8 Other manifestations of vitamin A deficiency,2269,E50.8,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E50.8,ORPHAcode: 199285 Hereditary hypercarotenemia and vitamin A deficiency,ICD-10 "E50.9 Vitamin A deficiency, unspecified",2270,E50.9,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E50.9,,ICD-10 E51 Thiamine deficiency,2271,E51,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E51,,ICD-10 E51.1 Thiamine deficiency - Beriberi,2272,E51.1,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E51.1,,ICD-10 -E51.2 Thiamine deficiency - Wernicke encephalopathy,2273,E51.2,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E51.2,ORPHAcode: 199348 Thiamine-responsive encephalopathy +E51.2 Thiamine deficiency - Wernicke encephalopathy,2273,E51.2,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E51.2,ORPHAcode: 199348 Thiamine-responsive encephalopathy,ICD-10 E51.8 Other manifestations of thiamine deficiency,2274,E51.8,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E51.8,,ICD-10 "E51.9 Thiamine deficiency, unspecified",2275,E51.9,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E51.9,,ICD-10 -E52 Niacin deficiency [pellagra],2276,E52,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E52,ORPHAcode: 97352 Pellagra +E52 Niacin deficiency [pellagra],2276,E52,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E52,ORPHAcode: 97352 Pellagra,ICD-10 E53 Deficiency of other B group vitamins,2277,E53,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E53,,ICD-10 E53.0 Riboflavin deficiency,2278,E53.0,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E53.0,,ICD-10 E53.1 Pyridoxine deficiency,2279,E53.1,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E53.1,,ICD-10 -E53.8 Deficiency of other specified B group vitamins,2280,E53.8,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E53.8,ORPHAcode: 2967 Transcobalamin I deficiency +E53.8 Deficiency of other specified B group vitamins,2280,E53.8,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E53.8,ORPHAcode: 2967 Transcobalamin I deficiency,ICD-10 "E53.9 Vitamin B deficiency, unspecified",2281,E53.9,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E53.9,,ICD-10 E54 Ascorbic acid deficiency,2282,E54,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E54,,ICD-10 E55 Vitamin D deficiency,2283,E55,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E55,,ICD-10 -"E55.0 Vitamin D deficiency - Rickets, active",2284,E55.0,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E55.0,ORPHAcode: 289157 Hypocalcemic vitamin D-dependent rickets +"E55.0 Vitamin D deficiency - Rickets, active",2284,E55.0,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E55.0,ORPHAcode: 289157 Hypocalcemic vitamin D-dependent rickets,ICD-10 "E55.9 Vitamin D deficiency, unspecified",2285,E55.9,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E55.9,,ICD-10 E56 Other vitamin deficiencies,2286,E56,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E56,,ICD-10 E56.0 Deficiency of vitamin E,2287,E56.0,E50-E64 Other nutritional deficiencies,http://identifiers.org/icd/E56.0,,ICD-10 @@ -2322,7 +2322,7 @@ E66 Obesity,2320,E66,E65-E68 Obesity and other hyperalimentation,http://identifi E66.0 Obesity due to excess calories,2321,E66.0,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E66.0,,ICD-10 E66.1 Drug-induced obesity,2322,E66.1,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E66.1,,ICD-10 E66.2 Extreme obesity with alveolar hypoventilation,2323,E66.2,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E66.2,,ICD-10 -E66.8 Other obesity,2324,E66.8,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E66.8,ORPHAcode: 98267 Genetic non-syndromic obesity +E66.8 Other obesity,2324,E66.8,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E66.8,ORPHAcode: 98267 Genetic non-syndromic obesity,ICD-10 "E66.9 Obesity, unspecified",2325,E66.9,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E66.9,,ICD-10 E67 Other hyperalimentation,2326,E67,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E67,,ICD-10 E67.0 Other hyperalimentation - Hypervitaminosis A,2327,E67.0,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E67.0,,ICD-10 @@ -2333,105 +2333,105 @@ E67.8 Other specified hyperalimentation,2331,E67.8,E65-E68 Obesity and other hyp E68 Sequelae of hyperalimentation,2332,E68,E65-E68 Obesity and other hyperalimentation,http://identifiers.org/icd/E68,,ICD-10 E70-E90 Metabolic disorders,2333,,"IV Endocrine, nutritional and metabolic diseases",,,ICD-10 E70 Disorders of aromatic amino-acid metabolism,2334,E70,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70,,ICD-10 -E72.5 Disorders of glycine metabolism,2335,E72.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.5,ORPHAcode: 407 Glycine encephalopathy -E70.0 Disorders of aromatic amino-acid metabolism - Classical phenylketonuria,2336,E70.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.0,ORPHAcode: 716 Phenylketonuria -E70.1 Disorders of aromatic amino-acid metabolism - Other hyperphenylalaninaemias,2337,E70.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.1,ORPHAcode: 2209 Maternal phenylketonuria -E70.2 Disorders of tyrosine metabolism,2338,E70.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.2,ORPHAcode: 56 Alkaptonuria -E70.3 Disorders of aromatic amino-acid metabolism - Albinism,2339,E70.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.3,ORPHAcode: 54 X-linked recessive ocular albinism -E70.8 Other disorders of aromatic amino-acid metabolism,2340,E70.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.8,ORPHAcode: 1361 Carnosinase deficiency +E72.5 Disorders of glycine metabolism,2335,E72.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.5,ORPHAcode: 407 Glycine encephalopathy,ICD-10 +E70.0 Disorders of aromatic amino-acid metabolism - Classical phenylketonuria,2336,E70.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.0,ORPHAcode: 716 Phenylketonuria,ICD-10 +E70.1 Disorders of aromatic amino-acid metabolism - Other hyperphenylalaninaemias,2337,E70.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.1,ORPHAcode: 2209 Maternal phenylketonuria,ICD-10 +E70.2 Disorders of tyrosine metabolism,2338,E70.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.2,ORPHAcode: 56 Alkaptonuria,ICD-10 +E70.3 Disorders of aromatic amino-acid metabolism - Albinism,2339,E70.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.3,ORPHAcode: 54 X-linked recessive ocular albinism,ICD-10 +E70.8 Other disorders of aromatic amino-acid metabolism,2340,E70.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.8,ORPHAcode: 1361 Carnosinase deficiency,ICD-10 "E70.9 Disorder of aromatic amino-acid metabolism, unspecified",2341,E70.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E70.9,,ICD-10 E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism,2342,E71,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71,,ICD-10 -E71.0 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism - Maple-syrup-urine disease,2343,E71.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71.0,ORPHAcode: 511 Maple syrup urine disease -E71.1 Other disorders of branched-chain amino-acid metabolism,2344,E71.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71.1,ORPHAcode: 6 3-methylcrotonyl-CoA carboxylase deficiency +E71.0 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism - Maple-syrup-urine disease,2343,E71.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71.0,ORPHAcode: 511 Maple syrup urine disease,ICD-10 +E71.1 Other disorders of branched-chain amino-acid metabolism,2344,E71.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71.1,ORPHAcode: 6 3-methylcrotonyl-CoA carboxylase deficiency,ICD-10 "E71.2 Disorder of branched-chain amino-acid metabolism, unspecified",2345,E71.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71.2,,ICD-10 -E71.3 Disorders of fatty-acid metabolism,2346,E71.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71.3,ORPHAcode: 5 Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency +E71.3 Disorders of fatty-acid metabolism,2346,E71.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E71.3,ORPHAcode: 5 Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency,ICD-10 E72 Other disorders of amino-acid metabolism,2347,E72,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72,,ICD-10 -E72.0 Disorders of amino-acid transport,2348,E72.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.0,ORPHAcode: 213 Cystinosis -E72.1 Disorders of sulfur-bearing amino-acid metabolism,2349,E72.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.1,ORPHAcode: 212 Cystathioninuria -E72.2 Disorders of urea cycle metabolism,2350,E72.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.2,ORPHAcode: 23 Argininosuccinic aciduria -E72.3 Disorders of lysine and hydroxylysine metabolism,2351,E72.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.3,ORPHAcode: 25 Glutaryl-CoA dehydrogenase deficiency -E72.4 Disorders of ornithine metabolism,2352,E72.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.4,ORPHAcode: 414 Gyrate atrophy of choroid and retina -E72.8 Other specified disorders of amino-acid metabolism,2353,E72.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.8,ORPHAcode: 22 Succinic semialdehyde dehydrogenase deficiency +E72.0 Disorders of amino-acid transport,2348,E72.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.0,ORPHAcode: 213 Cystinosis,ICD-10 +E72.1 Disorders of sulfur-bearing amino-acid metabolism,2349,E72.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.1,ORPHAcode: 212 Cystathioninuria,ICD-10 +E72.2 Disorders of urea cycle metabolism,2350,E72.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.2,ORPHAcode: 23 Argininosuccinic aciduria,ICD-10 +E72.3 Disorders of lysine and hydroxylysine metabolism,2351,E72.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.3,ORPHAcode: 25 Glutaryl-CoA dehydrogenase deficiency,ICD-10 +E72.4 Disorders of ornithine metabolism,2352,E72.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.4,ORPHAcode: 414 Gyrate atrophy of choroid and retina,ICD-10 +E72.8 Other specified disorders of amino-acid metabolism,2353,E72.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.8,ORPHAcode: 22 Succinic semialdehyde dehydrogenase deficiency,ICD-10 "E72.9 Disorder of amino-acid metabolism, unspecified",2354,E72.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E72.9,,ICD-10 E73 Lactose intolerance,2355,E73,E70-E90 Metabolic disorders,http://identifiers.org/icd/E73,,ICD-10 -E73.0 Lactose intolerance - Congenital lactase deficiency,2356,E73.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E73.0,ORPHAcode: 53690 Congenital lactase deficiency +E73.0 Lactose intolerance - Congenital lactase deficiency,2356,E73.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E73.0,ORPHAcode: 53690 Congenital lactase deficiency,ICD-10 E73.1 Lactose intolerance - Secondary lactase deficiency,2357,E73.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E73.1,,ICD-10 E73.8 Other lactose intolerance,2358,E73.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E73.8,,ICD-10 "E73.9 Lactose intolerance, unspecified",2359,E73.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E73.9,,ICD-10 E74 Other disorders of carbohydrate metabolism,2360,E74,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74,,ICD-10 -E74.0 Other disorders of carbohydrate metabolism - Glycogen storage disease,2361,E74.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.0,ORPHAcode: 57 Glycogen storage disease due to aldolase A deficiency -E74.1 Disorders of fructose metabolism,2362,E74.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.1,"ORPHAcode: 348 Fructose-1,6-bisphosphatase deficiency" -E74.2 Disorders of galactose metabolism,2363,E74.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.2,ORPHAcode: 79237 Galactokinase deficiency -E74.3 Other disorders of intestinal carbohydrate absorption,2364,E74.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.3,ORPHAcode: 35122 Congenital sucrase-isomaltase deficiency -E74.4 Disorders of pyruvate metabolism and gluconeogenesis,2365,E74.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.4,ORPHAcode: 765 Pyruvate dehydrogenase deficiency -E74.8 Other specified disorders of carbohydrate metabolism,2366,E74.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.8,ORPHAcode: 408 Isolated glycerol kinase deficiency +E74.0 Other disorders of carbohydrate metabolism - Glycogen storage disease,2361,E74.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.0,ORPHAcode: 57 Glycogen storage disease due to aldolase A deficiency,ICD-10 +E74.1 Disorders of fructose metabolism,2362,E74.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.1,"ORPHAcode: 348 Fructose-1,6-bisphosphatase deficiency",ICD-10 +E74.2 Disorders of galactose metabolism,2363,E74.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.2,ORPHAcode: 79237 Galactokinase deficiency,ICD-10 +E74.3 Other disorders of intestinal carbohydrate absorption,2364,E74.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.3,ORPHAcode: 35122 Congenital sucrase-isomaltase deficiency,ICD-10 +E74.4 Disorders of pyruvate metabolism and gluconeogenesis,2365,E74.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.4,ORPHAcode: 765 Pyruvate dehydrogenase deficiency,ICD-10 +E74.8 Other specified disorders of carbohydrate metabolism,2366,E74.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.8,ORPHAcode: 408 Isolated glycerol kinase deficiency,ICD-10 "E74.9 Disorder of carbohydrate metabolism, unspecified",2367,E74.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E74.9,,ICD-10 E75 Disorders of sphingolipid metabolism and other lipid storage disorders,2368,E75,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75,,ICD-10 -E75.0 Disorders of sphingolipid metabolism and other lipid storage disorders - gangliosidosis,2369,E75.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.0,ORPHAcode: 796 Sandhoff disease -E75.1 Other gangliosidosis,2370,E75.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.1,ORPHAcode: 354 GM1 gangliosidosis -E75.2 Other sphingolipidosis,2371,E75.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.2,ORPHAcode: 58 Alexander disease +E75.0 Disorders of sphingolipid metabolism and other lipid storage disorders - gangliosidosis,2369,E75.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.0,ORPHAcode: 796 Sandhoff disease,ICD-10 +E75.1 Other gangliosidosis,2370,E75.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.1,ORPHAcode: 354 GM1 gangliosidosis,ICD-10 +E75.2 Other sphingolipidosis,2371,E75.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.2,ORPHAcode: 58 Alexander disease,ICD-10 "E75.3 Sphingolipidosis, unspecified",2372,E75.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.3,,ICD-10 -E75.4 Neuronal ceroid lipofuscinosis,2373,E75.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.4,"ORPHAcode: 1947 Progressive epilepsy-intellectual disability syndrome, Finnish type" -E75.5 Other lipid storage disorders,2374,E75.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.5,ORPHAcode: 909 Cerebrotendinous xanthomatosis +E75.4 Neuronal ceroid lipofuscinosis,2373,E75.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.4,"ORPHAcode: 1947 Progressive epilepsy-intellectual disability syndrome, Finnish type",ICD-10 +E75.5 Other lipid storage disorders,2374,E75.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.5,ORPHAcode: 909 Cerebrotendinous xanthomatosis,ICD-10 "E75.6 Lipid storage disorder, unspecified",2375,E75.6,E70-E90 Metabolic disorders,http://identifiers.org/icd/E75.6,,ICD-10 E76 Disorders of glycosaminoglycan metabolism,2376,E76,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76,,ICD-10 -"E76.0 Disorders of glycosaminoglycan metabolism - Mucopolysaccharidosis, type I",2377,E76.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.0,ORPHAcode: 579 Mucopolysaccharidosis type 1 -"E76.1 Disorders of glycosaminoglycan metabolism - Mucopolysaccharidosis, type II",2378,E76.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.1,ORPHAcode: 580 Mucopolysaccharidosis type 2 -E76.2 Disorders of glycosaminoglycan metabolism - Other mucopolysaccharidoses,2379,E76.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.2,ORPHAcode: 581 Mucopolysaccharidosis type 3 +"E76.0 Disorders of glycosaminoglycan metabolism - Mucopolysaccharidosis, type I",2377,E76.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.0,ORPHAcode: 579 Mucopolysaccharidosis type 1,ICD-10 +"E76.1 Disorders of glycosaminoglycan metabolism - Mucopolysaccharidosis, type II",2378,E76.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.1,ORPHAcode: 580 Mucopolysaccharidosis type 2,ICD-10 +E76.2 Disorders of glycosaminoglycan metabolism - Other mucopolysaccharidoses,2379,E76.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.2,ORPHAcode: 581 Mucopolysaccharidosis type 3,ICD-10 "E76.3 Disorders of glycosaminoglycan metabolism - Mucopolysaccharidosis, unspecified",2380,E76.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.3,,ICD-10 E76.8 Other disorders of glucosaminoglycan metabolism,2381,E76.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.8,,ICD-10 "E76.9 Disorder of glucosaminoglycan metabolism, unspecified",2382,E76.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E76.9,,ICD-10 E77 Disorders of glycoprotein metabolism,2383,E77,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77,,ICD-10 -E77.0 Defects in post-translational modification of lysosomal enzymes,2384,E77.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77.0,ORPHAcode: 576 Mucolipidosis type II -E77.1 Defects in glycoprotein degradation,2385,E77.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77.1,ORPHAcode: 61 Alpha-mannosidosis -E77.8 Other disorders of glycoprotein metabolism,2386,E77.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77.8,ORPHAcode: 834 Free sialic acid storage disease +E77.0 Defects in post-translational modification of lysosomal enzymes,2384,E77.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77.0,ORPHAcode: 576 Mucolipidosis type II,ICD-10 +E77.1 Defects in glycoprotein degradation,2385,E77.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77.1,ORPHAcode: 61 Alpha-mannosidosis,ICD-10 +E77.8 Other disorders of glycoprotein metabolism,2386,E77.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77.8,ORPHAcode: 834 Free sialic acid storage disease,ICD-10 "E77.9 Disorder of glycoprotein metabolism, unspecified",2387,E77.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E77.9,,ICD-10 E78 Disorders of lipoprotein metabolism and other lipidaemias,2388,E78,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78,,ICD-10 -E78.0 Disorders of lipoprotein metabolism and other lipidaemias - Pure hypercholesterolaemia,2389,E78.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.0,ORPHAcode: 2882 Sitosterolemia +E78.0 Disorders of lipoprotein metabolism and other lipidaemias - Pure hypercholesterolaemia,2389,E78.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.0,ORPHAcode: 2882 Sitosterolemia,ICD-10 E78.1 Disorders of lipoprotein metabolism and other lipidaemias - Pure hyperglyceridaemia,2390,E78.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.1,,ICD-10 -E78.2 Disorders of lipoprotein metabolism and other lipidaemias - Mixed hyperlipidaemia,2391,E78.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.2,ORPHAcode: 412 Dysbetalipoproteinemia -E78.3 Disorders of lipoprotein metabolism and other lipidaemias - Hyperchylomicronaemia,2392,E78.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.3,ORPHAcode: 444490 Familial chylomicronemia syndrome -E78.4 Other hyperlipidaemia,2393,E78.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.4,ORPHAcode: 79506 Cholesterol-ester transfer protein deficiency +E78.2 Disorders of lipoprotein metabolism and other lipidaemias - Mixed hyperlipidaemia,2391,E78.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.2,ORPHAcode: 412 Dysbetalipoproteinemia,ICD-10 +E78.3 Disorders of lipoprotein metabolism and other lipidaemias - Hyperchylomicronaemia,2392,E78.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.3,ORPHAcode: 444490 Familial chylomicronemia syndrome,ICD-10 +E78.4 Other hyperlipidaemia,2393,E78.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.4,ORPHAcode: 79506 Cholesterol-ester transfer protein deficiency,ICD-10 "E78.5 Disorders of lipoprotein metabolism and other lipidaemias - Hyperlipidaemia, unspecified",2394,E78.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.5,,ICD-10 -E78.6 Lipoprotein deficiency,2395,E78.6,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.6,ORPHAcode: 14 Abetalipoproteinemia -E78.8 Other disorders of lipoprotein metabolism,2396,E78.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.8,ORPHAcode: 530 Lipoid proteinosis +E78.6 Lipoprotein deficiency,2395,E78.6,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.6,ORPHAcode: 14 Abetalipoproteinemia,ICD-10 +E78.8 Other disorders of lipoprotein metabolism,2396,E78.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.8,ORPHAcode: 530 Lipoid proteinosis,ICD-10 "E78.9 Disorder of lipoprotein metabolism, unspecified",2397,E78.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E78.9,,ICD-10 E79 Disorders of purine and pyrimidine metabolism,2398,E79,E70-E90 Metabolic disorders,http://identifiers.org/icd/E79,,ICD-10 E79.0 Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease,2399,E79.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E79.0,,ICD-10 -E79.1 Disorders of purine and pyrimidine metabolism - Lesch-Nyhan syndrome,2400,E79.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E79.1,ORPHAcode: 510 Lesch-Nyhan syndrome -E79.8 Other disorders of purine and pyrimidine metabolism,2401,E79.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E79.8,ORPHAcode: 30 Hereditary orotic aciduria +E79.1 Disorders of purine and pyrimidine metabolism - Lesch-Nyhan syndrome,2400,E79.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E79.1,ORPHAcode: 510 Lesch-Nyhan syndrome,ICD-10 +E79.8 Other disorders of purine and pyrimidine metabolism,2401,E79.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E79.8,ORPHAcode: 30 Hereditary orotic aciduria,ICD-10 "E79.9 Disorder of purine and pyrimidine metabolism, unspecified",2402,E79.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E79.9,,ICD-10 E80 Disorders of porphyrin and bilirubin metabolism,2403,E80,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80,,ICD-10 -E80.0 Disorders of porphyrin and bilirubin metabolism - Hereditary erythropoietic porphyria,2404,E80.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.0,ORPHAcode: 79277 Congenital erythropoietic porphyria -E80.1 Disorders of porphyrin and bilirubin metabolism - Porphyria cutanea tarda,2405,E80.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.1,ORPHAcode: 101330 Porphyria cutanea tarda -E80.2 Disorders of porphyrin and bilirubin metabolism - Other porphyria,2406,E80.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.2,ORPHAcode: 79273 Hereditary coproporphyria -E80.3 Defects of catalase and peroxidase,2407,E80.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.3,ORPHAcode: 926 Acatalasemia +E80.0 Disorders of porphyrin and bilirubin metabolism - Hereditary erythropoietic porphyria,2404,E80.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.0,ORPHAcode: 79277 Congenital erythropoietic porphyria,ICD-10 +E80.1 Disorders of porphyrin and bilirubin metabolism - Porphyria cutanea tarda,2405,E80.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.1,ORPHAcode: 101330 Porphyria cutanea tarda,ICD-10 +E80.2 Disorders of porphyrin and bilirubin metabolism - Other porphyria,2406,E80.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.2,ORPHAcode: 79273 Hereditary coproporphyria,ICD-10 +E80.3 Defects of catalase and peroxidase,2407,E80.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.3,ORPHAcode: 926 Acatalasemia,ICD-10 E80.4 Disorders of porphyrin and bilirubin metabolism - Gilbert syndrome,2408,E80.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.4,,ICD-10 -E80.5 Disorders of porphyrin and bilirubin metabolism - Crigler-Najjar syndrome,2409,E80.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.5,ORPHAcode: 205 Crigler-Najjar syndrome -E80.6 Other disorders of bilirubin metabolism,2410,E80.6,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.6,ORPHAcode: 234 Dubin-Johnson syndrome +E80.5 Disorders of porphyrin and bilirubin metabolism - Crigler-Najjar syndrome,2409,E80.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.5,ORPHAcode: 205 Crigler-Najjar syndrome,ICD-10 +E80.6 Other disorders of bilirubin metabolism,2410,E80.6,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.6,ORPHAcode: 234 Dubin-Johnson syndrome,ICD-10 "E80.7 Disorder of bilirubin metabolism, unspecified",2411,E80.7,E70-E90 Metabolic disorders,http://identifiers.org/icd/E80.7,,ICD-10 E83 Disorders of mineral metabolism,2412,E83,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83,,ICD-10 -E83.0 Disorders of copper metabolism,2413,E83.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.0,ORPHAcode: 198 Occipital horn syndrome -E83.1 Disorders of iron metabolism,2414,E83.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.1,ORPHAcode: 446 Neonatal hemochromatosis -E83.2 Disorders of zinc metabolism,2415,E83.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.2,ORPHAcode: 37 Acrodermatitis enteropathica -E83.3 Disorders of phosphorus metabolism and phosphatases,2416,E83.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.3,ORPHAcode: 436 Hypophosphatasia -E83.4 Disorders of magnesium metabolism,2417,E83.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.4,ORPHAcode: 2196 Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement -E83.5 Disorders of calcium metabolism,2418,E83.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.5,ORPHAcode: 405 Familial hypocalciuric hypercalcemia -E83.8 Other disorders of mineral metabolism,2419,E83.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.8,ORPHAcode: 521406 Dystonia-parkinsonism-hypermanganesemia syndrome +E83.0 Disorders of copper metabolism,2413,E83.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.0,ORPHAcode: 198 Occipital horn syndrome,ICD-10 +E83.1 Disorders of iron metabolism,2414,E83.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.1,ORPHAcode: 446 Neonatal hemochromatosis,ICD-10 +E83.2 Disorders of zinc metabolism,2415,E83.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.2,ORPHAcode: 37 Acrodermatitis enteropathica,ICD-10 +E83.3 Disorders of phosphorus metabolism and phosphatases,2416,E83.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.3,ORPHAcode: 436 Hypophosphatasia,ICD-10 +E83.4 Disorders of magnesium metabolism,2417,E83.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.4,ORPHAcode: 2196 Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement,ICD-10 +E83.5 Disorders of calcium metabolism,2418,E83.5,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.5,ORPHAcode: 405 Familial hypocalciuric hypercalcemia,ICD-10 +E83.8 Other disorders of mineral metabolism,2419,E83.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.8,ORPHAcode: 521406 Dystonia-parkinsonism-hypermanganesemia syndrome,ICD-10 "E83.9 Disorder of mineral metabolism, unspecified",2420,E83.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E83.9,,ICD-10 E84 Cystic fibrosis,2421,E84,E70-E90 Metabolic disorders,http://identifiers.org/icd/E84,,ICD-10 -E84.0 Cystic fibrosis with pulmonary manifestations,2422,E84.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E84.0,ORPHAcode: 586 Cystic fibrosis +E84.0 Cystic fibrosis with pulmonary manifestations,2422,E84.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E84.0,ORPHAcode: 586 Cystic fibrosis,ICD-10 E84.1 Cystic fibrosis with intestinal manifestations,2423,E84.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E84.1,,ICD-10 E84.8 Cystic fibrosis with other manifestations,2424,E84.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E84.8,,ICD-10 "E84.9 Cystic fibrosis, unspecified",2425,E84.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E84.9,,ICD-10 E85 Amyloidosis,2426,E85,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85,,ICD-10 -E85.0 Non-neuropathic heredofamilial amyloidosis,2427,E85.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.0,ORPHAcode: 342 Familial Mediterranean fever -E85.1 Neuropathic heredofamilial amyloidosis,2428,E85.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.1,ORPHAcode: 85448 AGel amyloidosis +E85.0 Non-neuropathic heredofamilial amyloidosis,2427,E85.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.0,ORPHAcode: 342 Familial Mediterranean fever,ICD-10 +E85.1 Neuropathic heredofamilial amyloidosis,2428,E85.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.1,ORPHAcode: 85448 AGel amyloidosis,ICD-10 "E85.2 Heredofamilial amyloidosis, unspecified",2429,E85.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.2,,ICD-10 -E85.3 Secondary systemic amyloidosis,2430,E85.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.3,ORPHAcode: 85445 AA amyloidosis +E85.3 Secondary systemic amyloidosis,2430,E85.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.3,ORPHAcode: 85445 AA amyloidosis,ICD-10 E85.4 Organ-limited amyloidosis,2431,E85.4,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.4,,ICD-10 -E85.8 Other amyloidosis,2432,E85.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.8,ORPHAcode: 330001 Wild type ATTR amyloidosis -"E85.9 Amyloidosis, unspecified",2433,E85.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.9,ORPHAcode: 85443 AL amyloidosis +E85.8 Other amyloidosis,2432,E85.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.8,ORPHAcode: 330001 Wild type ATTR amyloidosis,ICD-10 +"E85.9 Amyloidosis, unspecified",2433,E85.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E85.9,ORPHAcode: 85443 AL amyloidosis,ICD-10 E86 Volume depletion,2434,E86,E70-E90 Metabolic disorders,http://identifiers.org/icd/E86,,ICD-10 "E87 Other disorders of fluid, electrolyte and acid-base balance",2435,E87,E70-E90 Metabolic disorders,http://identifiers.org/icd/E87,,ICD-10 E87.0 Hyperosmolality and hypernatraemia,2436,E87.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E87.0,,ICD-10 @@ -2444,11 +2444,11 @@ E87.4 Mixed disorder of acid-base balance,2440,E87.4,E70-E90 Metabolic disorders E87.7 Fluid overload,2443,E87.7,E70-E90 Metabolic disorders,http://identifiers.org/icd/E87.7,,ICD-10 "E87.8 Other disorders of electrolyte and fluid balance, not elsewhere classified",2444,E87.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E87.8,,ICD-10 E88 Other metabolic disorders,2445,E88,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88,,ICD-10 -"E88.0 Disorders of plasma-protein metabolism, not elsewhere classified",2446,E88.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.0,ORPHAcode: 60 Alpha-1-antitrypsin deficiency -"E88.1 Other metabolic disorders - Lipodystrophy, not elsewhere classified",2447,E88.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.1,ORPHAcode: 528 Congenital generalized lipodystrophy -"E88.2 Other metabolic disorders - Lipomatosis, not elsewhere classified",2448,E88.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.2,ORPHAcode: 529 Roch-Leri mesosomatous lipomatosis +"E88.0 Disorders of plasma-protein metabolism, not elsewhere classified",2446,E88.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.0,ORPHAcode: 60 Alpha-1-antitrypsin deficiency,ICD-10 +"E88.1 Other metabolic disorders - Lipodystrophy, not elsewhere classified",2447,E88.1,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.1,ORPHAcode: 528 Congenital generalized lipodystrophy,ICD-10 +"E88.2 Other metabolic disorders - Lipomatosis, not elsewhere classified",2448,E88.2,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.2,ORPHAcode: 529 Roch-Leri mesosomatous lipomatosis,ICD-10 E88.3 Other metabolic disorders - Tumour lysis syndrome,2449,E88.3,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.3,,ICD-10 -E88.8 Other specified metabolic disorders,2450,E88.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.8,ORPHAcode: 24 Fumaric aciduria +E88.8 Other specified metabolic disorders,2450,E88.8,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.8,ORPHAcode: 24 Fumaric aciduria,ICD-10 "E88.9 Metabolic disorder, unspecified",2451,E88.9,E70-E90 Metabolic disorders,http://identifiers.org/icd/E88.9,,ICD-10 "E89 Postprocedural endocrine and metabolic disorders, not elsewhere classified",2452,E89,E70-E90 Metabolic disorders,http://identifiers.org/icd/E89,,ICD-10 E89.0 Postprocedural hypothyroidism,2453,E89.0,E70-E90 Metabolic disorders,http://identifiers.org/icd/E89.0,,ICD-10 @@ -2472,7 +2472,7 @@ F01.0 Vascular dementia of acute onset,2470,F01.0,"F00-F09 Organic, including sy F01.1 Multi-infarct dementia,2471,F01.1,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F01.1,,ICD-10 F01.2 Subcortical vascular dementia,2472,F01.2,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F01.2,,ICD-10 F01.3 Mixed cortical and subcortical vascular dementia,2473,F01.3,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F01.3,,ICD-10 -F01.8 Other vascular dementia,2474,F01.8,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F01.8,ORPHAcode: 97353 Dementia pugilistica +F01.8 Other vascular dementia,2474,F01.8,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F01.8,ORPHAcode: 97353 Dementia pugilistica,ICD-10 "F01.9 Vascular dementia, unspecified",2475,F01.9,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F01.9,,ICD-10 F02 Dementia in other diseases classified elsewhere,2476,F02,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F02,,ICD-10 F02.0 Dementia in Pick disease,2477,F02.0,"F00-F09 Organic, including symptomatic, mental disorders",http://identifiers.org/icd/F02.0,,ICD-10 @@ -2528,7 +2528,7 @@ F20.3 Undifferentiated schizophrenia,2526,F20.3,"F20-F29 Schizophrenia, schizoty F20.4 Schizophrenia - Post-schizophrenic depression,2527,F20.4,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F20.4,,ICD-10 F20.5 Residual schizophrenia,2528,F20.5,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F20.5,,ICD-10 F20.6 Simple schizophrenia,2529,F20.6,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F20.6,,ICD-10 -F20.8 Other schizophrenia,2530,F20.8,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F20.8,ORPHAcode: 96369 Early-onset schizophrenia +F20.8 Other schizophrenia,2530,F20.8,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F20.8,ORPHAcode: 96369 Early-onset schizophrenia,ICD-10 "F20.9 Schizophrenia, unspecified",2531,F20.9,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F20.9,,ICD-10 F21 Schizotypal disorder,2532,F21,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F21,,ICD-10 F22 Persistent delusional disorders,2533,F22,"F20-F29 Schizophrenia, schizotypal and delusional disorders",http://identifiers.org/icd/F22,,ICD-10 @@ -2625,7 +2625,7 @@ F44.0 Dissociative amnesia,2623,F44.0,"F40-F48 Neurotic, stress-related and soma F44.1 Dissociative fugue,2624,F44.1,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.1,,ICD-10 F44.2 Dissociative stupor,2625,F44.2,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.2,,ICD-10 F44.3 Trance and possession disorders,2626,F44.3,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.3,,ICD-10 -F44.4 Dissociative motor disorders,2627,F44.4,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.4,ORPHAcode: 71519 Psychogenic movement disorders +F44.4 Dissociative motor disorders,2627,F44.4,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.4,ORPHAcode: 71519 Psychogenic movement disorders,ICD-10 F44.5 Dissociative convulsions,2628,F44.5,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.5,,ICD-10 F44.6 Dissociative anaesthesia and sensory loss,2629,F44.6,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.6,,ICD-10 F44.7 Mixed dissociative [conversion] disorders,2630,F44.7,"F40-F48 Neurotic, stress-related and somatoform disorders",http://identifiers.org/icd/F44.7,,ICD-10 @@ -2647,7 +2647,7 @@ F48.8 Other specified neurotic disorders,2644,F48.8,"F40-F48 Neurotic, stress-re F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,2646,,V Mental and behavioural disorders,,,ICD-10 H26.3 Drug-induced cataract,2647,H26.3,H25-H28 Disorders of lens,http://identifiers.org/icd/H26.3,,ICD-10 F50 Eating disorders,2648,F50,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F50,,ICD-10 -F50.0 Eating disorders - Anorexia nervosa,2649,F50.0,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F50.0,ORPHAcode: 525738 Prepubertal anorexia nervosa +F50.0 Eating disorders - Anorexia nervosa,2649,F50.0,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F50.0,ORPHAcode: 525738 Prepubertal anorexia nervosa,ICD-10 F50.1 Eating disorders - Atypical anorexia nervosa,2650,F50.1,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F50.1,,ICD-10 F50.2 Eating disorders - Bulimia nervosa,2651,F50.2,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F50.2,,ICD-10 F50.3 Eating disorders - Atypical bulimia nervosa,2652,F50.3,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F50.3,,ICD-10 @@ -2657,7 +2657,7 @@ F50.8 Other eating disorders,2655,F50.8,F50-F59 Behavioural syndromes associated "F50.9 Eating disorder, unspecified",2656,F50.9,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F50.9,,ICD-10 F51 Nonorganic sleep disorders,2657,F51,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F51,,ICD-10 F51.0 Nonorganic insomnia,2658,F51.0,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F51.0,,ICD-10 -F51.1 Nonorganic hypersomnia,2659,F51.1,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F51.1,ORPHAcode: 33208 Idiopathic hypersomnia +F51.1 Nonorganic hypersomnia,2659,F51.1,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F51.1,ORPHAcode: 33208 Idiopathic hypersomnia,ICD-10 F51.2 Nonorganic disorder of the sleep-wake schedule,2660,F51.2,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F51.2,,ICD-10 F51.3 Sleepwalking [somnambulism],2661,F51.3,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F51.3,,ICD-10 F51.4 Sleep terrors [night terrors],2662,F51.4,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F51.4,,ICD-10 @@ -2669,7 +2669,7 @@ F51.8 Other nonorganic sleep disorders,2665,F51.8,F50-F59 Behavioural syndromes F52.0 Lack or loss of sexual desire,2668,F52.0,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.0,,ICD-10 F52.1 Sexual aversion and lack of sexual enjoyment,2669,F52.1,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.1,,ICD-10 "F52.2 Sexual dysfunction, not caused by organic disorder or disease - Failure of genital response",2670,F52.2,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.2,,ICD-10 -F52.3 Orgasmic dysfunction,2671,F52.3,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.3,ORPHAcode: 279947 Postorgasmic illness syndrome +F52.3 Orgasmic dysfunction,2671,F52.3,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.3,ORPHAcode: 279947 Postorgasmic illness syndrome,ICD-10 "F52.4 Sexual dysfunction, not caused by organic disorder or disease - Premature ejaculation",2672,F52.4,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.4,,ICD-10 F52.5 Nonorganic vaginismus,2673,F52.5,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.5,,ICD-10 F52.6 Nonorganic dyspareunia,2674,F52.6,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.6,,ICD-10 @@ -2678,7 +2678,7 @@ F52.7 Excessive sexual drive,2675,F52.7,F50-F59 Behavioural syndromes associated "F52.9 Unspecified sexual dysfunction, not caused by organic disorder or disease",2677,F52.9,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F52.9,,ICD-10 "F53 Mental and behavioural disorders associated with the puerperium, not elsewhere classified",2678,F53,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F53,,ICD-10 "F53.0 Mild mental and behavioural disorders associated with the puerperium, not elsewhere classified",2679,F53.0,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F53.0,,ICD-10 -"F53.1 Severe mental and behavioural disorders associated with the puerperium, not elsewhere classified",2680,F53.1,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F53.1,ORPHAcode: 443173 Postpartum psychosis +"F53.1 Severe mental and behavioural disorders associated with the puerperium, not elsewhere classified",2680,F53.1,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F53.1,ORPHAcode: 443173 Postpartum psychosis,ICD-10 "F53.8 Other mental and behavioural disorders associated with the puerperium, not elsewhere classified",2681,F53.8,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F53.8,,ICD-10 "F53.9 Puerperal mental disorder, unspecified",2682,F53.9,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F53.9,,ICD-10 F54 Psychological and behavioural factors associated with disorders or diseases classified elsewhere,2683,F54,F50-F59 Behavioural syndromes associated with physiological disturbances and physical factors,http://identifiers.org/icd/F54,,ICD-10 @@ -2741,36 +2741,36 @@ F69 Unspecified disorder of adult personality and behaviour,2739,F69,F60-F69 Dis F70-F79 Mental retardation,2740,,V Mental and behavioural disorders,,,ICD-10 F70 Mild mental retardation,2741,F70,F70-F79 Mental retardation,http://identifiers.org/icd/F70,,ICD-10 F71 Moderate mental retardation,2742,F71,F70-F79 Mental retardation,http://identifiers.org/icd/F71,,ICD-10 -F72 Severe mental retardation,2743,F72,F70-F79 Mental retardation,http://identifiers.org/icd/F72,ORPHAcode: 364028 X-linked intellectual disability due to GRIA3 mutations -F73 Profound mental retardation,2744,F73,F70-F79 Mental retardation,http://identifiers.org/icd/F73,ORPHAcode: 101685 Rare non-syndromic intellectual disability +F72 Severe mental retardation,2743,F72,F70-F79 Mental retardation,http://identifiers.org/icd/F72,ORPHAcode: 364028 X-linked intellectual disability due to GRIA3 mutations,ICD-10 +F73 Profound mental retardation,2744,F73,F70-F79 Mental retardation,http://identifiers.org/icd/F73,ORPHAcode: 101685 Rare non-syndromic intellectual disability,ICD-10 F78 Other mental retardation,2745,F78,F70-F79 Mental retardation,http://identifiers.org/icd/F78,,ICD-10 F79 Unspecified mental retardation,2746,F79,F70-F79 Mental retardation,http://identifiers.org/icd/F79,,ICD-10 F80-F89 Disorders of psychological development,2747,,V Mental and behavioural disorders,,,ICD-10 F80 Specific developmental disorders of speech and language,2748,F80,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80,,ICD-10 -F80.0 Specific speech articulation disorder,2749,F80.0,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.0,ORPHAcode: 209908 Childhood apraxia of speech -F80.1 Expressive language disorder,2750,F80.1,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.1,ORPHAcode: 1799 Familial developmental dysphasia +F80.0 Specific speech articulation disorder,2749,F80.0,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.0,ORPHAcode: 209908 Childhood apraxia of speech,ICD-10 +F80.1 Expressive language disorder,2750,F80.1,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.1,ORPHAcode: 1799 Familial developmental dysphasia,ICD-10 F80.2 Receptive language disorder,2751,F80.2,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.2,,ICD-10 -F80.3 Acquired aphasia with epilepsy [Landau-Kleffner],2752,F80.3,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.3,ORPHAcode: 725 Continuous spikes and waves during sleep +F80.3 Acquired aphasia with epilepsy [Landau-Kleffner],2752,F80.3,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.3,ORPHAcode: 725 Continuous spikes and waves during sleep,ICD-10 F80.8 Other developmental disorders of speech and language,2753,F80.8,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.8,,ICD-10 "F80.9 Developmental disorder of speech and language, unspecified",2754,F80.9,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F80.9,,ICD-10 F81 Specific developmental disorders of scholastic skills,2755,F81,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81,,ICD-10 F81.0 Specific reading disorder,2756,F81.0,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81.0,,ICD-10 F81.1 Specific spelling disorder,2757,F81.1,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81.1,,ICD-10 -F81.2 Specific disorder of arithmetical skills,2758,F81.2,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81.2,ORPHAcode: 221117 Gerstmann syndrome +F81.2 Specific disorder of arithmetical skills,2758,F81.2,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81.2,ORPHAcode: 221117 Gerstmann syndrome,ICD-10 F81.3 Mixed disorder of scholastic skills,2759,F81.3,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81.3,,ICD-10 F81.8 Other developmental disorders of scholastic skills,2760,F81.8,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81.8,,ICD-10 "F81.9 Developmental disorder of scholastic skills, unspecified",2761,F81.9,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F81.9,,ICD-10 F82 Specific developmental disorder of motor function,2762,F82,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F82,,ICD-10 F83 Mixed specific developmental disorders,2763,F83,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F83,,ICD-10 F84 Pervasive developmental disorders,2764,F84,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84,,ICD-10 -F84.0 Pervasive developmental disorders - Childhood autism,2765,F84.0,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.0,ORPHAcode: 137911 Autism-facial port-wine stain syndrome -F84.1 Pervasive developmental disorders - Atypical autism,2766,F84.1,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.1,ORPHAcode: 199627 Atypical autism -F84.2 Pervasive developmental disorders - Rett syndrome,2767,F84.2,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.2,ORPHAcode: 778 Rett syndrome -F84.3 Pervasive developmental disorders - Other childhood disintegrative disorder,2768,F84.3,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.3,ORPHAcode: 168782 Childhood disintegrative disorder +F84.0 Pervasive developmental disorders - Childhood autism,2765,F84.0,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.0,ORPHAcode: 137911 Autism-facial port-wine stain syndrome,ICD-10 +F84.1 Pervasive developmental disorders - Atypical autism,2766,F84.1,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.1,ORPHAcode: 199627 Atypical autism,ICD-10 +F84.2 Pervasive developmental disorders - Rett syndrome,2767,F84.2,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.2,ORPHAcode: 778 Rett syndrome,ICD-10 +F84.3 Pervasive developmental disorders - Other childhood disintegrative disorder,2768,F84.3,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.3,ORPHAcode: 168782 Childhood disintegrative disorder,ICD-10 F84.4 Pervasive developmental disorders - Overactive disorder associated with mental retardation and stereotyped movements,2769,F84.4,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.4,,ICD-10 Y04 Assault by bodily force,2770,Y04,X85-Y09 Assault,http://identifiers.org/icd/Y04,,ICD-10 F84.5 Pervasive developmental disorders - Asperger syndrome,2771,F84.5,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.5,,ICD-10 -F84.8 Other pervasive developmental disorders,2772,F84.8,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.8,ORPHAcode: 329195 Developmental delay with autism spectrum disorder and gait instability +F84.8 Other pervasive developmental disorders,2772,F84.8,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.8,ORPHAcode: 329195 Developmental delay with autism spectrum disorder and gait instability,ICD-10 "F84.9 Pervasive developmental disorder, unspecified",2773,F84.9,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F84.9,,ICD-10 F88 Other disorders of psychological development,2774,F88,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F88,,ICD-10 F89 Unspecified disorder of psychological development,2775,F89,F80-F89 Disorders of psychological development,http://identifiers.org/icd/F89,,ICD-10 @@ -2817,7 +2817,7 @@ F98.1 Other behavioural and emotional disorders with onset usually occurring in F98.2 Feeding disorder of infancy and childhood,2816,F98.2,F90-F98 Behavioural and emotional disorders with onset usually occurring in childhood and adolescence,http://identifiers.org/icd/F98.2,,ICD-10 G82.4 Spastic tetraplegia,2817,G82.4,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82.4,,ICD-10 F98.3 Pica of infancy and childhood,2818,F98.3,F90-F98 Behavioural and emotional disorders with onset usually occurring in childhood and adolescence,http://identifiers.org/icd/F98.3,,ICD-10 -F98.4 Stereotyped movement disorders,2819,F98.4,F90-F98 Behavioural and emotional disorders with onset usually occurring in childhood and adolescence,http://identifiers.org/icd/F98.4,ORPHAcode: 279882 Spasmus nutans +F98.4 Stereotyped movement disorders,2819,F98.4,F90-F98 Behavioural and emotional disorders with onset usually occurring in childhood and adolescence,http://identifiers.org/icd/F98.4,ORPHAcode: 279882 Spasmus nutans,ICD-10 F98.5 Stuttering [stammering],2820,F98.5,F90-F98 Behavioural and emotional disorders with onset usually occurring in childhood and adolescence,http://identifiers.org/icd/F98.5,,ICD-10 F98.6 Cluttering,2821,F98.6,F90-F98 Behavioural and emotional disorders with onset usually occurring in childhood and adolescence,http://identifiers.org/icd/F98.6,,ICD-10 F98.8 Other specified behavioural and emotional disorders with onset usually occurring in childhood and adolescence,2822,F98.8,F90-F98 Behavioural and emotional disorders with onset usually occurring in childhood and adolescence,http://identifiers.org/icd/F98.8,,ICD-10 @@ -2828,7 +2828,7 @@ VI Diseases of the nervous system,2826,,,,,ICD-10 G00-G09 Inflammatory diseases of the central nervous system,2827,,VI Diseases of the nervous system,,,ICD-10 "G00 Bacterial meningitis, not elsewhere classified",2828,G00,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G00,,ICD-10 G00.0 Haemophilus meningitis,2829,G00.0,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G00.0,,ICD-10 -G00.1 Pneumococcal meningitis,2830,G00.1,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G00.1,ORPHAcode: 55655 Pneumococcal meningitis +G00.1 Pneumococcal meningitis,2830,G00.1,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G00.1,ORPHAcode: 55655 Pneumococcal meningitis,ICD-10 G00.2 Streptococcal meningitis,2831,G00.2,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G00.2,,ICD-10 G00.3 Staphylococcal meningitis,2832,G00.3,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G00.3,,ICD-10 G00.8 Other bacterial meningitis,2833,G00.8,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G00.8,,ICD-10 @@ -2843,12 +2843,12 @@ G03.0 Nonpyogenic meningitis,2841,G03.0,G00-G09 Inflammatory diseases of the cen G03.1 Chronic meningitis,2842,G03.1,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G03.1,,ICD-10 G03.2 Benign recurrent meningitis [Mollaret],2843,G03.2,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G03.2,,ICD-10 G03.8 Meningitis due to other specified causes,2844,G03.8,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G03.8,,ICD-10 -"G03.9 Meningitis, unspecified",2845,G03.9,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G03.9,ORPHAcode: 137817 Arachnoiditis +"G03.9 Meningitis, unspecified",2845,G03.9,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G03.9,ORPHAcode: 137817 Arachnoiditis,ICD-10 "G04 Encephalitis, myelitis and encephalomyelitis",2846,G04,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04,,ICD-10 -G04.0 Acute disseminated encephalitis,2847,G04.0,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.0,ORPHAcode: 83597 Acute disseminated encephalomyelitis -"G04.1 Encephalitis, myelitis and encephalomyelitis - Tropical spastic paraplegia",2848,G04.1,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.1,ORPHAcode: 289326 Tropical spastic paraparesis +G04.0 Acute disseminated encephalitis,2847,G04.0,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.0,ORPHAcode: 83597 Acute disseminated encephalomyelitis,ICD-10 +"G04.1 Encephalitis, myelitis and encephalomyelitis - Tropical spastic paraplegia",2848,G04.1,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.1,ORPHAcode: 289326 Tropical spastic paraparesis,ICD-10 "G04.2 Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified",2849,G04.2,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.2,,ICD-10 -"G04.8 Other encephalitis, myelitis and encephalomyelitis",2850,G04.8,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.8,ORPHAcode: 1929 Rasmussen subacute encephalitis +"G04.8 Other encephalitis, myelitis and encephalomyelitis",2850,G04.8,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.8,ORPHAcode: 1929 Rasmussen subacute encephalitis,ICD-10 "G04.9 Encephalitis, myelitis and encephalomyelitis, unspecified",2851,G04.9,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G04.9,,ICD-10 "G05 Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere",2852,G05,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G05,,ICD-10 "G05.0 Encephalitis, myelitis and encephalomyelitis in bacterial diseases classified elsewhere",2853,G05.0,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G05.0,,ICD-10 @@ -2863,130 +2863,130 @@ G07 Intracranial and intraspinal abscess and granuloma in diseases classified el G08 Intracranial and intraspinal phlebitis and thrombophlebitis,2862,G08,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G08,,ICD-10 G09 Sequelae of inflammatory diseases of central nervous system,2863,G09,G00-G09 Inflammatory diseases of the central nervous system,http://identifiers.org/icd/G09,,ICD-10 G10-G14 Systemic atrophies primarily affecting the central nervous system,2864,,VI Diseases of the nervous system,,,ICD-10 -G10 Huntington disease,2865,G10,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G10,ORPHAcode: 399 Huntington disease +G10 Huntington disease,2865,G10,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G10,ORPHAcode: 399 Huntington disease,ICD-10 G11 Hereditary ataxia,2866,G11,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11,,ICD-10 -G11.0 Congenital nonprogressive ataxia,2867,G11.0,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.0,ORPHAcode: 1065 Aniridia-cerebellar ataxia-intellectual disability syndrome -G11.1 Early-onset cerebellar ataxia,2868,G11.1,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.1,ORPHAcode: 95 Friedreich ataxia +G11.0 Congenital nonprogressive ataxia,2867,G11.0,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.0,ORPHAcode: 1065 Aniridia-cerebellar ataxia-intellectual disability syndrome,ICD-10 +G11.1 Early-onset cerebellar ataxia,2868,G11.1,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.1,ORPHAcode: 95 Friedreich ataxia,ICD-10 H26.8 Other specified cataract,2869,H26.8,H25-H28 Disorders of lens,http://identifiers.org/icd/H26.8,,ICD-10 -G11.2 Late-onset cerebellar ataxia,2870,G11.2,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.2,ORPHAcode: 1368 Cataract-ataxia-deafness syndrome -G11.3 Cerebellar ataxia with defective DNA repair,2871,G11.3,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.3,ORPHAcode: 100 Ataxia-telangiectasia -G11.4 Hereditary spastic paraplegia,2872,G11.4,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.4,ORPHAcode: 1182 Spastic ataxia with congenital miosis -G11.8 Other hereditary ataxias,2873,G11.8,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.8,ORPHAcode: 97 Familial paroxysmal ataxia +G11.2 Late-onset cerebellar ataxia,2870,G11.2,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.2,ORPHAcode: 1368 Cataract-ataxia-deafness syndrome,ICD-10 +G11.3 Cerebellar ataxia with defective DNA repair,2871,G11.3,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.3,ORPHAcode: 100 Ataxia-telangiectasia,ICD-10 +G11.4 Hereditary spastic paraplegia,2872,G11.4,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.4,ORPHAcode: 1182 Spastic ataxia with congenital miosis,ICD-10 +G11.8 Other hereditary ataxias,2873,G11.8,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.8,ORPHAcode: 97 Familial paroxysmal ataxia,ICD-10 "G11.9 Hereditary ataxia, unspecified",2874,G11.9,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G11.9,,ICD-10 G12 Spinal muscular atrophy and related syndromes,2875,G12,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12,,ICD-10 -"G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]",2876,G12.0,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.0,ORPHAcode: 70 Proximal spinal muscular atrophy -G12.1 Other inherited spinal muscular atrophy,2877,G12.1,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.1,ORPHAcode: 1145 Infantile-onset X-linked spinal muscular atrophy -G12.2 Spinal muscular atrophy and related syndromes - Motor neuron disease,2878,G12.2,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.2,ORPHAcode: 481 Kennedy disease -G12.8 Other spinal muscular atrophies and related syndromes,2879,G12.8,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.8,ORPHAcode: 65684 Monomelic amyotrophy +"G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]",2876,G12.0,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.0,ORPHAcode: 70 Proximal spinal muscular atrophy,ICD-10 +G12.1 Other inherited spinal muscular atrophy,2877,G12.1,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.1,ORPHAcode: 1145 Infantile-onset X-linked spinal muscular atrophy,ICD-10 +G12.2 Spinal muscular atrophy and related syndromes - Motor neuron disease,2878,G12.2,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.2,ORPHAcode: 481 Kennedy disease,ICD-10 +G12.8 Other spinal muscular atrophies and related syndromes,2879,G12.8,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.8,ORPHAcode: 65684 Monomelic amyotrophy,ICD-10 "G12.9 Spinal muscular atrophy, unspecified",2880,G12.9,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G12.9,,ICD-10 G13 Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere,2881,G13,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G13,,ICD-10 G13.0 Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere - Paraneoplastic neuromyopathy and neuropathy,2882,G13.0,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G13.0,,ICD-10 -G13.1 Other systemic atrophy primarily affecting central nervous system in neoplastic disease,2883,G13.1,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G13.1,ORPHAcode: 163898 Classic paraneoplastic limbic encephalitis +G13.1 Other systemic atrophy primarily affecting central nervous system in neoplastic disease,2883,G13.1,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G13.1,ORPHAcode: 163898 Classic paraneoplastic limbic encephalitis,ICD-10 N60-N64 Disorders of breast,2884,,XIV Diseases of the genitourinary system,,,ICD-10 G13.2 Systemic atrophy primarily affecting central nervous system in myxoedema,2885,G13.2,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G13.2,,ICD-10 G13.8 Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere,2886,G13.8,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G13.8,,ICD-10 -G14 Postpolio syndrome,2887,G14,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G14,ORPHAcode: 2942 Postpoliomyelitis syndrome +G14 Postpolio syndrome,2887,G14,G10-G14 Systemic atrophies primarily affecting the central nervous system,http://identifiers.org/icd/G14,ORPHAcode: 2942 Postpoliomyelitis syndrome,ICD-10 G20-G26 Extrapyramidal and movement disorders,2888,,VI Diseases of the nervous system,,,ICD-10 -G20 Parkinson disease,2889,G20,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G20,ORPHAcode: 2379 Early-onset parkinsonism-intellectual disability syndrome +G20 Parkinson disease,2889,G20,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G20,ORPHAcode: 2379 Early-onset parkinsonism-intellectual disability syndrome,ICD-10 G21 Secondary parkinsonism,2890,G21,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21,,ICD-10 -G21.0 Secondary parkinsonism - Malignant neuroleptic syndrome,2891,G21.0,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.0,ORPHAcode: 94093 Neuroleptic malignant syndrome +G21.0 Secondary parkinsonism - Malignant neuroleptic syndrome,2891,G21.0,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.0,ORPHAcode: 94093 Neuroleptic malignant syndrome,ICD-10 G21.1 Other drug-induced secondary parkinsonism,2892,G21.1,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.1,,ICD-10 -G21.2 Secondary parkinsonism due to other external agents,2893,G21.2,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.2,ORPHAcode: 306686 Delayed encephalopathy due to carbon monoxide poisoning -G21.3 Postencephalitic parkinsonism,2894,G21.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.3,ORPHAcode: 97349 Postencephalitic parkinsonism +G21.2 Secondary parkinsonism due to other external agents,2893,G21.2,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.2,ORPHAcode: 306686 Delayed encephalopathy due to carbon monoxide poisoning,ICD-10 +G21.3 Postencephalitic parkinsonism,2894,G21.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.3,ORPHAcode: 97349 Postencephalitic parkinsonism,ICD-10 G21.4 Vascular parkinsonism,2895,G21.4,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.4,,ICD-10 G21.8 Other secondary parkinsonism,2896,G21.8,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.8,,ICD-10 "G21.9 Secondary parkinsonism, unspecified",2897,G21.9,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G21.9,,ICD-10 G22 Parkinsonism in diseases classified elsewhere,2898,G22,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G22,,ICD-10 G23 Other degenerative diseases of basal ganglia,2899,G23,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23,,ICD-10 -G23.0 Other degenerative diseases of basal ganglia - Hallervorden-Spatz disease,2900,G23.0,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.0,ORPHAcode: 35069 Infantile neuroaxonal dystrophy -G23.1 Other degenerative diseases of basal ganglia - Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski],2901,G23.1,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.1,ORPHAcode: 683 Progressive supranuclear palsy -"G23.2 Other degenerative diseases of basal ganglia - Multiple system atrophy, parkinsonian type [MSA-P]",2902,G23.2,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.2,ORPHAcode: 225147 Sporadic infantile bilateral striatal necrosis -"G23.3 Other degenerative diseases of basal ganglia - Multiple system atrophy, cerebellar type [MSA-C]",2903,G23.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.3,ORPHAcode: 102 Multiple system atrophy -G23.8 Other specified degenerative diseases of basal ganglia,2904,G23.8,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.8,ORPHAcode: 1980 Bilateral striopallidodentate calcinosis +G23.0 Other degenerative diseases of basal ganglia - Hallervorden-Spatz disease,2900,G23.0,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.0,ORPHAcode: 35069 Infantile neuroaxonal dystrophy,ICD-10 +G23.1 Other degenerative diseases of basal ganglia - Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski],2901,G23.1,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.1,ORPHAcode: 683 Progressive supranuclear palsy,ICD-10 +"G23.2 Other degenerative diseases of basal ganglia - Multiple system atrophy, parkinsonian type [MSA-P]",2902,G23.2,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.2,ORPHAcode: 225147 Sporadic infantile bilateral striatal necrosis,ICD-10 +"G23.3 Other degenerative diseases of basal ganglia - Multiple system atrophy, cerebellar type [MSA-C]",2903,G23.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.3,ORPHAcode: 102 Multiple system atrophy,ICD-10 +G23.8 Other specified degenerative diseases of basal ganglia,2904,G23.8,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.8,ORPHAcode: 1980 Bilateral striopallidodentate calcinosis,ICD-10 "G23.9 Degenerative disease of basal ganglia, unspecified",2905,G23.9,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G23.9,,ICD-10 G24 Dystonia,2906,G24,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24,,ICD-10 G24.0 Drug-induced dystonia,2907,G24.0,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.0,,ICD-10 -G24.1 Idiopathic familial dystonia,2908,G24.1,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.1,ORPHAcode: 256 Early-onset generalized limb-onset dystonia +G24.1 Idiopathic familial dystonia,2908,G24.1,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.1,ORPHAcode: 256 Early-onset generalized limb-onset dystonia,ICD-10 G24.2 Idiopathic nonfamilial dystonia,2909,G24.2,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.2,,ICD-10 -G24.3 Dystonia - Spasmodic torticollis,2910,G24.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.3,ORPHAcode: 71518 Benign paroxysmal torticollis of infancy -G24.4 Idiopathic orofacial dystonia,2911,G24.4,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.4,ORPHAcode: 93958 Oromandibular dystonia +G24.3 Dystonia - Spasmodic torticollis,2910,G24.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.3,ORPHAcode: 71518 Benign paroxysmal torticollis of infancy,ICD-10 +G24.4 Idiopathic orofacial dystonia,2911,G24.4,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.4,ORPHAcode: 93958 Oromandibular dystonia,ICD-10 G24.5 Dystonia - Blepharospasm,2912,G24.5,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.5,,ICD-10 -G24.8 Other dystonia,2913,G24.8,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.8,ORPHAcode: 35708 Aromatic L-amino acid decarboxylase deficiency +G24.8 Other dystonia,2913,G24.8,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.8,ORPHAcode: 35708 Aromatic L-amino acid decarboxylase deficiency,ICD-10 "G24.9 Dystonia, unspecified",2914,G24.9,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G24.9,,ICD-10 G25 Other extrapyramidal and movement disorders,2915,G25,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25,,ICD-10 -G25.0 Other extrapyramidal and movement disorders - Essential tremor,2916,G25.0,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.0,ORPHAcode: 3350 Tremor-nystagmus-duodenal ulcer syndrome +G25.0 Other extrapyramidal and movement disorders - Essential tremor,2916,G25.0,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.0,ORPHAcode: 3350 Tremor-nystagmus-duodenal ulcer syndrome,ICD-10 G25.1 Other extrapyramidal and movement disorders - Drug-induced tremor,2917,G25.1,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.1,,ICD-10 -G25.2 Other specified forms of tremor,2918,G25.2,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.2,ORPHAcode: 238606 Primary orthostatic tremor -G25.3 Other extrapyramidal and movement disorders - Myoclonus,2919,G25.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.3,ORPHAcode: 396 Chronic hiccup +G25.2 Other specified forms of tremor,2918,G25.2,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.2,ORPHAcode: 238606 Primary orthostatic tremor,ICD-10 +G25.3 Other extrapyramidal and movement disorders - Myoclonus,2919,G25.3,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.3,ORPHAcode: 396 Chronic hiccup,ICD-10 G25.4 Other extrapyramidal and movement disorders - Drug-induced chorea,2920,G25.4,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.4,,ICD-10 -G25.5 Other chorea,2921,G25.5,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.5,ORPHAcode: 1429 Benign hereditary chorea +G25.5 Other chorea,2921,G25.5,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.5,ORPHAcode: 1429 Benign hereditary chorea,ICD-10 G25.6 Drug-induced tics and other tics of organic origin,2922,G25.6,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.6,,ICD-10 -G25.8 Other specified extrapyramidal and movement disorders,2923,G25.8,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.8,ORPHAcode: 3197 Hereditary hyperekplexia +G25.8 Other specified extrapyramidal and movement disorders,2923,G25.8,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.8,ORPHAcode: 3197 Hereditary hyperekplexia,ICD-10 "G25.9 Extrapyramidal and movement disorder, unspecified",2924,G25.9,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G25.9,,ICD-10 G26 Extrapyramidal and movement disorders in diseases classified elsewhere,2925,G26,G20-G26 Extrapyramidal and movement disorders,http://identifiers.org/icd/G26,,ICD-10 G30-G32 Other degenerative diseases of the nervous system,2926,,VI Diseases of the nervous system,,,ICD-10 G30 Alzheimer disease,2927,G30,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G30,,ICD-10 -G30.0 Alzheimer disease with early onset,2928,G30.0,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G30.0,ORPHAcode: 1020 Early-onset autosomal dominant Alzheimer disease +G30.0 Alzheimer disease with early onset,2928,G30.0,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G30.0,ORPHAcode: 1020 Early-onset autosomal dominant Alzheimer disease,ICD-10 G30.1 Alzheimer disease with late onset,2929,G30.1,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G30.1,,ICD-10 G30.8 Other Alzheimer disease,2930,G30.8,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G30.8,,ICD-10 "G30.9 Alzheimer disease, unspecified",2931,G30.9,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G30.9,,ICD-10 "G31 Other degenerative diseases of nervous system, not elsewhere classified",2932,G31,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31,,ICD-10 -"G31.0 Other degenerative diseases of nervous system, not elsewhere classified - Circumscribed brain atrophy",2933,G31.0,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.0,ORPHAcode: 2289 Neuronal intranuclear inclusion disease -"G31.1 Senile degeneration of brain, not elsewhere classified",2934,G31.1,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.1,ORPHAcode: 54247 Posterior cortical atrophy +"G31.0 Other degenerative diseases of nervous system, not elsewhere classified - Circumscribed brain atrophy",2933,G31.0,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.0,ORPHAcode: 2289 Neuronal intranuclear inclusion disease,ICD-10 +"G31.1 Senile degeneration of brain, not elsewhere classified",2934,G31.1,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.1,ORPHAcode: 54247 Posterior cortical atrophy,ICD-10 G31.2 Degeneration of nervous system due to alcohol,2935,G31.2,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.2,,ICD-10 -G31.8 Other specified degenerative diseases of nervous system,2936,G31.8,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.8,ORPHAcode: 51 Aicardi-Gouti res sy +G31.8 Other specified degenerative diseases of nervous system,2936,G31.8,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.8,ORPHAcode: 51 Aicardi-Gouti res sy,ICD-10 "G31.9 Degenerative disease of nervous system, unspecified",2937,G31.9,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G31.9,,ICD-10 G32 Other degenerative disorders of nervous system in diseases classified elsewhere,2938,G32,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G32,,ICD-10 G32.0 Subacute combined degeneration of spinal cord in diseases classified elsewhere,2939,G32.0,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G32.0,,ICD-10 G32.8 Other specified degenerative disorders of nervous system in diseases classified elsewhere,2940,G32.8,G30-G32 Other degenerative diseases of the nervous system,http://identifiers.org/icd/G32.8,,ICD-10 G35-G37 Demyelinating diseases of the central nervous system,2941,,VI Diseases of the nervous system,,,ICD-10 -G35 Multiple sclerosis,2942,G35,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G35,ORPHAcode: 228157 Marburg acute multiple sclerosis +G35 Multiple sclerosis,2942,G35,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G35,ORPHAcode: 228157 Marburg acute multiple sclerosis,ICD-10 G36 Other acute disseminated demyelination,2943,G36,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G36,,ICD-10 -G36.0 Other acute disseminated demyelination - Neuromyelitis optica [Devic],2944,G36.0,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G36.0,ORPHAcode: 71211 Neuromyelitis optica spectrum disorder +G36.0 Other acute disseminated demyelination - Neuromyelitis optica [Devic],2944,G36.0,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G36.0,ORPHAcode: 71211 Neuromyelitis optica spectrum disorder,ICD-10 G36.1 Acute and subacute haemorrhagic leukoencephalitis [Hurst],2945,G36.1,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G36.1,,ICD-10 G36.8 Other specified acute disseminated demyelination,2946,G36.8,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G36.8,,ICD-10 "G36.9 Acute disseminated demyelination, unspecified",2947,G36.9,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G36.9,,ICD-10 G37 Other demyelinating diseases of central nervous system,2948,G37,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37,,ICD-10 -G37.0 Other demyelinating diseases of central nervous system - Diffuse sclerosis,2949,G37.0,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.0,ORPHAcode: 59298 Schilder disease -G37.1 Central demyelination of corpus callosum,2950,G37.1,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.1,ORPHAcode: 221074 Marchiafava-Bignami disease +G37.0 Other demyelinating diseases of central nervous system - Diffuse sclerosis,2949,G37.0,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.0,ORPHAcode: 59298 Schilder disease,ICD-10 +G37.1 Central demyelination of corpus callosum,2950,G37.1,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.1,ORPHAcode: 221074 Marchiafava-Bignami disease,ICD-10 G37.2 Central pontine myelinolysis,2951,G37.2,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.2,,ICD-10 -G37.3 Acute transverse myelitis in demyelinating disease of central nervous system,2952,G37.3,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.3,ORPHAcode: 139417 Acute transverse myelitis -G37.4 Other demyelinating diseases of central nervous system - Subacute necrotizing myelitis,2953,G37.4,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.4,ORPHAcode: 79093 Foix-Alajouanine syndrome -G37.5 Concentric sclerosis [Baló,2954,G37.5,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.5,ORPHAcode: 228165 Bal concentric scl -G37.8 Other specified demyelinating diseases of central nervous system,2955,G37.8,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.8,ORPHAcode: 3151 Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome +G37.3 Acute transverse myelitis in demyelinating disease of central nervous system,2952,G37.3,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.3,ORPHAcode: 139417 Acute transverse myelitis,ICD-10 +G37.4 Other demyelinating diseases of central nervous system - Subacute necrotizing myelitis,2953,G37.4,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.4,ORPHAcode: 79093 Foix-Alajouanine syndrome,ICD-10 +G37.5 Concentric sclerosis [Baló,2954,G37.5,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.5,ORPHAcode: 228165 Bal concentric scl,ICD-10 +G37.8 Other specified demyelinating diseases of central nervous system,2955,G37.8,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.8,ORPHAcode: 3151 Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome,ICD-10 "G37.9 Demyelinating disease of central nervous system, unspecified",2956,G37.9,G35-G37 Demyelinating diseases of the central nervous system,http://identifiers.org/icd/G37.9,,ICD-10 G40-G47 Episodic and paroxysmal disorders,2957,,VI Diseases of the nervous system,,,ICD-10 G40 Epilepsy,2958,G40,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40,,ICD-10 -G40.0 Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset,2959,G40.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.0,ORPHAcode: 1945 Rolandic epilepsy -G40.1 Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures,2960,G40.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.1,ORPHAcode: 166302 Benign partial epilepsy with secondarily generalized seizures in infancy -G40.2 Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures,2961,G40.2,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.2,ORPHAcode: 98819 Familial temporal lobe epilepsy -G40.3 Generalized idiopathic epilepsy and epileptic syndromes,2962,G40.3,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.3,ORPHAcode: 306 Benign familial infantile epilepsy -G40.4 Other generalized epilepsy and epileptic syndromes,2963,G40.4,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.4,ORPHAcode: 1935 Early myoclonic encephalopathy -G40.5 Epilepsy - Special epileptic syndromes,2964,G40.5,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.5,ORPHAcode: 86906 Hypothalamic hamartomas with gelastic seizures +G40.0 Localization-related (focal)(partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset,2959,G40.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.0,ORPHAcode: 1945 Rolandic epilepsy,ICD-10 +G40.1 Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures,2960,G40.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.1,ORPHAcode: 166302 Benign partial epilepsy with secondarily generalized seizures in infancy,ICD-10 +G40.2 Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures,2961,G40.2,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.2,ORPHAcode: 98819 Familial temporal lobe epilepsy,ICD-10 +G40.3 Generalized idiopathic epilepsy and epileptic syndromes,2962,G40.3,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.3,ORPHAcode: 306 Benign familial infantile epilepsy,ICD-10 +G40.4 Other generalized epilepsy and epileptic syndromes,2963,G40.4,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.4,ORPHAcode: 1935 Early myoclonic encephalopathy,ICD-10 +G40.5 Epilepsy - Special epileptic syndromes,2964,G40.5,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.5,ORPHAcode: 86906 Hypothalamic hamartomas with gelastic seizures,ICD-10 "G40.6 Epilepsy - Grand mal seizures, unspecified (with or without petit mal)",2965,G40.6,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.6,,ICD-10 "G40.7 Epilepsy - Petit mal, unspecified, without grand mal seizures",2966,G40.7,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.7,,ICD-10 -G40.8 Other epilepsy,2967,G40.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.8,ORPHAcode: 1544 Benign focal seizures of adolescence +G40.8 Other epilepsy,2967,G40.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.8,ORPHAcode: 1544 Benign focal seizures of adolescence,ICD-10 "G40.9 Epilepsy, unspecified",2968,G40.9,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G40.9,,ICD-10 G41 Status epilepticus,2969,G41,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G41,,ICD-10 G41.0 Grand mal status epilepticus,2970,G41.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G41.0,,ICD-10 G41.1 Petit mal status epilepticus,2971,G41.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G41.1,,ICD-10 G41.2 Complex partial status epilepticus,2972,G41.2,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G41.2,,ICD-10 -G41.8 Other status epilepticus,2973,G41.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G41.8,ORPHAcode: 363558 New-onset refractory status epilepticus +G41.8 Other status epilepticus,2973,G41.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G41.8,ORPHAcode: 363558 New-onset refractory status epilepticus,ICD-10 "G41.9 Status epilepticus, unspecified",2974,G41.9,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G41.9,,ICD-10 G43 Migraine,2975,G43,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43,,ICD-10 G43.0 Migraine without aura [common migraine],2976,G43.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43.0,,ICD-10 -G43.1 Migraine with aura [classical migraine],2977,G43.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43.1,ORPHAcode: 569 Familial or sporadic hemiplegic migraine +G43.1 Migraine with aura [classical migraine],2977,G43.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43.1,ORPHAcode: 569 Familial or sporadic hemiplegic migraine,ICD-10 G43.2 Migraine - Status migrainosus,2978,G43.2,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43.2,,ICD-10 G43.3 Complicated migraine,2979,G43.3,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43.3,,ICD-10 G43.8 Other migraine,2980,G43.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43.8,,ICD-10 "G43.9 Migraine, unspecified",2981,G43.9,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G43.9,,ICD-10 G44 Other headache syndromes,2982,G44,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44,,ICD-10 -G44.0 Cluster headache syndrome,2983,G44.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.0,ORPHAcode: 157835 Paroxysmal hemicrania +G44.0 Cluster headache syndrome,2983,G44.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.0,ORPHAcode: 157835 Paroxysmal hemicrania,ICD-10 "G44.1 Vascular headache, not elsewhere classified",2984,G44.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.1,,ICD-10 G44.2 Tension-type headache,2985,G44.2,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.2,,ICD-10 G44.3 Chronic post-traumatic headache,2986,G44.3,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.3,,ICD-10 "G44.4 Drug-induced headache, not elsewhere classified",2987,G44.4,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.4,,ICD-10 -G44.8 Other specified headache syndromes,2988,G44.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.8,ORPHAcode: 57145 SUNCT syndrome +G44.8 Other specified headache syndromes,2988,G44.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G44.8,ORPHAcode: 57145 SUNCT syndrome,ICD-10 G45 Transient cerebral ischaemic attacks and related syndromes,2989,G45,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G45,,ICD-10 G45.0 Transient cerebral ischaemic attacks and related syndromes - Vertebro-basilar artery syndrome,2990,G45.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G45.0,,ICD-10 G45.1 Transient cerebral ischaemic attacks and related syndromes - Carotid artery syndrome (hemispheric),2991,G45.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G45.1,,ICD-10 @@ -3008,32 +3008,32 @@ G46.8 Other vascular syndromes of brain in cerebrovascular diseases,3006,G46.8,G G47 Sleep disorders,3007,G47,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47,,ICD-10 G47.0 Disorders of initiating and maintaining sleep [insomnias],3008,G47.0,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.0,,ICD-10 G47.1 Disorders of excessive somnolence [hypersomnias],3009,G47.1,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.1,,ICD-10 -G47.2 Disorders of the sleep-wake schedule,3010,G47.2,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.2,ORPHAcode: 73267 Non-24-hour sleep-wake syndrome -G47.3 Sleep apnoea,3011,G47.3,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.3,ORPHAcode: 661 Ondine syndrome -G47.4 Sleep disorders - Narcolepsy and cataplexy,3012,G47.4,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.4,ORPHAcode: 2073 Narcolepsy type 1 -G47.8 Other sleep disorders,3013,G47.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.8,ORPHAcode: 33543 Kleine-Levin syndrome +G47.2 Disorders of the sleep-wake schedule,3010,G47.2,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.2,ORPHAcode: 73267 Non-24-hour sleep-wake syndrome,ICD-10 +G47.3 Sleep apnoea,3011,G47.3,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.3,ORPHAcode: 661 Ondine syndrome,ICD-10 +G47.4 Sleep disorders - Narcolepsy and cataplexy,3012,G47.4,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.4,ORPHAcode: 2073 Narcolepsy type 1,ICD-10 +G47.8 Other sleep disorders,3013,G47.8,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.8,ORPHAcode: 33543 Kleine-Levin syndrome,ICD-10 "G47.9 Sleep disorder, unspecified",3014,G47.9,G40-G47 Episodic and paroxysmal disorders,http://identifiers.org/icd/G47.9,,ICD-10 "G50-G59 Nerve, nerve root and plexus disorders",3015,,VI Diseases of the nervous system,,,ICD-10 G50 Disorders of trigeminal nerve,3016,G50,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50,,ICD-10 -G50.0 Trigeminal neuralgia,3017,G50.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50.0,ORPHAcode: 221091 Trigeminal neuralgia -G50.1 Disorders of trigeminal nerve - Atypical facial pain,3018,G50.1,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50.1,ORPHAcode: 398147 Persistent idiopathic facial pain -G50.8 Other disorders of trigeminal nerve,3019,G50.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50.8,ORPHAcode: 231013 Congenital trigeminal anesthesia +G50.0 Trigeminal neuralgia,3017,G50.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50.0,ORPHAcode: 221091 Trigeminal neuralgia,ICD-10 +G50.1 Disorders of trigeminal nerve - Atypical facial pain,3018,G50.1,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50.1,ORPHAcode: 398147 Persistent idiopathic facial pain,ICD-10 +G50.8 Other disorders of trigeminal nerve,3019,G50.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50.8,ORPHAcode: 231013 Congenital trigeminal anesthesia,ICD-10 "G50.9 Disorder of trigeminal nerve, unspecified",3020,G50.9,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G50.9,,ICD-10 G51 Facial nerve disorders,3021,G51,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51,,ICD-10 "H26.9 Cataract, unspecified",3022,H26.9,H25-H28 Disorders of lens,http://identifiers.org/icd/H26.9,,ICD-10 -G51.0 Facial nerve disorders - Bell palsy,3023,G51.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.0,ORPHAcode: 2809 Familial recurrent peripheral facial palsy +G51.0 Facial nerve disorders - Bell palsy,3023,G51.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.0,ORPHAcode: 2809 Familial recurrent peripheral facial palsy,ICD-10 G51.1 Facial nerve disorders - Geniculate ganglionitis,3024,G51.1,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.1,,ICD-10 -G51.2 Facial nerve disorders - Melkersson syndrome,3025,G51.2,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.2,ORPHAcode: 2483 Melkersson-Rosenthal syndrome -G51.3 Clonic hemifacial spasm,3026,G51.3,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.3,ORPHAcode: 221083 Hemifacial spasm -G51.4 Facial myokymia,3027,G51.4,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.4,ORPHAcode: 221106 Isolated facial myokymia -G51.8 Other disorders of facial nerve,3028,G51.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.8,ORPHAcode: 1214 Progressive hemifacial atrophy +G51.2 Facial nerve disorders - Melkersson syndrome,3025,G51.2,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.2,ORPHAcode: 2483 Melkersson-Rosenthal syndrome,ICD-10 +G51.3 Clonic hemifacial spasm,3026,G51.3,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.3,ORPHAcode: 221083 Hemifacial spasm,ICD-10 +G51.4 Facial myokymia,3027,G51.4,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.4,ORPHAcode: 221106 Isolated facial myokymia,ICD-10 +G51.8 Other disorders of facial nerve,3028,G51.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.8,ORPHAcode: 1214 Progressive hemifacial atrophy,ICD-10 "G51.9 Disorder of facial nerve, unspecified",3029,G51.9,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G51.9,,ICD-10 G52 Disorders of other cranial nerves,3030,G52,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52,,ICD-10 G52.0 Disorders of olfactory nerve,3031,G52.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.0,,ICD-10 -G52.1 Disorders of glossopharyngeal nerve,3032,G52.1,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.1,ORPHAcode: 221098 Glossopharyngeal neuralgia +G52.1 Disorders of glossopharyngeal nerve,3032,G52.1,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.1,ORPHAcode: 221098 Glossopharyngeal neuralgia,ICD-10 G52.2 Disorders of vagus nerve,3033,G52.2,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.2,,ICD-10 G52.3 Disorders of hypoglossal nerve,3034,G52.3,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.3,,ICD-10 -G52.7 Disorders of multiple cranial nerves,3035,G52.7,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.7,ORPHAcode: 221078 Combined hyperactive dysfunction syndrome of the cranial nerves +G52.7 Disorders of multiple cranial nerves,3035,G52.7,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.7,ORPHAcode: 221078 Combined hyperactive dysfunction syndrome of the cranial nerves,ICD-10 G52.8 Disorders of other specified cranial nerves,3036,G52.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.8,,ICD-10 "G52.9 Cranial nerve disorder, unspecified",3037,G52.9,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G52.9,,ICD-10 G53 Cranial nerve disorders in diseases classified elsewhere,3038,G53,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G53,,ICD-10 @@ -3044,15 +3044,15 @@ G53.2 Multiple cranial nerve palsies in sarcoidosis,3042,G53.2,"G50-G59 Nerve, n G53.3 Multiple cranial nerve palsies in neoplastic disease,3043,G53.3,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G53.3,,ICD-10 G53.8 Other cranial nerve disorders in other diseases classified elsewhere,3044,G53.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G53.8,,ICD-10 G54 Nerve root and plexus disorders,3045,G54,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54,,ICD-10 -G54.0 Brachial plexus disorders,3046,G54.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.0,ORPHAcode: 97330 Thoracic outlet syndrome +G54.0 Brachial plexus disorders,3046,G54.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.0,ORPHAcode: 97330 Thoracic outlet syndrome,ICD-10 G54.1 Lumbosacral plexus disorders,3047,G54.1,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.1,,ICD-10 "G54.2 Cervical root disorders, not elsewhere classified",3048,G54.2,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.2,,ICD-10 "G54.3 Thoracic root disorders, not elsewhere classified",3049,G54.3,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.3,,ICD-10 "G54.4 Lumbosacral root disorders, not elsewhere classified",3050,G54.4,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.4,,ICD-10 -G54.5 Nerve root and plexus disorders - Neuralgic amyotrophy,3051,G54.5,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.5,ORPHAcode: 2901 Neuralgic amyotrophy +G54.5 Nerve root and plexus disorders - Neuralgic amyotrophy,3051,G54.5,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.5,ORPHAcode: 2901 Neuralgic amyotrophy,ICD-10 G54.6 Nerve root and plexus disorders - Phantom limb syndrome with pain,3052,G54.6,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.6,,ICD-10 G54.7 Nerve root and plexus disorders - Phantom limb syndrome without pain,3053,G54.7,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.7,,ICD-10 -G54.8 Other nerve root and plexus disorders,3054,G54.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.8,ORPHAcode: 65250 Perineural cyst +G54.8 Other nerve root and plexus disorders,3054,G54.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.8,ORPHAcode: 65250 Perineural cyst,ICD-10 "G54.9 Nerve root and plexus disorder, unspecified",3055,G54.9,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G54.9,,ICD-10 G55 Nerve root and plexus compressions in diseases classified elsewhere,3056,G55,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G55,,ICD-10 G55.0 Nerve root and plexus compressions in neoplastic disease,3057,G55.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G55.0,,ICD-10 @@ -3076,10 +3076,10 @@ G57.2 Lesion of femoral nerve,3074,G57.2,"G50-G59 Nerve, nerve root and plexus d G57.3 Lesion of lateral popliteal nerve,3075,G57.3,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G57.3,,ICD-10 G57.4 Lesion of medial popliteal nerve,3076,G57.4,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G57.4,,ICD-10 G57.5 Mononeuropathies of lower limb - Tarsal tunnel syndrome,3077,G57.5,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G57.5,,ICD-10 -G57.8 Other mononeuropathies of lower limb,3078,G57.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G57.8,ORPHAcode: 60039 Pudendal neuralgia +G57.8 Other mononeuropathies of lower limb,3078,G57.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G57.8,ORPHAcode: 60039 Pudendal neuralgia,ICD-10 "G57.9 Mononeuropathy of lower limb, unspecified",3079,G57.9,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G57.9,,ICD-10 G58 Other mononeuropathies,3080,G58,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G58,,ICD-10 -G58.0 Other mononeuropathies - Intercostal neuropathy,3081,G58.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G58.0,ORPHAcode: 51890 Anterior cutaneous nerve entrapment syndrome +G58.0 Other mononeuropathies - Intercostal neuropathy,3081,G58.0,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G58.0,ORPHAcode: 51890 Anterior cutaneous nerve entrapment syndrome,ICD-10 G58.7 Other mononeuropathies - Mononeuritis multiplex,3082,G58.7,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G58.7,,ICD-10 G58.8 Other specified mononeuropathies,3083,G58.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G58.8,,ICD-10 "G58.9 Other mononeuropathies - Mononeuropathy, unspecified",3084,G58.9,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G58.9,,ICD-10 @@ -3088,16 +3088,16 @@ G59.0 Diabetic mononeuropathy,3086,G59.0,"G50-G59 Nerve, nerve root and plexus d G59.8 Other mononeuropathies in diseases classified elsewhere,3087,G59.8,"G50-G59 Nerve, nerve root and plexus disorders",http://identifiers.org/icd/G59.8,,ICD-10 G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,3088,,VI Diseases of the nervous system,,,ICD-10 G60 Hereditary and idiopathic neuropathy,3089,G60,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60,,ICD-10 -G60.0 Hereditary motor and sensory neuropathy,3090,G60.0,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.0,ORPHAcode: 640 Hereditary neuropathy with liability to pressure palsies -G60.1 Hereditary and idiopathic neuropathy - Refsum disease,3091,G60.1,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.1,ORPHAcode: 772 Infantile Refsum disease -G60.2 Neuropathy in association with hereditary ataxia,3092,G60.2,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.2,ORPHAcode: 1399 Richards-Rundle syndrome +G60.0 Hereditary motor and sensory neuropathy,3090,G60.0,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.0,ORPHAcode: 640 Hereditary neuropathy with liability to pressure palsies,ICD-10 +G60.1 Hereditary and idiopathic neuropathy - Refsum disease,3091,G60.1,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.1,ORPHAcode: 772 Infantile Refsum disease,ICD-10 +G60.2 Neuropathy in association with hereditary ataxia,3092,G60.2,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.2,ORPHAcode: 1399 Richards-Rundle syndrome,ICD-10 G60.3 Idiopathic progressive neuropathy,3093,G60.3,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.3,,ICD-10 -G60.8 Other hereditary and idiopathic neuropathies,3094,G60.8,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.8,ORPHAcode: 642 Hereditary sensory and autonomic neuropathy type 4 +G60.8 Other hereditary and idiopathic neuropathies,3094,G60.8,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.8,ORPHAcode: 642 Hereditary sensory and autonomic neuropathy type 4,ICD-10 "G60.9 Hereditary and idiopathic neuropathy, unspecified",3095,G60.9,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G60.9,,ICD-10 G61 Inflammatory polyneuropathy,3096,G61,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G61,,ICD-10 -G61.0 Guillain-Barré syndrom,3097,G61.0,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G61.0,ORPHAcode: 79138 Bickerstaff brainstem encephalitis +G61.0 Guillain-Barré syndrom,3097,G61.0,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G61.0,ORPHAcode: 79138 Bickerstaff brainstem encephalitis,ICD-10 G61.1 Inflammatory polyneuropathy - Serum neuropathy,3098,G61.1,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G61.1,,ICD-10 -G61.8 Other inflammatory polyneuropathies,3099,G61.8,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G61.8,ORPHAcode: 639 Polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG +G61.8 Other inflammatory polyneuropathies,3099,G61.8,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G61.8,ORPHAcode: 639 Polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG,ICD-10 "G61.9 Inflammatory polyneuropathy, unspecified",3100,G61.9,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G61.9,,ICD-10 G62 Other polyneuropathies,3101,G62,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G62,,ICD-10 G62.0 Other polyneuropathies - Drug-induced polyneuropathy,3102,G62.0,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G62.0,,ICD-10 @@ -3117,29 +3117,29 @@ G63.8 Polyneuropathy in other diseases classified elsewhere,3115,G63.8,G60-G64 P G64 Other disorders of peripheral nervous system,3116,G64,G60-G64 Polyneuropathies and other disorders of the peripheral nervous system,http://identifiers.org/icd/G64,,ICD-10 G70-G73 Diseases of myoneural junction and muscle,3117,,VI Diseases of the nervous system,,,ICD-10 G70 Myasthenia gravis and other myoneural disorders,3118,G70,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70,,ICD-10 -G70.0 Myasthenia gravis,3119,G70.0,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.0,ORPHAcode: 589 Myasthenia gravis +G70.0 Myasthenia gravis,3119,G70.0,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.0,ORPHAcode: 589 Myasthenia gravis,ICD-10 G70.1 Toxic myoneural disorders,3120,G70.1,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.1,,ICD-10 -G70.2 Congenital and developmental myasthenia,3121,G70.2,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.2,ORPHAcode: 590 Congenital myasthenic syndrome -G70.8 Other specified myoneural disorders,3122,G70.8,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.8,ORPHAcode: 206575 Rippling muscle disease with myasthenia gravis +G70.2 Congenital and developmental myasthenia,3121,G70.2,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.2,ORPHAcode: 590 Congenital myasthenic syndrome,ICD-10 +G70.8 Other specified myoneural disorders,3122,G70.8,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.8,ORPHAcode: 206575 Rippling muscle disease with myasthenia gravis,ICD-10 "G70.9 Myoneural disorder, unspecified",3123,G70.9,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G70.9,,ICD-10 G71 Primary disorders of muscles,3124,G71,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71,,ICD-10 -G71.0 Primary disorders of muscles - Muscular dystrophy,3125,G71.0,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.0,ORPHAcode: 62 Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3 -G71.1 Myotonic disorders,3126,G71.1,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.1,ORPHAcode: 273 Steinert myotonic dystrophy -G71.2 Primary disorders of muscles - Congenital myopathies,3127,G71.2,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.2,ORPHAcode: 258 Laminin subunit alpha 2-related congenital muscular dystrophy -"G71.3 Primary disorders of muscles - Mitochondrial myopathy, not elsewhere classified",3128,G71.3,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.3,ORPHAcode: 45 Adenosine monophosphate deaminase deficiency -G71.8 Other primary disorders of muscles,3129,G71.8,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.8,ORPHAcode: 602 GNE myopathy +G71.0 Primary disorders of muscles - Muscular dystrophy,3125,G71.0,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.0,ORPHAcode: 62 Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3,ICD-10 +G71.1 Myotonic disorders,3126,G71.1,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.1,ORPHAcode: 273 Steinert myotonic dystrophy,ICD-10 +G71.2 Primary disorders of muscles - Congenital myopathies,3127,G71.2,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.2,ORPHAcode: 258 Laminin subunit alpha 2-related congenital muscular dystrophy,ICD-10 +"G71.3 Primary disorders of muscles - Mitochondrial myopathy, not elsewhere classified",3128,G71.3,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.3,ORPHAcode: 45 Adenosine monophosphate deaminase deficiency,ICD-10 +G71.8 Other primary disorders of muscles,3129,G71.8,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.8,ORPHAcode: 602 GNE myopathy,ICD-10 "G71.9 Primary disorder of muscle, unspecified",3130,G71.9,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G71.9,,ICD-10 G72 Other myopathies,3131,G72,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72,,ICD-10 G72.0 Other myopathies - Drug-induced myopathy,3132,G72.0,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.0,,ICD-10 G72.1 Other myopathies - Alcoholic myopathy,3133,G72.1,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.1,,ICD-10 G72.2 Myopathy due to other toxic agents,3134,G72.2,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.2,,ICD-10 -G72.3 Other myopathies - Periodic paralysis,3135,G72.3,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.3,ORPHAcode: 681 Hypokalemic periodic paralysis -"G72.4 Other myopathies - Inflammatory myopathy, not elsewhere classified",3136,G72.4,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.4,ORPHAcode: 206569 Immune-mediated necrotizing myopathy -G72.8 Other specified myopathies,3137,G72.8,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.8,ORPHAcode: 171690 Metabolic myopathy due to lactate transporter defect +G72.3 Other myopathies - Periodic paralysis,3135,G72.3,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.3,ORPHAcode: 681 Hypokalemic periodic paralysis,ICD-10 +"G72.4 Other myopathies - Inflammatory myopathy, not elsewhere classified",3136,G72.4,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.4,ORPHAcode: 206569 Immune-mediated necrotizing myopathy,ICD-10 +G72.8 Other specified myopathies,3137,G72.8,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.8,ORPHAcode: 171690 Metabolic myopathy due to lactate transporter defect,ICD-10 "G72.9 Other myopathies - Myopathy, unspecified",3138,G72.9,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G72.9,,ICD-10 G73 Disorders of myoneural junction and muscle in diseases classified elsewhere,3139,G73,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G73,,ICD-10 G73.0 Myasthenic syndromes in endocrine diseases,3140,G73.0,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G73.0,,ICD-10 -G73.1 Disorders of myoneural junction and muscle in diseases classified elsewhere - Lambert-Eaton syndrome,3141,G73.1,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G73.1,ORPHAcode: 43393 Lambert-Eaton myasthenic syndrome +G73.1 Disorders of myoneural junction and muscle in diseases classified elsewhere - Lambert-Eaton syndrome,3141,G73.1,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G73.1,ORPHAcode: 43393 Lambert-Eaton myasthenic syndrome,ICD-10 G73.2 Other myasthenic syndromes in neoplastic disease,3142,G73.2,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G73.2,,ICD-10 G73.3 Myasthenic syndromes in other diseases classified elsewhere,3143,G73.3,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G73.3,,ICD-10 G73.4 Myopathy in infectious and parasitic diseases classified elsewhere,3144,G73.4,G70-G73 Diseases of myoneural junction and muscle,http://identifiers.org/icd/G73.4,,ICD-10 @@ -3147,19 +3147,19 @@ G73.7 Myopathy in other diseases classified elsewhere,3145,G73.7,G70-G73 Disease G80-G83 Cerebral palsy and other paralytic syndromes,3146,,VI Diseases of the nervous system,,,ICD-10 G80 Cerebral palsy,3147,G80,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80,,ICD-10 G80.0 Spastic quadriplegic cerebral palsy,3148,G80.0,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.0,,ICD-10 -G80.1 Spastic diplegic cerebral palsy,3149,G80.1,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.1,ORPHAcode: 404473 Severe intellectual disability-progressive spastic diplegia syndrome +G80.1 Spastic diplegic cerebral palsy,3149,G80.1,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.1,ORPHAcode: 404473 Severe intellectual disability-progressive spastic diplegia syndrome,ICD-10 G80.2 Spastic hemiplegic cerebral palsy,3150,G80.2,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.2,,ICD-10 G80.3 Dyskinetic cerebral palsy,3151,G80.3,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.3,,ICD-10 G80.4 Ataxic cerebral palsy,3152,G80.4,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.4,,ICD-10 -G80.8 Other cerebral palsy,3153,G80.8,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.8,ORPHAcode: 3465 Worster-Drought syndrome +G80.8 Other cerebral palsy,3153,G80.8,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.8,ORPHAcode: 3465 Worster-Drought syndrome,ICD-10 "G80.9 Cerebral palsy, unspecified",3154,G80.9,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G80.9,,ICD-10 G81 Hemiplegia,3155,G81,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G81,,ICD-10 G81.0 Flaccid hemiplegia,3156,G81.0,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G81.0,,ICD-10 G81.1 Spastic hemiplegia,3157,G81.1,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G81.1,,ICD-10 -"G81.9 Hemiplegia, unspecified",3158,G81.9,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G81.9,ORPHAcode: 209973 Benign nocturnal alternating hemiplegia of childhood +"G81.9 Hemiplegia, unspecified",3158,G81.9,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G81.9,ORPHAcode: 209973 Benign nocturnal alternating hemiplegia of childhood,ICD-10 G82 Paraplegia and tetraplegia,3159,G82,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82,,ICD-10 G82.0 Flaccid paraplegia,3160,G82.0,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82.0,,ICD-10 -G82.1 Spastic paraplegia,3161,G82.1,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82.1,ORPHAcode: 2824 Paraplegia-intellectual disability-hyperkeratosis syndrome +G82.1 Spastic paraplegia,3161,G82.1,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82.1,ORPHAcode: 2824 Paraplegia-intellectual disability-hyperkeratosis syndrome,ICD-10 "G82.2 Paraplegia, unspecified",3162,G82.2,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82.2,,ICD-10 G82.3 Flaccid tetraplegia,3163,G82.3,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82.3,,ICD-10 "G82.5 Tetraplegia, unspecified",3164,G82.5,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G82.5,,ICD-10 @@ -3170,16 +3170,16 @@ G83.2 Other paralytic syndromes - Monoplegia of upper limb,3168,G83.2,G80-G83 Ce "G83.3 Other paralytic syndromes - Monoplegia, unspecified",3169,G83.3,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G83.3,,ICD-10 G83.4 Other paralytic syndromes - Cauda equina syndrome,3170,G83.4,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G83.4,,ICD-10 G83.5 Other paralytic syndromes - Locked-in syndrome,3171,G83.5,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G83.5,,ICD-10 -G83.8 Other specified paralytic syndromes,3172,G83.8,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G83.8,ORPHAcode: 2406 Locked-in syndrome +G83.8 Other specified paralytic syndromes,3172,G83.8,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G83.8,ORPHAcode: 2406 Locked-in syndrome,ICD-10 "G83.9 Paralytic syndrome, unspecified",3173,G83.9,G80-G83 Cerebral palsy and other paralytic syndromes,http://identifiers.org/icd/G83.9,,ICD-10 G90-G99 Other disorders of the nervous system,3174,,VI Diseases of the nervous system,,,ICD-10 G90 Disorders of autonomic nervous system,3175,G90,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90,,ICD-10 G90.0 Idiopathic peripheral autonomic neuropathy,3176,G90.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.0,,ICD-10 -G90.1 Disorders of autonomic nervous system - Familial dysautonomia [Riley-Day],3177,G90.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.1,ORPHAcode: 1764 Familial dysautonomia -G90.2 Disorders of autonomic nervous system - Horner syndrome,3178,G90.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.2,ORPHAcode: 91413 Congenital Horner syndrome -G90.3 Multi-system degeneration,3179,G90.3,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.3,ORPHAcode: 441 Pure autonomic failure -G90.4 Autonomic dysreflexia,3180,G90.4,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.4,ORPHAcode: 443084 Baroreflex failure -G90.8 Other disorders of autonomic nervous system,3181,G90.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.8,ORPHAcode: 230 Dopamine beta-hydroxylase deficiency +G90.1 Disorders of autonomic nervous system - Familial dysautonomia [Riley-Day],3177,G90.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.1,ORPHAcode: 1764 Familial dysautonomia,ICD-10 +G90.2 Disorders of autonomic nervous system - Horner syndrome,3178,G90.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.2,ORPHAcode: 91413 Congenital Horner syndrome,ICD-10 +G90.3 Multi-system degeneration,3179,G90.3,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.3,ORPHAcode: 441 Pure autonomic failure,ICD-10 +G90.4 Autonomic dysreflexia,3180,G90.4,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.4,ORPHAcode: 443084 Baroreflex failure,ICD-10 +G90.8 Other disorders of autonomic nervous system,3181,G90.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.8,ORPHAcode: 230 Dopamine beta-hydroxylase deficiency,ICD-10 "G90.9 Disorder of autonomic nervous system, unspecified",3182,G90.9,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G90.9,,ICD-10 G91 Hydrocephalus,3183,G91,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G91,,ICD-10 G91.0 Communicating hydrocephalus,3184,G91.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G91.0,,ICD-10 @@ -3190,16 +3190,16 @@ G91.8 Other hydrocephalus,3188,G91.8,G90-G99 Other disorders of the nervous syst "G91.9 Hydrocephalus, unspecified",3189,G91.9,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G91.9,,ICD-10 G92 Toxic encephalopathy,3190,G92,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G92,,ICD-10 G93 Other disorders of brain,3191,G93,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93,,ICD-10 -G93.0 Other disorders of brain - Cerebral cysts,3192,G93.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.0,ORPHAcode: 2356 Arachnoid cyst +G93.0 Other disorders of brain - Cerebral cysts,3192,G93.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.0,ORPHAcode: 2356 Arachnoid cyst,ICD-10 "G93.1 Anoxic brain damage, not elsewhere classified",3193,G93.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.1,,ICD-10 -G93.2 Other disorders of brain - Benign intracranial hypertension,3194,G93.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.2,ORPHAcode: 238624 Idiopathic intracranial hypertension +G93.2 Other disorders of brain - Benign intracranial hypertension,3194,G93.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.2,ORPHAcode: 238624 Idiopathic intracranial hypertension,ICD-10 G93.3 Other disorders of brain - Postviral fatigue syndrome,3195,G93.3,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.3,,ICD-10 -"G93.4 Other disorders of brain - Encephalopathy, unspecified",3196,G93.4,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.4,ORPHAcode: 436271 Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy +"G93.4 Other disorders of brain - Encephalopathy, unspecified",3196,G93.4,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.4,ORPHAcode: 436271 Non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy,ICD-10 G93.5 Compression of brain,3197,G93.5,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.5,,ICD-10 G93.6 Other disorders of brain - Cerebral oedema,3198,G93.6,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.6,,ICD-10 -G93.7 Other disorders of brain - Reye syndrome,3199,G93.7,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.7,ORPHAcode: 3096 Reye syndrome +G93.7 Other disorders of brain - Reye syndrome,3199,G93.7,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.7,ORPHAcode: 3096 Reye syndrome,ICD-10 H01 Other inflammation of eyelid,3200,H01,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H01,,ICD-10 -G93.8 Other specified disorders of brain,3201,G93.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.8,ORPHAcode: 1313 Infantile choroidocerebral calcification syndrome +G93.8 Other specified disorders of brain,3201,G93.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.8,ORPHAcode: 1313 Infantile choroidocerebral calcification syndrome,ICD-10 "G93.9 Disorder of brain, unspecified",3202,G93.9,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G93.9,,ICD-10 G94 Other disorders of brain in diseases classified elsewhere,3203,G94,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G94,,ICD-10 G94.0 Hydrocephalus in infectious and parasitic diseases classified elsewhere,3204,G94.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G94.0,,ICD-10 @@ -3207,26 +3207,26 @@ G94.1 Hydrocephalus in neoplastic disease,3205,G94.1,G90-G99 Other disorders of G94.2 Hydrocephalus in other diseases classified elsewhere,3206,G94.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G94.2,,ICD-10 G94.8 Other specified disorders of brain in diseases classified elsewhere,3207,G94.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G94.8,,ICD-10 G95 Other diseases of spinal cord,3208,G95,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G95,,ICD-10 -G95.0 Other diseases of spinal cord - Syringomyelia and syringobulbia,3209,G95.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G95.0,ORPHAcode: 99857 Secondary syringomyelia +G95.0 Other diseases of spinal cord - Syringomyelia and syringobulbia,3209,G95.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G95.0,ORPHAcode: 99857 Secondary syringomyelia,ICD-10 G95.1 Other diseases of spinal cord - Vascular myelopathies,3210,G95.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G95.1,,ICD-10 "G95.2 Cord compression, unspecified",3211,G95.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G95.2,,ICD-10 G95.8 Other specified diseases of spinal cord,3212,G95.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G95.8,,ICD-10 "G95.9 Disease of spinal cord, unspecified",3213,G95.9,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G95.9,,ICD-10 G96 Other disorders of central nervous system,3214,G96,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G96,,ICD-10 -G96.0 Other disorders of central nervous system - Cerebrospinal fluid leak,3215,G96.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G96.0,ORPHAcode: 443180 Spontaneous intracranial hypotension +G96.0 Other disorders of central nervous system - Cerebrospinal fluid leak,3215,G96.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G96.0,ORPHAcode: 443180 Spontaneous intracranial hypotension,ICD-10 "G96.1 Disorders of meninges, not elsewhere classified",3216,G96.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G96.1,,ICD-10 -G96.8 Other specified disorders of central nervous system,3217,G96.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G96.8,ORPHAcode: 1179 Benign paroxysmal tonic upgaze of childhood with ataxia +G96.8 Other specified disorders of central nervous system,3217,G96.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G96.8,ORPHAcode: 1179 Benign paroxysmal tonic upgaze of childhood with ataxia,ICD-10 "G96.9 Disorder of central nervous system, unspecified",3218,G96.9,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G96.9,,ICD-10 "G97 Postprocedural disorders of nervous system, not elsewhere classified",3219,G97,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G97,,ICD-10 "G97.0 Postprocedural disorders of nervous system, not elsewhere classified - Cerebrospinal fluid leak from spinal puncture",3220,G97.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G97.0,,ICD-10 "G97.1 Postprocedural disorders of nervous system, not elsewhere classified - Other reaction to spinal and lumbar puncture",3221,G97.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G97.1,,ICD-10 "G97.2 Postprocedural disorders of nervous system, not elsewhere classified - Intracranial hypotension following ventricular shunting",3222,G97.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G97.2,,ICD-10 -G97.8 Other postprocedural disorders of nervous system,3223,G97.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G97.8,ORPHAcode: 90021 Radiation myelitis +G97.8 Other postprocedural disorders of nervous system,3223,G97.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G97.8,ORPHAcode: 90021 Radiation myelitis,ICD-10 "G97.9 Postprocedural disorder of nervous system, unspecified",3224,G97.9,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G97.9,,ICD-10 -"G98 Other disorders of nervous system, not elsewhere classified",3225,G98,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G98,ORPHAcode: 2131 Alternating hemiplegia of childhood +"G98 Other disorders of nervous system, not elsewhere classified",3225,G98,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G98,ORPHAcode: 2131 Alternating hemiplegia of childhood,ICD-10 G99 Other disorders of nervous system in diseases classified elsewhere,3226,G99,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G99,,ICD-10 G99.0 Autonomic neuropathy in endocrine and metabolic diseases,3227,G99.0,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G99.0,,ICD-10 -G99.1 Other disorders of autonomic nervous system in other diseases classified elsewhere,3228,G99.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G99.1,ORPHAcode: 306577 Sodium channelopathy-related small fiber neuropathy +G99.1 Other disorders of autonomic nervous system in other diseases classified elsewhere,3228,G99.1,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G99.1,ORPHAcode: 306577 Sodium channelopathy-related small fiber neuropathy,ICD-10 G99.2 Myelopathy in diseases classified elsewhere,3229,G99.2,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G99.2,,ICD-10 G99.8 Other specified disorders of nervous system in diseases classified elsewhere,3230,G99.8,G90-G99 Other disorders of the nervous system,http://identifiers.org/icd/G99.8,,ICD-10 VII Diseases of the eye and adnexa,3231,,,,,ICD-10 @@ -3261,13 +3261,13 @@ H04.2 Disorders of lacrimal system - Epiphora,3259,H04.2,"H00-H06 Disorders of e H04.3 Acute and unspecified inflammation of lacrimal passages,3260,H04.3,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H04.3,,ICD-10 H04.4 Chronic inflammation of lacrimal passages,3261,H04.4,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H04.4,,ICD-10 H04.5 Stenosis and insufficiency of lacrimal passages,3262,H04.5,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H04.5,,ICD-10 -H04.6 Other changes in lacrimal passages,3263,H04.6,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H04.6,ORPHAcode: 141083 Nasolacrimal duct cyst +H04.6 Other changes in lacrimal passages,3263,H04.6,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H04.6,ORPHAcode: 141083 Nasolacrimal duct cyst,ICD-10 H04.8 Other disorders of lacrimal system,3264,H04.8,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H04.8,,ICD-10 "H04.9 Disorder of lacrimal system, unspecified",3265,H04.9,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H04.9,,ICD-10 H05 Disorders of orbit,3266,H05,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05,,ICD-10 H05.0 Acute inflammation of orbit,3267,H05.0,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05.0,,ICD-10 H05.1 Chronic inflammatory disorders of orbit,3268,H05.1,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05.1,,ICD-10 -H05.2 Disorders of orbit - Exophthalmic conditions,3269,H05.2,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05.2,ORPHAcode: 466682 Euthyroid Graves orbitopathy +H05.2 Disorders of orbit - Exophthalmic conditions,3269,H05.2,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05.2,ORPHAcode: 466682 Euthyroid Graves orbitopathy,ICD-10 H05.3 Deformity of orbit,3270,H05.3,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05.3,,ICD-10 H05.4 Disorders of orbit - Enophthalmos,3271,H05.4,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05.4,,ICD-10 H05.5 Retained (old) foreign body following penetrating wound of orbit,3272,H05.5,"H00-H06 Disorders of eyelid, lacrimal system and orbit",http://identifiers.org/icd/H05.5,,ICD-10 @@ -3309,10 +3309,10 @@ H15.8 Other disorders of sclera,3306,H15.8,"H15-H22 Disorders of sclera, cornea, H16 Keratitis,3308,H16,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16,,ICD-10 H16.0 Keratitis - Corneal ulcer,3309,H16.0,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.0,,ICD-10 H16.1 Other superficial keratitis without conjunctivitis,3310,H16.1,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.1,,ICD-10 -H16.2 Keratitis - Keratoconjunctivitis,3311,H16.2,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.2,ORPHAcode: 70476 Vernal keratoconjunctivitis -H16.3 Interstitial and deep keratitis,3312,H16.3,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.3,ORPHAcode: 1467 Cogan syndrome +H16.2 Keratitis - Keratoconjunctivitis,3311,H16.2,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.2,ORPHAcode: 70476 Vernal keratoconjunctivitis,ICD-10 +H16.3 Interstitial and deep keratitis,3312,H16.3,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.3,ORPHAcode: 1467 Cogan syndrome,ICD-10 H16.4 Keratitis - Corneal neovascularization,3313,H16.4,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.4,,ICD-10 -H16.8 Other keratitis,3314,H16.8,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.8,ORPHAcode: 2334 Autosomal dominant keratitis +H16.8 Other keratitis,3314,H16.8,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.8,ORPHAcode: 2334 Autosomal dominant keratitis,ICD-10 "H16.9 Keratitis, unspecified",3315,H16.9,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H16.9,,ICD-10 H17 Corneal scars and opacities,3316,H17,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H17,,ICD-10 H17.0 Corneal scars and opacities - Adherent leukoma,3317,H17.0,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H17.0,,ICD-10 @@ -3325,9 +3325,9 @@ H18.1 Other disorders of cornea - Bullous keratopathy,3323,H18.1,"H15-H22 Disord H18.2 Other corneal oedema,3324,H18.2,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.2,,ICD-10 H18.3 Changes in corneal membranes,3325,H18.3,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.3,,ICD-10 H18.4 Corneal degeneration,3326,H18.4,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.4,,ICD-10 -H18.5 Hereditary corneal dystrophies,3327,H18.5,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.5,ORPHAcode: 1490 Corneal dystrophy-perceptive deafness syndrome +H18.5 Hereditary corneal dystrophies,3327,H18.5,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.5,ORPHAcode: 1490 Corneal dystrophy-perceptive deafness syndrome,ICD-10 H18.6 Other disorders of cornea - Keratoconus,3328,H18.6,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.6,,ICD-10 -H18.7 Other corneal deformities,3329,H18.7,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.7,ORPHAcode: 137672 Pellucid marginal degeneration +H18.7 Other corneal deformities,3329,H18.7,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.7,ORPHAcode: 137672 Pellucid marginal degeneration,ICD-10 H18.8 Other specified disorders of cornea,3330,H18.8,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.8,,ICD-10 "H18.9 Disorder of cornea, unspecified",3331,H18.9,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H18.9,,ICD-10 H19 Disorders of sclera and cornea in diseases classified elsewhere,3332,H19,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H19,,ICD-10 @@ -3337,15 +3337,15 @@ H19.2 Keratitis and keratoconjunctivitis in other infectious and parasitic disea H19.3 Keratitis and keratoconjunctivitis in other diseases classified elsewhere,3336,H19.3,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H19.3,,ICD-10 H19.8 Other disorders of sclera and cornea in diseases classified elsewhere,3337,H19.8,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H19.8,,ICD-10 H20 Iridocyclitis,3338,H20,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20,,ICD-10 -H20.0 Acute and subacute iridocyclitis,3339,H20.0,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.0,ORPHAcode: 279922 Infectious anterior uveitis +H20.0 Acute and subacute iridocyclitis,3339,H20.0,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.0,ORPHAcode: 279922 Infectious anterior uveitis,ICD-10 H20.1 Chronic iridocyclitis,3340,H20.1,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.1,,ICD-10 -H20.2 Lens-induced iridocyclitis,3341,H20.2,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.2,ORPHAcode: 209959 Phacoanaphylactic uveitis -H20.8 Other iridocyclitis,3342,H20.8,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.8,ORPHAcode: 3437 Vogt-Koyanagi-Harada disease +H20.2 Lens-induced iridocyclitis,3341,H20.2,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.2,ORPHAcode: 209959 Phacoanaphylactic uveitis,ICD-10 +H20.8 Other iridocyclitis,3342,H20.8,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.8,ORPHAcode: 3437 Vogt-Koyanagi-Harada disease,ICD-10 "H20.9 Iridocyclitis, unspecified",3343,H20.9,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H20.9,,ICD-10 H21 Other disorders of iris and ciliary body,3344,H21,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21,,ICD-10 H21.0 Other disorders of iris and ciliary body - Hyphaema,3345,H21.0,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.0,,ICD-10 -H21.1 Other vascular disorders of iris and ciliary body,3346,H21.1,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.1,ORPHAcode: 64734 Iridocorneal endothelial syndrome -H21.2 Degeneration of iris and ciliary body,3347,H21.2,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.2,ORPHAcode: 519392 Isolated iridoschisis +H21.1 Other vascular disorders of iris and ciliary body,3346,H21.1,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.1,ORPHAcode: 64734 Iridocorneal endothelial syndrome,ICD-10 +H21.2 Degeneration of iris and ciliary body,3347,H21.2,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.2,ORPHAcode: 519392 Isolated iridoschisis,ICD-10 "H21.3 Cyst of iris, ciliary body and anterior chamber",3348,H21.3,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.3,,ICD-10 H21.4 Other disorders of iris and ciliary body - Pupillary membranes,3349,H21.4,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.4,,ICD-10 H21.5 Other adhesions and disruptions of iris and ciliary body,3350,H21.5,"H15-H22 Disorders of sclera, cornea, iris and ciliary body",http://identifiers.org/icd/H21.5,,ICD-10 @@ -3363,7 +3363,7 @@ H25.1 Senile nuclear cataract,3360,H25.1,H25-H28 Disorders of lens,http://identi H25.8 Other senile cataract,3362,H25.8,H25-H28 Disorders of lens,http://identifiers.org/icd/H25.8,,ICD-10 "H25.9 Senile cataract, unspecified",3363,H25.9,H25-H28 Disorders of lens,http://identifiers.org/icd/H25.9,,ICD-10 H26 Other cataract,3364,H26,H25-H28 Disorders of lens,http://identifiers.org/icd/H26,,ICD-10 -"H26.0 Infantile, juvenile and presenile cataract",3365,H26.0,H25-H28 Disorders of lens,http://identifiers.org/icd/H26.0,ORPHAcode: 163 Hereditary hyperferritinemia-cataract syndrome +"H26.0 Infantile, juvenile and presenile cataract",3365,H26.0,H25-H28 Disorders of lens,http://identifiers.org/icd/H26.0,ORPHAcode: 163 Hereditary hyperferritinemia-cataract syndrome,ICD-10 H27 Other disorders of lens,3366,H27,H25-H28 Disorders of lens,http://identifiers.org/icd/H27,,ICD-10 H27.0 Other disorders of lens - Aphakia,3367,H27.0,H25-H28 Disorders of lens,http://identifiers.org/icd/H27.0,,ICD-10 H27.1 Dislocation of lens,3368,H27.1,H25-H28 Disorders of lens,http://identifiers.org/icd/H27.1,,ICD-10 @@ -3377,14 +3377,14 @@ H28.8 Other disorders of lens in diseases classified elsewhere,3375,H28.8,H25-H2 H30-H36 Disorders of choroid and retina,3376,,VII Diseases of the eye and adnexa,,,ICD-10 H30 Chorioretinal inflammation,3377,H30,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30,,ICD-10 H30.0 Focal chorioretinal inflammation,3378,H30.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.0,,ICD-10 -H30.1 Disseminated chorioretinal inflammation,3379,H30.1,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.1,ORPHAcode: 179 Birdshot chorioretinopathy -H30.2 Chorioretinal inflammation - Posterior cyclitis,3380,H30.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.2,ORPHAcode: 279914 Intermediate uveitis -H30.8 Other chorioretinal inflammations,3381,H30.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.8,ORPHAcode: 35686 Serpiginous choroiditis -"H30.9 Chorioretinal inflammation, unspecified",3382,H30.9,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.9,ORPHAcode: 279919 Infectious posterior uveitis +H30.1 Disseminated chorioretinal inflammation,3379,H30.1,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.1,ORPHAcode: 179 Birdshot chorioretinopathy,ICD-10 +H30.2 Chorioretinal inflammation - Posterior cyclitis,3380,H30.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.2,ORPHAcode: 279914 Intermediate uveitis,ICD-10 +H30.8 Other chorioretinal inflammations,3381,H30.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.8,ORPHAcode: 35686 Serpiginous choroiditis,ICD-10 +"H30.9 Chorioretinal inflammation, unspecified",3382,H30.9,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H30.9,ORPHAcode: 279919 Infectious posterior uveitis,ICD-10 H31 Other disorders of choroid,3383,H31,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31,,ICD-10 H31.0 Other disorders of choroid - Chorioretinal scars,3384,H31.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31.0,,ICD-10 H31.1 Choroidal degeneration,3385,H31.1,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31.1,,ICD-10 -H31.2 Hereditary choroidal dystrophy,3386,H31.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31.2,ORPHAcode: 180 Choroideremia +H31.2 Hereditary choroidal dystrophy,3386,H31.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31.2,ORPHAcode: 180 Choroideremia,ICD-10 H31.3 Choroidal haemorrhage and rupture,3387,H31.3,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31.3,,ICD-10 H31.4 Choroidal detachment,3388,H31.4,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31.4,,ICD-10 H31.8 Other specified disorders of choroid,3389,H31.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H31.8,,ICD-10 @@ -3393,7 +3393,7 @@ H32 Chorioretinal disorders in diseases classified elsewhere,3391,H32,H30-H36 Di H32.0 Chorioretinal inflammation in infectious and parasitic diseases classified elsewhere,3392,H32.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H32.0,,ICD-10 H32.8 Other chorioretinal disorders in diseases classified elsewhere,3393,H32.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H32.8,,ICD-10 H33 Retinal detachments and breaks,3394,H33,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H33,,ICD-10 -H33.0 Retinal detachment with retinal break,3395,H33.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H33.0,ORPHAcode: 209867 Autosomal dominant rhegmatogenous retinal detachment +H33.0 Retinal detachment with retinal break,3395,H33.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H33.0,ORPHAcode: 209867 Autosomal dominant rhegmatogenous retinal detachment,ICD-10 H33.1 Retinoschisis and retinal cysts,3396,H33.1,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H33.1,,ICD-10 H33.2 Serous retinal detachment,3397,H33.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H33.2,,ICD-10 H33.3 Retinal breaks without detachment,3398,H33.3,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H33.3,,ICD-10 @@ -3404,18 +3404,18 @@ H34.0 Transient retinal artery occlusion,3402,H34.0,H30-H36 Disorders of choroid H34.1 Central retinal artery occlusion,3403,H34.1,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H34.1,,ICD-10 H34.2 Other retinal artery occlusions,3404,H34.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H34.2,,ICD-10 H40.1 Primary open-angle glaucoma,3405,H40.1,H40-H42 Glaucoma,http://identifiers.org/icd/H40.1,,ICD-10 -H34.8 Other retinal vascular occlusions,3406,H34.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H34.8,ORPHAcode: 411527 Central retinal vein occlusion +H34.8 Other retinal vascular occlusions,3406,H34.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H34.8,ORPHAcode: 411527 Central retinal vein occlusion,ICD-10 "H34.9 Retinal vascular occlusion, unspecified",3407,H34.9,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H34.9,,ICD-10 H35 Other retinal disorders,3408,H35,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35,,ICD-10 -H35.0 Background retinopathy and retinal vascular changes,3409,H35.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.0,ORPHAcode: 190 Coats disease -H35.1 Other retinal disorders - Retinopathy of prematurity,3410,H35.1,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.1,ORPHAcode: 90050 Retinopathy of prematurity -H35.2 Other proliferative retinopathy,3411,H35.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.2,ORPHAcode: 329211 Autosomal dominant neovascular inflammatory vitreoretinopathy -H35.3 Other retinal disorders - Degeneration of macula and posterior pole,3412,H35.3,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.3,ORPHAcode: 178493 Myopic macular degeneration +H35.0 Background retinopathy and retinal vascular changes,3409,H35.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.0,ORPHAcode: 190 Coats disease,ICD-10 +H35.1 Other retinal disorders - Retinopathy of prematurity,3410,H35.1,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.1,ORPHAcode: 90050 Retinopathy of prematurity,ICD-10 +H35.2 Other proliferative retinopathy,3411,H35.2,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.2,ORPHAcode: 329211 Autosomal dominant neovascular inflammatory vitreoretinopathy,ICD-10 +H35.3 Other retinal disorders - Degeneration of macula and posterior pole,3412,H35.3,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.3,ORPHAcode: 178493 Myopic macular degeneration,ICD-10 H35.4 Peripheral retinal degeneration,3413,H35.4,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.4,,ICD-10 -H35.5 Hereditary retinal dystrophy,3414,H35.5,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.5,ORPHAcode: 65 Leber congenital amaurosis +H35.5 Hereditary retinal dystrophy,3414,H35.5,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.5,ORPHAcode: 65 Leber congenital amaurosis,ICD-10 H35.6 Retinal haemorrhage,3415,H35.6,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.6,,ICD-10 -H35.7 Separation of retinal layers,3416,H35.7,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.7,ORPHAcode: 443079 Central serous chorioretinopathy -H35.8 Other specified retinal disorders,3417,H35.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.8,ORPHAcode: 247691 Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations +H35.7 Separation of retinal layers,3416,H35.7,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.7,ORPHAcode: 443079 Central serous chorioretinopathy,ICD-10 +H35.8 Other specified retinal disorders,3417,H35.8,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.8,ORPHAcode: 247691 Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations,ICD-10 "H35.9 Retinal disorder, unspecified",3418,H35.9,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H35.9,,ICD-10 H36 Retinal disorders in diseases classified elsewhere,3419,H36,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H36,,ICD-10 H36.0 Diabetic retinopathy,3420,H36.0,H30-H36 Disorders of choroid and retina,http://identifiers.org/icd/H36.0,,ICD-10 @@ -3442,8 +3442,8 @@ H43.3 Other vitreous opacities,3440,H43.3,H43-H45 Disorders of vitreous body and H43.8 Other disorders of vitreous body,3441,H43.8,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H43.8,,ICD-10 "H43.9 Disorder of vitreous body, unspecified",3442,H43.9,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H43.9,,ICD-10 H44 Disorders of globe,3443,H44,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44,,ICD-10 -H44.0 Disorders of globe - Purulent endophthalmitis,3444,H44.0,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44.0,ORPHAcode: 199323 Endophthalmitis -H44.1 Disorders of globe - Other endophthalmitis,3445,H44.1,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44.1,ORPHAcode: 79098 Sympathetic ophthalmia +H44.0 Disorders of globe - Purulent endophthalmitis,3444,H44.0,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44.0,ORPHAcode: 199323 Endophthalmitis,ICD-10 +H44.1 Disorders of globe - Other endophthalmitis,3445,H44.1,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44.1,ORPHAcode: 79098 Sympathetic ophthalmia,ICD-10 H44.2 Disorders of globe - Degenerative myopia,3446,H44.2,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44.2,,ICD-10 H44.3 Other degenerative disorders of globe,3447,H44.3,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44.3,,ICD-10 H44.4 Hypotony of eye,3448,H44.4,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H44.4,,ICD-10 @@ -3457,15 +3457,15 @@ H45.0 Vitreous haemorrhage in diseases classified elsewhere,3455,H45.0,H43-H45 D H45.1 Endophthalmitis in diseases classified elsewhere,3456,H45.1,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H45.1,,ICD-10 H45.8 Other disorders of vitreous body and globe in diseases classified elsewhere,3457,H45.8,H43-H45 Disorders of vitreous body and globe,http://identifiers.org/icd/H45.8,,ICD-10 H46-H48 Disorders of optic nerve and visual pathways,3458,,VII Diseases of the eye and adnexa,,,ICD-10 -H46 Optic neuritis,3459,H46,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H46,ORPHAcode: 499085 Chronic relapsing inflammatory optic neuropathy +H46 Optic neuritis,3459,H46,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H46,ORPHAcode: 499085 Chronic relapsing inflammatory optic neuropathy,ICD-10 H47 Other disorders of optic [2nd] nerve and visual pathways,3460,H47,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47,,ICD-10 -"H47.0 Disorders of optic nerve, not elsewhere classified",3461,H47.0,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.0,ORPHAcode: 137902 Isolated optic nerve hypoplasia/aplasia +"H47.0 Disorders of optic nerve, not elsewhere classified",3461,H47.0,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.0,ORPHAcode: 137902 Isolated optic nerve hypoplasia/aplasia,ICD-10 "H47.1 Other disorders of optic [2nd] nerve and visual pathways - Papilloedema, unspecified",3462,H47.1,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.1,,ICD-10 -H47.2 Optic atrophy,3463,H47.2,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.2,ORPHAcode: 104 Leber hereditary optic neuropathy +H47.2 Optic atrophy,3463,H47.2,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.2,ORPHAcode: 104 Leber hereditary optic neuropathy,ICD-10 H47.3 Other disorders of optic disc,3464,H47.3,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.3,,ICD-10 -H47.4 Disorders of optic chiasm,3465,H47.4,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.4,ORPHAcode: 324353 Congenital achiasma +H47.4 Disorders of optic chiasm,3465,H47.4,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.4,ORPHAcode: 324353 Congenital achiasma,ICD-10 H47.5 Disorders of other visual pathways,3466,H47.5,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.5,,ICD-10 -H47.6 Disorders of visual cortex,3467,H47.6,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.6,ORPHAcode: 447788 Cerebral visual impairment +H47.6 Disorders of visual cortex,3467,H47.6,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.6,ORPHAcode: 447788 Cerebral visual impairment,ICD-10 "H47.7 Disorder of visual pathways, unspecified",3468,H47.7,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H47.7,,ICD-10 H48 Disorders of optic [2nd] nerve and visual pathways in diseases classified elsewhere,3469,H48,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H48,,ICD-10 H48.0 Optic atrophy in diseases classified elsewhere,3470,H48.0,H46-H48 Disorders of optic nerve and visual pathways,http://identifiers.org/icd/H48.0,,ICD-10 @@ -3474,11 +3474,11 @@ H48.8 Other disorders of optic nerve and visual pathways in diseases classified "H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",3473,,VII Diseases of the eye and adnexa,,,ICD-10 H49 Paralytic strabismus,3474,H49,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49,,ICD-10 H49.0 Paralytic strabismus - Third [oculomotor] nerve palsy,3475,H49.0,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.0,,ICD-10 -H49.1 Paralytic strabismus - Fourth [trochlear] nerve palsy,3476,H49.1,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.1,ORPHAcode: 91498 Familial congenital palsy of trochlear nerve +H49.1 Paralytic strabismus - Fourth [trochlear] nerve palsy,3476,H49.1,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.1,ORPHAcode: 91498 Familial congenital palsy of trochlear nerve,ICD-10 H49.2 Paralytic strabismus - Sixth [abducent] nerve palsy,3477,H49.2,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.2,,ICD-10 H49.3 Paralytic strabismus - Total (external) ophthalmoplegia,3478,H49.3,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.3,,ICD-10 -H49.4 Paralytic strabismus - Progressive external ophthalmoplegia,3479,H49.4,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.4,ORPHAcode: 663 Mitochondrial DNA-related progressive external ophthalmoplegia -H49.8 Other paralytic strabismus,3480,H49.8,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.8,ORPHAcode: 480 Kearns-Sayre syndrome +H49.4 Paralytic strabismus - Progressive external ophthalmoplegia,3479,H49.4,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.4,ORPHAcode: 663 Mitochondrial DNA-related progressive external ophthalmoplegia,ICD-10 +H49.8 Other paralytic strabismus,3480,H49.8,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.8,ORPHAcode: 480 Kearns-Sayre syndrome,ICD-10 "H49.9 Paralytic strabismus, unspecified",3481,H49.9,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H49.9,,ICD-10 H50 Other strabismus,3482,H50,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50,,ICD-10 H50.0 Convergent concomitant strabismus,3483,H50.0,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50.0,,ICD-10 @@ -3488,13 +3488,13 @@ H50.3 Other strabismus - Intermittent heterotropia,3486,H50.3,"H49-H52 Disorders H50.4 Other and unspecified heterotropia,3487,H50.4,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50.4,,ICD-10 H50.5 Other strabismus - Heterophoria,3488,H50.5,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50.5,,ICD-10 H50.6 Mechanical strabismus,3489,H50.6,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50.6,,ICD-10 -H50.8 Other specified strabismus,3490,H50.8,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50.8,ORPHAcode: 233 Duane retraction syndrome +H50.8 Other specified strabismus,3490,H50.8,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50.8,ORPHAcode: 233 Duane retraction syndrome,ICD-10 "H50.9 Strabismus, unspecified",3491,H50.9,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H50.9,,ICD-10 H51 Other disorders of binocular movement,3492,H51,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H51,,ICD-10 H51.0 Palsy of conjugate gaze,3493,H51.0,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H51.0,,ICD-10 H51.1 Other disorders of binocular movement - Convergence insufficiency and excess,3494,H51.1,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H51.1,,ICD-10 H51.2 Other disorders of binocular movement - Internuclear ophthalmoplegia,3495,H51.2,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H51.2,,ICD-10 -H51.8 Other specified disorders of binocular movement,3496,H51.8,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H51.8,"ORPHAcode: 1125 Ocular motor apraxia, Cogan type" +H51.8 Other specified disorders of binocular movement,3496,H51.8,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H51.8,"ORPHAcode: 1125 Ocular motor apraxia, Cogan type",ICD-10 "H51.9 Disorder of binocular movement, unspecified",3497,H51.9,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H51.9,,ICD-10 H52 Disorders of refraction and accommodation,3498,H52,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H52,,ICD-10 H52.0 Disorders of refraction and accommodation - Hypermetropia,3499,H52.0,"H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction",http://identifiers.org/icd/H52.0,,ICD-10 @@ -3512,9 +3512,9 @@ H53.1 Subjective visual disturbances,3510,H53.1,H53-H54 Visual disturbances and H53.2 Visual disturbances - Diplopia,3511,H53.2,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.2,,ICD-10 H53.3 Visual disturbances - Other disorders of binocular vision,3512,H53.3,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.3,,ICD-10 H53.4 Visual field defects,3513,H53.4,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.4,,ICD-10 -H53.5 Visual disturbances - Colour vision deficiencies,3514,H53.5,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.5,ORPHAcode: 16 Blue cone monochromatism -H53.6 Visual disturbances - Night blindness,3515,H53.6,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.6,ORPHAcode: 215 Congenital stationary night blindness -H53.8 Other visual disturbances,3516,H53.8,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.8,ORPHAcode: 75374 Bradyopsia +H53.5 Visual disturbances - Colour vision deficiencies,3514,H53.5,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.5,ORPHAcode: 16 Blue cone monochromatism,ICD-10 +H53.6 Visual disturbances - Night blindness,3515,H53.6,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.6,ORPHAcode: 215 Congenital stationary night blindness,ICD-10 +H53.8 Other visual disturbances,3516,H53.8,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.8,ORPHAcode: 75374 Bradyopsia,ICD-10 "H53.9 Visual disturbance, unspecified",3517,H53.9,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H53.9,,ICD-10 H54 Visual impairment including blindness (binocular or monocular),3518,H54,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H54,,ICD-10 "H54.0 Blindness, binocular",3519,H54.0,H53-H54 Visual disturbances and blindness,http://identifiers.org/icd/H54.0,,ICD-10 @@ -3528,7 +3528,7 @@ H54.9 Unspecified visual impairment (binocular),3526,H54.9,H53-H54 Visual distur H55-H59 Other disorders of eye and adnexa,3527,,VII Diseases of the eye and adnexa,,,ICD-10 H55 Nystagmus and other irregular eye movements,3528,H55,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H55,,ICD-10 H57 Other disorders of eye and adnexa,3529,H57,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H57,,ICD-10 -H57.0 Anomalies of pupillary function,3530,H57.0,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H57.0,ORPHAcode: 454718 Holmes-Adie syndrome +H57.0 Anomalies of pupillary function,3530,H57.0,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H57.0,ORPHAcode: 454718 Holmes-Adie syndrome,ICD-10 H57.1 Other disorders of eye and adnexa - Ocular pain,3531,H57.1,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H57.1,,ICD-10 H81.2 Vestibular neuronitis,3532,H81.2,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H81.2,,ICD-10 H57.8 Other specified disorders of eye and adnexa,3533,H57.8,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H57.8,,ICD-10 @@ -3539,7 +3539,7 @@ H58.1 Visual disturbances in diseases classified elsewhere,3537,H58.1,H55-H59 Ot H58.8 Other specified disorders of eye and adnexa in diseases classified elsewhere,3538,H58.8,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H58.8,,ICD-10 "H59 Postprocedural disorders of eye and adnexa, not elsewhere classified",3539,H59,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H59,,ICD-10 "H59.0 Postprocedural disorders of eye and adnexa, not elsewhere classified - Keratopathy (bullous aphakic) following cataract surgery",3540,H59.0,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H59.0,,ICD-10 -H59.8 Other postprocedural disorders of eye and adnexa,3541,H59.8,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H59.8,ORPHAcode: 90080 Scarring in glaucoma filtration surgical procedures +H59.8 Other postprocedural disorders of eye and adnexa,3541,H59.8,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H59.8,ORPHAcode: 90080 Scarring in glaucoma filtration surgical procedures,ICD-10 "H59.9 Postprocedural disorder of eye and adnexa, unspecified",3542,H59.9,H55-H59 Other disorders of eye and adnexa,http://identifiers.org/icd/H59.9,,ICD-10 VIII Diseases of the ear and mastoid process,3543,,,,,ICD-10 H60-H62 Diseases of external ear,3544,,VIII Diseases of the ear and mastoid process,,,ICD-10 @@ -3614,7 +3614,7 @@ H74 Other disorders of middle ear and mastoid,3612,H74,H65-H75 Diseases of middl H74.0 Other disorders of middle ear and mastoid - Tympanosclerosis,3613,H74.0,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.0,,ICD-10 H74.1 Adhesive middle ear disease,3614,H74.1,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.1,,ICD-10 H74.2 Discontinuity and dislocation of ear ossicles,3615,H74.2,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.2,,ICD-10 -H74.3 Other acquired abnormalities of ear ossicles,3616,H74.3,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.3,ORPHAcode: 3235 Progressive deafness with stapes fixation +H74.3 Other acquired abnormalities of ear ossicles,3616,H74.3,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.3,ORPHAcode: 3235 Progressive deafness with stapes fixation,ICD-10 H74.4 Polyp of middle ear,3617,H74.4,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.4,,ICD-10 H74.8 Other specified disorders of middle ear and mastoid,3618,H74.8,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.8,,ICD-10 "H74.9 Disorder of middle ear and mastoid, unspecified",3619,H74.9,H65-H75 Diseases of middle ear and mastoid,http://identifiers.org/icd/H74.9,,ICD-10 @@ -3633,25 +3633,25 @@ H81.0 Ménière disea,3631,H81.0,H80-H83 Diseases of inner ear,http://identifier H81.1 Disorders of vestibular function - Benign paroxysmal vertigo,3632,H81.1,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H81.1,,ICD-10 H81.3 Disorders of vestibular function - Other peripheral vertigo,3633,H81.3,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H81.3,,ICD-10 H81.4 Vertigo of central origin,3634,H81.4,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H81.4,,ICD-10 -H81.8 Other disorders of vestibular function,3635,H81.8,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H81.8,ORPHAcode: 171684 Idiopathic bilateral vestibulopathy +H81.8 Other disorders of vestibular function,3635,H81.8,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H81.8,ORPHAcode: 171684 Idiopathic bilateral vestibulopathy,ICD-10 "H81.9 Disorder of vestibular function, unspecified",3636,H81.9,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H81.9,,ICD-10 H82 Vertiginous syndromes in diseases classified elsewhere,3637,H82,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H82,,ICD-10 H83 Other diseases of inner ear,3638,H83,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83,,ICD-10 H83.0 Other diseases of inner ear - Labyrinthitis,3639,H83.0,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.0,,ICD-10 H83.1 Other diseases of inner ear - Labyrinthine fistula,3640,H83.1,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.1,,ICD-10 H83.2 Other diseases of inner ear - Labyrinthine dysfunction,3641,H83.2,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.2,,ICD-10 -H83.3 Noise effects on inner ear,3642,H83.3,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.3,ORPHAcode: 90059 Acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma -H83.8 Other specified diseases of inner ear,3643,H83.8,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.8,ORPHAcode: 420402 Semicircular canal dehiscence syndrome +H83.3 Noise effects on inner ear,3642,H83.3,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.3,ORPHAcode: 90059 Acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma,ICD-10 +H83.8 Other specified diseases of inner ear,3643,H83.8,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.8,ORPHAcode: 420402 Semicircular canal dehiscence syndrome,ICD-10 "H83.9 Disease of inner ear, unspecified",3644,H83.9,H80-H83 Diseases of inner ear,http://identifiers.org/icd/H83.9,,ICD-10 H90-H95 Other disorders of ear,3645,,VIII Diseases of the ear and mastoid process,,,ICD-10 H90 Conductive and sensorineural hearing loss,3646,H90,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90,,ICD-10 -"H90.0 Conductive hearing loss, bilateral",3647,H90.0,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.0,ORPHAcode: 2405 Thickened earlobes-conductive deafness syndrome +"H90.0 Conductive hearing loss, bilateral",3647,H90.0,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.0,ORPHAcode: 2405 Thickened earlobes-conductive deafness syndrome,ICD-10 "H90.1 Conductive hearing loss, unilateral with unrestricted hearing on the contralateral side",3648,H90.1,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.1,,ICD-10 "H90.2 Conductive hearing loss, unspecified",3649,H90.2,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.2,,ICD-10 -"H90.3 Sensorineural hearing loss, bilateral",3650,H90.3,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.3,ORPHAcode: 2027 Gingival fibromatosis-progressive deafness syndrome +"H90.3 Sensorineural hearing loss, bilateral",3650,H90.3,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.3,ORPHAcode: 2027 Gingival fibromatosis-progressive deafness syndrome,ICD-10 "H90.4 Sensorineural hearing loss, unilateral with unrestricted hearing on the contralateral side",3651,H90.4,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.4,,ICD-10 -"H90.5 Sensorineural hearing loss, unspecified",3652,H90.5,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.5,ORPHAcode: 998 Albinism-deafness syndrome -"H90.6 Mixed conductive and sensorineural hearing loss, bilateral",3653,H90.6,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.6,ORPHAcode: 90646 Deafness-hypogonadism syndrome +"H90.5 Sensorineural hearing loss, unspecified",3652,H90.5,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.5,ORPHAcode: 998 Albinism-deafness syndrome,ICD-10 +"H90.6 Mixed conductive and sensorineural hearing loss, bilateral",3653,H90.6,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.6,ORPHAcode: 90646 Deafness-hypogonadism syndrome,ICD-10 "H90.7 Mixed conductive and sensorineural hearing loss, unilateral with unrestricted hearing on the contralateral side",3654,H90.7,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.7,,ICD-10 "H90.8 Mixed conductive and sensorineural hearing loss, unspecified",3655,H90.8,H90-H95 Other disorders of ear,http://identifiers.org/icd/H90.8,,ICD-10 H91 Other hearing loss,3656,H91,H90-H95 Other disorders of ear,http://identifiers.org/icd/H91,,ICD-10 @@ -3659,7 +3659,7 @@ H91.0 Ototoxic hearing loss,3657,H91.0,H90-H95 Other disorders of ear,http://ide H91.1 Other hearing loss - Presbycusis,3658,H91.1,H90-H95 Other disorders of ear,http://identifiers.org/icd/H91.1,,ICD-10 H91.2 Sudden idiopathic hearing loss,3659,H91.2,H90-H95 Other disorders of ear,http://identifiers.org/icd/H91.2,,ICD-10 "H91.3 Other hearing loss - Deaf mutism, not elsewhere classified",3660,H91.3,H90-H95 Other disorders of ear,http://identifiers.org/icd/H91.3,,ICD-10 -H91.8 Other specified hearing loss,3661,H91.8,H90-H95 Other disorders of ear,http://identifiers.org/icd/H91.8,ORPHAcode: 324321 Sinoatrial node dysfunction and deafness +H91.8 Other specified hearing loss,3661,H91.8,H90-H95 Other disorders of ear,http://identifiers.org/icd/H91.8,ORPHAcode: 324321 Sinoatrial node dysfunction and deafness,ICD-10 "H91.9 Hearing loss, unspecified",3662,H91.9,H90-H95 Other disorders of ear,http://identifiers.org/icd/H91.9,,ICD-10 H92 Otalgia and effusion of ear,3663,H92,H90-H95 Other disorders of ear,http://identifiers.org/icd/H92,,ICD-10 H92.0 Otalgia,3664,H92.0,H90-H95 Other disorders of ear,http://identifiers.org/icd/H92.0,,ICD-10 @@ -3669,7 +3669,7 @@ H92.2 Otalgia and effusion of ear - Otorrhagia,3666,H92.2,H90-H95 Other disorder H93.0 Degenerative and vascular disorders of ear,3668,H93.0,H90-H95 Other disorders of ear,http://identifiers.org/icd/H93.0,,ICD-10 "H93.1 Other disorders of ear, not elsewhere classified - Tinnitus",3669,H93.1,H90-H95 Other disorders of ear,http://identifiers.org/icd/H93.1,,ICD-10 H93.2 Other abnormal auditory perceptions,3670,H93.2,H90-H95 Other disorders of ear,http://identifiers.org/icd/H93.2,,ICD-10 -H93.3 Disorders of acoustic nerve,3671,H93.3,H90-H95 Other disorders of ear,http://identifiers.org/icd/H93.3,ORPHAcode: 502318 Cochlear nerve deficiency +H93.3 Disorders of acoustic nerve,3671,H93.3,H90-H95 Other disorders of ear,http://identifiers.org/icd/H93.3,ORPHAcode: 502318 Cochlear nerve deficiency,ICD-10 H93.8 Other specified disorders of ear,3672,H93.8,H90-H95 Other disorders of ear,http://identifiers.org/icd/H93.8,,ICD-10 "H93.9 Disorder of ear, unspecified",3673,H93.9,H90-H95 Other disorders of ear,http://identifiers.org/icd/H93.9,,ICD-10 H94 Other disorders of ear in diseases classified elsewhere,3674,H94,H90-H95 Other disorders of ear,http://identifiers.org/icd/H94,,ICD-10 @@ -3682,7 +3682,7 @@ H95.8 Other postprocedural disorders of ear and mastoid process,3680,H95.8,H90-H "H95.9 Postprocedural disorder of ear and mastoid process, unspecified",3681,H95.9,H90-H95 Other disorders of ear,http://identifiers.org/icd/H95.9,,ICD-10 IX Diseases of the circulatory system,3682,,,,,ICD-10 I00-I02 Acute rheumatic fever,3683,I00-I02,,,,ICD-10 -I00 Rheumatic fever without mention of heart involvement,3684,I00,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I00,ORPHAcode: 3099 Rheumatic fever +I00 Rheumatic fever without mention of heart involvement,3684,I00,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I00,ORPHAcode: 3099 Rheumatic fever,ICD-10 I01 Rheumatic fever with heart involvement,3685,I01,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I01,,ICD-10 I01.0 Acute rheumatic pericarditis,3686,I01.0,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I01.0,,ICD-10 I01.1 Acute rheumatic endocarditis,3687,I01.1,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I01.1,,ICD-10 @@ -3690,7 +3690,7 @@ I01.2 Acute rheumatic myocarditis,3688,I01.2,I00-I02 Acute rheumatic fever,http: I01.8 Other acute rheumatic heart disease,3689,I01.8,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I01.8,,ICD-10 "I01.9 Acute rheumatic heart disease, unspecified",3690,I01.9,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I01.9,,ICD-10 I02 Rheumatic chorea,3691,I02,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I02,,ICD-10 -I02.0 Rheumatic chorea with heart involvement,3692,I02.0,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I02.0,ORPHAcode: 306731 Sydenham chorea +I02.0 Rheumatic chorea with heart involvement,3692,I02.0,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I02.0,ORPHAcode: 306731 Sydenham chorea,ICD-10 I02.9 Rheumatic chorea without heart involvement,3693,I02.9,I00-I02 Acute rheumatic fever,http://identifiers.org/icd/I02.9,,ICD-10 I05-I09 Chronic rheumatic heart diseases,3694,,IX Diseases of the circulatory system,,,ICD-10 I05 Rheumatic mitral valve diseases,3695,I05,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I05,,ICD-10 @@ -3721,7 +3721,7 @@ I08.8 Other multiple valve diseases,3718,I08.8,I05-I09 Chronic rheumatic heart d I09 Other rheumatic heart diseases,3720,I09,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I09,,ICD-10 I09.0 Rheumatic myocarditis,3721,I09.0,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I09.0,,ICD-10 "I09.1 Rheumatic diseases of endocardium, valve unspecified",3722,I09.1,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I09.1,,ICD-10 -I09.2 Chronic rheumatic pericarditis,3723,I09.2,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I09.2,ORPHAcode: 251307 Idiopathic recurrent pericarditis +I09.2 Chronic rheumatic pericarditis,3723,I09.2,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I09.2,ORPHAcode: 251307 Idiopathic recurrent pericarditis,ICD-10 I09.8 Other specified rheumatic heart diseases,3724,I09.8,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I09.8,,ICD-10 "I09.9 Rheumatic heart disease, unspecified",3725,I09.9,I05-I09 Chronic rheumatic heart diseases,http://identifiers.org/icd/I09.9,,ICD-10 I10-I15 Hypertensive diseases,3726,,IX Diseases of the circulatory system,,,ICD-10 @@ -3739,7 +3739,7 @@ I13.2 Hypertensive heart and renal disease with both (congestive) heart failure "I13.9 Hypertensive heart and renal disease, unspecified",3738,I13.9,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I13.9,,ICD-10 I15 Secondary hypertension,3739,I15,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I15,,ICD-10 I15.0 Renovascular hypertension,3740,I15.0,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I15.0,,ICD-10 -I15.1 Hypertension secondary to other renal disorders,3741,I15.1,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I15.1,ORPHAcode: 526 Liddle syndrome +I15.1 Hypertension secondary to other renal disorders,3741,I15.1,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I15.1,ORPHAcode: 526 Liddle syndrome,ICD-10 I15.2 Hypertension secondary to endocrine disorders,3742,I15.2,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I15.2,,ICD-10 I15.8 Other secondary hypertension,3743,I15.8,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I15.8,,ICD-10 "I15.9 Secondary hypertension, unspecified",3744,I15.9,I10-I15 Hypertensive diseases,http://identifiers.org/icd/I15.9,,ICD-10 @@ -3780,7 +3780,7 @@ I25 Chronic ischaemic heart disease,3777,I25,I20-I25 Ischaemic heart diseases,ht I25.1 Atherosclerotic heart disease,3779,I25.1,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.1,,ICD-10 I25.2 Chronic ischaemic heart disease - Old myocardial infarction,3780,I25.2,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.2,,ICD-10 I25.3 Aneurysm of heart,3781,I25.3,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.3,,ICD-10 -I25.4 Chronic ischaemic heart disease - Coronary artery aneurysm and dissection,3782,I25.4,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.4,ORPHAcode: 458718 Idiopathic spontaneous coronary artery dissection +I25.4 Chronic ischaemic heart disease - Coronary artery aneurysm and dissection,3782,I25.4,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.4,ORPHAcode: 458718 Idiopathic spontaneous coronary artery dissection,ICD-10 I25.5 Ischaemic cardiomyopathy,3783,I25.5,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.5,,ICD-10 I25.6 Chronic ischaemic heart disease - Silent myocardial ischaemia,3784,I25.6,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.6,,ICD-10 I25.8 Other forms of chronic ischaemic heart disease,3785,I25.8,I20-I25 Ischaemic heart diseases,http://identifiers.org/icd/I25.8,,ICD-10 @@ -3790,15 +3790,15 @@ I26 Pulmonary embolism,3788,I26,I26-I28 Pulmonary heart disease and diseases of I26.0 Pulmonary embolism with mention of acute cor pulmonale,3789,I26.0,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I26.0,,ICD-10 I26.9 Pulmonary embolism without mention of acute cor pulmonale,3790,I26.9,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I26.9,,ICD-10 I27 Other pulmonary heart diseases,3791,I27,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27,,ICD-10 -I27.0 Primary pulmonary hypertension,3792,I27.0,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27.0,ORPHAcode: 422 Idiopathic/heritable pulmonary arterial hypertension +I27.0 Primary pulmonary hypertension,3792,I27.0,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27.0,ORPHAcode: 422 Idiopathic/heritable pulmonary arterial hypertension,ICD-10 I27.1 Kyphoscoliotic heart disease,3793,I27.1,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27.1,,ICD-10 -I27.2 Other secondary pulmonary hypertension,3794,I27.2,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27.2,ORPHAcode: 97214 Eisenmenger syndrome +I27.2 Other secondary pulmonary hypertension,3794,I27.2,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27.2,ORPHAcode: 97214 Eisenmenger syndrome,ICD-10 I27.8 Other specified pulmonary heart diseases,3795,I27.8,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27.8,,ICD-10 "I27.9 Pulmonary heart disease, unspecified",3796,I27.9,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I27.9,,ICD-10 I28 Other diseases of pulmonary vessels,3797,I28,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I28,,ICD-10 I28.0 Arteriovenous fistula of pulmonary vessels,3798,I28.0,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I28.0,,ICD-10 I28.1 Aneurysm of pulmonary artery,3799,I28.1,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I28.1,,ICD-10 -I28.8 Other specified diseases of pulmonary vessels,3800,I28.8,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I28.8,ORPHAcode: 228116 Hughes-Stovin syndrome +I28.8 Other specified diseases of pulmonary vessels,3800,I28.8,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I28.8,ORPHAcode: 228116 Hughes-Stovin syndrome,ICD-10 "I28.9 Disease of pulmonary vessels, unspecified",3801,I28.9,I26-I28 Pulmonary heart disease and diseases of pulmonary circulation,http://identifiers.org/icd/I28.9,,ICD-10 I30-I52 Other forms of heart disease,3802,,IX Diseases of the circulatory system,,,ICD-10 I30 Acute pericarditis,3803,I30,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I30,,ICD-10 @@ -3818,11 +3818,11 @@ I32.0 Pericarditis in bacterial diseases classified elsewhere,3816,I32.0,I30-I52 I32.1 Pericarditis in other infectious and parasitic diseases classified elsewhere,3817,I32.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I32.1,,ICD-10 I32.8 Pericarditis in other diseases classified elsewhere,3818,I32.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I32.8,,ICD-10 I33 Acute and subacute endocarditis,3819,I33,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I33,,ICD-10 -I33.0 Acute and subacute infective endocarditis,3820,I33.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I33.0,ORPHAcode: 570762 Infective endocarditis +I33.0 Acute and subacute infective endocarditis,3820,I33.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I33.0,ORPHAcode: 570762 Infective endocarditis,ICD-10 "I33.9 Acute endocarditis, unspecified",3821,I33.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I33.9,,ICD-10 I34 Nonrheumatic mitral valve disorders,3822,I34,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I34,,ICD-10 I34.0 Mitral (valve) insufficiency,3823,I34.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I34.0,,ICD-10 -I34.1 Mitral (valve) prolapse,3824,I34.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I34.1,ORPHAcode: 741 Familial mitral valve prolapse +I34.1 Mitral (valve) prolapse,3824,I34.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I34.1,ORPHAcode: 741 Familial mitral valve prolapse,ICD-10 I34.2 Nonrheumatic mitral (valve) stenosis,3825,I34.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I34.2,,ICD-10 I34.8 Other nonrheumatic mitral valve disorders,3826,I34.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I34.8,,ICD-10 "I34.9 Nonrheumatic mitral valve disorder, unspecified",3827,I34.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I34.9,,ICD-10 @@ -3856,7 +3856,7 @@ I39.4 Multiple valve disorders in diseases classified elsewhere,3853,I39.4,I30-I I40 Acute myocarditis,3855,I40,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I40,,ICD-10 I40.0 Infective myocarditis,3856,I40.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I40.0,,ICD-10 I40.1 Isolated myocarditis,3857,I40.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I40.1,,ICD-10 -I40.8 Other acute myocarditis,3858,I40.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I40.8,ORPHAcode: 329874 Idiopathic giant cell myocarditis +I40.8 Other acute myocarditis,3858,I40.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I40.8,ORPHAcode: 329874 Idiopathic giant cell myocarditis,ICD-10 "I40.9 Acute myocarditis, unspecified",3859,I40.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I40.9,,ICD-10 I41 Myocarditis in diseases classified elsewhere,3860,I41,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I41,,ICD-10 I41.0 Myocarditis in bacterial diseases classified elsewhere,3861,I41.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I41.0,,ICD-10 @@ -3864,15 +3864,15 @@ I41.1 Myocarditis in viral diseases classified elsewhere,3862,I41.1,I30-I52 Othe I41.2 Myocarditis in other infectious and parasitic diseases classified elsewhere,3863,I41.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I41.2,,ICD-10 I41.8 Myocarditis in other diseases classified elsewhere,3864,I41.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I41.8,,ICD-10 I42 Cardiomyopathy,3865,I42,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42,,ICD-10 -I42.0 Dilated cardiomyopathy,3866,I42.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.0,ORPHAcode: 154 Familial isolated dilated cardiomyopathy +I42.0 Dilated cardiomyopathy,3866,I42.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.0,ORPHAcode: 154 Familial isolated dilated cardiomyopathy,ICD-10 I42.1 Obstructive hypertrophic cardiomyopathy,3867,I42.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.1,,ICD-10 -I42.2 Other hypertrophic cardiomyopathy,3868,I42.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.2,ORPHAcode: 217601 Hypertrophic cardiomyopathy due to intensive athletic training -I42.3 Cardiomyopathy - Endomyocardial (eosinophilic) disease,3869,I42.3,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.3,ORPHAcode: 75565 Tropical endomyocardial fibrosis -I42.4 Cardiomyopathy - Endocardial fibroelastosis,3870,I42.4,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.4,ORPHAcode: 2022 Endocardial fibroelastosis -I42.5 Other restrictive cardiomyopathy,3871,I42.5,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.5,ORPHAcode: 75249 Familial isolated restrictive cardiomyopathy +I42.2 Other hypertrophic cardiomyopathy,3868,I42.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.2,ORPHAcode: 217601 Hypertrophic cardiomyopathy due to intensive athletic training,ICD-10 +I42.3 Cardiomyopathy - Endomyocardial (eosinophilic) disease,3869,I42.3,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.3,ORPHAcode: 75565 Tropical endomyocardial fibrosis,ICD-10 +I42.4 Cardiomyopathy - Endocardial fibroelastosis,3870,I42.4,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.4,ORPHAcode: 2022 Endocardial fibroelastosis,ICD-10 +I42.5 Other restrictive cardiomyopathy,3871,I42.5,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.5,ORPHAcode: 75249 Familial isolated restrictive cardiomyopathy,ICD-10 I42.6 Alcoholic cardiomyopathy,3872,I42.6,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.6,,ICD-10 I42.7 Cardiomyopathy due to drugs and other external agents,3873,I42.7,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.7,,ICD-10 -I42.8 Cardiomyopathy - Other cardiomyopathies,3874,I42.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.8,ORPHAcode: 54260 Left ventricular noncompaction +I42.8 Cardiomyopathy - Other cardiomyopathies,3874,I42.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.8,ORPHAcode: 54260 Left ventricular noncompaction,ICD-10 "I42.9 Cardiomyopathy, unspecified",3875,I42.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I42.9,,ICD-10 I43 Cardiomyopathy in diseases classified elsewhere,3876,I43,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I43,,ICD-10 I43.0 Cardiomyopathy in infectious and parasitic diseases classified elsewhere,3877,I43.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I43.0,,ICD-10 @@ -3894,9 +3894,9 @@ I45.1 Other and unspecified right bundle-branch block,3892,I45.1,I30-I52 Other f I45.2 Other conduction disorders - Bifascicular block,3893,I45.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.2,,ICD-10 I45.3 Other conduction disorders - Trifascicular block,3894,I45.3,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.3,,ICD-10 I45.4 Other conduction disorders - Nonspecific intraventricular block,3895,I45.4,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.4,,ICD-10 -I45.5 Other specified heart block,3896,I45.5,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.5,ORPHAcode: 1344 Atrial standstill -I45.6 Other conduction disorders - Pre-excitation syndrome,3897,I45.6,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.6,ORPHAcode: 844 Lown-Ganong-Levine syndrome -I45.8 Other specified conduction disorders,3898,I45.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.8,ORPHAcode: 871 Familial progressive cardiac conduction defect +I45.5 Other specified heart block,3896,I45.5,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.5,ORPHAcode: 1344 Atrial standstill,ICD-10 +I45.6 Other conduction disorders - Pre-excitation syndrome,3897,I45.6,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.6,ORPHAcode: 844 Lown-Ganong-Levine syndrome,ICD-10 +I45.8 Other specified conduction disorders,3898,I45.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.8,ORPHAcode: 871 Familial progressive cardiac conduction defect,ICD-10 "I45.9 Conduction disorder, unspecified",3899,I45.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I45.9,,ICD-10 I46 Cardiac arrest,3900,I46,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I46,,ICD-10 I46.0 Cardiac arrest with successful resuscitation,3901,I46.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I46.0,,ICD-10 @@ -3904,9 +3904,9 @@ I46.0 Cardiac arrest with successful resuscitation,3901,I46.0,I30-I52 Other form "I46.9 Cardiac arrest, unspecified",3903,I46.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I46.9,,ICD-10 I47 Paroxysmal tachycardia,3904,I47,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I47,,ICD-10 I47.0 Paroxysmal tachycardia - Re-entry ventricular arrhythmia,3905,I47.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I47.0,,ICD-10 -I47.1 Supraventricular tachycardia,3906,I47.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I47.1,ORPHAcode: 3282 Multifocal atrial tachycardia +I47.1 Supraventricular tachycardia,3906,I47.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I47.1,ORPHAcode: 3282 Multifocal atrial tachycardia,ICD-10 Y06 Neglect and abandonment,3907,Y06,X85-Y09 Assault,http://identifiers.org/icd/Y06,,ICD-10 -I47.2 Ventricular tachycardia,3908,I47.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I47.2,ORPHAcode: 3286 Catecholaminergic polymorphic ventricular tachycardia +I47.2 Ventricular tachycardia,3908,I47.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I47.2,ORPHAcode: 3286 Catecholaminergic polymorphic ventricular tachycardia,ICD-10 "I47.9 Paroxysmal tachycardia, unspecified",3909,I47.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I47.9,,ICD-10 I48 Atrial fibrillation and flutter,3910,I48,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I48,,ICD-10 I48.0 Paroxysmal atrial fibrillation,3911,I48.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I48.0,,ICD-10 @@ -3914,15 +3914,15 @@ I48.1 Persistent atrial fibrillation,3912,I48.1,I30-I52 Other forms of heart dis I48.2 Chronic atrial fibrillation,3913,I48.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I48.2,,ICD-10 I48.3 Typical atrial flutter,3914,I48.3,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I48.3,,ICD-10 I48.4 Atypical atrial flutter,3915,I48.4,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I48.4,,ICD-10 -"I48.9 Atrial fibrillation and atrial flutter, unspecified",3916,I48.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I48.9,ORPHAcode: 334 Familial atrial fibrillation +"I48.9 Atrial fibrillation and atrial flutter, unspecified",3916,I48.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I48.9,ORPHAcode: 334 Familial atrial fibrillation,ICD-10 I49 Other cardiac arrhythmias,3917,I49,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49,,ICD-10 -I49.0 Other cardiac arrhythmias - Ventricular fibrillation and flutter,3918,I49.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.0,"ORPHAcode: 228140 Idiopathic ventricular fibrillation, non Brugada type" +I49.0 Other cardiac arrhythmias - Ventricular fibrillation and flutter,3918,I49.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.0,"ORPHAcode: 228140 Idiopathic ventricular fibrillation, non Brugada type",ICD-10 I49.1 Other cardiac arrhythmias - Atrial premature depolarization,3919,I49.1,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.1,,ICD-10 I49.2 Other cardiac arrhythmias - Junctional premature depolarization,3920,I49.2,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.2,,ICD-10 I49.3 Other cardiac arrhythmias - Ventricular premature depolarization,3921,I49.3,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.3,,ICD-10 I49.4 Other and unspecified premature depolarization,3922,I49.4,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.4,,ICD-10 -I49.5 Other cardiac arrhythmias - Sick sinus syndrome,3923,I49.5,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.5,ORPHAcode: 166282 Familial sick sinus syndrome -I49.8 Other specified cardiac arrhythmias,3924,I49.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.8,ORPHAcode: 130 Brugada syndrome +I49.5 Other cardiac arrhythmias - Sick sinus syndrome,3923,I49.5,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.5,ORPHAcode: 166282 Familial sick sinus syndrome,ICD-10 +I49.8 Other specified cardiac arrhythmias,3924,I49.8,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.8,ORPHAcode: 130 Brugada syndrome,ICD-10 "I49.9 Cardiac arrhythmia, unspecified",3925,I49.9,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I49.9,,ICD-10 I50 Heart failure,3926,I50,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I50,,ICD-10 I50.0 Congestive heart failure,3927,I50.0,I30-I52 Other forms of heart disease,http://identifiers.org/icd/I50.0,,ICD-10 @@ -3954,7 +3954,7 @@ I60.5 Subarachnoid haemorrhage from vertebral artery,3952,I60.5,I60-I69 Cerebrov I60.6 Subarachnoid haemorrhage from other intracranial arteries,3953,I60.6,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I60.6,,ICD-10 "I60.7 Subarachnoid haemorrhage from intracranial artery, unspecified",3954,I60.7,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I60.7,,ICD-10 I60.8 Other subarachnoid haemorrhage,3955,I60.8,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I60.8,,ICD-10 -"I60.9 Subarachnoid haemorrhage, unspecified",3956,I60.9,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I60.9,ORPHAcode: 90065 Acquired aneurysmal subarachnoid hemorrhage +"I60.9 Subarachnoid haemorrhage, unspecified",3956,I60.9,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I60.9,ORPHAcode: 90065 Acquired aneurysmal subarachnoid hemorrhage,ICD-10 I61 Intracerebral haemorrhage,3957,I61,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I61,,ICD-10 "I61.0 Intracerebral haemorrhage in hemisphere, subcortical",3958,I61.0,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I61.0,,ICD-10 "I61.1 Intracerebral haemorrhage in hemisphere, cortical",3959,I61.1,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I61.1,,ICD-10 @@ -3975,7 +3975,7 @@ I63.1 Cerebral infarction due to embolism of precerebral arteries,3973,I63.1,I60 I63.2 Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries,3974,I63.2,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.2,,ICD-10 I63.3 Cerebral infarction due to thrombosis of cerebral arteries,3975,I63.3,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.3,,ICD-10 I63.4 Cerebral infarction due to embolism of cerebral arteries,3976,I63.4,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.4,,ICD-10 -I63.5 Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries,3977,I63.5,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.5,ORPHAcode: 439175 Pediatric arterial ischemic stroke +I63.5 Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries,3977,I63.5,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.5,ORPHAcode: 439175 Pediatric arterial ischemic stroke,ICD-10 "I63.6 Cerebral infarction due to cerebral venous thrombosis, nonpyogenic",3978,I63.6,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.6,,ICD-10 I63.8 Other cerebral infarction,3979,I63.8,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.8,,ICD-10 "I63.9 Cerebral infarction, unspecified",3980,I63.9,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I63.9,,ICD-10 @@ -3997,15 +3997,15 @@ I66.8 Occlusion and stenosis of other cerebral artery,3995,I66.8,I60-I69 Cerebro I66.9 Occlusion and stenosis of unspecified cerebral artery,3996,I66.9,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I66.9,,ICD-10 I67 Other cerebrovascular diseases,3997,I67,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67,,ICD-10 "I67.0 Other cerebrovascular diseases - Dissection of cerebral arteries, nonruptured",3998,I67.0,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.0,,ICD-10 -"I67.1 Other cerebrovascular diseases - Cerebral aneurysm, nonruptured",3999,I67.1,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.1,ORPHAcode: 231160 Familial cerebral saccular aneurysm +"I67.1 Other cerebrovascular diseases - Cerebral aneurysm, nonruptured",3999,I67.1,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.1,ORPHAcode: 231160 Familial cerebral saccular aneurysm,ICD-10 I67.2 Other cerebrovascular diseases - Cerebral atherosclerosis,4000,I67.2,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.2,,ICD-10 I67.3 Other cerebrovascular diseases - Progressive vascular leukoencephalopathy,4001,I67.3,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.3,,ICD-10 I67.4 Other cerebrovascular diseases - Hypertensive encephalopathy,4002,I67.4,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.4,,ICD-10 I70 Atherosclerosis,4003,I70,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I70,,ICD-10 -I67.5 Other cerebrovascular diseases - Moyamoya disease,4004,I67.5,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.5,ORPHAcode: 2573 Moyamoya disease -I67.6 Other cerebrovascular diseases - Nonpyogenic thrombosis of intracranial venous system,4005,I67.6,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.6,ORPHAcode: 329217 Cerebral sinovenous thrombosis -"I67.7 Other cerebrovascular diseases - Cerebral arteritis, not elsewhere classified",4006,I67.7,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.7,ORPHAcode: 838 Susac syndrome -I67.8 Other specified cerebrovascular diseases,4007,I67.8,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.8,ORPHAcode: 136 Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy +I67.5 Other cerebrovascular diseases - Moyamoya disease,4004,I67.5,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.5,ORPHAcode: 2573 Moyamoya disease,ICD-10 +I67.6 Other cerebrovascular diseases - Nonpyogenic thrombosis of intracranial venous system,4005,I67.6,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.6,ORPHAcode: 329217 Cerebral sinovenous thrombosis,ICD-10 +"I67.7 Other cerebrovascular diseases - Cerebral arteritis, not elsewhere classified",4006,I67.7,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.7,ORPHAcode: 838 Susac syndrome,ICD-10 +I67.8 Other specified cerebrovascular diseases,4007,I67.8,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.8,ORPHAcode: 136 Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy,ICD-10 "I67.9 Cerebrovascular disease, unspecified",4008,I67.9,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I67.9,,ICD-10 I68 Cerebrovascular disorders in diseases classified elsewhere,4009,I68,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I68,,ICD-10 I68.0 Cerebrovascular disorders in diseases classified elsewhere - Cerebral amyloid angiopathy,4010,I68.0,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I68.0,,ICD-10 @@ -4013,7 +4013,7 @@ I68.1 Cerebral arteritis in infectious and parasitic diseases classified elsewhe I68.2 Cerebral arteritis in other diseases classified elsewhere,4012,I68.2,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I68.2,,ICD-10 I68.8 Other cerebrovascular disorders in diseases classified elsewhere,4013,I68.8,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I68.8,,ICD-10 I69 Sequelae of cerebrovascular disease,4014,I69,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I69,,ICD-10 -I69.0 Sequelae of subarachnoid haemorrhage,4015,I69.0,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I69.0,ORPHAcode: 247245 Superficial siderosis +I69.0 Sequelae of subarachnoid haemorrhage,4015,I69.0,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I69.0,ORPHAcode: 247245 Superficial siderosis,ICD-10 I69.1 Sequelae of intracerebral haemorrhage,4016,I69.1,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I69.1,,ICD-10 I69.2 Sequelae of other nontraumatic intracranial haemorrhage,4017,I69.2,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I69.2,,ICD-10 I69.3 Sequelae of cerebral infarction,4018,I69.3,I60-I69 Cerebrovascular diseases,http://identifiers.org/icd/I69.3,,ICD-10 @@ -4024,19 +4024,19 @@ I70.0 Atherosclerosis of aorta,4022,I70.0,"I70-I79 Diseases of arteries, arterio I70.1 Atherosclerosis of renal artery,4023,I70.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I70.1,,ICD-10 I70.2 Atherosclerosis of arteries of extremities,4024,I70.2,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I70.2,,ICD-10 I70.8 Atherosclerosis of other arteries,4025,I70.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I70.8,,ICD-10 -I70.9 Generalized and unspecified atherosclerosis,4026,I70.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I70.9,ORPHAcode: 1192 Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome +I70.9 Generalized and unspecified atherosclerosis,4026,I70.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I70.9,ORPHAcode: 1192 Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome,ICD-10 I71 Aortic aneurysm and dissection,4027,I71,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71,,ICD-10 -I71.0 Dissection of aorta [any part],4028,I71.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.0,ORPHAcode: 229 Familial aortic dissection +I71.0 Dissection of aorta [any part],4028,I71.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.0,ORPHAcode: 229 Familial aortic dissection,ICD-10 "I71.1 Thoracic aortic aneurysm, ruptured",4029,I71.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.1,,ICD-10 -"I71.2 Thoracic aortic aneurysm, without mention of rupture",4030,I71.2,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.2,ORPHAcode: 91387 Familial thoracic aortic aneurysm and aortic dissection +"I71.2 Thoracic aortic aneurysm, without mention of rupture",4030,I71.2,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.2,ORPHAcode: 91387 Familial thoracic aortic aneurysm and aortic dissection,ICD-10 "I71.3 Abdominal aortic aneurysm, ruptured",4031,I71.3,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.3,,ICD-10 -"I71.4 Abdominal aortic aneurysm, without mention of rupture",4032,I71.4,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.4,ORPHAcode: 86 Familial abdominal aortic aneurysm +"I71.4 Abdominal aortic aneurysm, without mention of rupture",4032,I71.4,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.4,ORPHAcode: 86 Familial abdominal aortic aneurysm,ICD-10 "I71.5 Thoracoabdominal aortic aneurysm, ruptured",4033,I71.5,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.5,,ICD-10 "I71.6 Thoracoabdominal aortic aneurysm, without mention of rupture",4034,I71.6,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.6,,ICD-10 "I71.8 Aortic aneurysm of unspecified site, ruptured",4035,I71.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.8,,ICD-10 "I71.9 Aortic aneurysm of unspecified site, without mention of rupture",4036,I71.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I71.9,,ICD-10 I72 Other aneurysm and dissection,4037,I72,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I72,,ICD-10 -I72.0 Aneurysm and dissection of carotid artery,4038,I72.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I72.0,ORPHAcode: 36382 Familial cervical artery dissection +I72.0 Aneurysm and dissection of carotid artery,4038,I72.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I72.0,ORPHAcode: 36382 Familial cervical artery dissection,ICD-10 I72.1 Aneurysm and dissection of artery of upper extremity,4039,I72.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I72.1,,ICD-10 I72.2 Aneurysm and dissection of renal artery,4040,I72.2,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I72.2,,ICD-10 I72.3 Aneurysm and dissection of iliac artery,4041,I72.3,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I72.3,,ICD-10 @@ -4047,33 +4047,33 @@ I72.8 Aneurysm and dissection of other specified arteries,4045,I72.8,"I70-I79 Di I72.9 Aneurysm and dissection of unspecified site,4046,I72.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I72.9,,ICD-10 I73 Other peripheral vascular diseases,4047,I73,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I73,,ICD-10 I73.0 Other peripheral vascular diseases - Raynaud syndrome,4048,I73.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I73.0,,ICD-10 -I73.1 Other peripheral vascular diseases - Thromboangiitis obliterans [Buerger],4049,I73.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I73.1,ORPHAcode: 36258 Buerger disease -I73.8 Other specified peripheral vascular diseases,4050,I73.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I73.8,ORPHAcode: 90026 Primary erythromelalgia +I73.1 Other peripheral vascular diseases - Thromboangiitis obliterans [Buerger],4049,I73.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I73.1,ORPHAcode: 36258 Buerger disease,ICD-10 +I73.8 Other specified peripheral vascular diseases,4050,I73.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I73.8,ORPHAcode: 90026 Primary erythromelalgia,ICD-10 "I73.9 Peripheral vascular disease, unspecified",4051,I73.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I73.9,,ICD-10 I74 Arterial embolism and thrombosis,4052,I74,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74,,ICD-10 I74.0 Embolism and thrombosis of abdominal aorta,4053,I74.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.0,,ICD-10 I74.1 Embolism and thrombosis of other and unspecified parts of aorta,4054,I74.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.1,,ICD-10 I74.2 Embolism and thrombosis of arteries of upper extremities,4055,I74.2,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.2,,ICD-10 I74.3 Embolism and thrombosis of arteries of lower extremities,4056,I74.3,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.3,,ICD-10 -"I74.4 Embolism and thrombosis of arteries of extremities, unspecified",4057,I74.4,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.4,ORPHAcode: 90064 Acute peripheral arterial occlusion +"I74.4 Embolism and thrombosis of arteries of extremities, unspecified",4057,I74.4,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.4,ORPHAcode: 90064 Acute peripheral arterial occlusion,ICD-10 I74.5 Embolism and thrombosis of iliac artery,4058,I74.5,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.5,,ICD-10 I74.8 Embolism and thrombosis of other arteries,4059,I74.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.8,,ICD-10 I74.9 Embolism and thrombosis of unspecified artery,4060,I74.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I74.9,,ICD-10 I77 Other disorders of arteries and arterioles,4061,I77,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77,,ICD-10 "I77.0 Other disorders of arteries and arterioles - Arteriovenous fistula, acquired",4062,I77.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.0,,ICD-10 -I77.1 Stricture of artery,4063,I77.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.1,ORPHAcode: 3342 Arterial tortuosity syndrome +I77.1 Stricture of artery,4063,I77.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.1,ORPHAcode: 3342 Arterial tortuosity syndrome,ICD-10 I77.2 Rupture of artery,4064,I77.2,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.2,,ICD-10 I77.3 Other disorders of arteries and arterioles - Arterial fibromuscular dysplasia,4065,I77.3,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.3,,ICD-10 -I77.4 Other disorders of arteries and arterioles - Coeliac artery compression syndrome,4066,I77.4,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.4,ORPHAcode: 293208 Celiac artery compression syndrome +I77.4 Other disorders of arteries and arterioles - Coeliac artery compression syndrome,4066,I77.4,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.4,ORPHAcode: 293208 Celiac artery compression syndrome,ICD-10 I77.5 Necrosis of artery,4067,I77.5,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.5,,ICD-10 -"I77.6 Other disorders of arteries and arterioles - Arteritis, unspecified",4068,I77.6,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.6,ORPHAcode: 48435 Postinfectious vasculitis -I77.8 Other specified disorders of arteries and arterioles,4069,I77.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.8,ORPHAcode: 679 Malignant atrophic papulosis +"I77.6 Other disorders of arteries and arterioles - Arteritis, unspecified",4068,I77.6,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.6,ORPHAcode: 48435 Postinfectious vasculitis,ICD-10 +I77.8 Other specified disorders of arteries and arterioles,4069,I77.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.8,ORPHAcode: 679 Malignant atrophic papulosis,ICD-10 "I77.9 Disorder of arteries and arterioles, unspecified",4070,I77.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I77.9,,ICD-10 I78 Diseases of capillaries,4071,I78,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I78,,ICD-10 J01 Acute sinusitis,4072,J01,J00-J06 Acute upper respiratory infections,http://identifiers.org/icd/J01,,ICD-10 -I78.0 Diseases of capillaries - Hereditary haemorrhagic telangiectasia,4073,I78.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I78.0,ORPHAcode: 774 Hereditary hemorrhagic telangiectasia +I78.0 Diseases of capillaries - Hereditary haemorrhagic telangiectasia,4073,I78.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I78.0,ORPHAcode: 774 Hereditary hemorrhagic telangiectasia,ICD-10 "I78.1 Diseases of capillaries - Naevus, non-neoplastic",4074,I78.1,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I78.1,,ICD-10 -I78.8 Other diseases of capillaries,4075,I78.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I78.8,ORPHAcode: 188 Systemic capillary leak syndrome +I78.8 Other diseases of capillaries,4075,I78.8,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I78.8,ORPHAcode: 188 Systemic capillary leak syndrome,ICD-10 "I78.9 Disease of capillaries, unspecified",4076,I78.9,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I78.9,,ICD-10 "I79 Disorders of arteries, arterioles and capillaries in diseases classified elsewhere",4077,I79,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I79,,ICD-10 I79.0 Aneurysm of aorta in diseases classified elsewhere,4078,I79.0,"I70-I79 Diseases of arteries, arterioles and capillaries",http://identifiers.org/icd/I79.0,,ICD-10 @@ -4086,15 +4086,15 @@ I80.0 Phlebitis and thrombophlebitis of superficial vessels of lower extremities I80.1 Phlebitis and thrombophlebitis of femoral vein,4085,I80.1,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I80.1,,ICD-10 I80.2 Phlebitis and thrombophlebitis of other deep vessels of lower extremities,4086,I80.2,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I80.2,,ICD-10 "I80.3 Phlebitis and thrombophlebitis of lower extremities, unspecified",4087,I80.3,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I80.3,,ICD-10 -I80.8 Phlebitis and thrombophlebitis of other sites,4088,I80.8,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I80.8,ORPHAcode: 137839 Lemierre syndrome +I80.8 Phlebitis and thrombophlebitis of other sites,4088,I80.8,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I80.8,ORPHAcode: 137839 Lemierre syndrome,ICD-10 I80.9 Phlebitis and thrombophlebitis of unspecified site,4089,I80.9,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I80.9,,ICD-10 -I81 Portal vein thrombosis,4090,I81,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I81,ORPHAcode: 854 Primitive portal vein thrombosis +I81 Portal vein thrombosis,4090,I81,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I81,ORPHAcode: 854 Primitive portal vein thrombosis,ICD-10 I82 Other venous embolism and thrombosis,4091,I82,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82,,ICD-10 -I82.0 Other venous embolism and thrombosis - Budd-Chiari syndrome,4092,I82.0,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.0,ORPHAcode: 131 Budd-Chiari syndrome +I82.0 Other venous embolism and thrombosis - Budd-Chiari syndrome,4092,I82.0,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.0,ORPHAcode: 131 Budd-Chiari syndrome,ICD-10 I82.1 Other venous embolism and thrombosis - Thrombophlebitis migrans,4093,I82.1,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.1,,ICD-10 I82.2 Embolism and thrombosis of vena cava,4094,I82.2,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.2,,ICD-10 I82.3 Embolism and thrombosis of renal vein,4095,I82.3,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.3,,ICD-10 -I82.8 Embolism and thrombosis of other specified veins,4096,I82.8,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.8,ORPHAcode: 583856 Isolated splenic vein thrombosis +I82.8 Embolism and thrombosis of other specified veins,4096,I82.8,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.8,ORPHAcode: 583856 Isolated splenic vein thrombosis,ICD-10 I82.9 Embolism and thrombosis of unspecified vein,4097,I82.9,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I82.9,,ICD-10 I83 Varicose veins of lower extremities,4098,I83,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I83,,ICD-10 I83.0 Varicose veins of lower extremities with ulcer,4099,I83.0,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I83.0,,ICD-10 @@ -4119,18 +4119,18 @@ I87.8 Other specified disorders of veins,4117,I87.8,"I80-I89 Diseases of veins, "I87.9 Disorder of vein, unspecified",4118,I87.9,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I87.9,,ICD-10 I88 Nonspecific lymphadenitis,4119,I88,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I88,,ICD-10 I88.0 Nonspecific mesenteric lymphadenitis,4120,I88.0,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I88.0,,ICD-10 -"I88.1 Chronic lymphadenitis, except mesenteric",4121,I88.1,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I88.1,ORPHAcode: 50918 Kikuchi-Fujimoto disease +"I88.1 Chronic lymphadenitis, except mesenteric",4121,I88.1,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I88.1,ORPHAcode: 50918 Kikuchi-Fujimoto disease,ICD-10 I88.8 Other nonspecific lymphadenitis,4122,I88.8,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I88.8,,ICD-10 "I88.9 Nonspecific lymphadenitis, unspecified",4123,I88.9,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I88.9,,ICD-10 I89 Other noninfective disorders of lymphatic vessels and lymph nodes,4124,I89,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I89,,ICD-10 -"I89.0 Lymphoedema, not elsewhere classified",4125,I89.0,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I89.0,ORPHAcode: 90362 Primary intestinal lymphangiectasia +"I89.0 Lymphoedema, not elsewhere classified",4125,I89.0,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I89.0,ORPHAcode: 90362 Primary intestinal lymphangiectasia,ICD-10 I89.1 Lymphangitis,4126,I89.1,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I89.1,,ICD-10 -I89.8 Other specified noninfective disorders of lymphatic vessels and lymph nodes,4127,I89.8,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I89.8,ORPHAcode: 482 Kimura disease +I89.8 Other specified noninfective disorders of lymphatic vessels and lymph nodes,4127,I89.8,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I89.8,ORPHAcode: 482 Kimura disease,ICD-10 "I89.9 Noninfective disorder of lymphatic vessels and lymph nodes, unspecified",4128,I89.9,"I80-I89 Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified",http://identifiers.org/icd/I89.9,,ICD-10 I95-I99 Other and unspecified disorders of the circulatory system,4129,,IX Diseases of the circulatory system,,,ICD-10 I95 Hypotension,4130,I95,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I95,,ICD-10 I95.0 Idiopathic hypotension,4131,I95.0,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I95.0,,ICD-10 -I95.1 Orthostatic hypotension,4132,I95.1,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I95.1,ORPHAcode: 443236 Postural orthostatic tachycardia syndrome due to NET deficiency +I95.1 Orthostatic hypotension,4132,I95.1,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I95.1,ORPHAcode: 443236 Postural orthostatic tachycardia syndrome due to NET deficiency,ICD-10 I95.2 Hypotension due to drugs,4133,I95.2,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I95.2,,ICD-10 I95.8 Other hypotension,4134,I95.8,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I95.8,,ICD-10 "I95.9 Hypotension, unspecified",4135,I95.9,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I95.9,,ICD-10 @@ -4138,7 +4138,7 @@ I95.8 Other hypotension,4134,I95.8,I95-I99 Other and unspecified disorders of th "I97.0 Postprocedural disorders of circulatory system, not elsewhere classified - Postcardiotomy syndrome",4137,I97.0,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I97.0,,ICD-10 "I97.1 Postprocedural disorders of circulatory system, not elsewhere classified - Other functional disturbances following cardiac surgery",4138,I97.1,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I97.1,,ICD-10 "I97.2 Postprocedural disorders of circulatory system, not elsewhere classified - Postmastectomy lymphoedema syndrome",4139,I97.2,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I97.2,,ICD-10 -"I97.8 Other postprocedural disorders of circulatory system, not elsewhere classified",4140,I97.8,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I97.8,ORPHAcode: 263352 Postcardiotomy right ventricular failure +"I97.8 Other postprocedural disorders of circulatory system, not elsewhere classified",4140,I97.8,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I97.8,ORPHAcode: 263352 Postcardiotomy right ventricular failure,ICD-10 "I97.9 Postprocedural disorder of circulatory system, unspecified",4141,I97.9,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I97.9,,ICD-10 I98 Other disorders of circulatory system in diseases classified elsewhere,4142,I98,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I98,,ICD-10 I98.0 Other disorders of circulatory system in diseases classified elsewhere - Cardiovascular syphilis,4143,I98.0,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I98.0,,ICD-10 @@ -4146,7 +4146,7 @@ I98.1 Cardiovascular disorders in other infectious and parasitic diseases classi I98.2 Oesophageal varices without bleeding in diseases classified elsewhere,4145,I98.2,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I98.2,,ICD-10 I98.3 Oesophageal varices with bleeding in diseases classified elsewhere,4146,I98.3,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I98.3,,ICD-10 I98.8 Other specified disorders of circulatory system in diseases classified elsewhere,4147,I98.8,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I98.8,,ICD-10 -I99 Other and unspecified disorders of circulatory system,4148,I99,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I99,ORPHAcode: 73229 HANAC syndrome +I99 Other and unspecified disorders of circulatory system,4148,I99,I95-I99 Other and unspecified disorders of the circulatory system,http://identifiers.org/icd/I99,ORPHAcode: 73229 HANAC syndrome,ICD-10 X Diseases of the respiratory system,4149,,,,,ICD-10 J00-J06 Acute upper respiratory infections,4150,,X Diseases of the respiratory system,,,ICD-10 J00 Acute nasopharyngitis [common cold],4151,J00,J00-J06 Acute upper respiratory infections,http://identifiers.org/icd/J00,,ICD-10 @@ -4177,7 +4177,7 @@ J06.0 Acute laryngopharyngitis,4175,J06.0,J00-J06 Acute upper respiratory infect J06.8 Other acute upper respiratory infections of multiple sites,4176,J06.8,J00-J06 Acute upper respiratory infections,http://identifiers.org/icd/J06.8,,ICD-10 "J06.9 Acute upper respiratory infection, unspecified",4177,J06.9,J00-J06 Acute upper respiratory infections,http://identifiers.org/icd/J06.9,,ICD-10 J09-J18 Influenza and pneumonia,4178,,X Diseases of the respiratory system,,,ICD-10 -J09 Influenza due to identified zoonotic or pandemic influenza virus,4179,J09,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J09,ORPHAcode: 454836 Avian influenza +J09 Influenza due to identified zoonotic or pandemic influenza virus,4179,J09,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J09,ORPHAcode: 454836 Avian influenza,ICD-10 J10 influenza due to identified seasonal influenza virus,4180,J10,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J10,,ICD-10 "J10.0 Influenza with pneumonia, seasonal influenza virus identified",4181,J10.0,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J10.0,,ICD-10 "J10.1 Influenza with other respiratory manifestations, seasonal influenza virus identified",4182,J10.1,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J10.1,,ICD-10 @@ -4197,8 +4197,8 @@ J13 Pneumonia due to Streptococcus pneumoniae,4195,J13,J09-J18 Influenza and pne J14 Pneumonia due to Haemophilus influenzae,4196,J14,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J14,,ICD-10 "J15 Bacterial pneumonia, not elsewhere classified",4197,J15,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15,,ICD-10 J15.0 Pneumonia due to Klebsiella pneumoniae,4198,J15.0,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.0,,ICD-10 -J15.1 Pneumonia due to Pseudomonas,4199,J15.1,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.1,ORPHAcode: 90066 Pneumonia caused by Pseudomonas aeruginosa infection -J15.2 Pneumonia due to staphylococcus,4200,J15.2,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.2,ORPHAcode: 36238 Staphylococcal necrotizing pneumonia +J15.1 Pneumonia due to Pseudomonas,4199,J15.1,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.1,ORPHAcode: 90066 Pneumonia caused by Pseudomonas aeruginosa infection,ICD-10 +J15.2 Pneumonia due to staphylococcus,4200,J15.2,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.2,ORPHAcode: 36238 Staphylococcal necrotizing pneumonia,ICD-10 "J15.3 Pneumonia due to streptococcus, group B",4201,J15.3,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.3,,ICD-10 J15.4 Pneumonia due to other streptococci,4202,J15.4,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.4,,ICD-10 J15.5 Pneumonia due to Escherichia coli,4203,J15.5,J09-J18 Influenza and pneumonia,http://identifiers.org/icd/J15.5,,ICD-10 @@ -4268,7 +4268,7 @@ J34 Other disorders of nose and nasal sinuses,4265,J34,J30-J39 Other diseases of J34.1 Cyst and mucocele of nose and nasal sinus,4267,J34.1,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J34.1,,ICD-10 J34.2 Deviated nasal septum,4268,J34.2,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J34.2,,ICD-10 J34.3 Hypertrophy of nasal turbinates,4269,J34.3,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J34.3,,ICD-10 -J34.8 Other specified disorders of nose and nasal sinuses,4270,J34.8,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J34.8,ORPHAcode: 71276 Silent sinus syndrome +J34.8 Other specified disorders of nose and nasal sinuses,4270,J34.8,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J34.8,ORPHAcode: 71276 Silent sinus syndrome,ICD-10 J35 Chronic diseases of tonsils and adenoids,4271,J35,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J35,,ICD-10 J35.0 Chronic tonsillitis,4272,J35.0,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J35.0,,ICD-10 J35.1 Hypertrophy of tonsils,4273,J35.1,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J35.1,,ICD-10 @@ -4281,7 +4281,7 @@ J37 Chronic laryngitis and laryngotracheitis,4279,J37,J30-J39 Other diseases of J37.0 Chronic laryngitis,4280,J37.0,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J37.0,,ICD-10 J37.1 Chronic laryngotracheitis,4281,J37.1,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J37.1,,ICD-10 "J38 Diseases of vocal cords and larynx, not elsewhere classified",4282,J38,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J38,,ICD-10 -J38.0 Paralysis of vocal cords and larynx,4283,J38.0,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J38.0,ORPHAcode: 2375 Laryngeal abductor paralysis-intellectual disability syndrome +J38.0 Paralysis of vocal cords and larynx,4283,J38.0,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J38.0,ORPHAcode: 2375 Laryngeal abductor paralysis-intellectual disability syndrome,ICD-10 J38.1 Polyp of vocal cord and larynx,4284,J38.1,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J38.1,,ICD-10 J38.2 Nodules of vocal cords,4285,J38.2,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J38.2,,ICD-10 J38.3 Other diseases of vocal cords,4286,J38.3,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J38.3,,ICD-10 @@ -4292,9 +4292,9 @@ J38.7 Other diseases of larynx,4290,J38.7,J30-J39 Other diseases of upper respir J39 Other diseases of upper respiratory tract,4291,J39,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39,,ICD-10 J39.0 Other diseases of upper respiratory tract - Retropharyngeal and parapharyngeal abscess,4292,J39.0,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.0,,ICD-10 J39.1 Other abscess of pharynx,4293,J39.1,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.1,,ICD-10 -J39.2 Other diseases of pharynx,4294,J39.2,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.2,ORPHAcode: 2291 Congenital velopharyngeal incompetence +J39.2 Other diseases of pharynx,4294,J39.2,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.2,ORPHAcode: 2291 Congenital velopharyngeal incompetence,ICD-10 "J39.3 Upper respiratory tract hypersensitivity reaction, site unspecified",4295,J39.3,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.3,,ICD-10 -J39.8 Other specified diseases of upper respiratory tract,4296,J39.8,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.8,ORPHAcode: 449566 Eosinophilic angiocentric fibrosis +J39.8 Other specified diseases of upper respiratory tract,4296,J39.8,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.8,ORPHAcode: 449566 Eosinophilic angiocentric fibrosis,ICD-10 "J39.9 Disease of upper respiratory tract, unspecified",4297,J39.9,J30-J39 Other diseases of upper respiratory tract,http://identifiers.org/icd/J39.9,,ICD-10 J40-J47 Chronic lower respiratory diseases,4298,,X Diseases of the respiratory system,,,ICD-10 "J40 Bronchitis, not specified as acute or chronic",4299,J40,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J40,,ICD-10 @@ -4313,7 +4313,7 @@ K38.3 Fistula of appendix,4311,K38.3,K35-K38 Diseases of appendix,http://identif J44 Other chronic obstructive pulmonary disease,4312,J44,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J44,,ICD-10 J44.0 Chronic obstructive pulmonary disease with acute lower respiratory infection,4313,J44.0,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J44.0,,ICD-10 "J44.1 Chronic obstructive pulmonary disease with acute exacerbation, unspecified",4314,J44.1,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J44.1,,ICD-10 -J44.8 Other specified chronic obstructive pulmonary disease,4315,J44.8,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J44.8,ORPHAcode: 1303 Bronchiolitis obliterans with obstructive pulmonary disease +J44.8 Other specified chronic obstructive pulmonary disease,4315,J44.8,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J44.8,ORPHAcode: 1303 Bronchiolitis obliterans with obstructive pulmonary disease,ICD-10 "J44.9 Chronic obstructive pulmonary disease, unspecified",4316,J44.9,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J44.9,,ICD-10 J45 Asthma,4317,J45,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J45,,ICD-10 J45.0 Predominantly allergic asthma,4318,J45.0,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J45.0,,ICD-10 @@ -4321,10 +4321,10 @@ J45.1 Nonallergic asthma,4319,J45.1,J40-J47 Chronic lower respiratory diseases,h J45.8 Mixed asthma,4320,J45.8,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J45.8,,ICD-10 "J45.9 Asthma, unspecified",4321,J45.9,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J45.9,,ICD-10 J46 Status asthmaticus,4322,J46,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J46,,ICD-10 -J47 Bronchiectasis,4323,J47,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J47,ORPHAcode: 60033 Idiopathic bronchiectasis +J47 Bronchiectasis,4323,J47,J40-J47 Chronic lower respiratory diseases,http://identifiers.org/icd/J47,ORPHAcode: 60033 Idiopathic bronchiectasis,ICD-10 J60-J70 Lung diseases due to external agents,4324,,X Diseases of the respiratory system,,,ICD-10 J60 Coalworker pneumoconiosis,4325,J60,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J60,,ICD-10 -J61 Pneumoconiosis due to asbestos and other mineral fibres,4326,J61,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J61,ORPHAcode: 2302 Asbestos intoxication +J61 Pneumoconiosis due to asbestos and other mineral fibres,4326,J61,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J61,ORPHAcode: 2302 Asbestos intoxication,ICD-10 J62 Pneumoconiosis due to dust containing silica,4327,J62,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J62,,ICD-10 J62.0 Pneumoconiosis due to talc dust,4328,J62.0,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J62.0,,ICD-10 J62.8 Pneumoconiosis due to other dust containing silica,4329,J62.8,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J62.8,,ICD-10 @@ -4332,7 +4332,7 @@ J63 Pneumoconiosis due to other inorganic dusts,4330,J63,J60-J70 Lung diseases d K50-K52 Noninfective enteritis and colitis,4331,,XI Diseases of the digestive system,,,ICD-10 J63.0 Pneumoconiosis due to other inorganic dusts - Aluminosis (of lung),4332,J63.0,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J63.0,,ICD-10 J63.1 Pneumoconiosis due to other inorganic dusts - Bauxite fibrosis (of lung),4333,J63.1,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J63.1,,ICD-10 -J63.2 Pneumoconiosis due to other inorganic dusts - Berylliosis,4334,J63.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J63.2,ORPHAcode: 133 Chronic beryllium disease +J63.2 Pneumoconiosis due to other inorganic dusts - Berylliosis,4334,J63.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J63.2,ORPHAcode: 133 Chronic beryllium disease,ICD-10 J63.3 Pneumoconiosis due to other inorganic dusts - Graphite fibrosis (of lung),4335,J63.3,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J63.3,,ICD-10 J63.4 Pneumoconiosis due to other inorganic dusts - Siderosis,4336,J63.4,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J63.4,,ICD-10 J63.5 Pneumoconiosis due to other inorganic dusts - Stannosis,4337,J63.5,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J63.5,,ICD-10 @@ -4345,22 +4345,22 @@ J66.1 Flax-dresser disease,4343,J66.1,J60-J70 Lung diseases due to external agen J66.2 Airway disease due to specific organic dust - Cannabinosis,4344,J66.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J66.2,,ICD-10 J66.8 Airway disease due to other specific organic dusts,4345,J66.8,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J66.8,,ICD-10 J67 Hypersensitivity pneumonitis due to organic dust,4346,J67,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67,,ICD-10 -J67.0 Hypersensitivity pneumonitis due to organic dust - Farmer lung,4347,J67.0,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.0,ORPHAcode: 99906 Farmer's lung disease +J67.0 Hypersensitivity pneumonitis due to organic dust - Farmer lung,4347,J67.0,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.0,ORPHAcode: 99906 Farmer's lung disease,ICD-10 J67.1 Hypersensitivity pneumonitis due to organic dust - Bagassosis,4348,J67.1,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.1,,ICD-10 -J67.2 Hypersensitivity pneumonitis due to organic dust - Bird fancier lung,4349,J67.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.2,ORPHAcode: 99908 Pigeon-breeder lung disease +J67.2 Hypersensitivity pneumonitis due to organic dust - Bird fancier lung,4349,J67.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.2,ORPHAcode: 99908 Pigeon-breeder lung disease,ICD-10 J67.3 Hypersensitivity pneumonitis due to organic dust - Suberosis,4350,J67.3,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.3,,ICD-10 J67.4 Hypersensitivity pneumonitis due to organic dust - Maltworker lung,4351,J67.4,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.4,,ICD-10 J67.5 Hypersensitivity pneumonitis due to organic dust - Mushroom-worker lung,4352,J67.5,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.5,,ICD-10 J67.6 Hypersensitivity pneumonitis due to organic dust - Maple-bark-stripper lung,4353,J67.6,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.6,,ICD-10 J67.7 Hypersensitivity pneumonitis due to organic dust - Air-conditioner and humidifier lung,4354,J67.7,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.7,,ICD-10 -J67.8 Hypersensitivity pneumonitis due to other organic dusts,4355,J67.8,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.8,ORPHAcode: 99907 House allergic alveolitis +J67.8 Hypersensitivity pneumonitis due to other organic dusts,4355,J67.8,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.8,ORPHAcode: 99907 House allergic alveolitis,ICD-10 J67.9 Hypersensitivity pneumonitis due to unspecified organic dust,4356,J67.9,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J67.9,,ICD-10 "J68 Respiratory conditions due to inhalation of chemicals, gases, fumes and vapours",4357,J68,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68,,ICD-10 "J68.0 Bronchitis and pneumonitis due to chemicals, gases, fumes and vapours",4358,J68.0,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.0,,ICD-10 "J68.1 Pulmonary oedema due to chemicals, gases, fumes and vapours",4359,J68.1,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.1,,ICD-10 "J68.2 Upper respiratory inflammation due to chemicals, gases, fumes and vapours, not elsewhere classified",4360,J68.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.2,,ICD-10 "J68.3 Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapours",4361,J68.3,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.3,,ICD-10 -"J68.4 Chronic respiratory conditions due to chemicals, gases, fumes and vapours",4362,J68.4,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.4,ORPHAcode: 79127 Respiratory bronchiolitis-interstitial lung disease syndrome +"J68.4 Chronic respiratory conditions due to chemicals, gases, fumes and vapours",4362,J68.4,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.4,ORPHAcode: 79127 Respiratory bronchiolitis-interstitial lung disease syndrome,ICD-10 "J68.8 Other respiratory conditions due to chemicals, gases, fumes and vapours",4363,J68.8,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.8,,ICD-10 "J68.9 Unspecified respiratory condition due to chemicals, gases, fumes and vapours",4364,J68.9,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J68.9,,ICD-10 J69 Pneumonitis due to solids and liquids,4365,J69,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J69,,ICD-10 @@ -4371,20 +4371,20 @@ J69.8 Pneumonitis due to other solids and liquids,4369,J69.8,J60-J70 Lung diseas J70 Respiratory conditions due to other external agents,4370,J70,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70,,ICD-10 J70.0 Acute pulmonary manifestations due to radiation,4371,J70.0,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.0,,ICD-10 J70.1 Chronic and other pulmonary manifestations due to radiation,4372,J70.1,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.1,,ICD-10 -J70.2 Respiratory conditions due to other external agents - Acute drug-induced interstitial lung disorders,4373,J70.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.2,ORPHAcode: 264978 Drug or radiation exposure-related interstitial lung disease +J70.2 Respiratory conditions due to other external agents - Acute drug-induced interstitial lung disorders,4373,J70.2,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.2,ORPHAcode: 264978 Drug or radiation exposure-related interstitial lung disease,ICD-10 J70.3 Respiratory conditions due to other external agents - Chronic drug-induced interstitial lung disorders,4374,J70.3,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.3,,ICD-10 "J70.4 Respiratory conditions due to other external agents - Drug-induced interstitial lung disorders, unspecified",4375,J70.4,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.4,,ICD-10 J70.8 Respiratory conditions due to other specified external agents,4376,J70.8,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.8,,ICD-10 J70.9 Respiratory conditions due to unspecified external agent,4377,J70.9,J60-J70 Lung diseases due to external agents,http://identifiers.org/icd/J70.9,,ICD-10 J80-J84 Other respiratory diseases principally affecting the interstitium,4378,,X Diseases of the respiratory system,,,ICD-10 -J80 Adult respiratory distress syndrome,4379,J80,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J80,ORPHAcode: 70578 Adult acute respiratory distress syndrome -J81 Pulmonary oedema,4380,J81,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J81,ORPHAcode: 330012 High altitude pulmonary edema -"J82 Pulmonary eosinophilia, not elsewhere classified",4381,J82,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J82,ORPHAcode: 724 Idiopathic acute eosinophilic pneumonia +J80 Adult respiratory distress syndrome,4379,J80,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J80,ORPHAcode: 70578 Adult acute respiratory distress syndrome,ICD-10 +J81 Pulmonary oedema,4380,J81,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J81,ORPHAcode: 330012 High altitude pulmonary edema,ICD-10 +"J82 Pulmonary eosinophilia, not elsewhere classified",4381,J82,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J82,ORPHAcode: 724 Idiopathic acute eosinophilic pneumonia,ICD-10 J84 Other interstitial pulmonary diseases,4382,J84,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84,,ICD-10 J92.9 Pleural plaque without asbestos,4383,J92.9,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J92.9,,ICD-10 -J84.0 Other interstitial pulmonary diseases - Alveolar and parietoalveolar conditions,4384,J84.0,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84.0,ORPHAcode: 747 Autoimmune pulmonary alveolar proteinosis -J84.1 Other interstitial pulmonary diseases with fibrosis,4385,J84.1,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84.1,ORPHAcode: 1302 Cryptogenic organizing pneumonia -J84.8 Other specified interstitial pulmonary diseases,4386,J84.8,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84.8,ORPHAcode: 91364 Non-specific interstitial pneumonia +J84.0 Other interstitial pulmonary diseases - Alveolar and parietoalveolar conditions,4384,J84.0,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84.0,ORPHAcode: 747 Autoimmune pulmonary alveolar proteinosis,ICD-10 +J84.1 Other interstitial pulmonary diseases with fibrosis,4385,J84.1,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84.1,ORPHAcode: 1302 Cryptogenic organizing pneumonia,ICD-10 +J84.8 Other specified interstitial pulmonary diseases,4386,J84.8,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84.8,ORPHAcode: 91364 Non-specific interstitial pneumonia,ICD-10 "J84.9 Interstitial pulmonary disease, unspecified",4387,J84.9,J80-J84 Other respiratory diseases principally affecting the interstitium,http://identifiers.org/icd/J84.9,,ICD-10 J85-J86 Suppurative and necrotic conditions of lower respiratory tract,4388,,X Diseases of the respiratory system,,,ICD-10 J85 Abscess of lung and mediastinum,4389,J85,J85-J86 Suppurative and necrotic conditions of lower respiratory tract,http://identifiers.org/icd/J85,,ICD-10 @@ -4401,7 +4401,7 @@ J91 Pleural effusion in conditions classified elsewhere,4399,J91,J90-J94 Other d J92 Pleural plaque,4400,J92,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J92,,ICD-10 J92.0 Pleural plaque with presence of asbestos,4401,J92.0,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J92.0,,ICD-10 J93.0 Spontaneous tension pneumothorax,4402,J93.0,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J93.0,,ICD-10 -J93.1 Other spontaneous pneumothorax,4403,J93.1,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J93.1,ORPHAcode: 2903 Familial spontaneous pneumothorax +J93.1 Other spontaneous pneumothorax,4403,J93.1,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J93.1,ORPHAcode: 2903 Familial spontaneous pneumothorax,ICD-10 J93.8 Other pneumothorax,4404,J93.8,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J93.8,,ICD-10 "J93.9 Pneumothorax, unspecified",4405,J93.9,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J93.9,,ICD-10 J94 Other pleural conditions,4406,J94,J90-J94 Other diseases of pleura,http://identifiers.org/icd/J94,,ICD-10 @@ -4426,11 +4426,11 @@ J96.0 Acute respiratory failure,4424,J96.0,J95-J99 Other diseases of the respira J96.1 Chronic respiratory failure,4425,J96.1,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J96.1,,ICD-10 "J96.9 Respiratory failure, unspecified",4426,J96.9,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J96.9,,ICD-10 J98 Other respiratory disorders,4427,J98,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98,,ICD-10 -"J98.0 Other respiratory disorders - Diseases of bronchus, not elsewhere classified",4428,J98.0,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.0,ORPHAcode: 3347 Mounier-K hn sy +"J98.0 Other respiratory disorders - Diseases of bronchus, not elsewhere classified",4428,J98.0,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.0,ORPHAcode: 3347 Mounier-K hn sy,ICD-10 J98.1 Other respiratory disorders - Pulmonary collapse,4429,J98.1,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.1,,ICD-10 J98.2 Other respiratory disorders - Interstitial emphysema,4430,J98.2,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.2,,ICD-10 J98.3 Other respiratory disorders - Compensatory emphysema,4431,J98.3,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.3,,ICD-10 -J98.4 Other disorders of lung,4432,J98.4,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.4,ORPHAcode: 2357 Bronchogenic cyst +J98.4 Other disorders of lung,4432,J98.4,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.4,ORPHAcode: 2357 Bronchogenic cyst,ICD-10 "J98.5 Other respiratory disorders - Diseases of mediastinum, not elsewhere classified",4433,J98.5,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.5,,ICD-10 J98.6 Disorders of diaphragm,4434,J98.6,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.6,,ICD-10 J98.8 Other specified respiratory disorders,4435,J98.8,J95-J99 Other diseases of the respiratory system,http://identifiers.org/icd/J98.8,,ICD-10 @@ -4442,15 +4442,15 @@ J99.8 Respiratory disorders in other diseases classified elsewhere,4440,J99.8,J9 XI Diseases of the digestive system,4441,,,,,ICD-10 "K00-K14 Diseases of oral cavity, salivary glands and jaws",4442,,XI Diseases of the digestive system,,,ICD-10 K00 Disorders of tooth development and eruption,4443,K00,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00,,ICD-10 -K00.0 Disorders of tooth development and eruption - Anodontia,4444,K00.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.0,ORPHAcode: 99797 Anodontia +K00.0 Disorders of tooth development and eruption - Anodontia,4444,K00.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.0,ORPHAcode: 99797 Anodontia,ICD-10 K00.1 Disorders of tooth development and eruption - Supernumerary teeth,4445,K00.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.1,,ICD-10 -K00.2 Abnormalities of size and form of teeth,4446,K00.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.2,ORPHAcode: 2287 Fused mandibular incisors +K00.2 Abnormalities of size and form of teeth,4446,K00.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.2,ORPHAcode: 2287 Fused mandibular incisors,ICD-10 K00.3 Disorders of tooth development and eruption - Mottled teeth,4447,K00.3,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.3,,ICD-10 -K00.4 Disturbances in tooth formation,4448,K00.4,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.4,ORPHAcode: 67039 Segmental odontomaxillary dysplasia -"K00.5 Hereditary disturbances in tooth structure, not elsewhere classified",4449,K00.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.5,ORPHAcode: 1031 Enamel-renal syndrome +K00.4 Disturbances in tooth formation,4448,K00.4,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.4,ORPHAcode: 67039 Segmental odontomaxillary dysplasia,ICD-10 +"K00.5 Hereditary disturbances in tooth structure, not elsewhere classified",4449,K00.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.5,ORPHAcode: 1031 Enamel-renal syndrome,ICD-10 K00.6 Disturbances in tooth eruption,4450,K00.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.6,,ICD-10 K00.7 Disorders of tooth development and eruption - Teething syndrome,4451,K00.7,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.7,,ICD-10 -K00.8 Other disorders of tooth development,4452,K00.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.8,ORPHAcode: 412206 Primary failure of tooth eruption +K00.8 Other disorders of tooth development,4452,K00.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.8,ORPHAcode: 412206 Primary failure of tooth eruption,ICD-10 "K00.9 Disorder of tooth development, unspecified",4453,K00.9,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K00.9,,ICD-10 K01 Embedded and impacted teeth,4454,K01,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K01,,ICD-10 K01.0 Embedded teeth,4455,K01.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K01.0,,ICD-10 @@ -4470,7 +4470,7 @@ K03.1 Abrasion of teeth,4468,K03.1,"K00-K14 Diseases of oral cavity, salivary gl K03.2 Erosion of teeth,4469,K03.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.2,,ICD-10 K03.3 Pathological resorption of teeth,4470,K03.3,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.3,,ICD-10 K03.4 Other diseases of hard tissues of teeth - Hypercementosis,4471,K03.4,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.4,,ICD-10 -K03.5 Ankylosis of teeth,4472,K03.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.5,ORPHAcode: 1077 Dental ankylosis +K03.5 Ankylosis of teeth,4472,K03.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.5,ORPHAcode: 1077 Dental ankylosis,ICD-10 K03.6 Deposits [accretions] on teeth,4473,K03.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.6,,ICD-10 K03.7 Posteruptive colour changes of dental hard tissues,4474,K03.7,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.7,,ICD-10 K03.8 Other specified diseases of hard tissues of teeth,4475,K03.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K03.8,,ICD-10 @@ -4496,19 +4496,19 @@ K05.5 Other periodontal diseases,4494,K05.5,"K00-K14 Diseases of oral cavity, sa "K05.6 Periodontal disease, unspecified",4495,K05.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K05.6,,ICD-10 K06 Other disorders of gingiva and edentulous alveolar ridge,4496,K06,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06,,ICD-10 K06.0 Gingival recession,4497,K06.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06.0,,ICD-10 -K06.1 Gingival enlargement,4498,K06.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06.1,ORPHAcode: 2024 Hereditary gingival fibromatosis +K06.1 Gingival enlargement,4498,K06.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06.1,ORPHAcode: 2024 Hereditary gingival fibromatosis,ICD-10 K06.2 Gingival and edentulous alveolar ridge lesions associated with trauma,4499,K06.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06.2,,ICD-10 -K06.8 Other specified disorders of gingiva and edentulous alveolar ridge,4500,K06.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06.8,ORPHAcode: 157826 Congenital epulis +K06.8 Other specified disorders of gingiva and edentulous alveolar ridge,4500,K06.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06.8,ORPHAcode: 157826 Congenital epulis,ICD-10 "K06.9 Disorder of gingiva and edentulous alveolar ridge, unspecified",4501,K06.9,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K06.9,,ICD-10 K07 Dentofacial anomalies [including malocclusion],4502,K07,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07,,ICD-10 -K07.0 Major anomalies of jaw size,4503,K07.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.0,ORPHAcode: 477781 Primary condylar hyperplasia -K07.1 Anomalies of jaw-cranial base relationship,4504,K07.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.1,ORPHAcode: 2964 Autosomal dominant prognathism +K07.0 Major anomalies of jaw size,4503,K07.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.0,ORPHAcode: 477781 Primary condylar hyperplasia,ICD-10 +K07.1 Anomalies of jaw-cranial base relationship,4504,K07.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.1,ORPHAcode: 2964 Autosomal dominant prognathism,ICD-10 K07.2 Anomalies of dental arch relationship,4505,K07.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.2,,ICD-10 K07.3 Anomalies of tooth position,4506,K07.3,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.3,,ICD-10 "K07.4 Malocclusion, unspecified",4507,K07.4,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.4,,ICD-10 K07.5 Dentofacial functional abnormalities,4508,K07.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.5,,ICD-10 -K07.6 Dentofacial anomalies [including malocclusion] - Temporomandibular joint disorders,4509,K07.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.6,ORPHAcode: 210576 Congenital temporomandibular joint ankylosis -K07.8 Other dentofacial anomalies,4510,K07.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.8,ORPHAcode: 99806 Oculootodental syndrome +K07.6 Dentofacial anomalies [including malocclusion] - Temporomandibular joint disorders,4509,K07.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.6,ORPHAcode: 210576 Congenital temporomandibular joint ankylosis,ICD-10 +K07.8 Other dentofacial anomalies,4510,K07.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.8,ORPHAcode: 99806 Oculootodental syndrome,ICD-10 "K07.9 Dentofacial anomaly, unspecified",4511,K07.9,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K07.9,,ICD-10 K08 Other disorders of teeth and supporting structures,4512,K08,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K08,,ICD-10 K08.0 Exfoliation of teeth due to systemic causes,4513,K08.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K08.0,,ICD-10 @@ -4526,9 +4526,9 @@ K09.2 Other cysts of jaw,4522,K09.2,"K00-K14 Diseases of oral cavity, salivary g K10 Other diseases of jaws,4525,K10,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10,,ICD-10 K10.0 Developmental disorders of jaws,4526,K10.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.0,,ICD-10 "K10.1 Other diseases of jaws - Giant cell granuloma, central",4527,K10.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.1,,ICD-10 -K10.2 Inflammatory conditions of jaws,4528,K10.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.2,ORPHAcode: 399293 Osteonecrosis of the jaw +K10.2 Inflammatory conditions of jaws,4528,K10.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.2,ORPHAcode: 399293 Osteonecrosis of the jaw,ICD-10 K10.3 Alveolitis of jaws,4529,K10.3,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.3,,ICD-10 -K10.8 Other specified diseases of jaws,4530,K10.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.8,ORPHAcode: 184 Cherubism +K10.8 Other specified diseases of jaws,4530,K10.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.8,ORPHAcode: 184 Cherubism,ICD-10 "K10.9 Disease of jaws, unspecified",4531,K10.9,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K10.9,,ICD-10 K11 Diseases of salivary glands,4532,K11,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K11,,ICD-10 K11.0 Atrophy of salivary gland,4533,K11.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K11.0,,ICD-10 @@ -4547,14 +4547,14 @@ K12.1 Other forms of stomatitis,4545,K12.1,"K00-K14 Diseases of oral cavity, sal K12.2 Cellulitis and abscess of mouth,4546,K12.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K12.2,,ICD-10 K12.3 Stomatitis and related lesions - Oral mucositis (ulcerative),4547,K12.3,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K12.3,,ICD-10 K13 Other diseases of lip and oral mucosa,4548,K13,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13,,ICD-10 -K13.0 Diseases of lips,4549,K13.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.0,ORPHAcode: 1221 Cheilitis glandularis +K13.0 Diseases of lips,4549,K13.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.0,ORPHAcode: 1221 Cheilitis glandularis,ICD-10 K13.1 Cheek and lip biting,4550,K13.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.1,,ICD-10 "K13.2 Leukoplakia and other disturbances of oral epithelium, including tongue",4551,K13.2,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.2,,ICD-10 K13.3 Other diseases of lip and oral mucosa - Hairy leukoplakia,4552,K13.3,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.3,,ICD-10 K13.4 Granuloma and granuloma-like lesions of oral mucosa,4553,K13.4,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.4,,ICD-10 -K13.5 Oral submucous fibrosis,4554,K13.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.5,ORPHAcode: 357154 Oral submucous fibrosis +K13.5 Oral submucous fibrosis,4554,K13.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.5,ORPHAcode: 357154 Oral submucous fibrosis,ICD-10 K13.6 Irritative hyperplasia of oral mucosa,4555,K13.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.6,,ICD-10 -K13.7 Other and unspecified lesions of oral mucosa,4556,K13.7,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.7,ORPHAcode: 1839 Hereditary mucoepithelial dysplasia +K13.7 Other and unspecified lesions of oral mucosa,4556,K13.7,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K13.7,ORPHAcode: 1839 Hereditary mucoepithelial dysplasia,ICD-10 K14 Diseases of tongue,4557,K14,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14,,ICD-10 K14.0 Diseases of tongue - Glossitis,4558,K14.0,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.0,,ICD-10 K14.1 Geographic tongue,4559,K14.1,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.1,,ICD-10 @@ -4562,16 +4562,16 @@ K14.2 Diseases of tongue - Median rhomboid glossitis,4560,K14.2,"K00-K14 Disease K14.3 Hypertrophy of tongue papillae,4561,K14.3,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.3,,ICD-10 K14.4 Atrophy of tongue papillae,4562,K14.4,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.4,,ICD-10 K14.5 Plicated tongue,4563,K14.5,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.5,,ICD-10 -K14.6 Diseases of tongue - Glossodynia,4564,K14.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.6,ORPHAcode: 353253 Burning mouth syndrome +K14.6 Diseases of tongue - Glossodynia,4564,K14.6,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.6,ORPHAcode: 353253 Burning mouth syndrome,ICD-10 K14.8 Other diseases of tongue,4565,K14.8,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.8,,ICD-10 "K14.9 Disease of tongue, unspecified",4566,K14.9,"K00-K14 Diseases of oral cavity, salivary glands and jaws",http://identifiers.org/icd/K14.9,,ICD-10 "K20-K31 Diseases of oesophagus, stomach and duodenum",4567,,XI Diseases of the digestive system,,,ICD-10 -K20 Oesophagitis,4568,K20,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K20,ORPHAcode: 73247 Eosinophilic esophagitis +K20 Oesophagitis,4568,K20,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K20,ORPHAcode: 73247 Eosinophilic esophagitis,ICD-10 K21 Gastro-oesophageal reflux disease,4569,K21,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K21,,ICD-10 K21.0 Gastro-oesophageal reflux disease with oesophagitis,4570,K21.0,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K21.0,,ICD-10 K21.9 Gastro-oesophageal reflux disease without oesophagitis,4571,K21.9,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K21.9,,ICD-10 K22 Other diseases of oesophagus,4572,K22,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K22,,ICD-10 -K22.0 Achalasia of cardia,4573,K22.0,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K22.0,ORPHAcode: 930 Idiopathic achalasia +K22.0 Achalasia of cardia,4573,K22.0,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K22.0,ORPHAcode: 930 Idiopathic achalasia,ICD-10 K22.1 Ulcer of oesophagus,4574,K22.1,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K22.1,,ICD-10 K22.2 Other diseases of oesophagus - Oesophageal obstruction,4575,K22.2,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K22.2,,ICD-10 K22.3 Perforation of oesophagus,4576,K22.3,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K22.3,,ICD-10 @@ -4596,7 +4596,7 @@ K29.2 Alcoholic gastritis,4594,K29.2,"K20-K31 Diseases of oesophagus, stomach an K29.3 Chronic superficial gastritis,4595,K29.3,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.3,,ICD-10 K29.4 Chronic atrophic gastritis,4596,K29.4,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.4,,ICD-10 "K29.5 Chronic gastritis, unspecified",4597,K29.5,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.5,,ICD-10 -K29.6 Other gastritis,4598,K29.6,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.6,ORPHAcode: 2494 M n t +K29.6 Other gastritis,4598,K29.6,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.6,ORPHAcode: 2494 M n t,ICD-10 "K29.7 Gastritis, unspecified",4599,K29.7,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.7,,ICD-10 K29.8 Duodenitis,4600,K29.8,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.8,,ICD-10 "K29.9 Gastroduodenitis, unspecified",4601,K29.9,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K29.9,,ICD-10 @@ -4610,7 +4610,7 @@ K31.4 Other diseases of stomach and duodenum - Gastric diverticulum,4608,K31.4," K31.5 Obstruction of duodenum,4609,K31.5,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K31.5,,ICD-10 K31.6 Fistula of stomach and duodenum,4610,K31.6,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K31.6,,ICD-10 K31.7 Polyp of stomach and duodenum,4611,K31.7,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K31.7,,ICD-10 -K31.8 Other specified diseases of stomach and duodenum,4612,K31.8,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K31.8,ORPHAcode: 558411 Idiopathic gastroparesis +K31.8 Other specified diseases of stomach and duodenum,4612,K31.8,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K31.8,ORPHAcode: 558411 Idiopathic gastroparesis,ICD-10 "K31.9 Disease of stomach and duodenum, unspecified",4613,K31.9,"K20-K31 Diseases of oesophagus, stomach and duodenum",http://identifiers.org/icd/K31.9,,ICD-10 K35-K38 Diseases of appendix,4614,,XI Diseases of the digestive system,,,ICD-10 K35 Acute appendicitis,4615,K35,K35-K38 Diseases of appendix,http://identifiers.org/icd/K35,,ICD-10 @@ -4651,7 +4651,7 @@ K43.2 Incisional hernia without obstruction or gangrene,4649,K43.2,K40-K46 Herni "K43.3 Parastomal hernia with obstruction, without gangrene",4650,K43.3,K40-K46 Hernia,http://identifiers.org/icd/K43.3,,ICD-10 K43.4 Parastomal hernia with gangrene,4651,K43.4,K40-K46 Hernia,http://identifiers.org/icd/K43.4,,ICD-10 K43.5 Parastomal hernia without obstruction or gangrene,4652,K43.5,K40-K46 Hernia,http://identifiers.org/icd/K43.5,,ICD-10 -K43.6 Other and unspecified ventral hernia with obstruction without gangrene,4653,K43.6,K40-K46 Hernia,http://identifiers.org/icd/K43.6,ORPHAcode: 314432 Spigelian hernia-cryptorchidism syndrome +K43.6 Other and unspecified ventral hernia with obstruction without gangrene,4653,K43.6,K40-K46 Hernia,http://identifiers.org/icd/K43.6,ORPHAcode: 314432 Spigelian hernia-cryptorchidism syndrome,ICD-10 K43.7 Other and unspecified ventral hernia with gangrene,4654,K43.7,K40-K46 Hernia,http://identifiers.org/icd/K43.7,,ICD-10 K43.9 Other and unspecified ventral hernia without obstruction or gangrene,4655,K43.9,K40-K46 Hernia,http://identifiers.org/icd/K43.9,,ICD-10 K44 Diaphragmatic hernia,4656,K44,K40-K46 Hernia,http://identifiers.org/icd/K44,,ICD-10 @@ -4683,17 +4683,17 @@ K52 Other noninfective gastroenteritis and colitis,4681,K52,K50-K52 Noninfective K52.0 Gastroenteritis and colitis due to radiation,4682,K52.0,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.0,,ICD-10 K52.1 Toxic gastroenteritis and colitis,4683,K52.1,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.1,,ICD-10 K52.2 Allergic and dietetic gastroenteritis and colitis,4684,K52.2,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.2,,ICD-10 -K52.3 Indeterminate colitis,4685,K52.3,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.3,ORPHAcode: 103920 Undetermined colitis -K52.8 Other specified noninfective gastroenteritis and colitis,4686,K52.8,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.8,ORPHAcode: 2070 Eosinophilic gastroenteritis +K52.3 Indeterminate colitis,4685,K52.3,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.3,ORPHAcode: 103920 Undetermined colitis,ICD-10 +K52.8 Other specified noninfective gastroenteritis and colitis,4686,K52.8,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.8,ORPHAcode: 2070 Eosinophilic gastroenteritis,ICD-10 "K52.9 Noninfective gastroenteritis and colitis, unspecified",4687,K52.9,K50-K52 Noninfective enteritis and colitis,http://identifiers.org/icd/K52.9,,ICD-10 K55 Vascular disorders of intestine,4688,K55,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K55,,ICD-10 -K55.0 Acute vascular disorders of intestine,4689,K55.0,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K55.0,ORPHAcode: 583861 Isolated mesenteric vein thrombosis +K55.0 Acute vascular disorders of intestine,4689,K55.0,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K55.0,ORPHAcode: 583861 Isolated mesenteric vein thrombosis,ICD-10 K55.1 Chronic vascular disorders of intestine,4690,K55.1,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K55.1,,ICD-10 K55.2 Angiodysplasia of colon,4691,K55.2,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K55.2,,ICD-10 K55.8 Other vascular disorders of intestine,4692,K55.8,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K55.8,,ICD-10 "K55.9 Vascular disorder of intestine, unspecified",4693,K55.9,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K55.9,,ICD-10 K56 Paralytic ileus and intestinal obstruction without hernia,4694,K56,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K56,,ICD-10 -K56.0 Paralytic ileus,4695,K56.0,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K56.0,ORPHAcode: 2604 Familial visceral myopathy +K56.0 Paralytic ileus,4695,K56.0,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K56.0,ORPHAcode: 2604 Familial visceral myopathy,ICD-10 K56.1 Paralytic ileus and intestinal obstruction without hernia - Intussusception,4696,K56.1,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K56.1,,ICD-10 K56.2 Paralytic ileus and intestinal obstruction without hernia - Volvulus,4697,K56.2,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K56.2,,ICD-10 K56.3 Gallstone ileus,4698,K56.3,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K56.3,,ICD-10 @@ -4715,16 +4715,16 @@ K58.0 Irritable bowel syndrome with diarrhoea,4713,K58.0,K55-K64 Other diseases K58.9 Irritable bowel syndrome without diarrhoea,4714,K58.9,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K58.9,,ICD-10 K59 Other functional intestinal disorders,4715,K59,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59,,ICD-10 K59.0 Other functional intestinal disorders - Constipation,4716,K59.0,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.0,,ICD-10 -K59.1 Functional diarrhoea,4717,K59.1,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.1,ORPHAcode: 1670 Chronic diarrhea with villous atrophy +K59.1 Functional diarrhoea,4717,K59.1,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.1,ORPHAcode: 1670 Chronic diarrhea with villous atrophy,ICD-10 "K59.2 Other functional intestinal disorders - Neurogenic bowel, not elsewhere classified",4718,K59.2,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.2,,ICD-10 "K59.3 Other functional intestinal disorders - Megacolon, not elsewhere classified",4719,K59.3,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.3,,ICD-10 K59.4 Other functional intestinal disorders - Anal spasm,4720,K59.4,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.4,,ICD-10 -K59.8 Other specified functional intestinal disorders,4721,K59.8,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.8,ORPHAcode: 2978 Chronic intestinal pseudoobstruction +K59.8 Other specified functional intestinal disorders,4721,K59.8,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.8,ORPHAcode: 2978 Chronic intestinal pseudoobstruction,ICD-10 "K59.9 Functional intestinal disorder, unspecified",4722,K59.9,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K59.9,,ICD-10 K60 Fissure and fistula of anal and rectal regions,4723,K60,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K60,,ICD-10 K60.0 Acute anal fissure,4724,K60.0,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K60.0,,ICD-10 "K60.2 Anal fissure, unspecified",4725,K60.2,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K60.2,,ICD-10 -K60.3 Anal fistula,4726,K60.3,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K60.3,ORPHAcode: 228113 Anal fistula +K60.3 Anal fistula,4726,K60.3,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K60.3,ORPHAcode: 228113 Anal fistula,ICD-10 K60.4 Rectal fistula,4727,K60.4,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K60.4,,ICD-10 K60.5 Anorectal fistula,4728,K60.5,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K60.5,,ICD-10 K61 Abscess of anal and rectal regions,4729,K61,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K61,,ICD-10 @@ -4740,8 +4740,8 @@ K62.2 Other diseases of anus and rectum - Anal prolapse,4738,K62.2,K55-K64 Other K62.3 Other diseases of anus and rectum - Rectal prolapse,4739,K62.3,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.3,,ICD-10 K62.4 Stenosis of anus and rectum,4740,K62.4,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.4,,ICD-10 K62.5 Haemorrhage of anus and rectum,4741,K62.5,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.5,,ICD-10 -K62.6 Ulcer of anus and rectum,4742,K62.6,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.6,ORPHAcode: 209964 Solitary rectal ulcer syndrome -K62.7 Other diseases of anus and rectum - Radiation proctitis,4743,K62.7,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.7,ORPHAcode: 70475 Radiation proctitis +K62.6 Ulcer of anus and rectum,4742,K62.6,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.6,ORPHAcode: 209964 Solitary rectal ulcer syndrome,ICD-10 +K62.7 Other diseases of anus and rectum - Radiation proctitis,4743,K62.7,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.7,ORPHAcode: 70475 Radiation proctitis,ICD-10 K62.8 Other specified diseases of anus and rectum,4744,K62.8,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.8,,ICD-10 "K62.9 Disease of anus and rectum, unspecified",4745,K62.9,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K62.9,,ICD-10 K63 Other diseases of intestine,4746,K63,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63,,ICD-10 @@ -4751,8 +4751,8 @@ K63.2 Fistula of intestine,4749,K63.2,K55-K64 Other diseases of intestines,http: K63.3 Ulcer of intestine,4750,K63.3,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63.3,,ICD-10 K63.4 Other diseases of intestine - Enteroptosis,4751,K63.4,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63.4,,ICD-10 K63.5 Polyp of colon,4752,K63.5,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63.5,,ICD-10 -K63.8 Other specified diseases of intestine,4753,K63.8,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63.8,ORPHAcode: 263665 NK-cell enteropathy -"K63.9 Disease of intestine, unspecified",4754,K63.9,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63.9,ORPHAcode: 391487 Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome +K63.8 Other specified diseases of intestine,4753,K63.8,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63.8,ORPHAcode: 263665 NK-cell enteropathy,ICD-10 +"K63.9 Disease of intestine, unspecified",4754,K63.9,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K63.9,ORPHAcode: 391487 Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome,ICD-10 K64 Haemorrhoids and perianal venous thrombosis,4755,K64,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K64,,ICD-10 K64.0 First degree haemorrhoids,4756,K64.0,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K64.0,,ICD-10 K64.1 Second degree haemorrhoids,4757,K64.1,K55-K64 Other diseases of intestines,http://identifiers.org/icd/K64.1,,ICD-10 @@ -4796,8 +4796,8 @@ K71.5 Toxic liver disease with chronic active hepatitis,4793,K71.5,K70-K77 Disea K71.7 Toxic liver disease with fibrosis and cirrhosis of liver,4795,K71.7,K70-K77 Diseases of liver,http://identifiers.org/icd/K71.7,,ICD-10 K71.8 Toxic liver disease with other disorders of liver,4796,K71.8,K70-K77 Diseases of liver,http://identifiers.org/icd/K71.8,,ICD-10 "K71.9 Toxic liver disease, unspecified",4797,K71.9,K70-K77 Diseases of liver,http://identifiers.org/icd/K71.9,,ICD-10 -"K72 Hepatic failure, not elsewhere classified",4798,K72,K70-K77 Diseases of liver,http://identifiers.org/icd/K72,ORPHAcode: 35063 Fulminant viral hepatitis -K72.0 Acute and subacute hepatic failure,4799,K72.0,K70-K77 Diseases of liver,http://identifiers.org/icd/K72.0,ORPHAcode: 90062 Acute liver failure +"K72 Hepatic failure, not elsewhere classified",4798,K72,K70-K77 Diseases of liver,http://identifiers.org/icd/K72,ORPHAcode: 35063 Fulminant viral hepatitis,ICD-10 +K72.0 Acute and subacute hepatic failure,4799,K72.0,K70-K77 Diseases of liver,http://identifiers.org/icd/K72.0,ORPHAcode: 90062 Acute liver failure,ICD-10 K72.1 Chronic hepatic failure,4800,K72.1,K70-K77 Diseases of liver,http://identifiers.org/icd/K72.1,,ICD-10 "K72.9 Hepatic failure, unspecified",4801,K72.9,K70-K77 Diseases of liver,http://identifiers.org/icd/K72.9,,ICD-10 "K73 Chronic hepatitis, not elsewhere classified",4802,K73,K70-K77 Diseases of liver,http://identifiers.org/icd/K73,,ICD-10 @@ -4810,28 +4810,28 @@ K74 Fibrosis and cirrhosis of liver,4808,K74,K70-K77 Diseases of liver,http://id K74.0 Hepatic fibrosis,4809,K74.0,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.0,,ICD-10 K74.1 Fibrosis and cirrhosis of liver - Hepatic sclerosis,4810,K74.1,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.1,,ICD-10 K74.2 Hepatic fibrosis with hepatic sclerosis,4811,K74.2,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.2,,ICD-10 -K74.3 Primary biliary cirrhosis,4812,K74.3,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.3,ORPHAcode: 186 Primary biliary cholangitis +K74.3 Primary biliary cirrhosis,4812,K74.3,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.3,ORPHAcode: 186 Primary biliary cholangitis,ICD-10 K74.4 Secondary biliary cirrhosis,4813,K74.4,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.4,,ICD-10 "K74.5 Biliary cirrhosis, unspecified",4814,K74.5,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.5,,ICD-10 -K74.6 Other and unspecified cirrhosis of liver,4815,K74.6,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.6,ORPHAcode: 209919 Idiopathic copper-associated cirrhosis +K74.6 Other and unspecified cirrhosis of liver,4815,K74.6,K70-K77 Diseases of liver,http://identifiers.org/icd/K74.6,ORPHAcode: 209919 Idiopathic copper-associated cirrhosis,ICD-10 K75 Other inflammatory liver diseases,4816,K75,K70-K77 Diseases of liver,http://identifiers.org/icd/K75,,ICD-10 K75.0 Abscess of liver,4817,K75.0,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.0,,ICD-10 K75.1 Other inflammatory liver diseases - Phlebitis of portal vein,4818,K75.1,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.1,,ICD-10 K75.2 Other inflammatory liver diseases - Nonspecific reactive hepatitis,4819,K75.2,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.2,,ICD-10 "K75.3 Other inflammatory liver diseases - Granulomatous hepatitis, not elsewhere classified",4820,K75.3,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.3,,ICD-10 -K75.4 Other inflammatory liver diseases - Autoimmune hepatitis,4821,K75.4,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.4,ORPHAcode: 2137 Autoimmune hepatitis -K75.8 Other specified inflammatory liver diseases,4822,K75.8,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.8,ORPHAcode: 90003 Inflammatory pseudotumor of the liver +K75.4 Other inflammatory liver diseases - Autoimmune hepatitis,4821,K75.4,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.4,ORPHAcode: 2137 Autoimmune hepatitis,ICD-10 +K75.8 Other specified inflammatory liver diseases,4822,K75.8,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.8,ORPHAcode: 90003 Inflammatory pseudotumor of the liver,ICD-10 "K75.9 Inflammatory liver disease, unspecified",4823,K75.9,K70-K77 Diseases of liver,http://identifiers.org/icd/K75.9,,ICD-10 K76 Other diseases of liver,4824,K76,K70-K77 Diseases of liver,http://identifiers.org/icd/K76,,ICD-10 -"K76.0 Fatty (change of) liver, not elsewhere classified",4825,K76.0,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.0,ORPHAcode: 300293 Transient infantile hypertriglyceridemia and hepatosteatosis +"K76.0 Fatty (change of) liver, not elsewhere classified",4825,K76.0,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.0,ORPHAcode: 300293 Transient infantile hypertriglyceridemia and hepatosteatosis,ICD-10 K76.1 Chronic passive congestion of liver,4826,K76.1,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.1,,ICD-10 K76.2 Central haemorrhagic necrosis of liver,4827,K76.2,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.2,,ICD-10 K76.3 Infarction of liver,4828,K76.3,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.3,,ICD-10 K76.4 Other diseases of liver - Peliosis hepatis,4829,K76.4,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.4,,ICD-10 -K76.5 Other diseases of liver - Hepatic veno-occlusive disease,4830,K76.5,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.5,ORPHAcode: 890 Hepatic veno-occlusive disease +K76.5 Other diseases of liver - Hepatic veno-occlusive disease,4830,K76.5,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.5,ORPHAcode: 890 Hepatic veno-occlusive disease,ICD-10 K76.6 Other diseases of liver - Portal hypertension,4831,K76.6,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.6,,ICD-10 K76.7 Other diseases of liver - Hepatorenal syndrome,4832,K76.7,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.7,,ICD-10 -K76.8 Other specified diseases of liver,4833,K76.8,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.8,ORPHAcode: 172 Progressive familial intrahepatic cholestasis +K76.8 Other specified diseases of liver,4833,K76.8,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.8,ORPHAcode: 172 Progressive familial intrahepatic cholestasis,ICD-10 "K76.9 Liver disease, unspecified",4834,K76.9,K70-K77 Diseases of liver,http://identifiers.org/icd/K76.9,,ICD-10 K77 Liver disorders in diseases classified elsewhere,4835,K77,K70-K77 Diseases of liver,http://identifiers.org/icd/K77,,ICD-10 K77.0 Liver disorders in infectious and parasitic diseases classified elsewhere,4836,K77.0,K70-K77 Diseases of liver,http://identifiers.org/icd/K77.0,,ICD-10 @@ -4841,10 +4841,10 @@ K80 Cholelithiasis,4839,K80,"K80-K87 Disorders of gallbladder, biliary tract and K80.0 Cholelithiasis - Calculus of gallbladder with acute cholecystitis,4840,K80.0,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.0,,ICD-10 K80.1 Cholelithiasis - Calculus of gallbladder with other cholecystitis,4841,K80.1,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.1,,ICD-10 K80.2 Cholelithiasis - Calculus of gallbladder without cholecystitis,4842,K80.2,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.2,,ICD-10 -K80.3 Cholelithiasis - Calculus of bile duct with cholangitis,4843,K80.3,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.3,ORPHAcode: 480506 Primary intrahepatic lithiasis +K80.3 Cholelithiasis - Calculus of bile duct with cholangitis,4843,K80.3,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.3,ORPHAcode: 480506 Primary intrahepatic lithiasis,ICD-10 K80.4 Cholelithiasis - Calculus of bile duct with cholecystitis,4844,K80.4,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.4,,ICD-10 K80.5 Cholelithiasis - Calculus of bile duct without cholangitis or cholecystitis,4845,K80.5,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.5,,ICD-10 -K80.8 Other cholelithiasis,4846,K80.8,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.8,ORPHAcode: 69663 Low phospholipid-associated cholelithiasis +K80.8 Other cholelithiasis,4846,K80.8,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K80.8,ORPHAcode: 69663 Low phospholipid-associated cholelithiasis,ICD-10 K81 Cholecystitis,4847,K81,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K81,,ICD-10 K81.0 Acute cholecystitis,4848,K81.0,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K81.0,,ICD-10 K81.1 Chronic cholecystitis,4849,K81.1,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K81.1,,ICD-10 @@ -4859,13 +4859,13 @@ K82.4 Cholesterolosis of gallbladder,4857,K82.4,"K80-K87 Disorders of gallbladde K82.8 Other specified diseases of gallbladder,4858,K82.8,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K82.8,,ICD-10 "K82.9 Disease of gallbladder, unspecified",4859,K82.9,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K82.9,,ICD-10 K83 Other diseases of biliary tract,4860,K83,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83,,ICD-10 -K83.0 Other diseases of biliary tract - Cholangitis,4861,K83.0,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.0,ORPHAcode: 171 Primary sclerosing cholangitis -K83.1 Obstruction of bile duct,4862,K83.1,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.1,ORPHAcode: 65682 Benign recurrent intrahepatic cholestasis +K83.0 Other diseases of biliary tract - Cholangitis,4861,K83.0,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.0,ORPHAcode: 171 Primary sclerosing cholangitis,ICD-10 +K83.1 Obstruction of bile duct,4862,K83.1,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.1,ORPHAcode: 65682 Benign recurrent intrahepatic cholestasis,ICD-10 K83.2 Perforation of bile duct,4863,K83.2,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.2,,ICD-10 K83.3 Fistula of bile duct,4864,K83.3,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.3,,ICD-10 K83.4 Spasm of sphincter of Oddi,4865,K83.4,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.4,,ICD-10 K83.5 Biliary cyst,4866,K83.5,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.5,,ICD-10 -K83.8 Other specified diseases of biliary tract,4867,K83.8,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.8,ORPHAcode: 480512 Idiopathic ductopenia +K83.8 Other specified diseases of biliary tract,4867,K83.8,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.8,ORPHAcode: 480512 Idiopathic ductopenia,ICD-10 "K83.9 Disease of biliary tract, unspecified",4868,K83.9,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K83.9,,ICD-10 K85 Acute pancreatitis,4869,K85,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K85,,ICD-10 K85.0 Idiopathic acute pancreatitis,4870,K85.0,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K85.0,,ICD-10 @@ -4876,7 +4876,7 @@ K85.8 Other acute pancreatitis,4874,K85.8,"K80-K87 Disorders of gallbladder, bil "K85.9 Acute pancreatitis, unspecified",4875,K85.9,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K85.9,,ICD-10 K86 Other diseases of pancreas,4876,K86,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K86,,ICD-10 K86.0 Other diseases of pancreas - Alcohol-induced chronic pancreatitis,4877,K86.0,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K86.0,,ICD-10 -K86.1 Other chronic pancreatitis,4878,K86.1,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K86.1,ORPHAcode: 676 Hereditary chronic pancreatitis +K86.1 Other chronic pancreatitis,4878,K86.1,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K86.1,ORPHAcode: 676 Hereditary chronic pancreatitis,ICD-10 K86.2 Cyst of pancreas,4879,K86.2,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K86.2,,ICD-10 K86.3 Pseudocyst of pancreas,4880,K86.3,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K86.3,,ICD-10 K86.8 Other specified diseases of pancreas,4881,K86.8,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K86.8,,ICD-10 @@ -4887,17 +4887,17 @@ K87.0 Disorders of gallbladder and biliary tract in diseases classified elsewher K87.1 Disorders of pancreas in diseases classified elsewhere,4886,K87.1,"K80-K87 Disorders of gallbladder, biliary tract and pancreas",http://identifiers.org/icd/K87.1,,ICD-10 K90-K93 Other diseases of the digestive system,4887,,XI Diseases of the digestive system,,,ICD-10 K90 Intestinal malabsorption,4888,K90,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90,,ICD-10 -K90.0 Intestinal malabsorption - Coeliac disease,4889,K90.0,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.0,ORPHAcode: 398063 Refractory celiac disease +K90.0 Intestinal malabsorption - Coeliac disease,4889,K90.0,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.0,ORPHAcode: 398063 Refractory celiac disease,ICD-10 K90.1 Intestinal malabsorption - Tropical sprue,4890,K90.1,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.1,,ICD-10 "K90.2 Intestinal malabsorption - Blind loop syndrome, not elsewhere classified",4891,K90.2,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.2,,ICD-10 -K90.3 Intestinal malabsorption - Pancreatic steatorrhoea,4892,K90.3,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.3,ORPHAcode: 309031 Pancreatic triacylglycerol lipase deficiency +K90.3 Intestinal malabsorption - Pancreatic steatorrhoea,4892,K90.3,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.3,ORPHAcode: 309031 Pancreatic triacylglycerol lipase deficiency,ICD-10 "K90.4 Malabsorption due to intolerance, not elsewhere classified",4893,K90.4,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.4,,ICD-10 -K90.8 Other intestinal malabsorption,4894,K90.8,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.8,ORPHAcode: 84065 Idiopathic malabsorption due to bile acid synthesis defects +K90.8 Other intestinal malabsorption,4894,K90.8,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.8,ORPHAcode: 84065 Idiopathic malabsorption due to bile acid synthesis defects,ICD-10 "K90.9 Intestinal malabsorption, unspecified",4895,K90.9,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K90.9,,ICD-10 "K91 Postprocedural disorders of digestive system, not elsewhere classified",4896,K91,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91,,ICD-10 "K91.0 Postprocedural disorders of digestive system, not elsewhere classified - Vomiting following gastrointestinal surgery",4897,K91.0,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91.0,,ICD-10 "K91.1 Postprocedural disorders of digestive system, not elsewhere classified - Postgastric surgery syndromes",4898,K91.1,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91.1,,ICD-10 -"K91.2 Postsurgical malabsorption, not elsewhere classified",4899,K91.2,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91.2,ORPHAcode: 95427 Secondary short bowel syndrome +"K91.2 Postsurgical malabsorption, not elsewhere classified",4899,K91.2,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91.2,ORPHAcode: 95427 Secondary short bowel syndrome,ICD-10 "K91.3 Postprocedural disorders of digestive system, not elsewhere classified - Postoperative intestinal obstruction",4900,K91.3,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91.3,,ICD-10 "K91.4 Postprocedural disorders of digestive system, not elsewhere classified - Colostomy and enterostomy malfunction",4901,K91.4,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91.4,,ICD-10 "K91.5 Postprocedural disorders of digestive system, not elsewhere classified - Postcholecystectomy syndrome",4902,K91.5,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K91.5,,ICD-10 @@ -4915,8 +4915,8 @@ K93.1 Megacolon in Chagas disease,4913,K93.1,K90-K93 Other diseases of the diges K93.8 Disorders of other specified digestive organs in diseases classified elsewhere,4914,K93.8,K90-K93 Other diseases of the digestive system,http://identifiers.org/icd/K93.8,,ICD-10 XII Diseases of the skin and subcutaneous tissue,4915,,,,,ICD-10 L00-L08 Infections of the skin and subcutaneous tissue,4916,,XII Diseases of the skin and subcutaneous tissue,,,ICD-10 -L00 Staphylococcal scalded skin syndrome,4917,L00,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L00,ORPHAcode: 36236 Staphylococcal scalded skin syndrome -L01.0 Impetigo [any organism] [any site],4918,L01.0,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L01.0,ORPHAcode: 36237 Bullous impetigo +L00 Staphylococcal scalded skin syndrome,4917,L00,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L00,ORPHAcode: 36236 Staphylococcal scalded skin syndrome,ICD-10 +L01.0 Impetigo [any organism] [any site],4918,L01.0,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L01.0,ORPHAcode: 36237 Bullous impetigo,ICD-10 L01.1 Impetigo - Impetiginization of other dermatoses,4919,L01.1,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L01.1,,ICD-10 "L02 Cutaneous abscess, furuncle and carbuncle",4920,L02,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L02,,ICD-10 "L02.0 Cutaneous abscess, furuncle and carbuncle of face",4921,L02.0,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L02.0,,ICD-10 @@ -4947,16 +4947,16 @@ L05.9 Pilonidal cyst without abscess,4945,L05.9,L00-L08 Infections of the skin a L08 Other local infections of skin and subcutaneous tissue,4946,L08,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L08,,ICD-10 L08.0 Other local infections of skin and subcutaneous tissue - Pyoderma,4947,L08.0,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L08.0,,ICD-10 L08.1 Other local infections of skin and subcutaneous tissue - Erythrasma,4948,L08.1,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L08.1,,ICD-10 -L08.8 Other specified local infections of skin and subcutaneous tissue,4949,L08.8,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L08.8,ORPHAcode: 345 Dissecting cellulitis of the scalp +L08.8 Other specified local infections of skin and subcutaneous tissue,4949,L08.8,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L08.8,ORPHAcode: 345 Dissecting cellulitis of the scalp,ICD-10 "L08.9 Local infection of skin and subcutaneous tissue, unspecified",4950,L08.9,L00-L08 Infections of the skin and subcutaneous tissue,http://identifiers.org/icd/L08.9,,ICD-10 L10-L14 Bullous disorders,4951,,XII Diseases of the skin and subcutaneous tissue,,,ICD-10 L10 Pemphigus,4952,L10,L10-L14 Bullous disorders,http://identifiers.org/icd/L10,,ICD-10 -L10.0 Pemphigus vulgaris,4953,L10.0,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.0,ORPHAcode: 704 Pemphigus vulgaris -L10.1 Pemphigus vegetans,4954,L10.1,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.1,ORPHAcode: 79479 Pemphigus vegetans -L10.2 Pemphigus foliaceus,4955,L10.2,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.2,ORPHAcode: 79481 Pemphigus foliaceus -L10.4 Pemphigus erythematosus,4956,L10.4,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.4,ORPHAcode: 79480 Pemphigus erythematosus +L10.0 Pemphigus vulgaris,4953,L10.0,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.0,ORPHAcode: 704 Pemphigus vulgaris,ICD-10 +L10.1 Pemphigus vegetans,4954,L10.1,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.1,ORPHAcode: 79479 Pemphigus vegetans,ICD-10 +L10.2 Pemphigus foliaceus,4955,L10.2,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.2,ORPHAcode: 79481 Pemphigus foliaceus,ICD-10 +L10.4 Pemphigus erythematosus,4956,L10.4,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.4,ORPHAcode: 79480 Pemphigus erythematosus,ICD-10 L10.5 Drug-induced pemphigus,4957,L10.5,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.5,,ICD-10 -L10.8 Other pemphigus,4958,L10.8,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.8,ORPHAcode: 46488 Linear IgA dermatosis +L10.8 Other pemphigus,4958,L10.8,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.8,ORPHAcode: 46488 Linear IgA dermatosis,ICD-10 "L10.9 Pemphigus, unspecified",4959,L10.9,L10-L14 Bullous disorders,http://identifiers.org/icd/L10.9,,ICD-10 L11 Other acantholytic disorders,4960,L11,L10-L14 Bullous disorders,http://identifiers.org/icd/L11,,ICD-10 L11.0 Other acantholytic disorders - Acquired keratosis follicularis,4961,L11.0,L10-L14 Bullous disorders,http://identifiers.org/icd/L11.0,,ICD-10 @@ -4964,15 +4964,15 @@ L11.1 Transient acantholytic dermatosis [Grover],4962,L11.1,L10-L14 Bullous diso L11.8 Other specified acantholytic disorders,4963,L11.8,L10-L14 Bullous disorders,http://identifiers.org/icd/L11.8,,ICD-10 "L11.9 Acantholytic disorder, unspecified",4964,L11.9,L10-L14 Bullous disorders,http://identifiers.org/icd/L11.9,,ICD-10 L12 Pemphigoid,4965,L12,L10-L14 Bullous disorders,http://identifiers.org/icd/L12,,ICD-10 -L12.0 Bullous pemphigoid,4966,L12.0,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.0,ORPHAcode: 703 Bullous pemphigoid -L12.1 Cicatricial pemphigoid,4967,L12.1,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.1,ORPHAcode: 46486 Mucous membrane pemphigoid +L12.0 Bullous pemphigoid,4966,L12.0,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.0,ORPHAcode: 703 Bullous pemphigoid,ICD-10 +L12.1 Cicatricial pemphigoid,4967,L12.1,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.1,ORPHAcode: 46486 Mucous membrane pemphigoid,ICD-10 L12.2 Pemphigoid - Chronic bullous disease of childhood,4968,L12.2,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.2,,ICD-10 -L12.3 Pemphigoid - Acquired epidermolysis bullosa,4969,L12.3,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.3,ORPHAcode: 46487 Epidermolysis bullosa acquisita -L12.8 Other pemphigoid,4970,L12.8,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.8,ORPHAcode: 63275 Pemphigoid gestationis +L12.3 Pemphigoid - Acquired epidermolysis bullosa,4969,L12.3,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.3,ORPHAcode: 46487 Epidermolysis bullosa acquisita,ICD-10 +L12.8 Other pemphigoid,4970,L12.8,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.8,ORPHAcode: 63275 Pemphigoid gestationis,ICD-10 "L12.9 Pemphigoid, unspecified",4971,L12.9,L10-L14 Bullous disorders,http://identifiers.org/icd/L12.9,,ICD-10 L13 Other bullous disorders,4972,L13,L10-L14 Bullous disorders,http://identifiers.org/icd/L13,,ICD-10 -L13.0 Other bullous disorders - Dermatitis herpetiformis,4973,L13.0,L10-L14 Bullous disorders,http://identifiers.org/icd/L13.0,ORPHAcode: 1656 Dermatitis herpetiformis -L13.1 Other bullous disorders - Subcorneal pustular dermatitis,4974,L13.1,L10-L14 Bullous disorders,http://identifiers.org/icd/L13.1,ORPHAcode: 48377 Subcorneal pustular dermatosis +L13.0 Other bullous disorders - Dermatitis herpetiformis,4973,L13.0,L10-L14 Bullous disorders,http://identifiers.org/icd/L13.0,ORPHAcode: 1656 Dermatitis herpetiformis,ICD-10 +L13.1 Other bullous disorders - Subcorneal pustular dermatitis,4974,L13.1,L10-L14 Bullous disorders,http://identifiers.org/icd/L13.1,ORPHAcode: 48377 Subcorneal pustular dermatosis,ICD-10 L13.8 Other specified bullous disorders,4975,L13.8,L10-L14 Bullous disorders,http://identifiers.org/icd/L13.8,,ICD-10 "L13.9 Bullous disorder, unspecified",4976,L13.9,L10-L14 Bullous disorders,http://identifiers.org/icd/L13.9,,ICD-10 L14 Bullous disorders in diseases classified elsewhere,4977,L14,L10-L14 Bullous disorders,http://identifiers.org/icd/L14,,ICD-10 @@ -4983,7 +4983,7 @@ L20.8 Other atopic dermatitis,4981,L20.8,L20-L30 Dermatitis and eczema,http://id "L20.9 Atopic dermatitis, unspecified",4982,L20.9,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L20.9,,ICD-10 L21 Seborrhoeic dermatitis,4983,L21,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L21,,ICD-10 L21.0 Seborrhoeic dermatitis - Seborrhoea capitis,4984,L21.0,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L21.0,,ICD-10 -L21.1 Seborrhoeic infantile dermatitis,4985,L21.1,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L21.1,ORPHAcode: 314 Erythroderma desquamativum +L21.1 Seborrhoeic infantile dermatitis,4985,L21.1,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L21.1,ORPHAcode: 314 Erythroderma desquamativum,ICD-10 L21.8 Other seborrhoeic dermatitis,4986,L21.8,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L21.8,,ICD-10 "L21.9 Seborrhoeic dermatitis, unspecified",4987,L21.9,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L21.9,,ICD-10 L22 Diaper [napkin] dermatitis,4988,L22,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L22,,ICD-10 @@ -5034,13 +5034,13 @@ L29.0 Pruritus ani,5032,L29.0,L20-L30 Dermatitis and eczema,http://identifiers.o L29.1 Pruritus scroti,5033,L29.1,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L29.1,,ICD-10 L29.2 Pruritus vulvae,5034,L29.2,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L29.2,,ICD-10 "L29.3 Anogenital pruritus, unspecified",5035,L29.3,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L29.3,,ICD-10 -L29.8 Other pruritus,5036,L29.8,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L29.8,ORPHAcode: 94059 Uremic pruritus +L29.8 Other pruritus,5036,L29.8,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L29.8,ORPHAcode: 94059 Uremic pruritus,ICD-10 "L29.9 Pruritus, unspecified",5037,L29.9,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L29.9,,ICD-10 L30 Other dermatitis,5038,L30,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30,,ICD-10 L30.0 Nummular dermatitis,5039,L30.0,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.0,,ICD-10 L30.1 Other dermatitis - Dyshidrosis [pompholyx],5040,L30.1,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.1,,ICD-10 L30.2 Other dermatitis - Cutaneous autosensitization,5041,L30.2,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.2,,ICD-10 -L30.3 Infective dermatitis,5042,L30.3,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.3,ORPHAcode: 289347 Infective dermatitis associated with HTLV-1 +L30.3 Infective dermatitis,5042,L30.3,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.3,ORPHAcode: 289347 Infective dermatitis associated with HTLV-1,ICD-10 L30.4 Other dermatitis - Erythema intertrigo,5043,L30.4,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.4,,ICD-10 L30.5 Other dermatitis - Pityriasis alba,5044,L30.5,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.5,,ICD-10 L30.8 Other specified dermatitis,5045,L30.8,L20-L30 Dermatitis and eczema,http://identifiers.org/icd/L30.8,,ICD-10 @@ -5048,9 +5048,9 @@ L30.8 Other specified dermatitis,5045,L30.8,L20-L30 Dermatitis and eczema,http:/ L40-L45 Papulosquamous disorders,5047,,XII Diseases of the skin and subcutaneous tissue,,,ICD-10 L40 Psoriasis,5048,L40,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40,,ICD-10 L40.0 Psoriasis vulgaris,5049,L40.0,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.0,,ICD-10 -L40.1 Generalized pustular psoriasis,5050,L40.1,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.1,ORPHAcode: 247353 Generalized pustular psoriasis -L40.2 Psoriasis - Acrodermatitis continua,5051,L40.2,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.2,ORPHAcode: 163931 Acrodermatitis continua of Hallopeau -L40.3 Psoriasis - Pustulosis palmaris et plantaris,5052,L40.3,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.3,ORPHAcode: 163927 Pustulosis palmaris et plantaris +L40.1 Generalized pustular psoriasis,5050,L40.1,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.1,ORPHAcode: 247353 Generalized pustular psoriasis,ICD-10 +L40.2 Psoriasis - Acrodermatitis continua,5051,L40.2,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.2,ORPHAcode: 163931 Acrodermatitis continua of Hallopeau,ICD-10 +L40.3 Psoriasis - Pustulosis palmaris et plantaris,5052,L40.3,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.3,ORPHAcode: 163927 Pustulosis palmaris et plantaris,ICD-10 L40.4 Guttate psoriasis,5053,L40.4,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.4,,ICD-10 L40.5 Arthropathic psoriasis,5054,L40.5,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.5,,ICD-10 L40.8 Other psoriasis,5055,L40.8,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L40.8,,ICD-10 @@ -5066,13 +5066,13 @@ L41.8 Other parapsoriasis,5063,L41.8,L40-L45 Papulosquamous disorders,http://ide L42 Pityriasis rosea,5065,L42,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L42,,ICD-10 L43 Lichen planus,5066,L43,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43,,ICD-10 L43.0 Hypertrophic lichen planus,5067,L43.0,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.0,,ICD-10 -L43.1 Bullous lichen planus,5068,L43.1,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.1,ORPHAcode: 33408 Bullous lichen planus +L43.1 Bullous lichen planus,5068,L43.1,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.1,ORPHAcode: 33408 Bullous lichen planus,ICD-10 L43.2 Lichenoid drug reaction,5069,L43.2,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.2,,ICD-10 L43.3 Subacute (active) lichen planus,5070,L43.3,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.3,,ICD-10 -L43.8 Other lichen planus,5071,L43.8,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.8,ORPHAcode: 31142 Oral erosive lichen +L43.8 Other lichen planus,5071,L43.8,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.8,ORPHAcode: 31142 Oral erosive lichen,ICD-10 "L43.9 Lichen planus, unspecified",5072,L43.9,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L43.9,,ICD-10 L44 Other papulosquamous disorders,5073,L44,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L44,,ICD-10 -L44.0 Other papulosquamous disorders - Pityriasis rubra pilaris,5074,L44.0,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L44.0,ORPHAcode: 2897 Pityriasis rubra pilaris +L44.0 Other papulosquamous disorders - Pityriasis rubra pilaris,5074,L44.0,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L44.0,ORPHAcode: 2897 Pityriasis rubra pilaris,ICD-10 L44.1 Other papulosquamous disorders - Lichen nitidus,5075,L44.1,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L44.1,,ICD-10 L44.2 Other papulosquamous disorders - Lichen striatus,5076,L44.2,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L44.2,,ICD-10 L44.3 Other papulosquamous disorders - Lichen ruber moniliformis,5077,L44.3,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L44.3,,ICD-10 @@ -5082,17 +5082,17 @@ L44.8 Other specified papulosquamous disorders,5079,L44.8,L40-L45 Papulosquamous L45 Papulosquamous disorders in diseases classified elsewhere,5081,L45,L40-L45 Papulosquamous disorders,http://identifiers.org/icd/L45,,ICD-10 L50.0 Allergic urticaria,5082,L50.0,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.0,,ICD-10 L50.1 Idiopathic urticaria,5083,L50.1,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.1,,ICD-10 -L50.2 Urticaria due to cold and heat,5084,L50.2,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.2,ORPHAcode: 47045 Familial cold urticaria +L50.2 Urticaria due to cold and heat,5084,L50.2,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.2,ORPHAcode: 47045 Familial cold urticaria,ICD-10 L50.3 Dermatographic urticaria,5085,L50.3,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.3,,ICD-10 L50.4 Vibratory urticaria,5086,L50.4,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.4,,ICD-10 L50.5 Cholinergic urticaria,5087,L50.5,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.5,,ICD-10 L50.6 Contact urticaria,5088,L50.6,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.6,,ICD-10 -L50.8 Other urticaria,5089,L50.8,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.8,ORPHAcode: 37748 Schnitzler syndrome +L50.8 Other urticaria,5089,L50.8,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.8,ORPHAcode: 37748 Schnitzler syndrome,ICD-10 "L50.9 Urticaria, unspecified",5090,L50.9,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L50.9,,ICD-10 L51 Erythema multiforme,5091,L51,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L51,,ICD-10 L51.0 Nonbullous erythema multiforme,5092,L51.0,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L51.0,,ICD-10 L51.1 Bullous erythema multiforme,5093,L51.1,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L51.1,,ICD-10 -L51.2 Erythema multiforme - Toxic epidermal necrolysis [Lyell],5094,L51.2,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L51.2,ORPHAcode: 95455 Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum +L51.2 Erythema multiforme - Toxic epidermal necrolysis [Lyell],5094,L51.2,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L51.2,ORPHAcode: 95455 Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum,ICD-10 L51.8 Other erythema multiforme,5095,L51.8,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L51.8,,ICD-10 "L51.9 Erythema multiforme, unspecified",5096,L51.9,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L51.9,,ICD-10 L52 Erythema nodosum,5097,L52,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L52,,ICD-10 @@ -5101,7 +5101,7 @@ L53.0 Other erythematous conditions - Toxic erythema,5099,L53.0,L50-L54 Urticari L53.1 Other erythematous conditions - Erythema annulare centrifugum,5100,L53.1,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L53.1,,ICD-10 L53.2 Other erythematous conditions - Erythema marginatum,5101,L53.2,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L53.2,,ICD-10 L53.3 Other chronic figurate erythema,5102,L53.3,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L53.3,,ICD-10 -L53.8 Other specified erythematous conditions,5103,L53.8,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L53.8,ORPHAcode: 439196 Zinc-responsive necrolytic acral erythema +L53.8 Other specified erythematous conditions,5103,L53.8,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L53.8,ORPHAcode: 439196 Zinc-responsive necrolytic acral erythema,ICD-10 "L53.9 Erythematous condition, unspecified",5104,L53.9,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L53.9,,ICD-10 L54 Erythema in diseases classified elsewhere,5105,L54,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L54,,ICD-10 L54.0 Erythema marginatum in acute rheumatic fever,5106,L54.0,L50-L54 Urticaria and erythema,http://identifiers.org/icd/L54.0,,ICD-10 @@ -5117,18 +5117,18 @@ L56 Other acute skin changes due to ultraviolet radiation,5115,L56,L55-L59 Radia L56.0 Drug phototoxic response,5116,L56.0,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.0,,ICD-10 L56.1 Drug photoallergic response,5117,L56.1,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.1,,ICD-10 L56.2 Photocontact dermatitis [berloque dermatitis],5118,L56.2,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.2,,ICD-10 -L56.3 Other acute skin changes due to ultraviolet radiation - Solar urticaria,5119,L56.3,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.3,ORPHAcode: 97230 Solar urticaria -L56.4 Other acute skin changes due to ultraviolet radiation - Polymorphous light eruption,5120,L56.4,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.4,ORPHAcode: 330058 Hydroa vacciniforme +L56.3 Other acute skin changes due to ultraviolet radiation - Solar urticaria,5119,L56.3,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.3,ORPHAcode: 97230 Solar urticaria,ICD-10 +L56.4 Other acute skin changes due to ultraviolet radiation - Polymorphous light eruption,5120,L56.4,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.4,ORPHAcode: 330058 Hydroa vacciniforme,ICD-10 L56.8 Other specified acute skin changes due to ultraviolet radiation,5121,L56.8,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.8,,ICD-10 "L56.9 Acute skin change due to ultraviolet radiation, unspecified",5122,L56.9,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L56.9,,ICD-10 L57 Skin changes due to chronic exposure to nonionizing radiation,5123,L57,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57,,ICD-10 L57.0 Actinic keratosis,5124,L57.0,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.0,,ICD-10 -L57.1 Skin changes due to chronic exposure to nonionizing radiation - Actinic reticuloid,5125,L57.1,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.1,ORPHAcode: 330064 Chronic actinic dermatitis +L57.1 Skin changes due to chronic exposure to nonionizing radiation - Actinic reticuloid,5125,L57.1,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.1,ORPHAcode: 330064 Chronic actinic dermatitis,ICD-10 L57.2 Skin changes due to chronic exposure to nonionizing radiation - Cutis rhomboidalis nuchae,5126,L57.2,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.2,,ICD-10 L57.3 Skin changes due to chronic exposure to nonionizing radiation - Poikiloderma of Civatte,5127,L57.3,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.3,,ICD-10 L57.4 Skin changes due to chronic exposure to nonionizing radiation - Cutis laxa senilis,5128,L57.4,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.4,,ICD-10 L57.5 Skin changes due to chronic exposure to nonionizing radiation - Actinic granuloma,5129,L57.5,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.5,,ICD-10 -L57.8 Other skin changes due to chronic exposure to nonionizing radiation,5130,L57.8,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.8,ORPHAcode: 2881 Cutaneous photosensitivity-lethal colitis syndrome +L57.8 Other skin changes due to chronic exposure to nonionizing radiation,5130,L57.8,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.8,ORPHAcode: 2881 Cutaneous photosensitivity-lethal colitis syndrome,ICD-10 "L57.9 Skin changes due to chronic exposure to nonionizing radiation, unspecified",5131,L57.9,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L57.9,,ICD-10 L58 Radiodermatitis,5132,L58,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L58,,ICD-10 L58.0 Acute radiodermatitis,5133,L58.0,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L58.0,,ICD-10 @@ -5137,24 +5137,24 @@ L58.1 Chronic radiodermatitis,5134,L58.1,L55-L59 Radiation-related disorders of L70.4 Infantile acne,5136,L70.4,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.4,,ICD-10 L59 Other disorders of skin and subcutaneous tissue related to radiation,5137,L59,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L59,,ICD-10 L59.0 Other disorders of skin and subcutaneous tissue related to radiation - Erythema ab igne [dermatitis ab igne],5138,L59.0,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L59.0,,ICD-10 -L59.8 Other specified disorders of skin and subcutaneous tissue related to radiation,5139,L59.8,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L59.8,ORPHAcode: 231031 Erythema palmare hereditarium +L59.8 Other specified disorders of skin and subcutaneous tissue related to radiation,5139,L59.8,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L59.8,ORPHAcode: 231031 Erythema palmare hereditarium,ICD-10 "L59.9 Disorder of skin and subcutaneous tissue related to radiation, unspecified",5140,L59.9,L55-L59 Radiation-related disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L59.9,,ICD-10 L60-L75 Disorders of skin appendages,5141,,XII Diseases of the skin and subcutaneous tissue,,,ICD-10 L60 Nail disorders,5142,L60,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60,,ICD-10 L60.0 Ingrowing nail,5143,L60.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.0,,ICD-10 L60.1 Nail disorders - Onycholysis,5144,L60.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.1,,ICD-10 L60.2 Nail disorders - Onychogryphosis,5145,L60.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.2,,ICD-10 -L60.3 Nail dystrophy,5146,L60.3,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.3,ORPHAcode: 79153 Idiopathic trachyonychia +L60.3 Nail dystrophy,5146,L60.3,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.3,ORPHAcode: 79153 Idiopathic trachyonychia,ICD-10 L60.4 Nail disorders - Beau lines,5147,L60.4,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.4,,ICD-10 -L60.5 Yellow nail syndrome,5148,L60.5,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.5,ORPHAcode: 662 Yellow nail syndrome -L60.8 Other nail disorders,5149,L60.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.8,ORPHAcode: 2045 FLOTCH syndrome +L60.5 Yellow nail syndrome,5148,L60.5,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.5,ORPHAcode: 662 Yellow nail syndrome,ICD-10 +L60.8 Other nail disorders,5149,L60.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.8,ORPHAcode: 2045 FLOTCH syndrome,ICD-10 "L60.9 Nail disorder, unspecified",5150,L60.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L60.9,,ICD-10 L62 Nail disorders in diseases classified elsewhere,5151,L62,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L62,,ICD-10 L62.0 Clubbed nail pachydermoperiostosis,5152,L62.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L62.0,,ICD-10 L62.8 Nail disorders in other diseases classified elsewhere,5153,L62.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L62.8,,ICD-10 L63 Alopecia areata,5154,L63,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63,,ICD-10 -L63.0 Alopecia (capitis) totalis,5155,L63.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63.0,ORPHAcode: 700 Alopecia totalis -L63.1 Alopecia universalis,5156,L63.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63.1,ORPHAcode: 701 Alopecia universalis +L63.0 Alopecia (capitis) totalis,5155,L63.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63.0,ORPHAcode: 700 Alopecia totalis,ICD-10 +L63.1 Alopecia universalis,5156,L63.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63.1,ORPHAcode: 701 Alopecia universalis,ICD-10 L63.2 Alopecia areata - Ophiasis,5157,L63.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63.2,,ICD-10 L63.8 Other alopecia areata,5158,L63.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63.8,,ICD-10 "L63.9 Alopecia areata, unspecified",5159,L63.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L63.9,,ICD-10 @@ -5164,36 +5164,36 @@ L64.8 Other androgenic alopecia,5162,L64.8,L60-L75 Disorders of skin appendages, "L64.9 Androgenic alopecia, unspecified",5163,L64.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L64.9,,ICD-10 L65 Other nonscarring hair loss,5164,L65,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65,,ICD-10 L65.0 Other nonscarring hair loss - Telogen effluvium,5165,L65.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65.0,,ICD-10 -L65.1 Other nonscarring hair loss - Anagen effluvium,5166,L65.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65.1,ORPHAcode: 168 Loose anagen syndrome +L65.1 Other nonscarring hair loss - Anagen effluvium,5166,L65.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65.1,ORPHAcode: 168 Loose anagen syndrome,ICD-10 L65.2 Other nonscarring hair loss - Alopecia mucinosa,5167,L65.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65.2,,ICD-10 -L65.8 Other specified nonscarring hair loss,5168,L65.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65.8,ORPHAcode: 55654 Hypotrichosis simplex +L65.8 Other specified nonscarring hair loss,5168,L65.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65.8,ORPHAcode: 55654 Hypotrichosis simplex,ICD-10 "L65.9 Nonscarring hair loss, unspecified",5169,L65.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L65.9,,ICD-10 L66 Cicatricial alopecia [scarring hair loss],5170,L66,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66,,ICD-10 -L66.0 Cicatricial alopecia [scarring hair loss] - Pseudopelade,5171,L66.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.0,ORPHAcode: 129 Pseudopelade of Brocq -L66.1 Cicatricial alopecia [scarring hair loss] - Lichen planopilaris,5172,L66.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.1,ORPHAcode: 505 Graham Little-Piccardi-Lassueur syndrome -L66.2 Cicatricial alopecia [scarring hair loss] - Folliculitis decalvans,5173,L66.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.2,ORPHAcode: 346 Quinquaud folliculitis decalvans +L66.0 Cicatricial alopecia [scarring hair loss] - Pseudopelade,5171,L66.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.0,ORPHAcode: 129 Pseudopelade of Brocq,ICD-10 +L66.1 Cicatricial alopecia [scarring hair loss] - Lichen planopilaris,5172,L66.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.1,ORPHAcode: 505 Graham Little-Piccardi-Lassueur syndrome,ICD-10 +L66.2 Cicatricial alopecia [scarring hair loss] - Folliculitis decalvans,5173,L66.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.2,ORPHAcode: 346 Quinquaud folliculitis decalvans,ICD-10 L66.3 Cicatricial alopecia [scarring hair loss] - Perifolliculitis capitis abscedens,5174,L66.3,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.3,,ICD-10 -L66.4 Cicatricial alopecia [scarring hair loss] - Folliculitis ulerythematosa reticulata,5175,L66.4,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.4,ORPHAcode: 79100 Atrophoderma vermiculata +L66.4 Cicatricial alopecia [scarring hair loss] - Folliculitis ulerythematosa reticulata,5175,L66.4,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.4,ORPHAcode: 79100 Atrophoderma vermiculata,ICD-10 L66.8 Other cicatricial alopecia,5176,L66.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.8,,ICD-10 "L66.9 Cicatricial alopecia, unspecified",5177,L66.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L66.9,,ICD-10 L67 Hair colour and hair shaft abnormalities,5178,L67,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L67,,ICD-10 L67.0 Hair colour and hair shaft abnormalities - Trichorrhexis nodosa,5179,L67.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L67.0,,ICD-10 L67.1 Variations in hair colour,5180,L67.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L67.1,,ICD-10 -L67.8 Other hair colour and hair shaft abnormalities,5181,L67.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L67.8,ORPHAcode: 720 Pili bifurcati +L67.8 Other hair colour and hair shaft abnormalities,5181,L67.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L67.8,ORPHAcode: 720 Pili bifurcati,ICD-10 "L67.9 Hair colour and hair shaft abnormality, unspecified",5182,L67.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L67.9,,ICD-10 L68 Hypertrichosis,5183,L68,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68,,ICD-10 L68.0 Hypertrichosis - Hirsutism,5184,L68.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.0,,ICD-10 -L68.1 Acquired hypertrichosis lanuginosa,5185,L68.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.1,ORPHAcode: 2221 Acquired hypertrichosis lanuginosa -L68.2 Localized hypertrichosis,5186,L68.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.2,ORPHAcode: 3387 Isolated anterior cervical hypertrichosis +L68.1 Acquired hypertrichosis lanuginosa,5185,L68.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.1,ORPHAcode: 2221 Acquired hypertrichosis lanuginosa,ICD-10 +L68.2 Localized hypertrichosis,5186,L68.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.2,ORPHAcode: 3387 Isolated anterior cervical hypertrichosis,ICD-10 L68.3 Hypertrichosis - Polytrichia,5187,L68.3,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.3,,ICD-10 -L68.8 Other hypertrichosis,5188,L68.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.8,ORPHAcode: 2026 Gingival fibromatosis-hypertrichosis syndrome +L68.8 Other hypertrichosis,5188,L68.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.8,ORPHAcode: 2026 Gingival fibromatosis-hypertrichosis syndrome,ICD-10 "L68.9 Hypertrichosis, unspecified",5189,L68.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L68.9,,ICD-10 L70 Acne,5190,L70,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70,,ICD-10 L70.0 Acne vulgaris,5191,L70.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.0,,ICD-10 L70.1 Acne conglobata,5192,L70.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.1,,ICD-10 L70.2 Acne varioliformis,5193,L70.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.2,,ICD-10 L70.3 Acne tropica,5194,L70.3,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.3,,ICD-10 -L70.5 Acné excori ,5195,L70.5,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.5,,ICD-10 +L70.5 Acné excori,5195,L70.5,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.5,,ICD-10 L70.8 Other acne,5196,L70.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.8,,ICD-10 "L70.9 Acne, unspecified",5197,L70.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L70.9,,ICD-10 L71 Rosacea,5198,L71,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L71,,ICD-10 @@ -5203,9 +5203,9 @@ L71.8 Other rosacea,5201,L71.8,L60-L75 Disorders of skin appendages,http://ident "L71.9 Rosacea, unspecified",5202,L71.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L71.9,,ICD-10 L72 Follicular cysts of skin and subcutaneous tissue,5203,L72,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72,,ICD-10 L72.0 Follicular cysts of skin and subcutaneous tissue - Epidermal cyst,5204,L72.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.0,,ICD-10 -L72.1 Follicular cysts of skin and subcutaneous tissue - Trichilemmal cyst,5205,L72.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.1,ORPHAcode: 492 Proliferating trichilemmal cyst -L72.2 Follicular cysts of skin and subcutaneous tissue - Steatocystoma multiplex,5206,L72.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.2,ORPHAcode: 841 Sebocystomatosis -L72.8 Other follicular cysts of skin and subcutaneous tissue,5207,L72.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.8,ORPHAcode: 587 Muir-Torre syndrome +L72.1 Follicular cysts of skin and subcutaneous tissue - Trichilemmal cyst,5205,L72.1,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.1,ORPHAcode: 492 Proliferating trichilemmal cyst,ICD-10 +L72.2 Follicular cysts of skin and subcutaneous tissue - Steatocystoma multiplex,5206,L72.2,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.2,ORPHAcode: 841 Sebocystomatosis,ICD-10 +L72.8 Other follicular cysts of skin and subcutaneous tissue,5207,L72.8,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.8,ORPHAcode: 587 Muir-Torre syndrome,ICD-10 "L72.9 Follicular cyst of skin and subcutaneous tissue, unspecified",5208,L72.9,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L72.9,,ICD-10 L73 Other follicular disorders,5209,L73,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L73,,ICD-10 L73.0 Other follicular disorders - Acne keloid,5210,L73.0,L60-L75 Disorders of skin appendages,http://identifiers.org/icd/L73.0,,ICD-10 @@ -5233,31 +5233,31 @@ L81 Other disorders of pigmentation,5231,L81,L80-L99 Other disorders of the skin L81.0 Postinflammatory hyperpigmentation,5232,L81.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.0,,ICD-10 L81.1 Other disorders of pigmentation - Chloasma,5233,L81.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.1,,ICD-10 L81.2 Other disorders of pigmentation - Freckles,5234,L81.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.2,,ICD-10 -L81.3 Café au lait spot,5235,L81.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.3,ORPHAcode: 2678 Neurofibromatosis type 6 -L81.4 Other melanin hyperpigmentation,5236,L81.4,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.4,ORPHAcode: 39 Acromelanosis +L81.3 Café au lait spot,5235,L81.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.3,ORPHAcode: 2678 Neurofibromatosis type 6,ICD-10 +L81.4 Other melanin hyperpigmentation,5236,L81.4,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.4,ORPHAcode: 39 Acromelanosis,ICD-10 "L81.5 Other disorders of pigmentation - Leukoderma, not elsewhere classified",5237,L81.5,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.5,,ICD-10 L81.6 Other disorders of diminished melanin formation,5238,L81.6,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.6,,ICD-10 -L81.7 Other disorders of pigmentation - Pigmented purpuric dermatosis,5239,L81.7,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.7,ORPHAcode: 95429 Angioma serpiginosum -L81.8 Other specified disorders of pigmentation,5240,L81.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.8,ORPHAcode: 41 Dyschromatosis symmetrica hereditaria +L81.7 Other disorders of pigmentation - Pigmented purpuric dermatosis,5239,L81.7,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.7,ORPHAcode: 95429 Angioma serpiginosum,ICD-10 +L81.8 Other specified disorders of pigmentation,5240,L81.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.8,ORPHAcode: 41 Dyschromatosis symmetrica hereditaria,ICD-10 "L81.9 Disorder of pigmentation, unspecified",5241,L81.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L81.9,,ICD-10 L82 Seborrhoeic keratosis,5242,L82,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L82,,ICD-10 L83 Acanthosis nigricans,5243,L83,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L83,,ICD-10 L84 Corns and callosities,5244,L84,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L84,,ICD-10 L85 Other epidermal thickening,5245,L85,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85,,ICD-10 -L85.0 Other epidermal thickening - Acquired ichthyosis,5246,L85.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.0,ORPHAcode: 454 Acquired ichthyosis +L85.0 Other epidermal thickening - Acquired ichthyosis,5246,L85.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.0,ORPHAcode: 454 Acquired ichthyosis,ICD-10 L85.1 Other epidermal thickening - Acquired keratosis [keratoderma] palmaris et plantaris,5247,L85.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.1,,ICD-10 L85.2 Other epidermal thickening - Keratosis punctata (palmaris et plantaris),5248,L85.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.2,,ICD-10 L85.3 Other epidermal thickening - Xerosis cutis,5249,L85.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.3,,ICD-10 -L85.8 Other specified epidermal thickening,5250,L85.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.8,ORPHAcode: 493 Familial keratoacanthoma +L85.8 Other specified epidermal thickening,5250,L85.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.8,ORPHAcode: 493 Familial keratoacanthoma,ICD-10 "L85.9 Epidermal thickening, unspecified",5251,L85.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L85.9,,ICD-10 L86 Keratoderma in diseases classified elsewhere,5252,L86,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L86,,ICD-10 L87 Transepidermal elimination disorders,5253,L87,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87,,ICD-10 L87.0 Transepidermal elimination disorders - Keratosis follicularis et parafollicularis in cutem penetrans [Kyrle],5254,L87.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87.0,,ICD-10 -L87.1 Transepidermal elimination disorders - Reactive perforating collagenosis,5255,L87.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87.1,ORPHAcode: 79147 Familial reactive perforating collagenosis -L87.2 Transepidermal elimination disorders - Elastosis perforans serpiginosa,5256,L87.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87.2,ORPHAcode: 79148 Elastosis perforans serpiginosa +L87.1 Transepidermal elimination disorders - Reactive perforating collagenosis,5255,L87.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87.1,ORPHAcode: 79147 Familial reactive perforating collagenosis,ICD-10 +L87.2 Transepidermal elimination disorders - Elastosis perforans serpiginosa,5256,L87.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87.2,ORPHAcode: 79148 Elastosis perforans serpiginosa,ICD-10 L87.8 Other transepidermal elimination disorders,5257,L87.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87.8,,ICD-10 "L87.9 Transepidermal elimination disorder, unspecified",5258,L87.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L87.9,,ICD-10 -L88 Pyoderma gangrenosum,5259,L88,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L88,ORPHAcode: 48104 Pyoderma gangrenosum +L88 Pyoderma gangrenosum,5259,L88,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L88,ORPHAcode: 48104 Pyoderma gangrenosum,ICD-10 L89 Decubitus ulcer and pressure area,5260,L89,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L89,,ICD-10 L89.0 Stage I decubitus ulcer and pressure area,5261,L89.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L89.0,,ICD-10 L89.1 Stage II decubitus ulcer,5262,L89.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L89.1,,ICD-10 @@ -5266,56 +5266,56 @@ L89.3 Stage IV decubitus ulcer,5264,L89.3,L80-L99 Other disorders of the skin an "L89.9 Decubitus ulcer and pressure area, unspecified",5265,L89.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L89.9,,ICD-10 L90 Atrophic disorders of skin,5266,L90,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90,,ICD-10 L90.0 Lichen sclerosus et atrophicus,5267,L90.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.0,,ICD-10 -L90.1 Anetoderma of Schweninger-Buzzi,5268,L90.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.1,ORPHAcode: 228272 Primary anetoderma +L90.1 Anetoderma of Schweninger-Buzzi,5268,L90.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.1,ORPHAcode: 228272 Primary anetoderma,ICD-10 L90.2 Anetoderma of Jadassohn-Pellizzari,5269,L90.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.2,,ICD-10 L90.3 Atrophoderma of Pasini and Pierini,5270,L90.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.3,,ICD-10 L90.4 Acrodermatitis chronica atrophicans,5271,L90.4,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.4,,ICD-10 -L90.5 Scar conditions and fibrosis of skin,5272,L90.5,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.5,ORPHAcode: 722 Hypoplasminogenemia +L90.5 Scar conditions and fibrosis of skin,5272,L90.5,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.5,ORPHAcode: 722 Hypoplasminogenemia,ICD-10 L90.6 Striae atrophicae,5273,L90.6,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.6,,ICD-10 -L90.8 Other atrophic disorders of skin,5274,L90.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.8,ORPHAcode: 2500 Acrogeria +L90.8 Other atrophic disorders of skin,5274,L90.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.8,ORPHAcode: 2500 Acrogeria,ICD-10 "L90.9 Atrophic disorder of skin, unspecified",5275,L90.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L90.9,,ICD-10 L91 Hypertrophic disorders of skin,5276,L91,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L91,,ICD-10 L91.0 Hypertrophic scar,5277,L91.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L91.0,,ICD-10 -L91.8 Other hypertrophic disorders of skin,5278,L91.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L91.8,ORPHAcode: 2812 Parana hard skin syndrome +L91.8 Other hypertrophic disorders of skin,5278,L91.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L91.8,ORPHAcode: 2812 Parana hard skin syndrome,ICD-10 "L91.9 Hypertrophic disorder of skin, unspecified",5279,L91.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L91.9,,ICD-10 L92 Granulomatous disorders of skin and subcutaneous tissue,5280,L92,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92,,ICD-10 L92.0 Granulomatous disorders of skin and subcutaneous tissue - Granuloma annulare,5281,L92.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92.0,,ICD-10 -"L92.1 Granulomatous disorders of skin and subcutaneous tissue - Necrobiosis lipoidica, not elsewhere classified",5282,L92.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92.1,ORPHAcode: 542592 Necrobiosis lipoidica +"L92.1 Granulomatous disorders of skin and subcutaneous tissue - Necrobiosis lipoidica, not elsewhere classified",5282,L92.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92.1,ORPHAcode: 542592 Necrobiosis lipoidica,ICD-10 L92.2 Granuloma faciale [eosinophilic granuloma of skin],5283,L92.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92.2,,ICD-10 L92.3 Foreign body granuloma of skin and subcutaneous tissue,5284,L92.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92.3,,ICD-10 L92.8 Other granulomatous disorders of skin and subcutaneous tissue,5285,L92.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92.8,,ICD-10 "L92.9 Granulomatous disorder of skin and subcutaneous tissue, unspecified",5286,L92.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L92.9,,ICD-10 L93 Lupus erythematosus,5287,L93,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L93,,ICD-10 -L93.0 Discoid lupus erythematosus,5288,L93.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L93.0,ORPHAcode: 90281 Discoid lupus erythematosus -L93.1 Subacute cutaneous lupus erythematosus,5289,L93.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L93.1,ORPHAcode: 163525 Subacute cutaneous lupus erythematosus -L93.2 Other local lupus erythematosus,5290,L93.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L93.2,ORPHAcode: 90280 Chilblain lupus +L93.0 Discoid lupus erythematosus,5288,L93.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L93.0,ORPHAcode: 90281 Discoid lupus erythematosus,ICD-10 +L93.1 Subacute cutaneous lupus erythematosus,5289,L93.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L93.1,ORPHAcode: 163525 Subacute cutaneous lupus erythematosus,ICD-10 +L93.2 Other local lupus erythematosus,5290,L93.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L93.2,ORPHAcode: 90280 Chilblain lupus,ICD-10 L94 Other localized connective tissue disorders,5291,L94,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94,,ICD-10 -L94.0 Localized scleroderma [morphea],5292,L94.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.0,ORPHAcode: 90289 Localized scleroderma +L94.0 Localized scleroderma [morphea],5292,L94.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.0,ORPHAcode: 90289 Localized scleroderma,ICD-10 L94.1 Other localized connective tissue disorders - Linear scleroderma,5293,L94.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.1,,ICD-10 L94.2 Other localized connective tissue disorders - Calcinosis cutis,5294,L94.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.2,,ICD-10 L94.3 Other localized connective tissue disorders - Sclerodactyly,5295,L94.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.3,,ICD-10 L94.4 Other localized connective tissue disorders - Gottron papules,5296,L94.4,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.4,,ICD-10 L94.5 Other localized connective tissue disorders - Poikiloderma vasculare atrophicans,5297,L94.5,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.5,,ICD-10 L94.6 Other localized connective tissue disorders - Ainhum,5298,L94.6,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.6,,ICD-10 -L94.8 Other specified localized connective tissue disorders,5299,L94.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.8,ORPHAcode: 53296 Familial cutaneous collagenoma +L94.8 Other specified localized connective tissue disorders,5299,L94.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.8,ORPHAcode: 53296 Familial cutaneous collagenoma,ICD-10 "L94.9 Localized connective tissue disorder, unspecified",5300,L94.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L94.9,,ICD-10 "L95 Vasculitis limited to skin, not elsewhere classified",5301,L95,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95,,ICD-10 M08 Juvenile arthritis,5302,M08,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08,,ICD-10 -L95.0 Livedoid vasculitis,5303,L95.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95.0,ORPHAcode: 542643 Livedoid vasculopathy -"L95.1 Vasculitis limited to skin, not elsewhere classified - Erythema elevatum diutinum",5304,L95.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95.1,ORPHAcode: 90000 Erythema elevatum diutinum -L95.8 Other vasculitis limited to skin,5305,L95.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95.8,ORPHAcode: 26137 Juvenile temporal arteritis +L95.0 Livedoid vasculitis,5303,L95.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95.0,ORPHAcode: 542643 Livedoid vasculopathy,ICD-10 +"L95.1 Vasculitis limited to skin, not elsewhere classified - Erythema elevatum diutinum",5304,L95.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95.1,ORPHAcode: 90000 Erythema elevatum diutinum,ICD-10 +L95.8 Other vasculitis limited to skin,5305,L95.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95.8,ORPHAcode: 26137 Juvenile temporal arteritis,ICD-10 "L95.9 Vasculitis limited to skin, unspecified",5306,L95.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L95.9,,ICD-10 "L97 Ulcer of lower limb, not elsewhere classified",5307,L97,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L97,,ICD-10 "L98 Other disorders of skin and subcutaneous tissue, not elsewhere classified",5308,L98,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98,,ICD-10 "L98.0 Other disorders of skin and subcutaneous tissue, not elsewhere classified - Pyogenic granuloma",5309,L98.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.0,,ICD-10 "L98.1 Other disorders of skin and subcutaneous tissue, not elsewhere classified - Factitial dermatitis",5310,L98.1,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.1,,ICD-10 -"L98.2 Other disorders of skin and subcutaneous tissue, not elsewhere classified - Febrile neutrophilic dermatosis [Sweet]",5311,L98.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.2,ORPHAcode: 3243 Sweet syndrome -"L98.3 Other disorders of skin and subcutaneous tissue, not elsewhere classified - Eosinophilic cellulitis [Wells]",5312,L98.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.3,ORPHAcode: 901 Wells syndrome +"L98.2 Other disorders of skin and subcutaneous tissue, not elsewhere classified - Febrile neutrophilic dermatosis [Sweet]",5311,L98.2,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.2,ORPHAcode: 3243 Sweet syndrome,ICD-10 +"L98.3 Other disorders of skin and subcutaneous tissue, not elsewhere classified - Eosinophilic cellulitis [Wells]",5312,L98.3,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.3,ORPHAcode: 901 Wells syndrome,ICD-10 "L98.4 Chronic ulcer of skin, not elsewhere classified",5313,L98.4,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.4,,ICD-10 -L98.5 Mucinosis of skin,5314,L98.5,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.5,ORPHAcode: 86797 Atypical lichen myxedematosus -L98.6 Other infiltrative disorders of skin and subcutaneous tissue,5315,L98.6,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.6,ORPHAcode: 33314 Jessner lymphocytic infiltration of the skin +L98.5 Mucinosis of skin,5314,L98.5,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.5,ORPHAcode: 86797 Atypical lichen myxedematosus,ICD-10 +L98.6 Other infiltrative disorders of skin and subcutaneous tissue,5315,L98.6,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.6,ORPHAcode: 33314 Jessner lymphocytic infiltration of the skin,ICD-10 L98.7 Excessive and redundant skin and subcutaneous tissue,5316,L98.7,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.7,,ICD-10 -L98.8 Other specified disorders of skin and subcutaneous tissue,5317,L98.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.8,ORPHAcode: 113 Bazex-Dupr -Christol sy +L98.8 Other specified disorders of skin and subcutaneous tissue,5317,L98.8,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.8,ORPHAcode: 113 Bazex-Dupr -Christol sy,ICD-10 "L98.9 Disorder of skin and subcutaneous tissue, unspecified",5318,L98.9,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L98.9,,ICD-10 L99 Other disorders of skin and subcutaneous tissue in diseases classified elsewhere,5319,L99,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L99,,ICD-10 L99.0 Amyloidosis of skin,5320,L99.0,L80-L99 Other disorders of the skin and subcutaneous tissue,http://identifiers.org/icd/L99.0,,ICD-10 @@ -5342,7 +5342,7 @@ M02 Reactive arthropathies,5340,M02,M00-M03 Infectious arthropathies,http://iden M02.0 Reactive arthropathies - Arthropathy following intestinal bypass,5341,M02.0,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M02.0,,ICD-10 M02.1 Reactive arthropathies - Postdysenteric arthropathy,5342,M02.1,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M02.1,,ICD-10 M02.2 Reactive arthropathies - Postimmunization arthropathy,5343,M02.2,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M02.2,,ICD-10 -M02.3 Reactive arthropathies - Reiter disease,5344,M02.3,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M02.3,ORPHAcode: 29207 Reactive arthritis +M02.3 Reactive arthropathies - Reiter disease,5344,M02.3,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M02.3,ORPHAcode: 29207 Reactive arthritis,ICD-10 M02.8 Other reactive arthropathies,5345,M02.8,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M02.8,,ICD-10 "M02.9 Reactive arthropathy, unspecified",5346,M02.9,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M02.9,,ICD-10 M03 Postinfective and reactive arthropathies in diseases classified elsewhere,5347,M03,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M03,,ICD-10 @@ -5352,7 +5352,7 @@ M03.2 Other postinfectious arthropathies in diseases classified elsewhere,5350,M M03.6 Reactive arthropathy in other diseases classified elsewhere,5351,M03.6,M00-M03 Infectious arthropathies,http://identifiers.org/icd/M03.6,,ICD-10 M05-M14 Inflammatory polyarthropathies,5352,M05-M14,M00-M25 Arthropathies,,,ICD-10 M05 Seropositive rheumatoid arthritis,5353,M05,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M05,,ICD-10 -M05.0 Seropositive rheumatoid arthritis - Felty syndrome,5354,M05.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M05.0,ORPHAcode: 47612 Felty syndrome +M05.0 Seropositive rheumatoid arthritis - Felty syndrome,5354,M05.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M05.0,ORPHAcode: 47612 Felty syndrome,ICD-10 M05.1 Rheumatoid lung disease,5355,M05.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M05.1,,ICD-10 M05.2 Rheumatoid vasculitis,5356,M05.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M05.2,,ICD-10 M05.3 Rheumatoid arthritis with involvement of other organs and systems,5357,M05.3,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M05.3,,ICD-10 @@ -5360,11 +5360,11 @@ M05.8 Other seropositive rheumatoid arthritis,5358,M05.8,M05-M14 Inflammatory po "M05.9 Seropositive rheumatoid arthritis, unspecified",5359,M05.9,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M05.9,,ICD-10 M06 Other rheumatoid arthritis,5360,M06,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06,,ICD-10 M06.0 Seronegative rheumatoid arthritis,5361,M06.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.0,,ICD-10 -M06.1 Other rheumatoid arthritis - Adult-onset Still disease,5362,M06.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.1,ORPHAcode: 829 Adult-onset Still disease +M06.1 Other rheumatoid arthritis - Adult-onset Still disease,5362,M06.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.1,ORPHAcode: 829 Adult-onset Still disease,ICD-10 M06.2 Rheumatoid bursitis,5363,M06.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.2,,ICD-10 M06.3 Rheumatoid nodule,5364,M06.3,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.3,,ICD-10 -M06.4 Other rheumatoid arthritis - Inflammatory polyarthropathy,5365,M06.4,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.4,ORPHAcode: 477650 Fibroblastic rheumatism -M06.8 Other specified rheumatoid arthritis,5366,M06.8,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.8,ORPHAcode: 85169 Familial digital arthropathy-brachydactyly +M06.4 Other rheumatoid arthritis - Inflammatory polyarthropathy,5365,M06.4,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.4,ORPHAcode: 477650 Fibroblastic rheumatism,ICD-10 +M06.8 Other specified rheumatoid arthritis,5366,M06.8,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.8,ORPHAcode: 85169 Familial digital arthropathy-brachydactyly,ICD-10 "M06.9 Rheumatoid arthritis, unspecified",5367,M06.9,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M06.9,,ICD-10 M07 Psoriatic and enteropathic arthropathies,5368,M07,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M07,,ICD-10 M07.0 Distal interphalangeal psoriatic arthropathy,5369,M07.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M07.0,,ICD-10 @@ -5374,12 +5374,12 @@ M07.3 Other psoriatic arthropathies,5372,M07.3,M05-M14 Inflammatory polyarthropa M07.4 Psoriatic and enteropathic arthropathies - Arthropathy in Crohn disease [regional enteritis],5373,M07.4,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M07.4,,ICD-10 M07.5 Psoriatic and enteropathic arthropathies - Arthropathy in ulcerative colitis,5374,M07.5,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M07.5,,ICD-10 M07.6 Other enteropathic arthropathies,5375,M07.6,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M07.6,,ICD-10 -M08.0 Juvenile rheumatoid arthritis,5376,M08.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.0,ORPHAcode: 85435 Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis +M08.0 Juvenile rheumatoid arthritis,5376,M08.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.0,ORPHAcode: 85435 Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis,ICD-10 M08.1 Juvenile ankylosing spondylitis,5377,M08.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.1,,ICD-10 -M08.2 Juvenile arthritis with systemic onset,5378,M08.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.2,ORPHAcode: 85414 Systemic-onset juvenile idiopathic arthritis -M08.3 Juvenile polyarthritis (seronegative),5379,M08.3,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.3,ORPHAcode: 85408 Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis -M08.4 Pauciarticular juvenile arthritis,5380,M08.4,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.4,ORPHAcode: 85410 Oligoarticular juvenile idiopathic arthritis -M08.8 Other juvenile arthritis,5381,M08.8,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.8,ORPHAcode: 85438 Enthesitis-related juvenile idiopathic arthritis +M08.2 Juvenile arthritis with systemic onset,5378,M08.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.2,ORPHAcode: 85414 Systemic-onset juvenile idiopathic arthritis,ICD-10 +M08.3 Juvenile polyarthritis (seronegative),5379,M08.3,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.3,ORPHAcode: 85408 Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis,ICD-10 +M08.4 Pauciarticular juvenile arthritis,5380,M08.4,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.4,ORPHAcode: 85410 Oligoarticular juvenile idiopathic arthritis,ICD-10 +M08.8 Other juvenile arthritis,5381,M08.8,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.8,ORPHAcode: 85438 Enthesitis-related juvenile idiopathic arthritis,ICD-10 "M08.9 Juvenile arthritis, unspecified",5382,M08.9,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M08.9,,ICD-10 M09 Juvenile arthritis in diseases classified elsewhere,5383,M09,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M09,,ICD-10 M09.0 Juvenile arthritis in psoriasis,5384,M09.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M09.0,,ICD-10 @@ -5395,18 +5395,18 @@ M10.4 Other secondary gout,5393,M10.4,M05-M14 Inflammatory polyarthropathies,htt "M10.9 Gout, unspecified",5394,M10.9,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M10.9,,ICD-10 M11 Other crystal arthropathies,5395,M11,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11,,ICD-10 M11.0 Other crystal arthropathies - Hydroxyapatite deposition disease,5396,M11.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11.0,,ICD-10 -M11.1 Other crystal arthropathies - Familial chondrocalcinosis,5397,M11.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11.1,ORPHAcode: 1416 Familial calcium pyrophosphate deposition -M11.2 Other chondrocalcinosis,5398,M11.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11.2,ORPHAcode: 53715 Familial tumoral calcinosis +M11.1 Other crystal arthropathies - Familial chondrocalcinosis,5397,M11.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11.1,ORPHAcode: 1416 Familial calcium pyrophosphate deposition,ICD-10 +M11.2 Other chondrocalcinosis,5398,M11.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11.2,ORPHAcode: 53715 Familial tumoral calcinosis,ICD-10 M11.8 Other specified crystal arthropathies,5399,M11.8,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11.8,,ICD-10 "M11.9 Crystal arthropathy, unspecified",5400,M11.9,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M11.9,,ICD-10 M12 Other specific arthropathies,5401,M12,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12,,ICD-10 M12.0 Other specific arthropathies - Chronic postrheumatic arthropathy [Jaccoud],5402,M12.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.0,,ICD-10 M12.1 Other specific arthropathies - Kaschin-Beck disease,5403,M12.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.1,,ICD-10 -M12.2 Other specific arthropathies - Villonodular synovitis (pigmented),5404,M12.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.2,ORPHAcode: 66627 Pigmented villonodular synovitis +M12.2 Other specific arthropathies - Villonodular synovitis (pigmented),5404,M12.2,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.2,ORPHAcode: 66627 Pigmented villonodular synovitis,ICD-10 M12.3 Other specific arthropathies - Palindromic rheumatism,5405,M12.3,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.3,,ICD-10 -M12.4 Other specific arthropathies - Intermittent hydrarthrosis,5406,M12.4,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.4,ORPHAcode: 329967 Intermittent hydrarthrosis +M12.4 Other specific arthropathies - Intermittent hydrarthrosis,5406,M12.4,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.4,ORPHAcode: 329967 Intermittent hydrarthrosis,ICD-10 M12.5 Other specific arthropathies - Traumatic arthropathy,5407,M12.5,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.5,,ICD-10 -"M12.8 Other specific arthropathies, not elsewhere classified",5408,M12.8,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.8,ORPHAcode: 2848 Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome +"M12.8 Other specific arthropathies, not elsewhere classified",5408,M12.8,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M12.8,ORPHAcode: 2848 Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome,ICD-10 M13 Other arthritis,5409,M13,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M13,,ICD-10 "M13.0 Polyarthritis, unspecified",5410,M13.0,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M13.0,,ICD-10 "M13.1 Monoarthritis, not elsewhere classified",5411,M13.1,M05-M14 Inflammatory polyarthropathies,http://identifiers.org/icd/M13.1,,ICD-10 @@ -5480,14 +5480,14 @@ M21.4 Flat foot [pes planus] (acquired),5478,M21.4,M20-M25 Other joint disorders "M21.5 Acquired clawhand, clubhand, clawfoot and clubfoot",5479,M21.5,M20-M25 Other joint disorders,http://identifiers.org/icd/M21.5,,ICD-10 M21.6 Other acquired deformities of ankle and foot,5480,M21.6,M20-M25 Other joint disorders,http://identifiers.org/icd/M21.6,,ICD-10 M21.7 Unequal limb length (acquired),5481,M21.7,M20-M25 Other joint disorders,http://identifiers.org/icd/M21.7,,ICD-10 -M21.8 Other specified acquired deformities of limbs,5482,M21.8,M20-M25 Other joint disorders,http://identifiers.org/icd/M21.8,ORPHAcode: 2771 Bruck syndrome +M21.8 Other specified acquired deformities of limbs,5482,M21.8,M20-M25 Other joint disorders,http://identifiers.org/icd/M21.8,ORPHAcode: 2771 Bruck syndrome,ICD-10 "M21.9 Acquired deformity of limb, unspecified",5483,M21.9,M20-M25 Other joint disorders,http://identifiers.org/icd/M21.9,,ICD-10 M22 Disorders of patella,5484,M22,M20-M25 Other joint disorders,http://identifiers.org/icd/M22,,ICD-10 M22.0 Recurrent dislocation of patella,5485,M22.0,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.0,,ICD-10 M22.1 Recurrent subluxation of patella,5486,M22.1,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.1,,ICD-10 M22.2 Patellofemoral disorders,5487,M22.2,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.2,,ICD-10 M22.3 Other derangements of patella,5488,M22.3,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.3,,ICD-10 -M22.4 Chondromalacia patellae,5489,M22.4,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.4,ORPHAcode: 1428 Familial chondromalacia patellae +M22.4 Chondromalacia patellae,5489,M22.4,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.4,ORPHAcode: 1428 Familial chondromalacia patellae,ICD-10 M22.8 Other disorders of patella,5490,M22.8,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.8,,ICD-10 "M22.9 Disorder of patella, unspecified",5491,M22.9,M20-M25 Other joint disorders,http://identifiers.org/icd/M22.9,,ICD-10 M23 Internal derangement of knee,5492,M23,M20-M25 Other joint disorders,http://identifiers.org/icd/M23,,ICD-10 @@ -5524,50 +5524,50 @@ M25.8 Other specified joint disorders,5522,M25.8,M20-M25 Other joint disorders,h "M25.9 Joint disorder, unspecified",5523,M25.9,M20-M25 Other joint disorders,http://identifiers.org/icd/M25.9,,ICD-10 M30-M36 Systemic connective tissue disorders,5524,M30-M36,XIII Diseases of the musculoskeletal system and connective tissue,,,ICD-10 M30 Polyarteritis nodosa and related conditions,5525,M30,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30,,ICD-10 -M30.0 Polyarteritis nodosa,5526,M30.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.0,ORPHAcode: 767 Polyarteritis nodosa -M30.1 Polyarteritis with lung involvement [Churg-Strauss],5527,M30.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.1,ORPHAcode: 183 Eosinophilic granulomatosis with polyangiitis +M30.0 Polyarteritis nodosa,5526,M30.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.0,ORPHAcode: 767 Polyarteritis nodosa,ICD-10 +M30.1 Polyarteritis with lung involvement [Churg-Strauss],5527,M30.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.1,ORPHAcode: 183 Eosinophilic granulomatosis with polyangiitis,ICD-10 M30.2 Juvenile polyarteritis,5528,M30.2,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.2,,ICD-10 -M30.3 Polyarteritis nodosa and related conditions - Mucocutaneous lymph node syndrome [Kawasaki],5529,M30.3,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.3,ORPHAcode: 2331 Kawasaki disease -M30.8 Other conditions related to polyarteritis nodosa,5530,M30.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.8,ORPHAcode: 404553 Vasculitis due to ADA2 deficiency +M30.3 Polyarteritis nodosa and related conditions - Mucocutaneous lymph node syndrome [Kawasaki],5529,M30.3,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.3,ORPHAcode: 2331 Kawasaki disease,ICD-10 +M30.8 Other conditions related to polyarteritis nodosa,5530,M30.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M30.8,ORPHAcode: 404553 Vasculitis due to ADA2 deficiency,ICD-10 M31 Other necrotizing vasculopathies,5531,M31,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31,,ICD-10 -M31.0 Other necrotizing vasculopathies - Hypersensitivity angiitis,5532,M31.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.0,ORPHAcode: 889 Cutaneous small vessel vasculitis -M31.1 Other necrotizing vasculopathies - Thrombotic microangiopathy,5533,M31.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.1,ORPHAcode: 54057 Thrombotic thrombocytopenic purpura +M31.0 Other necrotizing vasculopathies - Hypersensitivity angiitis,5532,M31.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.0,ORPHAcode: 889 Cutaneous small vessel vasculitis,ICD-10 +M31.1 Other necrotizing vasculopathies - Thrombotic microangiopathy,5533,M31.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.1,ORPHAcode: 54057 Thrombotic thrombocytopenic purpura,ICD-10 M31.2 Other necrotizing vasculopathies - Lethal midline granuloma,5534,M31.2,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.2,,ICD-10 -M31.3 Other necrotizing vasculopathies - Wegener granulomatosis,5535,M31.3,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.3,ORPHAcode: 900 Granulomatosis with polyangiitis -M31.4 Other necrotizing vasculopathies - Aortic arch syndrome [Takayasu],5536,M31.4,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.4,ORPHAcode: 3287 Takayasu arteritis +M31.3 Other necrotizing vasculopathies - Wegener granulomatosis,5535,M31.3,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.3,ORPHAcode: 900 Granulomatosis with polyangiitis,ICD-10 +M31.4 Other necrotizing vasculopathies - Aortic arch syndrome [Takayasu],5536,M31.4,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.4,ORPHAcode: 3287 Takayasu arteritis,ICD-10 M62.6 Muscle strain,5537,M62.6,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.6,,ICD-10 M31.5 Other necrotizing vasculopathies - Giant cell arteritis with polymyalgia rheumatica,5538,M31.5,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.5,,ICD-10 -M31.6 Other giant cell arteritis,5539,M31.6,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.6,ORPHAcode: 397 Giant cell arteritis -M31.7 Other necrotizing vasculopathies - Microscopic polyangiitis,5540,M31.7,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.7,ORPHAcode: 727 Microscopic polyangiitis -M31.8 Other specified necrotizing vasculopathies,5541,M31.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.8,ORPHAcode: 36412 Hypocomplementemic urticarial vasculitis +M31.6 Other giant cell arteritis,5539,M31.6,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.6,ORPHAcode: 397 Giant cell arteritis,ICD-10 +M31.7 Other necrotizing vasculopathies - Microscopic polyangiitis,5540,M31.7,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.7,ORPHAcode: 727 Microscopic polyangiitis,ICD-10 +M31.8 Other specified necrotizing vasculopathies,5541,M31.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.8,ORPHAcode: 36412 Hypocomplementemic urticarial vasculitis,ICD-10 "M31.9 Necrotizing vasculopathy, unspecified",5542,M31.9,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M31.9,,ICD-10 M32 Systemic lupus erythematosus,5543,M32,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M32,,ICD-10 -M32.0 Drug-induced systemic lupus erythematosus,5544,M32.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M32.0,ORPHAcode: 536 Systemic lupus erythematosus +M32.0 Drug-induced systemic lupus erythematosus,5544,M32.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M32.0,ORPHAcode: 536 Systemic lupus erythematosus,ICD-10 M32.1 Systemic lupus erythematosus with organ or system involvement,5545,M32.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M32.1,,ICD-10 -M32.8 Other forms of systemic lupus erythematosus,5546,M32.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M32.8,ORPHAcode: 300345 Autosomal systemic lupus erythematosus +M32.8 Other forms of systemic lupus erythematosus,5546,M32.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M32.8,ORPHAcode: 300345 Autosomal systemic lupus erythematosus,ICD-10 "M32.9 Systemic lupus erythematosus, unspecified",5547,M32.9,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M32.9,,ICD-10 M33 Dermatopolymyositis,5548,M33,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33,,ICD-10 -M33.0 Dermatopolymyositis - Juvenile dermatomyositis,5549,M33.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33.0,ORPHAcode: 93672 Juvenile dermatomyositis -M33.1 Dermatopolymyositis - Other dermatomyositis,5550,M33.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33.1,ORPHAcode: 221 Dermatomyositis -M33.2 Dermatopolymyositis - Polymyositis,5551,M33.2,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33.2,ORPHAcode: 732 Polymyositis +M33.0 Dermatopolymyositis - Juvenile dermatomyositis,5549,M33.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33.0,ORPHAcode: 93672 Juvenile dermatomyositis,ICD-10 +M33.1 Dermatopolymyositis - Other dermatomyositis,5550,M33.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33.1,ORPHAcode: 221 Dermatomyositis,ICD-10 +M33.2 Dermatopolymyositis - Polymyositis,5551,M33.2,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33.2,ORPHAcode: 732 Polymyositis,ICD-10 "M33.9 Dermatopolymyositis, unspecified",5552,M33.9,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M33.9,,ICD-10 M34 Systemic sclerosis,5553,M34,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34,,ICD-10 -M34.0 Progressive systemic sclerosis,5554,M34.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34.0,ORPHAcode: 90291 Systemic sclerosis +M34.0 Progressive systemic sclerosis,5554,M34.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34.0,ORPHAcode: 90291 Systemic sclerosis,ICD-10 M41.5 Other secondary scoliosis,5555,M41.5,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M41.5,,ICD-10 M34.1 Systemic sclerosis - CR(E)ST syndrome,5556,M34.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34.1,,ICD-10 M34.2 Systemic sclerosis induced by drugs and chemicals,5557,M34.2,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34.2,,ICD-10 -M34.8 Other forms of systemic sclerosis,5558,M34.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34.8,ORPHAcode: 352763 Scleredema +M34.8 Other forms of systemic sclerosis,5558,M34.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34.8,ORPHAcode: 352763 Scleredema,ICD-10 "M34.9 Systemic sclerosis, unspecified",5559,M34.9,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M34.9,,ICD-10 M35 Other systemic involvement of connective tissue,5560,M35,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35,,ICD-10 -M35.0 Other systemic involvement of connective tissue - Sicca syndrome [Sjögren],5561,M35.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.0,ORPHAcode: 289390 Primary Sjögren syndrome -M35.1 Other overlap syndromes,5562,M35.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.1,ORPHAcode: 809 Mixed connective tissue disease -M35.2 Other systemic involvement of connective tissue - Behçet disease,5563,M35.2,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.2,ORPHAcode: 117 Beh et d -M35.3 Other systemic involvement of connective tissue - Polymyalgia rheumatica,5564,M35.3,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.3,ORPHAcode: 93569 Polymyalgia rheumatica -M35.4 Other systemic involvement of connective tissue - Diffuse (eosinophilic) fasciitis,5565,M35.4,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.4,ORPHAcode: 3165 Eosinophilic fasciitis +M35.0 Other systemic involvement of connective tissue - Sicca syndrome [Sjögren],5561,M35.0,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.0,ORPHAcode: 289390 Primary Sjögren syndrome,ICD-10 +M35.1 Other overlap syndromes,5562,M35.1,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.1,ORPHAcode: 809 Mixed connective tissue disease,ICD-10 +M35.2 Other systemic involvement of connective tissue - Behçet disease,5563,M35.2,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.2,ORPHAcode: 117 Beh et d,ICD-10 +M35.3 Other systemic involvement of connective tissue - Polymyalgia rheumatica,5564,M35.3,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.3,ORPHAcode: 93569 Polymyalgia rheumatica,ICD-10 +M35.4 Other systemic involvement of connective tissue - Diffuse (eosinophilic) fasciitis,5565,M35.4,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.4,ORPHAcode: 3165 Eosinophilic fasciitis,ICD-10 M35.5 Other systemic involvement of connective tissue - Multifocal fibrosclerosis,5566,M35.5,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.5,,ICD-10 -M35.6 Other systemic involvement of connective tissue - Relapsing panniculitis [Weber-Christian],5567,M35.6,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.6,ORPHAcode: 33577 Nodular non-suppurative panniculitis +M35.6 Other systemic involvement of connective tissue - Relapsing panniculitis [Weber-Christian],5567,M35.6,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.6,ORPHAcode: 33577 Nodular non-suppurative panniculitis,ICD-10 M35.7 Other systemic involvement of connective tissue - Hypermobility syndrome,5568,M35.7,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.7,,ICD-10 -M35.8 Other specified systemic involvement of connective tissue,5569,M35.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.8,ORPHAcode: 81 Antisynthetase syndrome +M35.8 Other specified systemic involvement of connective tissue,5569,M35.8,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.8,ORPHAcode: 81 Antisynthetase syndrome,ICD-10 "M35.9 Systemic involvement of connective tissue, unspecified",5570,M35.9,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M35.9,,ICD-10 M41.3 Thoracogenic scoliosis,5571,M41.3,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M41.3,,ICD-10 M36 Systemic disorders of connective tissue in diseases classified elsewhere,5572,M36,M30-M36 Systemic connective tissue disorders,http://identifiers.org/icd/M36,,ICD-10 @@ -5595,7 +5595,7 @@ M41.4 Neuromuscular scoliosis,5593,M41.4,M40-M43 Deforming dorsopathies,http://i M41.8 Other forms of scoliosis,5594,M41.8,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M41.8,,ICD-10 "M41.9 Scoliosis, unspecified",5595,M41.9,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M41.9,,ICD-10 M42 Spinal osteochondrosis,5596,M42,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M42,,ICD-10 -M42.0 Juvenile osteochondrosis of spine,5597,M42.0,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M42.0,ORPHAcode: 3135 Familial Scheuermann disease +M42.0 Juvenile osteochondrosis of spine,5597,M42.0,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M42.0,ORPHAcode: 3135 Familial Scheuermann disease,ICD-10 M42.1 Adult osteochondrosis of spine,5598,M42.1,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M42.1,,ICD-10 "M42.9 Spinal osteochondrosis, unspecified",5599,M42.9,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M42.9,,ICD-10 M43 Other deforming dorsopathies,5600,M43,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M43,,ICD-10 @@ -5606,7 +5606,7 @@ M43.3 Other deforming dorsopathies - Recurrent atlantoaxial subluxation with mye M43.4 Other recurrent atlantoaxial subluxation,5605,M43.4,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M43.4,,ICD-10 M43.5 Other recurrent vertebral subluxation,5606,M43.5,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M43.5,,ICD-10 M43.6 Other deforming dorsopathies - Torticollis,5607,M43.6,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M43.6,,ICD-10 -M43.8 Other specified deforming dorsopathies,5608,M43.8,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M43.8,ORPHAcode: 1320 Idiopathic camptocormia +M43.8 Other specified deforming dorsopathies,5608,M43.8,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M43.8,ORPHAcode: 1320 Idiopathic camptocormia,ICD-10 "M43.9 Deforming dorsopathy, unspecified",5609,M43.9,M40-M43 Deforming dorsopathies,http://identifiers.org/icd/M43.9,,ICD-10 M45-M49 Spondylopathies,5610,M45-M49,M40-M54 Dorsopathies,,,ICD-10 M45 Ankylosing spondylitis,5611,M45,M45-M49 Spondylopathies,http://identifiers.org/icd/M45,,ICD-10 @@ -5627,7 +5627,7 @@ M47.8 Other spondylosis,5625,M47.8,M45-M49 Spondylopathies,http://identifiers.or "M47.9 Spondylosis, unspecified",5626,M47.9,M45-M49 Spondylopathies,http://identifiers.org/icd/M47.9,,ICD-10 M48 Other spondylopathies,5627,M48,M45-M49 Spondylopathies,http://identifiers.org/icd/M48,,ICD-10 M48.0 Other spondylopathies - Spinal stenosis,5628,M48.0,M45-M49 Spondylopathies,http://identifiers.org/icd/M48.0,,ICD-10 -M48.1 Other spondylopathies - Ankylosing hyperostosis [Forestier],5629,M48.1,M45-M49 Spondylopathies,http://identifiers.org/icd/M48.1,ORPHAcode: 2206 Ankylosing vertebral hyperostosis with tylosis +M48.1 Other spondylopathies - Ankylosing hyperostosis [Forestier],5629,M48.1,M45-M49 Spondylopathies,http://identifiers.org/icd/M48.1,ORPHAcode: 2206 Ankylosing vertebral hyperostosis with tylosis,ICD-10 M48.2 Other spondylopathies - Kissing spine,5630,M48.2,M45-M49 Spondylopathies,http://identifiers.org/icd/M48.2,,ICD-10 M48.3 Other spondylopathies - Traumatic spondylopathy,5631,M48.3,M45-M49 Spondylopathies,http://identifiers.org/icd/M48.3,,ICD-10 M48.4 Other spondylopathies - Fatigue fracture of vertebra,5632,M48.4,M45-M49 Spondylopathies,http://identifiers.org/icd/M48.4,,ICD-10 @@ -5676,18 +5676,18 @@ M54.6 Dorsalgia - Pain in thoracic spine,5674,M54.6,M50-M54 Other dorsopathies,h M54.8 Other dorsalgia,5675,M54.8,M50-M54 Other dorsopathies,http://identifiers.org/icd/M54.8,,ICD-10 "M54.9 Dorsalgia, unspecified",5676,M54.9,M50-M54 Other dorsopathies,http://identifiers.org/icd/M54.9,,ICD-10 M60-M79 Soft tissue disorders,5677,,XIII Diseases of the musculoskeletal system and connective tissue,,,ICD-10 -M60.0 Infective myositis,5678,M60.0,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60.0,ORPHAcode: 764 Pyomyositis +M60.0 Infective myositis,5678,M60.0,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60.0,ORPHAcode: 764 Pyomyositis,ICD-10 M60.1 Interstitial myositis,5679,M60.1,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60.1,,ICD-10 "M60.2 Myositis - Foreign body granuloma of soft tissue, not elsewhere classified",5680,M60.2,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60.2,,ICD-10 -M60.8 Other myositis,5681,M60.8,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60.8,ORPHAcode: 592 Macrophagic myofasciitis +M60.8 Other myositis,5681,M60.8,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60.8,ORPHAcode: 592 Macrophagic myofasciitis,ICD-10 "M60.9 Myositis, unspecified",5682,M60.9,M60-M63 Disorders of muscles,http://identifiers.org/icd/M60.9,,ICD-10 M61 Calcification and ossification of muscle,5683,M61,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61,,ICD-10 M61.0 Calcification and ossification of muscle - Myositis ossificans traumatica,5684,M61.0,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.0,,ICD-10 -M61.1 Calcification and ossification of muscle - Myositis ossificans progressiva,5685,M61.1,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.1,ORPHAcode: 337 Fibrodysplasia ossificans progressiva +M61.1 Calcification and ossification of muscle - Myositis ossificans progressiva,5685,M61.1,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.1,ORPHAcode: 337 Fibrodysplasia ossificans progressiva,ICD-10 M61.2 Paralytic calcification and ossification of muscle,5686,M61.2,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.2,,ICD-10 M61.3 Calcification and ossification of muscles associated with burns,5687,M61.3,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.3,,ICD-10 M61.4 Other calcification of muscle,5688,M61.4,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.4,,ICD-10 -M61.5 Other ossification of muscle,5689,M61.5,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.5,ORPHAcode: 2762 Progressive osseous heteroplasia +M61.5 Other ossification of muscle,5689,M61.5,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.5,ORPHAcode: 2762 Progressive osseous heteroplasia,ICD-10 "M61.9 Calcification and ossification of muscle, unspecified",5690,M61.9,M60-M63 Disorders of muscles,http://identifiers.org/icd/M61.9,,ICD-10 M62 Other disorders of muscle,5691,M62,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62,,ICD-10 M62.0 Diastasis of muscle,5692,M62.0,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.0,,ICD-10 @@ -5696,7 +5696,7 @@ M62.2 Ischaemic infarction of muscle,5694,M62.2,M60-M63 Disorders of muscles,htt M62.3 Other disorders of muscle - Immobility syndrome (paraplegic),5695,M62.3,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.3,,ICD-10 M62.4 Contracture of muscle,5696,M62.4,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.4,,ICD-10 "M62.5 Muscle wasting and atrophy, not elsewhere classified",5697,M62.5,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.5,,ICD-10 -M62.8 Other specified disorders of muscle,5698,M62.8,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.8,ORPHAcode: 275534 Myostatin-related muscle hypertrophy +M62.8 Other specified disorders of muscle,5698,M62.8,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.8,ORPHAcode: 275534 Myostatin-related muscle hypertrophy,ICD-10 "M62.9 Disorder of muscle, unspecified",5699,M62.9,M60-M63 Disorders of muscles,http://identifiers.org/icd/M62.9,,ICD-10 M63 Disorders of muscle in diseases classified elsewhere,5700,M63,M60-M63 Disorders of muscles,http://identifiers.org/icd/M63,,ICD-10 M63.0 Myositis in bacterial diseases classified elsewhere,5701,M63.0,M60-M63 Disorders of muscles,http://identifiers.org/icd/M63.0,,ICD-10 @@ -5757,10 +5757,10 @@ M71.8 Other specified bursopathies,5754,M71.8,M70-M79 Other soft tissue disorder M72 Fibroblastic disorders,5756,M72,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72,,ICD-10 M72.0 Fibroblastic disorders - Palmar fascial fibromatosis [Dupuytren],5757,M72.0,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.0,,ICD-10 M72.1 Fibroblastic disorders - Knuckle pads,5758,M72.1,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.1,,ICD-10 -M72.2 Fibroblastic disorders - Plantar fascial fibromatosis,5759,M72.2,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.2,ORPHAcode: 199251 Ledderhose disease +M72.2 Fibroblastic disorders - Plantar fascial fibromatosis,5759,M72.2,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.2,ORPHAcode: 199251 Ledderhose disease,ICD-10 M72.4 Fibroblastic disorders - Pseudosarcomatous fibromatosis,5760,M72.4,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.4,,ICD-10 -M72.6 Fibroblastic disorders - Necrotizing fasciitis,5761,M72.6,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.6,ORPHAcode: 440368 Necrotizing soft tissue infection -M72.8 Other fibroblastic disorders,5762,M72.8,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.8,ORPHAcode: 199260 Calcifying aponeurotic fibroma +M72.6 Fibroblastic disorders - Necrotizing fasciitis,5761,M72.6,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.6,ORPHAcode: 440368 Necrotizing soft tissue infection,ICD-10 +M72.8 Other fibroblastic disorders,5762,M72.8,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.8,ORPHAcode: 199260 Calcifying aponeurotic fibroma,ICD-10 "M72.9 Fibroblastic disorder, unspecified",5763,M72.9,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M72.9,,ICD-10 M73 Soft tissue disorders in diseases classified elsewhere,5764,M73,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M73,,ICD-10 M73.0 Soft tissue disorders in diseases classified elsewhere - Gonococcal bursitis,5765,M73.0,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M73.0,,ICD-10 @@ -5803,9 +5803,9 @@ M77.5 Other enthesopathy of foot,5795,M77.5,M70-M79 Other soft tissue disorders, "M79.3 Other soft tissue disorders, not elsewhere classified - Panniculitis, unspecified",5802,M79.3,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.3,,ICD-10 "M79.4 Other soft tissue disorders, not elsewhere classified - Hypertrophy of (infrapatellar) fat pad",5803,M79.4,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.4,,ICD-10 M79.5 Residual foreign body in soft tissue,5804,M79.5,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.5,,ICD-10 -"M79.6 Other soft tissue disorders, not elsewhere classified - Pain in limb",5805,M79.6,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.6,ORPHAcode: 391384 Familial episodic pain syndrome +"M79.6 Other soft tissue disorders, not elsewhere classified - Pain in limb",5805,M79.6,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.6,ORPHAcode: 391384 Familial episodic pain syndrome,ICD-10 "M79.7 Other soft tissue disorders, not elsewhere classified - Fibromyalgia",5806,M79.7,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.7,,ICD-10 -M79.8 Other specified soft tissue disorders,5807,M79.8,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.8,ORPHAcode: 306553 Myospherulosis +M79.8 Other specified soft tissue disorders,5807,M79.8,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.8,ORPHAcode: 306553 Myospherulosis,ICD-10 "M79.9 Soft tissue disorder, unspecified",5808,M79.9,M70-M79 Other soft tissue disorders,http://identifiers.org/icd/M79.9,,ICD-10 M80-M94 Osteopathies and chondropathies,5809,,XIII Diseases of the musculoskeletal system and connective tissue,,,ICD-10 M80-M85 Disorders of bone density and structure,5810,M80-M85,M80-M94 Osteopathies and chondropathies,,,ICD-10 @@ -5815,7 +5815,7 @@ M80.1 Postoophorectomy osteoporosis with pathological fracture,5813,M80.1,M80-M8 M80.2 Osteoporosis of disuse with pathological fracture,5814,M80.2,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M80.2,,ICD-10 M80.3 Postsurgical malabsorption osteoporosis with pathological fracture,5815,M80.3,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M80.3,,ICD-10 M80.4 Drug-induced osteoporosis with pathological fracture,5816,M80.4,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M80.4,,ICD-10 -M80.5 Idiopathic osteoporosis with pathological fracture,5817,M80.5,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M80.5,ORPHAcode: 391330 X-linked osteoporosis with fractures +M80.5 Idiopathic osteoporosis with pathological fracture,5817,M80.5,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M80.5,ORPHAcode: 391330 X-linked osteoporosis with fractures,ICD-10 M80.8 Other osteoporosis with pathological fracture,5818,M80.8,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M80.8,,ICD-10 M80.9 Unspecified osteoporosis with pathological fracture,5819,M80.9,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M80.9,,ICD-10 M81 Osteoporosis without pathological fracture,5820,M81,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81,,ICD-10 @@ -5824,7 +5824,7 @@ M81.1 Postoophorectomy osteoporosis,5822,M81.1,M80-M85 Disorders of bone density M81.2 Osteoporosis of disuse,5823,M81.2,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.2,,ICD-10 M81.3 Postsurgical malabsorption osteoporosis,5824,M81.3,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.3,,ICD-10 M81.4 Drug-induced osteoporosis,5825,M81.4,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.4,,ICD-10 -M81.5 Idiopathic osteoporosis,5826,M81.5,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.5,ORPHAcode: 85193 Idiopathic juvenile osteoporosis +M81.5 Idiopathic osteoporosis,5826,M81.5,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.5,ORPHAcode: 85193 Idiopathic juvenile osteoporosis,ICD-10 M81.6 Localized osteoporosis [Lequesne],5827,M81.6,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.6,,ICD-10 M81.8 Other osteoporosis,5828,M81.8,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.8,,ICD-10 "M81.9 Osteoporosis, unspecified",5829,M81.9,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M81.9,,ICD-10 @@ -5839,7 +5839,7 @@ M83.2 Adult osteomalacia due to malabsorption,5837,M83.2,M80-M85 Disorders of bo M83.3 Adult osteomalacia due to malnutrition,5838,M83.3,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M83.3,,ICD-10 M83.4 Adult osteomalacia - Aluminium bone disease,5839,M83.4,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M83.4,,ICD-10 M83.5 Other drug-induced osteomalacia in adults,5840,M83.5,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M83.5,,ICD-10 -M83.8 Other adult osteomalacia,5841,M83.8,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M83.8,ORPHAcode: 352540 Oncogenic osteomalacia +M83.8 Other adult osteomalacia,5841,M83.8,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M83.8,ORPHAcode: 352540 Oncogenic osteomalacia,ICD-10 "M83.9 Adult osteomalacia, unspecified",5842,M83.9,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M83.9,,ICD-10 M84 Disorders of continuity of bone,5843,M84,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M84,,ICD-10 M84.0 Malunion of fracture,5844,M84.0,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M84.0,,ICD-10 @@ -5850,35 +5850,35 @@ M84.2 Delayed union of fracture,5846,M84.2,M80-M85 Disorders of bone density and M84.8 Other disorders of continuity of bone,5849,M84.8,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M84.8,,ICD-10 "M84.9 Disorder of continuity of bone, unspecified",5850,M84.9,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M84.9,,ICD-10 M85 Other disorders of bone density and structure,5851,M85,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85,,ICD-10 -M85.0 Other disorders of bone density and structure - Fibrous dysplasia (monostotic),5852,M85.0,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.0,ORPHAcode: 57782 Mazabraud syndrome +M85.0 Other disorders of bone density and structure - Fibrous dysplasia (monostotic),5852,M85.0,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.0,ORPHAcode: 57782 Mazabraud syndrome,ICD-10 M85.1 Other disorders of bone density and structure - Skeletal fluorosis,5853,M85.1,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.1,,ICD-10 -M85.2 Hyperostosis of skull,5854,M85.2,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.2,ORPHAcode: 1513 Craniodiaphyseal dysplasia -M85.3 Other disorders of bone density and structure - Osteitis condensans,5855,M85.3,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.3,ORPHAcode: 57196 Medial condensing osteitis of the clavicle -M85.4 Solitary bone cyst,5856,M85.4,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.4,ORPHAcode: 83468 Solitary bone cyst +M85.2 Hyperostosis of skull,5854,M85.2,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.2,ORPHAcode: 1513 Craniodiaphyseal dysplasia,ICD-10 +M85.3 Other disorders of bone density and structure - Osteitis condensans,5855,M85.3,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.3,ORPHAcode: 57196 Medial condensing osteitis of the clavicle,ICD-10 +M85.4 Solitary bone cyst,5856,M85.4,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.4,ORPHAcode: 83468 Solitary bone cyst,ICD-10 M85.5 Aneurysmal bone cyst,5857,M85.5,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.5,,ICD-10 M85.6 Other cyst of bone,5858,M85.6,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.6,,ICD-10 -M85.8 Other specified disorders of bone density and structure,5859,M85.8,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.8,ORPHAcode: 1879 Melorheostosis with osteopoikilosis +M85.8 Other specified disorders of bone density and structure,5859,M85.8,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.8,ORPHAcode: 1879 Melorheostosis with osteopoikilosis,ICD-10 "M85.9 Disorder of bone density and structure, unspecified",5860,M85.9,M80-M85 Disorders of bone density and structure,http://identifiers.org/icd/M85.9,,ICD-10 M86-M90 Other osteopathies,5861,M86-M90,M80-M94 Osteopathies and chondropathies,,,ICD-10 M86 Osteomyelitis,5862,M86,M86-M90 Other osteopathies,http://identifiers.org/icd/M86,,ICD-10 M86.0 Acute haematogenous osteomyelitis,5863,M86.0,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.0,,ICD-10 M86.1 Other acute osteomyelitis,5864,M86.1,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.1,,ICD-10 M86.2 Subacute osteomyelitis,5865,M86.2,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.2,,ICD-10 -M86.3 Chronic multifocal osteomyelitis,5866,M86.3,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.3,ORPHAcode: 793 SAPHO syndrome +M86.3 Chronic multifocal osteomyelitis,5866,M86.3,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.3,ORPHAcode: 793 SAPHO syndrome,ICD-10 M86.4 Chronic osteomyelitis with draining sinus,5867,M86.4,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.4,,ICD-10 M86.5 Other chronic haematogenous osteomyelitis,5868,M86.5,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.5,,ICD-10 M86.6 Other chronic osteomyelitis,5869,M86.6,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.6,,ICD-10 M86.8 Other osteomyelitis,5870,M86.8,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.8,,ICD-10 "M86.9 Osteomyelitis, unspecified",5871,M86.9,M86-M90 Other osteopathies,http://identifiers.org/icd/M86.9,,ICD-10 M87 Osteonecrosis,5872,M87,M86-M90 Other osteopathies,http://identifiers.org/icd/M87,,ICD-10 -M87.0 Osteonecrosis - Idiopathic aseptic necrosis of bone,5873,M87.0,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.0,ORPHAcode: 399307 Idiopathic avascular necrosis -M87.1 Osteonecrosis due to drugs,5874,M87.1,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.1,ORPHAcode: 399180 Secondary non-traumatic avascular necrosis -M87.2 Osteonecrosis due to previous trauma,5875,M87.2,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.2,ORPHAcode: 399175 Traumatic avascular necrosis +M87.0 Osteonecrosis - Idiopathic aseptic necrosis of bone,5873,M87.0,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.0,ORPHAcode: 399307 Idiopathic avascular necrosis,ICD-10 +M87.1 Osteonecrosis due to drugs,5874,M87.1,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.1,ORPHAcode: 399180 Secondary non-traumatic avascular necrosis,ICD-10 +M87.2 Osteonecrosis due to previous trauma,5875,M87.2,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.2,ORPHAcode: 399175 Traumatic avascular necrosis,ICD-10 M87.3 Other secondary osteonecrosis,5876,M87.3,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.3,,ICD-10 -M87.8 Other osteonecrosis,5877,M87.8,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.8,ORPHAcode: 86820 Familial avascular necrosis of femoral head +M87.8 Other osteonecrosis,5877,M87.8,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.8,ORPHAcode: 86820 Familial avascular necrosis of femoral head,ICD-10 "M87.9 Osteonecrosis, unspecified",5878,M87.9,M86-M90 Other osteopathies,http://identifiers.org/icd/M87.9,,ICD-10 M88 Paget disease of bone [osteitis deformans],5879,M88,M86-M90 Other osteopathies,http://identifiers.org/icd/M88,,ICD-10 -M88.0 Paget disease of skull,5880,M88.0,M86-M90 Other osteopathies,http://identifiers.org/icd/M88.0,ORPHAcode: 2801 Juvenile Paget disease +M88.0 Paget disease of skull,5880,M88.0,M86-M90 Other osteopathies,http://identifiers.org/icd/M88.0,ORPHAcode: 2801 Juvenile Paget disease,ICD-10 M88.8 Paget disease of other bones,5881,M88.8,M86-M90 Other osteopathies,http://identifiers.org/icd/M88.8,,ICD-10 "M88.9 Paget disease of bone, unspecified",5882,M88.9,M86-M90 Other osteopathies,http://identifiers.org/icd/M88.9,,ICD-10 M89 Other disorders of bone,5883,M89,M86-M90 Other osteopathies,http://identifiers.org/icd/M89,,ICD-10 @@ -5886,11 +5886,11 @@ M89.0 Other disorders of bone - Algoneurodystrophy,5884,M89.0,M86-M90 Other oste M89.1 Other disorders of bone - Epiphyseal arrest,5885,M89.1,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.1,,ICD-10 M89.2 Other disorders of bone development and growth,5886,M89.2,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.2,,ICD-10 M89.3 Hypertrophy of bone,5887,M89.3,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.3,,ICD-10 -M89.4 Other hypertrophic osteoarthropathy,5888,M89.4,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.4,ORPHAcode: 1525 Cranio-osteoarthropathy +M89.4 Other hypertrophic osteoarthropathy,5888,M89.4,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.4,ORPHAcode: 1525 Cranio-osteoarthropathy,ICD-10 M94 Other disorders of cartilage,5889,M94,M91-M94 Chondropathies,http://identifiers.org/icd/M94,,ICD-10 -M89.5 Other disorders of bone - Osteolysis,5890,M89.5,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.5,ORPHAcode: 73 Gorham-Stout disease +M89.5 Other disorders of bone - Osteolysis,5890,M89.5,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.5,ORPHAcode: 73 Gorham-Stout disease,ICD-10 M89.6 Other disorders of bone - Osteopathy after poliomyelitis,5891,M89.6,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.6,,ICD-10 -M89.8 Other specified disorders of bone,5892,M89.8,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.8,ORPHAcode: 1310 Caffey disease +M89.8 Other specified disorders of bone,5892,M89.8,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.8,ORPHAcode: 1310 Caffey disease,ICD-10 "M89.9 Disorder of bone, unspecified",5893,M89.9,M86-M90 Other osteopathies,http://identifiers.org/icd/M89.9,,ICD-10 M90 Osteopathies in diseases classified elsewhere,5894,M90,M86-M90 Other osteopathies,http://identifiers.org/icd/M90,,ICD-10 M90.0 Osteopathies in diseases classified elsewhere - Tuberculosis of bone,5895,M90.0,M86-M90 Other osteopathies,http://identifiers.org/icd/M90.0,,ICD-10 @@ -5905,31 +5905,31 @@ M90.8 Osteopathy in other diseases classified elsewhere,5903,M90.8,M86-M90 Other M91-M94 Chondropathies,5904,M91-M94,M80-M94 Osteopathies and chondropathies,,,ICD-10 M91 Juvenile osteochondrosis of hip and pelvis,5905,M91,M91-M94 Chondropathies,http://identifiers.org/icd/M91,,ICD-10 M91.0 Juvenile osteochondrosis of pelvis,5906,M91.0,M91-M94 Chondropathies,http://identifiers.org/icd/M91.0,,ICD-10 -M91.1 Juvenile osteochondrosis of head of femur [Legg-Calvé-Perthes,5907,M91.1,M91-M94 Chondropathies,http://identifiers.org/icd/M91.1,ORPHAcode: 2380 Legg-Calv -Perthes d +M91.1 Juvenile osteochondrosis of head of femur [Legg-Calvé-Perthes,5907,M91.1,M91-M94 Chondropathies,http://identifiers.org/icd/M91.1,ORPHAcode: 2380 Legg-Calv -Perthes d,ICD-10 M91.2 Juvenile osteochondrosis of hip and pelvis - Coxa plana,5908,M91.2,M91-M94 Chondropathies,http://identifiers.org/icd/M91.2,,ICD-10 M91.3 Juvenile osteochondrosis of hip and pelvis - Pseudocoxalgia,5909,M91.3,M91-M94 Chondropathies,http://identifiers.org/icd/M91.3,,ICD-10 -M91.8 Other juvenile osteochondrosis of hip and pelvis,5910,M91.8,M91-M94 Chondropathies,http://identifiers.org/icd/M91.8,ORPHAcode: 3408 Upington disease +M91.8 Other juvenile osteochondrosis of hip and pelvis,5910,M91.8,M91-M94 Chondropathies,http://identifiers.org/icd/M91.8,ORPHAcode: 3408 Upington disease,ICD-10 "M91.9 Juvenile osteochondrosis of hip and pelvis, unspecified",5911,M91.9,M91-M94 Chondropathies,http://identifiers.org/icd/M91.9,,ICD-10 M92 Other juvenile osteochondrosis,5912,M92,M91-M94 Chondropathies,http://identifiers.org/icd/M92,,ICD-10 -M92.0 Juvenile osteochondrosis of humerus,5913,M92.0,M91-M94 Chondropathies,http://identifiers.org/icd/M92.0,ORPHAcode: 97336 Panner disease +M92.0 Juvenile osteochondrosis of humerus,5913,M92.0,M91-M94 Chondropathies,http://identifiers.org/icd/M92.0,ORPHAcode: 97336 Panner disease,ICD-10 M92.1 Juvenile osteochondrosis of radius and ulna,5914,M92.1,M91-M94 Chondropathies,http://identifiers.org/icd/M92.1,,ICD-10 -M92.2 Juvenile osteochondrosis of hand,5915,M92.2,M91-M94 Chondropathies,http://identifiers.org/icd/M92.2,ORPHAcode: 97332 Kienbock disease +M92.2 Juvenile osteochondrosis of hand,5915,M92.2,M91-M94 Chondropathies,http://identifiers.org/icd/M92.2,ORPHAcode: 97332 Kienbock disease,ICD-10 M92.3 Other juvenile osteochondrosis of upper limb,5916,M92.3,M91-M94 Chondropathies,http://identifiers.org/icd/M92.3,,ICD-10 -M92.4 Juvenile osteochondrosis of patella,5917,M92.4,M91-M94 Chondropathies,http://identifiers.org/icd/M92.4,ORPHAcode: 97337 Sinding-Larsen-Johansson disease -M92.5 Juvenile osteochondrosis of tibia and fibula,5918,M92.5,M91-M94 Chondropathies,http://identifiers.org/icd/M92.5,ORPHAcode: 2768 Blount disease -M92.6 Juvenile osteochondrosis of tarsus,5919,M92.6,M91-M94 Chondropathies,http://identifiers.org/icd/M92.6,ORPHAcode: 563991 Osteochondrosis of the tarsal bone -M92.7 Juvenile osteochondrosis of metatarsus,5920,M92.7,M91-M94 Chondropathies,http://identifiers.org/icd/M92.7,ORPHAcode: 564003 Osteochondrosis of the metatarsal bone +M92.4 Juvenile osteochondrosis of patella,5917,M92.4,M91-M94 Chondropathies,http://identifiers.org/icd/M92.4,ORPHAcode: 97337 Sinding-Larsen-Johansson disease,ICD-10 +M92.5 Juvenile osteochondrosis of tibia and fibula,5918,M92.5,M91-M94 Chondropathies,http://identifiers.org/icd/M92.5,ORPHAcode: 2768 Blount disease,ICD-10 +M92.6 Juvenile osteochondrosis of tarsus,5919,M92.6,M91-M94 Chondropathies,http://identifiers.org/icd/M92.6,ORPHAcode: 563991 Osteochondrosis of the tarsal bone,ICD-10 +M92.7 Juvenile osteochondrosis of metatarsus,5920,M92.7,M91-M94 Chondropathies,http://identifiers.org/icd/M92.7,ORPHAcode: 564003 Osteochondrosis of the metatarsal bone,ICD-10 M92.8 Other specified juvenile osteochondrosis,5921,M92.8,M91-M94 Chondropathies,http://identifiers.org/icd/M92.8,,ICD-10 "M92.9 Juvenile osteochondrosis, unspecified",5922,M92.9,M91-M94 Chondropathies,http://identifiers.org/icd/M92.9,,ICD-10 M93 Other osteochondropathies,5923,M93,M91-M94 Chondropathies,http://identifiers.org/icd/M93,,ICD-10 M93.0 Other osteochondropathies - Slipped upper femoral epiphysis (nontraumatic),5924,M93.0,M91-M94 Chondropathies,http://identifiers.org/icd/M93.0,,ICD-10 M93.1 Kienböck disease of adult,5925,M93.1,M91-M94 Chondropathies,http://identifiers.org/icd/M93.1,,ICD-10 -M93.2 Other osteochondropathies - Osteochondritis dissecans,5926,M93.2,M91-M94 Chondropathies,http://identifiers.org/icd/M93.2,ORPHAcode: 2764 Osteochondritis dissecans +M93.2 Other osteochondropathies - Osteochondritis dissecans,5926,M93.2,M91-M94 Chondropathies,http://identifiers.org/icd/M93.2,ORPHAcode: 2764 Osteochondritis dissecans,ICD-10 M93.8 Other specified osteochondropathies,5927,M93.8,M91-M94 Chondropathies,http://identifiers.org/icd/M93.8,,ICD-10 -"M93.9 Other osteochondropathies - Osteochondropathy, unspecified",5928,M93.9,M91-M94 Chondropathies,http://identifiers.org/icd/M93.9,ORPHAcode: 399329 Epiphysiolysis of the hip +"M93.9 Other osteochondropathies - Osteochondropathy, unspecified",5928,M93.9,M91-M94 Chondropathies,http://identifiers.org/icd/M93.9,ORPHAcode: 399329 Epiphysiolysis of the hip,ICD-10 M94.0 Other disorders of cartilage - Chondrocostal junction syndrome [Tietze],5929,M94.0,M91-M94 Chondropathies,http://identifiers.org/icd/M94.0,,ICD-10 N08.3 Glomerular disorders in diabetes mellitus,5930,N08.3,N00-N08 Glomerular diseases,http://identifiers.org/icd/N08.3,,ICD-10 -M94.1 Other disorders of cartilage - Relapsing polychondritis,5931,M94.1,M91-M94 Chondropathies,http://identifiers.org/icd/M94.1,ORPHAcode: 728 Relapsing polychondritis +M94.1 Other disorders of cartilage - Relapsing polychondritis,5931,M94.1,M91-M94 Chondropathies,http://identifiers.org/icd/M94.1,ORPHAcode: 728 Relapsing polychondritis,ICD-10 O83 Other assisted single delivery,5932,O83,O80-O84 Delivery,http://identifiers.org/icd/O83,,ICD-10 M94.2 Other disorders of cartilage - Chondromalacia,5933,M94.2,M91-M94 Chondropathies,http://identifiers.org/icd/M94.2,,ICD-10 M94.3 Other disorders of cartilage - Chondrolysis,5934,M94.3,M91-M94 Chondropathies,http://identifiers.org/icd/M94.3,,ICD-10 @@ -5977,7 +5977,7 @@ N02.8 Recurrent and persistent haematuria - Recurrent and persistent haematuria: N03 Chronic nephritic syndrome,5975,N03,N00-N08 Glomerular diseases,http://identifiers.org/icd/N03,,ICD-10 N04 Nephrotic syndrome,5976,N04,N00-N08 Glomerular diseases,http://identifiers.org/icd/N04,,ICD-10 N04.5 Nephrotic syndrome - Nephrotic syndrome: Diffuse mesangiocapillary glomerulonephritis,,N04.5,N00-N08 Glomerular diseases,http://identifiers.org/icd/N04.5,,ICD-10 -N05 Unspecified nephritic syndrome,5977,N05,N00-N08 Glomerular diseases,http://identifiers.org/icd/N05,ORPHAcode: 567544 Idiopathic non-lupus full-house nephropathy +N05 Unspecified nephritic syndrome,5977,N05,N00-N08 Glomerular diseases,http://identifiers.org/icd/N05,ORPHAcode: 567544 Idiopathic non-lupus full-house nephropathy,ICD-10 N05.5 Unspecified nephritic syndrome - Unspecified nephritic syndrome: Diffuse mesangiocapillary glomerulonephritis,,N05.5,N00-N08 Glomerular diseases,http://identifiers.org/icd/N05.5,,ICD-10 N06 Isolated proteinuria with specified morphological lesion,5978,N06,N00-N08 Glomerular diseases,http://identifiers.org/icd/N06,,ICD-10 "N07 Hereditary nephropathy, not elsewhere classified",5979,N07,N00-N08 Glomerular diseases,http://identifiers.org/icd/N07,,ICD-10 @@ -5988,11 +5988,11 @@ N08.2 Glomerular disorders in blood diseases and disorders involving the immune N08.5 Glomerular disorders in systemic connective tissue disorders,5984,N08.5,N00-N08 Glomerular diseases,http://identifiers.org/icd/N08.5,,ICD-10 N08.8 Glomerular disorders in other diseases classified elsewhere,5985,N08.8,N00-N08 Glomerular diseases,http://identifiers.org/icd/N08.8,,ICD-10 N10-N16 Renal tubulo-interstitial diseases,5986,,XIV Diseases of the genitourinary system,,,ICD-10 -N10 Acute tubulo-interstitial nephritis,5987,N10,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N10,ORPHAcode: 91500 Tubulointerstitial nephritis and uveitis syndrome +N10 Acute tubulo-interstitial nephritis,5987,N10,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N10,ORPHAcode: 91500 Tubulointerstitial nephritis and uveitis syndrome,ICD-10 N11 Chronic tubulo-interstitial nephritis,5988,N11,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N11,,ICD-10 N11.0 Nonobstructive reflux-associated chronic pyelonephritis,5989,N11.0,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N11.0,,ICD-10 N11.1 Chronic obstructive pyelonephritis,5990,N11.1,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N11.1,,ICD-10 -N11.8 Other chronic tubulo-interstitial nephritis,5991,N11.8,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N11.8,ORPHAcode: 401996 Karyomegalic interstitial nephritis +N11.8 Other chronic tubulo-interstitial nephritis,5991,N11.8,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N11.8,ORPHAcode: 401996 Karyomegalic interstitial nephritis,ICD-10 "N11.9 Chronic tubulo-interstitial nephritis, unspecified",5992,N11.9,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N11.9,,ICD-10 "N12 Tubulo-interstitial nephritis, not specified as acute or chronic",5993,N12,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N12,,ICD-10 N13 Obstructive and reflux uropathy,5994,N13,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13,,ICD-10 @@ -6003,7 +6003,7 @@ N13.3 Other and unspecified hydronephrosis,5998,N13.3,N10-N16 Renal tubulo-inter N13.4 Obstructive and reflux uropathy - Hydroureter,5999,N13.4,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13.4,,ICD-10 N13.5 Kinking and stricture of ureter without hydronephrosis,6000,N13.5,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13.5,,ICD-10 N13.6 Obstructive and reflux uropathy - Pyonephrosis,6001,N13.6,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13.6,,ICD-10 -N13.7 Vesicoureteral-reflux-associated uropathy,6002,N13.7,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13.7,ORPHAcode: 289365 Familial vesicoureteral reflux +N13.7 Vesicoureteral-reflux-associated uropathy,6002,N13.7,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13.7,ORPHAcode: 289365 Familial vesicoureteral reflux,ICD-10 N13.8 Other obstructive and reflux uropathy,6003,N13.8,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13.8,,ICD-10 "N13.9 Obstructive and reflux uropathy, unspecified",6004,N13.9,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N13.9,,ICD-10 N14 Drug- and heavy-metal-induced tubulo-interstitial and tubular conditions,6005,N14,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N14,,ICD-10 @@ -6015,7 +6015,7 @@ N14.3 Drug- and heavy-metal-induced tubulo-interstitial and tubular conditions - N15 Other renal tubulo-interstitial diseases,6011,N15,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N15,,ICD-10 N15.0 Other renal tubulo-interstitial diseases - Balkan nephropathy,6012,N15.0,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N15.0,,ICD-10 N15.1 Renal and perinephric abscess,6013,N15.1,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N15.1,,ICD-10 -N15.8 Other specified renal tubulo-interstitial diseases,6014,N15.8,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N15.8,ORPHAcode: 358 Gitelman syndrome +N15.8 Other specified renal tubulo-interstitial diseases,6014,N15.8,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N15.8,ORPHAcode: 358 Gitelman syndrome,ICD-10 "N18.4 Chronic kidney disease, stage 4",6015,N18.4,N17-N19 Renal failure,http://identifiers.org/icd/N18.4,,ICD-10 "N15.9 Renal tubulo-interstitial disease, unspecified",6016,N15.9,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N15.9,,ICD-10 N16 Renal tubulo-interstitial disorders in diseases classified elsewhere,6017,N16,N10-N16 Renal tubulo-interstitial diseases,http://identifiers.org/icd/N16,,ICD-10 @@ -6055,8 +6055,8 @@ N23 Unspecified renal colic,6050,N23,N20-N23 Urolithiasis,http://identifiers.org N25-N29 Other disorders of kidney and ureter,6051,,XIV Diseases of the genitourinary system,,,ICD-10 N25 Disorders resulting from impaired renal tubular function,6052,N25,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N25,,ICD-10 N25.0 Renal osteodystrophy,6053,N25.0,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N25.0,,ICD-10 -N25.1 Disorders resulting from impaired renal tubular function - Nephrogenic diabetes insipidus,6054,N25.1,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N25.1,ORPHAcode: 223 Nephrogenic diabetes insipidus -N25.8 Other disorders resulting from impaired renal tubular function,6055,N25.8,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N25.8,ORPHAcode: 18 Distal renal tubular acidosis +N25.1 Disorders resulting from impaired renal tubular function - Nephrogenic diabetes insipidus,6054,N25.1,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N25.1,ORPHAcode: 223 Nephrogenic diabetes insipidus,ICD-10 +N25.8 Other disorders resulting from impaired renal tubular function,6055,N25.8,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N25.8,ORPHAcode: 18 Distal renal tubular acidosis,ICD-10 "N25.9 Disorder resulting from impaired renal tubular function, unspecified",6056,N25.9,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N25.9,,ICD-10 N26 Unspecified contracted kidney,6057,N26,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N26,,ICD-10 N26.9 DMS,,N26.9,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N26.9,,ICD-10 @@ -6067,7 +6067,7 @@ N27 Small kidney of unknown cause,6058,N27,N25-N29 Other disorders of kidney and "N28 Other disorders of kidney and ureter, not elsewhere classified",6062,N28,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N28,,ICD-10 N28.0 Ischaemia and infarction of kidney,6063,N28.0,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N28.0,,ICD-10 N28.1 Cyst of kidney,6064,N28.1,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N28.1,,ICD-10 -N28.8 Other specified disorders of kidney and ureter,6065,N28.8,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N28.8,ORPHAcode: 556 Malakoplakia +N28.8 Other specified disorders of kidney and ureter,6065,N28.8,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N28.8,ORPHAcode: 556 Malakoplakia,ICD-10 "N28.9 Disorder of kidney and ureter, unspecified",6066,N28.9,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N28.9,,ICD-10 N29 Other disorders of kidney and ureter in diseases classified elsewhere,6067,N29,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N29,,ICD-10 N29.0 Late syphilis of kidney,6068,N29.0,N25-N29 Other disorders of kidney and ureter,http://identifiers.org/icd/N29.0,,ICD-10 @@ -6076,7 +6076,7 @@ N29.8 Other disorders of kidney and ureter in other diseases classified elsewher N30-N39 Other diseases of urinary system,6071,,XIV Diseases of the genitourinary system,,,ICD-10 N30 Cystitis,6072,N30,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N30,,ICD-10 N30.0 Acute cystitis,6073,N30.0,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N30.0,,ICD-10 -N30.1 Interstitial cystitis (chronic),6074,N30.1,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N30.1,ORPHAcode: 37202 Interstitial cystitis +N30.1 Interstitial cystitis (chronic),6074,N30.1,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N30.1,ORPHAcode: 37202 Interstitial cystitis,ICD-10 N30.2 Other chronic cystitis,6075,N30.2,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N30.2,,ICD-10 N30.3 Cystitis - Trigonitis,6076,N30.3,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N30.3,,ICD-10 N30.4 Irradiation cystitis,6077,N30.4,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N30.4,,ICD-10 @@ -6086,7 +6086,7 @@ N30.8 Other cystitis,6078,N30.8,N30-N39 Other diseases of urinary system,http:// "N31.0 Uninhibited neuropathic bladder, not elsewhere classified",6081,N31.0,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N31.0,,ICD-10 "N31.1 Reflex neuropathic bladder, not elsewhere classified",6082,N31.1,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N31.1,,ICD-10 "N31.2 Flaccid neuropathic bladder, not elsewhere classified",6083,N31.2,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N31.2,,ICD-10 -N31.8 Other neuromuscular dysfunction of bladder,6084,N31.8,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N31.8,ORPHAcode: 2704 Ochoa syndrome +N31.8 Other neuromuscular dysfunction of bladder,6084,N31.8,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N31.8,ORPHAcode: 2704 Ochoa syndrome,ICD-10 "N31.9 Neuromuscular dysfunction of bladder, unspecified",6085,N31.9,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N31.9,,ICD-10 N32 Other disorders of bladder,6086,N32,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32,,ICD-10 N32.0 Bladder-neck obstruction,6087,N32.0,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32.0,,ICD-10 @@ -6094,7 +6094,7 @@ N32.1 Other disorders of bladder - Vesicointestinal fistula,6088,N32.1,N30-N39 O "N32.2 Other disorders of bladder - Vesical fistula, not elsewhere classified",6089,N32.2,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32.2,,ICD-10 N32.3 Diverticulum of bladder,6090,N32.3,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32.3,,ICD-10 "N32.4 Rupture of bladder, nontraumatic",6091,N32.4,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32.4,,ICD-10 -N32.8 Other specified disorders of bladder,6092,N32.8,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32.8,ORPHAcode: 84085 Hinman syndrome +N32.8 Other specified disorders of bladder,6092,N32.8,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32.8,ORPHAcode: 84085 Hinman syndrome,ICD-10 "N32.9 Bladder disorder, unspecified",6093,N32.9,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N32.9,,ICD-10 N33 Bladder disorders in diseases classified elsewhere,6094,N33,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N33,,ICD-10 N33.0 Bladder disorders in diseases classified elsewhere - Tuberculous cystitis,6095,N33.0,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N33.0,,ICD-10 @@ -6126,7 +6126,7 @@ N48.6 Induratio penis plastica,6119,N48.6,N40-N51 Diseases of male genital organ "N39.2 Other disorders of urinary system - Orthostatic proteinuria, unspecified",6121,N39.2,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N39.2,,ICD-10 N39.3 Other disorders of urinary system - Stress incontinence,6122,N39.3,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N39.3,,ICD-10 N39.4 Other specified urinary incontinence,6123,N39.4,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N39.4,,ICD-10 -N39.8 Other specified disorders of urinary system,6124,N39.8,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N39.8,ORPHAcode: 2795 Fowler urethral sphincter dysfunction syndrome +N39.8 Other specified disorders of urinary system,6124,N39.8,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N39.8,ORPHAcode: 2795 Fowler urethral sphincter dysfunction syndrome,ICD-10 "N39.9 Disorder of urinary system, unspecified",6125,N39.9,N30-N39 Other diseases of urinary system,http://identifiers.org/icd/N39.9,,ICD-10 N40-N51 Diseases of male genital organs,6126,,XIV Diseases of the genitourinary system,,,ICD-10 N40 Hyperplasia of prostate,6127,N40,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N40,,ICD-10 @@ -6154,13 +6154,13 @@ N44 Torsion of testis,6148,N44,N40-N51 Diseases of male genital organs,http://id N45 Orchitis and epididymitis,6149,N45,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N45,,ICD-10 "N45.0 Orchitis, epididymitis and epididymo-orchitis with abscess",6150,N45.0,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N45.0,,ICD-10 "N45.9 Orchitis, epididymitis and epididymo-orchitis without abscess",6151,N45.9,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N45.9,,ICD-10 -N46 Male infertility,6152,N46,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N46,ORPHAcode: 3471 Young syndrome +N46 Male infertility,6152,N46,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N46,ORPHAcode: 3471 Young syndrome,ICD-10 "N47 Redundant prepuce, phimosis and paraphimosis",6153,N47,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N47,,ICD-10 N48 Other disorders of penis,6154,N48,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48,,ICD-10 N48.0 Leukoplakia of penis,6155,N48.0,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.0,,ICD-10 N48.1 Other disorders of penis - Balanoposthitis,6156,N48.1,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.1,,ICD-10 N48.2 Other inflammatory disorders of penis,6157,N48.2,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.2,,ICD-10 -N48.3 Other disorders of penis - Priapism,6158,N48.3,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.3,ORPHAcode: 140949 Low-flow priapism +N48.3 Other disorders of penis - Priapism,6158,N48.3,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.3,ORPHAcode: 140949 Low-flow priapism,ICD-10 N48.4 Impotence of organic origin,6159,N48.4,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.4,,ICD-10 N48.5 Ulcer of penis,6160,N48.5,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.5,,ICD-10 N48.8 Other specified disorders of penis,6161,N48.8,N40-N51 Diseases of male genital organs,http://identifiers.org/icd/N48.8,,ICD-10 @@ -6189,8 +6189,8 @@ N60.3 Benign mammary dysplasia - Fibrosclerosis of breast,6182,N60.3,N60-N64 Dis N60.4 Mammary duct ectasia,6183,N60.4,N60-N64 Disorders of breast,http://identifiers.org/icd/N60.4,,ICD-10 N60.8 Other benign mammary dysplasias,6184,N60.8,N60-N64 Disorders of breast,http://identifiers.org/icd/N60.8,,ICD-10 "N60.9 Benign mammary dysplasia, unspecified",6185,N60.9,N60-N64 Disorders of breast,http://identifiers.org/icd/N60.9,,ICD-10 -N61 Inflammatory disorders of breast,6186,N61,N60-N64 Disorders of breast,http://identifiers.org/icd/N61,ORPHAcode: 64722 Granulomatous mastitis -N62 Hypertrophy of breast,6187,N62,N60-N64 Disorders of breast,http://identifiers.org/icd/N62,ORPHAcode: 180176 Familial juvenile hypertrophy of the breast +N61 Inflammatory disorders of breast,6186,N61,N60-N64 Disorders of breast,http://identifiers.org/icd/N61,ORPHAcode: 64722 Granulomatous mastitis,ICD-10 +N62 Hypertrophy of breast,6187,N62,N60-N64 Disorders of breast,http://identifiers.org/icd/N62,ORPHAcode: 180176 Familial juvenile hypertrophy of the breast,ICD-10 N63 Unspecified lump in breast,6188,N63,N60-N64 Disorders of breast,http://identifiers.org/icd/N63,,ICD-10 N64 Other disorders of breast,6189,N64,N60-N64 Disorders of breast,http://identifiers.org/icd/N64,,ICD-10 N64.0 Fissure and fistula of nipple,6190,N64.0,N60-N64 Disorders of breast,http://identifiers.org/icd/N64.0,,ICD-10 @@ -6248,7 +6248,7 @@ N77.0 Ulceration of vulva in infectious and parasitic diseases classified elsewh N77.8 Vulvovaginal ulceration and inflammation in other diseases classified elsewhere,6242,N77.8,N70-N77 Inflammatory diseases of female pelvic organs,http://identifiers.org/icd/N77.8,,ICD-10 N80-N98 Noninflammatory disorders of female genital tract,6243,,XIV Diseases of the genitourinary system,,,ICD-10 N80 Endometriosis,6244,N80,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N80,,ICD-10 -N80.0 Endometriosis of uterus,6245,N80.0,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N80.0,ORPHAcode: 137820 Extrapelvic endometriosis +N80.0 Endometriosis of uterus,6245,N80.0,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N80.0,ORPHAcode: 137820 Extrapelvic endometriosis,ICD-10 N80.1 Endometriosis of ovary,6246,N80.1,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N80.1,,ICD-10 N80.2 Endometriosis of fallopian tube,6247,N80.2,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N80.2,,ICD-10 N80.3 Endometriosis of pelvic peritoneum,6248,N80.3,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N80.3,,ICD-10 @@ -6303,7 +6303,7 @@ N85.2 Hypertrophy of uterus,6296,N85.2,N80-N98 Noninflammatory disorders of fema N85.3 Subinvolution of uterus,6297,N85.3,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.3,,ICD-10 N85.4 Malposition of uterus,6298,N85.4,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.4,,ICD-10 N85.5 Inversion of uterus,6299,N85.5,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.5,,ICD-10 -"N85.6 Other noninflammatory disorders of uterus, except cervix - Intrauterine synechiae",6300,N85.6,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.6,ORPHAcode: 137686 Asherman syndrome +"N85.6 Other noninflammatory disorders of uterus, except cervix - Intrauterine synechiae",6300,N85.6,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.6,ORPHAcode: 137686 Asherman syndrome,ICD-10 "N85.7 Other noninflammatory disorders of uterus, except cervix - Haematometra",6301,N85.7,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.7,,ICD-10 N85.8 Other specified noninflammatory disorders of uterus,6302,N85.8,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.8,,ICD-10 "N85.9 Noninflammatory disorder of uterus, unspecified",6303,N85.9,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N85.9,,ICD-10 @@ -6371,7 +6371,7 @@ N94.3 Premenstrual tension syndrome,6364,N94.3,N80-N98 Noninflammatory disorders N94.4 Pain and other conditions associated with female genital organs and menstrual cycle - Primary dysmenorrhoea,6365,N94.4,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N94.4,,ICD-10 N94.5 Pain and other conditions associated with female genital organs and menstrual cycle - Secondary dysmenorrhoea,6366,N94.5,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N94.5,,ICD-10 "N94.6 Pain and other conditions associated with female genital organs and menstrual cycle - Dysmenorrhoea, unspecified",6367,N94.6,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N94.6,,ICD-10 -N94.8 Other specified conditions associated with female genital organs and menstrual cycle,6368,N94.8,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N94.8,ORPHAcode: 498251 Menstrual cycle-dependent periodic fever +N94.8 Other specified conditions associated with female genital organs and menstrual cycle,6368,N94.8,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N94.8,ORPHAcode: 498251 Menstrual cycle-dependent periodic fever,ICD-10 N94.9 Unspecified condition associated with female genital organs and menstrual cycle,6369,N94.9,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N94.9,,ICD-10 N95 Menopausal and other perimenopausal disorders,6370,N95,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N95,,ICD-10 N95.0 Postmenopausal bleeding,6371,N95.0,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N95.0,,ICD-10 @@ -6388,11 +6388,11 @@ N97.1 Female infertility of tubal origin,6381,N97.1,N80-N98 Noninflammatory diso N97.2 Female infertility of uterine origin,6382,N97.2,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N97.2,,ICD-10 N97.3 Female infertility of cervical origin,6383,N97.3,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N97.3,,ICD-10 N97.4 Female infertility associated with male factors,6384,N97.4,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N97.4,,ICD-10 -N97.8 Female infertility of other origin,6385,N97.8,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N97.8,ORPHAcode: 404466 Female infertility due to zona pellucida defect +N97.8 Female infertility of other origin,6385,N97.8,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N97.8,ORPHAcode: 404466 Female infertility due to zona pellucida defect,ICD-10 "N97.9 Female infertility, unspecified",6386,N97.9,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N97.9,,ICD-10 N98 Complications associated with artificial fertilization,6387,N98,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N98,,ICD-10 N98.0 Infection associated with artificial insemination,6388,N98.0,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N98.0,,ICD-10 -N98.1 Complications associated with artificial fertilization - Hyperstimulation of ovaries,6389,N98.1,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N98.1,ORPHAcode: 64739 Ovarian hyperstimulation syndrome +N98.1 Complications associated with artificial fertilization - Hyperstimulation of ovaries,6389,N98.1,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N98.1,ORPHAcode: 64739 Ovarian hyperstimulation syndrome,ICD-10 N98.2 Complications of attempted introduction of fertilized ovum following in vitro fertilization,6390,N98.2,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N98.2,,ICD-10 N98.3 Complications of attempted introduction of embryo in embryo transfer,6391,N98.3,N80-N98 Noninflammatory disorders of female genital tract,http://identifiers.org/icd/N98.3,,ICD-10 O81.0 Low forceps delivery,6392,O81.0,O80-O84 Delivery,http://identifiers.org/icd/O81.0,,ICD-10 @@ -6416,7 +6416,7 @@ O00.1 Tubal pregnancy,6409,O00.1,O00-O08 Pregnancy with abortive outcome,http:// O00.2 Ovarian pregnancy,6410,O00.2,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O00.2,,ICD-10 O00.8 Other ectopic pregnancy,6411,O00.8,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O00.8,,ICD-10 "O00.9 Ectopic pregnancy, unspecified",6412,O00.9,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O00.9,,ICD-10 -O01.0 Classical hydatidiform mole,6413,O01.0,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O01.0,ORPHAcode: 99927 Hydatidiform mole +O01.0 Classical hydatidiform mole,6413,O01.0,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O01.0,ORPHAcode: 99927 Hydatidiform mole,ICD-10 O01.1 Incomplete and partial hydatidiform mole,6414,O01.1,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O01.1,,ICD-10 "O01.9 Hydatidiform mole, unspecified",6415,O01.9,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O01.9,,ICD-10 O02 Other abnormal products of conception,6416,O02,O00-O08 Pregnancy with abortive outcome,http://identifiers.org/icd/O02,,ICD-10 @@ -6470,7 +6470,7 @@ O13 Gestational [pregnancy-induced] hypertension,6463,O13,"O10-O16 Oedema, prote O14 Pre-eclampsia,6464,O14,"O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium",http://identifiers.org/icd/O14,,ICD-10 O14.0 Pre-eclampsia - Mild to moderate pre-eclampsia,6465,O14.0,"O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium",http://identifiers.org/icd/O14.0,,ICD-10 O14.1 Pre-eclampsia - Severe pre-eclampsia,6466,O14.1,"O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium",http://identifiers.org/icd/O14.1,,ICD-10 -O14.2 Pre-eclampsia - HELLP syndrome,6467,O14.2,"O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium",http://identifiers.org/icd/O14.2,ORPHAcode: 244242 HELLP syndrome +O14.2 Pre-eclampsia - HELLP syndrome,6467,O14.2,"O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium",http://identifiers.org/icd/O14.2,ORPHAcode: 244242 HELLP syndrome,ICD-10 "O21.9 Vomiting of pregnancy, unspecified",6468,O21.9,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O21.9,,ICD-10 "O14.9 Pre-eclampsia - Pre-eclampsia, unspecified",6469,O14.9,"O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium",http://identifiers.org/icd/O14.9,,ICD-10 O15 Eclampsia,6470,O15,"O10-O16 Oedema, proteinuria and hypertensive disorders in pregnancy, childbirth and the puerperium",http://identifiers.org/icd/O15,,ICD-10 @@ -6523,10 +6523,10 @@ O26.2 Pregnancy care of habitual aborter,6516,O26.2,O20-O29 Other maternal disor O26.3 Retained intrauterine contraceptive device in pregnancy,6517,O26.3,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.3,,ICD-10 O26.4 Maternal care for other conditions predominantly related to pregnancy - Herpes gestationis,6518,O26.4,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.4,,ICD-10 O26.5 Maternal hypotension syndrome,6519,O26.5,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.5,,ICD-10 -"O26.6 Liver disorders in pregnancy, childbirth and the puerperium",6520,O26.6,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.6,ORPHAcode: 69665 Intrahepatic cholestasis of pregnancy +"O26.6 Liver disorders in pregnancy, childbirth and the puerperium",6520,O26.6,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.6,ORPHAcode: 69665 Intrahepatic cholestasis of pregnancy,ICD-10 "O26.7 Subluxation of symphysis (pubis) in pregnancy, childbirth and the puerperium",6521,O26.7,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.7,,ICD-10 O60.0 Preterm labour without delivery,6522,O60.0,O60-O75 Complications of labour and delivery,http://identifiers.org/icd/O60.0,,ICD-10 -O26.8 Other specified pregnancy-related conditions,6523,O26.8,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.8,ORPHAcode: 64745 Pruritic urticarial papules and plaques of pregnancy +O26.8 Other specified pregnancy-related conditions,6523,O26.8,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.8,ORPHAcode: 64745 Pruritic urticarial papules and plaques of pregnancy,ICD-10 "O26.9 Pregnancy-related condition, unspecified",6524,O26.9,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O26.9,,ICD-10 O28 Abnormal findings on antenatal screening of mother,6525,O28,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O28,,ICD-10 O28.0 Abnormal haematological finding on antenatal screening of mother,6526,O28.0,O20-O29 Other maternal disorders predominantly related to pregnancy,http://identifiers.org/icd/O28.0,,ICD-10 @@ -6610,7 +6610,7 @@ O36.1 Maternal care for other isoimmunization,6603,O36.1,O30-O48 Maternal care r O36.2 Maternal care for hydrops fetalis,6604,O36.2,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.2,,ICD-10 O36.3 Maternal care for signs of fetal hypoxia,6605,O36.3,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.3,,ICD-10 O36.4 Maternal care for intrauterine death,6606,O36.4,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.4,,ICD-10 -O36.5 Maternal care for poor fetal growth,6607,O36.5,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.5,ORPHAcode: 439167 Placental insufficiency +O36.5 Maternal care for poor fetal growth,6607,O36.5,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.5,ORPHAcode: 439167 Placental insufficiency,ICD-10 O36.6 Maternal care for excessive fetal growth,6608,O36.6,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.6,,ICD-10 O36.7 Maternal care for viable fetus in abdominal pregnancy,6609,O36.7,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.7,,ICD-10 O36.8 Maternal care for other specified fetal problems,6610,O36.8,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O36.8,,ICD-10 @@ -6629,7 +6629,7 @@ O42 Premature rupture of membranes,6619,O42,O30-O48 Maternal care related to the "O42.2 Premature rupture of membranes, labour delayed by therapy",6623,O42.2,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O42.2,,ICD-10 "O42.9 Premature rupture of membranes, unspecified",6624,O42.9,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O42.9,,ICD-10 O43 Placental disorders,6625,O43,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O43,,ICD-10 -O43.0 Placental transfusion syndromes,6626,O43.0,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O43.0,ORPHAcode: 95431 Twin to twin transfusion syndrome +O43.0 Placental transfusion syndromes,6626,O43.0,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O43.0,ORPHAcode: 95431 Twin to twin transfusion syndrome,ICD-10 O43.1 Placental disorders - Malformation of placenta,6627,O43.1,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O43.1,,ICD-10 O43.2 Placental disorders - Morbidly adherent placenta,6628,O43.2,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O43.2,,ICD-10 O43.8 Other placental disorders,6629,O43.8,O30-O48 Maternal care related to the fetus and amniotic cavity and possible delivery problems,http://identifiers.org/icd/O43.8,,ICD-10 @@ -6829,7 +6829,7 @@ O89.8 Other complications of anaesthesia during the puerperium,6820,O89.8,O85-O9 O90.0 Disruption of caesarean section wound,6823,O90.0,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.0,,ICD-10 O90.1 Disruption of perineal obstetric wound,6824,O90.1,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.1,,ICD-10 O90.2 Haematoma of obstetric wound,6825,O90.2,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.2,,ICD-10 -O90.3 Cardiomyopathy in the puerperium,6826,O90.3,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.3,ORPHAcode: 563 Peripartum cardiomyopathy +O90.3 Cardiomyopathy in the puerperium,6826,O90.3,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.3,ORPHAcode: 563 Peripartum cardiomyopathy,ICD-10 "O90.4 Complications of the puerperium, not elsewhere classified - Postpartum acute renal failure",6827,O90.4,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.4,,ICD-10 "O90.5 Complications of the puerperium, not elsewhere classified - Postpartum thyroiditis",6828,O90.5,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.5,,ICD-10 "O90.8 Other complications of the puerperium, not elsewhere classified",6829,O90.8,O85-O92 Complications predominantly related to the puerperium,http://identifiers.org/icd/O90.8,,ICD-10 @@ -6886,7 +6886,7 @@ P00.0 Fetus and newborn affected by maternal hypertensive disorders,6879,P00.0," P00.1 Fetus and newborn affected by maternal renal and urinary tract diseases,6880,P00.1,"P00-P04 Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery",http://identifiers.org/icd/P00.1,,ICD-10 P00.2 Fetus and newborn affected by maternal infectious and parasitic diseases,6881,P00.2,"P00-P04 Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery",http://identifiers.org/icd/P00.2,,ICD-10 P00.3 Fetus and newborn affected by other maternal circulatory and respiratory diseases,6882,P00.3,"P00-P04 Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery",http://identifiers.org/icd/P00.3,,ICD-10 -P00.4 Fetus and newborn affected by maternal nutritional disorders,6883,P00.4,"P00-P04 Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery",http://identifiers.org/icd/P00.4,ORPHAcode: 1926 Diabetic embryopathy +P00.4 Fetus and newborn affected by maternal nutritional disorders,6883,P00.4,"P00-P04 Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery",http://identifiers.org/icd/P00.4,ORPHAcode: 1926 Diabetic embryopathy,ICD-10 P00.5 Fetus and newborn affected by maternal injury,6884,P00.5,"P00-P04 Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery",http://identifiers.org/icd/P00.5,,ICD-10 P15.1 Birth injury to spleen,6885,P15.1,P10-P15 Birth trauma,http://identifiers.org/icd/P15.1,,ICD-10 P00.6 Fetus and newborn affected by surgical procedure on mother,6886,P00.6,"P00-P04 Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery",http://identifiers.org/icd/P00.6,,ICD-10 @@ -6982,7 +6982,7 @@ P14 Birth injury to peripheral nervous system,6975,P14,P10-P15 Birth trauma,http P14.0 Erb paralysis due to birth injury,6976,P14.0,P10-P15 Birth trauma,http://identifiers.org/icd/P14.0,,ICD-10 P14.1 Klumpke paralysis due to birth injury,6977,P14.1,P10-P15 Birth trauma,http://identifiers.org/icd/P14.1,,ICD-10 P14.2 Phrenic nerve paralysis due to birth injury,6978,P14.2,P10-P15 Birth trauma,http://identifiers.org/icd/P14.2,,ICD-10 -P14.3 Other brachial plexus birth injuries,6979,P14.3,P10-P15 Birth trauma,http://identifiers.org/icd/P14.3,ORPHAcode: 439202 Non-recovering obstetric brachial plexus lesion +P14.3 Other brachial plexus birth injuries,6979,P14.3,P10-P15 Birth trauma,http://identifiers.org/icd/P14.3,ORPHAcode: 439202 Non-recovering obstetric brachial plexus lesion,ICD-10 P14.8 Birth injuries to other parts of peripheral nervous system,6980,P14.8,P10-P15 Birth trauma,http://identifiers.org/icd/P14.8,,ICD-10 "P14.9 Birth injury to peripheral nervous system, unspecified",6981,P14.9,P10-P15 Birth trauma,http://identifiers.org/icd/P14.9,,ICD-10 P15 Other birth injuries,6982,P15,P10-P15 Birth trauma,http://identifiers.org/icd/P15,,ICD-10 @@ -7003,9 +7003,9 @@ P21.0 Severe birth asphyxia,6996,P21.0,P20-P29 Respiratory and cardiovascular di P21.1 Mild and moderate birth asphyxia,6997,P21.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P21.1,,ICD-10 "P21.9 Birth asphyxia, unspecified",6998,P21.9,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P21.9,,ICD-10 P22 Respiratory distress of newborn,6999,P22,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P22,,ICD-10 -P22.0 Respiratory distress syndrome of newborn,7000,P22.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P22.0,ORPHAcode: 70587 Infant acute respiratory distress syndrome +P22.0 Respiratory distress syndrome of newborn,7000,P22.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P22.0,ORPHAcode: 70587 Infant acute respiratory distress syndrome,ICD-10 P22.1 Transient tachypnoea of newborn,7001,P22.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P22.1,,ICD-10 -P22.8 Other respiratory distress of newborn,7002,P22.8,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P22.8,ORPHAcode: 217557 Pulmonary interstitial glycogenosis +P22.8 Other respiratory distress of newborn,7002,P22.8,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P22.8,ORPHAcode: 217557 Pulmonary interstitial glycogenosis,ICD-10 "P22.9 Respiratory distress of newborn, unspecified",7003,P22.9,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P22.9,,ICD-10 P23 Congenital pneumonia,7004,P23,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P23,,ICD-10 P23.0 Congenital pneumonia due to viral agent,7005,P23.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P23.0,,ICD-10 @@ -7020,7 +7020,7 @@ P23.6 Congenital pneumonia due to other bacterial agents,7013,P23.6,P20-P29 Resp P23.8 Congenital pneumonia due to other organisms,7014,P23.8,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P23.8,,ICD-10 "P23.9 Congenital pneumonia, unspecified",7015,P23.9,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P23.9,,ICD-10 P24 Neonatal aspiration syndromes,7016,P24,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P24,,ICD-10 -P24.0 Neonatal aspiration of meconium,7017,P24.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P24.0,ORPHAcode: 70588 Meconium aspiration syndrome +P24.0 Neonatal aspiration of meconium,7017,P24.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P24.0,ORPHAcode: 70588 Meconium aspiration syndrome,ICD-10 R34 Anuria and oliguria,7018,R34,R30-R39 Symptoms and signs involving the urinary system,http://identifiers.org/icd/R34,,ICD-10 P24.1 Neonatal aspiration of amniotic fluid and mucus,7019,P24.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P24.1,,ICD-10 P24.2 Neonatal aspiration of blood,7020,P24.2,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P24.2,,ICD-10 @@ -7041,21 +7041,21 @@ R35 Polyuria,7034,R35,R30-R39 Symptoms and signs involving the urinary system,ht P26.9 Unspecified pulmonary haemorrhage originating in the perinatal period,7035,P26.9,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P26.9,,ICD-10 P27 Chronic respiratory disease originating in the perinatal period,7036,P27,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P27,,ICD-10 P27.0 Chronic respiratory disease originating in the perinatal period - Wilson-Mikity syndrome,7037,P27.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P27.0,,ICD-10 -P27.1 Bronchopulmonary dysplasia originating in the perinatal period,7038,P27.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P27.1,ORPHAcode: 70589 Bronchopulmonary dysplasia +P27.1 Bronchopulmonary dysplasia originating in the perinatal period,7038,P27.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P27.1,ORPHAcode: 70589 Bronchopulmonary dysplasia,ICD-10 P27.8 Other chronic respiratory diseases originating in the perinatal period,7039,P27.8,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P27.8,,ICD-10 P27.9 Unspecified chronic respiratory disease originating in the perinatal period,7040,P27.9,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P27.9,,ICD-10 P28 Other respiratory conditions originating in the perinatal period,7041,P28,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28,,ICD-10 -P28.0 Other respiratory conditions originating in the perinatal period - Primary atelectasis of newborn,7042,P28.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.0,ORPHAcode: 217563 Neonatal acute respiratory distress due to SP-B deficiency +P28.0 Other respiratory conditions originating in the perinatal period - Primary atelectasis of newborn,7042,P28.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.0,ORPHAcode: 217563 Neonatal acute respiratory distress due to SP-B deficiency,ICD-10 P28.1 Other and unspecified atelectasis of newborn,7043,P28.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.1,,ICD-10 P28.2 Other respiratory conditions originating in the perinatal period - Cyanotic attacks of newborn,7044,P28.2,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.2,,ICD-10 P28.3 Other respiratory conditions originating in the perinatal period - Primary sleep apnoea of newborn,7045,P28.3,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.3,,ICD-10 -P28.4 Other apnoea of newborn,7046,P28.4,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.4,ORPHAcode: 70590 Infantile apnea +P28.4 Other apnoea of newborn,7046,P28.4,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.4,ORPHAcode: 70590 Infantile apnea,ICD-10 P28.5 Respiratory failure of newborn,7047,P28.5,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.5,,ICD-10 P28.8 Other specified respiratory conditions of newborn,7048,P28.8,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.8,,ICD-10 "P28.9 Respiratory condition of newborn, unspecified",7049,P28.9,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P28.9,,ICD-10 P29 Cardiovascular disorders originating in the perinatal period,7050,P29,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29,,ICD-10 P29.0 Cardiovascular disorders originating in the perinatal period - Neonatal cardiac failure,7051,P29.0,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29.0,,ICD-10 -P29.1 Cardiovascular disorders originating in the perinatal period - Neonatal cardiac dysrhythmia,7052,P29.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29.1,ORPHAcode: 45452 Idiopathic neonatal atrial flutter +P29.1 Cardiovascular disorders originating in the perinatal period - Neonatal cardiac dysrhythmia,7052,P29.1,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29.1,ORPHAcode: 45452 Idiopathic neonatal atrial flutter,ICD-10 P29.2 Cardiovascular disorders originating in the perinatal period - Neonatal hypertension,7053,P29.2,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29.2,,ICD-10 P29.3 Cardiovascular disorders originating in the perinatal period - Persistent fetal circulation,7054,P29.3,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29.3,,ICD-10 P29.4 Cardiovascular disorders originating in the perinatal period - Transient myocardial ischaemia of newborn,7055,P29.4,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29.4,,ICD-10 @@ -7063,14 +7063,14 @@ P29.8 Other cardiovascular disorders originating in the perinatal period,7056,P2 "P29.9 Cardiovascular disorder originating in the perinatal period, unspecified",7057,P29.9,P20-P29 Respiratory and cardiovascular disorders specific to the perinatal period,http://identifiers.org/icd/P29.9,,ICD-10 P35-P39 Infections specific to the perinatal period,7058,,XVI Certain conditions originating in the perinatal period,,,ICD-10 P35 Congenital viral diseases,7059,P35,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35,,ICD-10 -P35.0 Congenital rubella syndrome,7060,P35.0,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.0,ORPHAcode: 290 Congenital rubella syndrome -P35.1 Congenital cytomegalovirus infection,7061,P35.1,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.1,ORPHAcode: 294 Fetal cytomegalovirus syndrome -P35.2 Congenital herpesviral [herpes simplex] infection,7062,P35.2,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.2,ORPHAcode: 293 Congenital herpes simplex virus infection +P35.0 Congenital rubella syndrome,7060,P35.0,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.0,ORPHAcode: 290 Congenital rubella syndrome,ICD-10 +P35.1 Congenital cytomegalovirus infection,7061,P35.1,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.1,ORPHAcode: 294 Fetal cytomegalovirus syndrome,ICD-10 +P35.2 Congenital herpesviral [herpes simplex] infection,7062,P35.2,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.2,ORPHAcode: 293 Congenital herpes simplex virus infection,ICD-10 P35.3 Congenital viral hepatitis,7063,P35.3,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.3,,ICD-10 -P35.8 Other congenital viral diseases,7064,P35.8,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.8,ORPHAcode: 291 Congenital varicella syndrome +P35.8 Other congenital viral diseases,7064,P35.8,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.8,ORPHAcode: 291 Congenital varicella syndrome,ICD-10 "P35.9 Congenital viral disease, unspecified",7065,P35.9,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P35.9,,ICD-10 P36 Bacterial sepsis of newborn,7066,P36,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P36,,ICD-10 -"P36.0 Sepsis of newborn due to streptococcus, group B",7067,P36.0,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P36.0,ORPHAcode: 90051 Sepsis in premature infants +"P36.0 Sepsis of newborn due to streptococcus, group B",7067,P36.0,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P36.0,ORPHAcode: 90051 Sepsis in premature infants,ICD-10 P36.1 Sepsis of newborn due to other and unspecified streptococci,7068,P36.1,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P36.1,,ICD-10 P36.2 Sepsis of newborn due to Staphylococcus aureus,7069,P36.2,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P36.2,,ICD-10 P36.3 Sepsis of newborn due to other and unspecified staphylococci,7070,P36.3,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P36.3,,ICD-10 @@ -7079,7 +7079,7 @@ P36.8 Other bacterial sepsis of newborn,7072,P36.8,P35-P39 Infections specific t "P36.9 Bacterial sepsis of newborn, unspecified",7073,P36.9,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P36.9,,ICD-10 P37 Other congenital infectious and parasitic diseases,7074,P37,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P37,,ICD-10 P37.0 Congenital tuberculosis,7075,P37.0,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P37.0,,ICD-10 -P37.1 Congenital toxoplasmosis,7076,P37.1,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P37.1,ORPHAcode: 858 Congenital toxoplasmosis +P37.1 Congenital toxoplasmosis,7076,P37.1,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P37.1,ORPHAcode: 858 Congenital toxoplasmosis,ICD-10 P37.2 Other congenital infectious and parasitic diseases - Neonatal (disseminated) listeriosis,7077,P37.2,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P37.2,,ICD-10 P37.3 Congenital falciparum malaria,7078,P37.3,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P37.3,,ICD-10 P37.4 Other congenital malaria,7079,P37.4,P35-P39 Infections specific to the perinatal period,http://identifiers.org/icd/P37.4,,ICD-10 @@ -7136,14 +7136,14 @@ P54.8 Other specified neonatal haemorrhages,7129,P54.8,P50-P61 Haemorrhagic and "P54.9 Neonatal haemorrhage, unspecified",7130,P54.9,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P54.9,,ICD-10 P55 Haemolytic disease of fetus and newborn,7131,P55,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P55,,ICD-10 P55.0 Rh isoimmunization of fetus and newborn,7132,P55.0,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P55.0,,ICD-10 -P55.8 Other haemolytic diseases of fetus and newborn,7133,P55.8,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P55.8,ORPHAcode: 275944 Hemolytic disease of the newborn with Kell alloimmunization +P55.8 Other haemolytic diseases of fetus and newborn,7133,P55.8,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P55.8,ORPHAcode: 275944 Hemolytic disease of the newborn with Kell alloimmunization,ICD-10 "P55.9 Haemolytic disease of fetus and newborn, unspecified",7134,P55.9,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P55.9,,ICD-10 P56 Hydrops fetalis due to haemolytic disease,7135,P56,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P56,,ICD-10 P56.0 Hydrops fetalis due to isoimmunization,7136,P56.0,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P56.0,,ICD-10 P56.9 Hydrops fetalis due to other and unspecified haemolytic disease,7137,P56.9,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P56.9,,ICD-10 P57 Kernicterus,7138,P57,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P57,,ICD-10 P57.0 Kernicterus due to isoimmunization,7139,P57.0,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P57.0,,ICD-10 -P57.8 Other specified kernicterus,7140,P57.8,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P57.8,ORPHAcode: 529799 Acute bilirubin encephalopathy +P57.8 Other specified kernicterus,7140,P57.8,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P57.8,ORPHAcode: 529799 Acute bilirubin encephalopathy,ICD-10 "P57.9 Kernicterus, unspecified",7141,P57.9,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P57.9,,ICD-10 P58 Neonatal jaundice due to other excessive haemolysis,7142,P58,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P58,,ICD-10 P58.0 Neonatal jaundice due to bruising,7143,P58.0,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P58.0,,ICD-10 @@ -7160,16 +7160,16 @@ P59.0 Neonatal jaundice associated with preterm delivery,7153,P59.0,P50-P61 Haem P59.1 Neonatal jaundice from other and unspecified causes - Inspissated bile syndrome,7154,P59.1,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P59.1,,ICD-10 P59.2 Neonatal jaundice from other and unspecified hepatocellular damage,7155,P59.2,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P59.2,,ICD-10 P59.3 Neonatal jaundice from breast milk inhibitor,7156,P59.3,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P59.3,,ICD-10 -P59.8 Neonatal jaundice from other specified causes,7157,P59.8,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P59.8,ORPHAcode: 2312 Transient familial neonatal hyperbilirubinemia +P59.8 Neonatal jaundice from other specified causes,7157,P59.8,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P59.8,ORPHAcode: 2312 Transient familial neonatal hyperbilirubinemia,ICD-10 "P59.9 Neonatal jaundice, unspecified",7158,P59.9,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P59.9,,ICD-10 P60 Disseminated intravascular coagulation of fetus and newborn,7159,P60,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P60,,ICD-10 P61 Other perinatal haematological disorders,7160,P61,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61,,ICD-10 -P61.0 Other perinatal haematological disorders - Transient neonatal thrombocytopenia,7161,P61.0,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.0,ORPHAcode: 853 Fetal and neonatal alloimmune thrombocytopenia +P61.0 Other perinatal haematological disorders - Transient neonatal thrombocytopenia,7161,P61.0,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.0,ORPHAcode: 853 Fetal and neonatal alloimmune thrombocytopenia,ICD-10 P61.1 Other perinatal haematological disorders - Polycythaemia neonatorum,7162,P61.1,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.1,,ICD-10 P61.2 Other perinatal haematological disorders - Anaemia of prematurity,7163,P61.2,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.2,,ICD-10 P61.3 Other perinatal haematological disorders - Congenital anaemia from fetal blood loss,7164,P61.3,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.3,,ICD-10 "P61.4 Other congenital anaemias, not elsewhere classified",7165,P61.4,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.4,,ICD-10 -P61.5 Other perinatal haematological disorders - Transient neonatal neutropenia,7166,P61.5,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.5,ORPHAcode: 464370 Neonatal alloimmune neutropenia +P61.5 Other perinatal haematological disorders - Transient neonatal neutropenia,7166,P61.5,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.5,ORPHAcode: 464370 Neonatal alloimmune neutropenia,ICD-10 P61.6 Other transient neonatal disorders of coagulation,7167,P61.6,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.6,,ICD-10 P61.8 Other specified perinatal haematological disorders,7168,P61.8,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.8,,ICD-10 "P61.9 Perinatal haematological disorder, unspecified",7169,P61.9,P50-P61 Haemorrhagic and haematological disorders of fetus and newborn,http://identifiers.org/icd/P61.9,,ICD-10 @@ -7178,7 +7178,7 @@ P70 Transitory disorders of carbohydrate metabolism specific to fetus and newbor P70.0 Syndrome of infant of mother with gestational diabetes,7172,P70.0,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P70.0,,ICD-10 P70.1 Syndrome of infant of a diabetic mother,7173,P70.1,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P70.1,,ICD-10 Q90 Down syndrome,7174,Q90,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q90,,ICD-10 -P70.2 Transitory disorders of carbohydrate metabolism specific to fetus and newborn - Neonatal diabetes mellitus,7175,P70.2,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P70.2,ORPHAcode: 65288 Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome +P70.2 Transitory disorders of carbohydrate metabolism specific to fetus and newborn - Neonatal diabetes mellitus,7175,P70.2,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P70.2,ORPHAcode: 65288 Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome,ICD-10 P70.3 Transitory disorders of carbohydrate metabolism specific to fetus and newborn - Iatrogenic neonatal hypoglycaemia,7176,P70.3,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P70.3,,ICD-10 P70.4 Transitory disorders of carbohydrate metabolism specific to fetus and newborn - Other neonatal hypoglycaemia,7177,P70.4,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P70.4,,ICD-10 P70.8 Other transitory disorders of carbohydrate metabolism of fetus and newborn,7178,P70.8,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P70.8,,ICD-10 @@ -7194,7 +7194,7 @@ P71.8 Other transitory neonatal disorders of calcium and magnesium metabolism,71 P72 Other transitory neonatal endocrine disorders,7188,P72,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P72,,ICD-10 "P72.0 Neonatal goitre, not elsewhere classified",7189,P72.0,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P72.0,,ICD-10 P72.1 Transitory neonatal hyperthyroidism,7190,P72.1,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P72.1,,ICD-10 -"P72.2 Other transitory neonatal disorders of thyroid function, not elsewhere classified",7191,P72.2,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P72.2,ORPHAcode: 1910 Fetal iodine syndrome +"P72.2 Other transitory neonatal disorders of thyroid function, not elsewhere classified",7191,P72.2,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P72.2,ORPHAcode: 1910 Fetal iodine syndrome,ICD-10 P72.8 Other specified transitory neonatal endocrine disorders,7192,P72.8,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P72.8,,ICD-10 "P72.9 Transitory neonatal endocrine disorder, unspecified",7193,P72.9,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P72.9,,ICD-10 P74 Other transitory neonatal electrolyte and metabolic disturbances,7194,P74,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74,,ICD-10 @@ -7203,23 +7203,23 @@ P74.1 Other transitory neonatal electrolyte and metabolic disturbances - Dehydra P74.2 Disturbances of sodium balance of newborn,7197,P74.2,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.2,,ICD-10 P74.3 Disturbances of potassium balance of newborn,7198,P74.3,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.3,,ICD-10 P74.4 Other transitory electrolyte disturbances of newborn,7199,P74.4,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.4,,ICD-10 -P74.5 Transitory tyrosinaemia of newborn,7200,P74.5,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.5,ORPHAcode: 3402 Transient tyrosinemia of the newborn -P74.8 Other transitory metabolic disturbances of newborn,7201,P74.8,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.8,ORPHAcode: 289877 Transient hyperammonemia of the newborn +P74.5 Transitory tyrosinaemia of newborn,7200,P74.5,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.5,ORPHAcode: 3402 Transient tyrosinemia of the newborn,ICD-10 +P74.8 Other transitory metabolic disturbances of newborn,7201,P74.8,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.8,ORPHAcode: 289877 Transient hyperammonemia of the newborn,ICD-10 "P74.9 Transitory metabolic disturbance of newborn, unspecified",7202,P74.9,P70-P74 Transitory endocrine and metabolic disorders specific to fetus and newborn,http://identifiers.org/icd/P74.9,,ICD-10 P75-P78 Digestive system disorders of fetus and newborn,7203,,XVI Certain conditions originating in the perinatal period,,,ICD-10 P76 Other intestinal obstruction of newborn,7204,P76,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P76,,ICD-10 -P76.0 Other intestinal obstruction of newborn - Meconium plug syndrome,7205,P76.0,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P76.0,ORPHAcode: 314376 Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency +P76.0 Other intestinal obstruction of newborn - Meconium plug syndrome,7205,P76.0,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P76.0,ORPHAcode: 314376 Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency,ICD-10 P76.1 Transitory ileus of newborn,7206,P76.1,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P76.1,,ICD-10 P76.2 Intestinal obstruction due to inspissated milk,7207,P76.2,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P76.2,,ICD-10 P76.8 Other specified intestinal obstruction of newborn,7208,P76.8,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P76.8,,ICD-10 "P76.9 Intestinal obstruction of newborn, unspecified",7209,P76.9,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P76.9,,ICD-10 "XVII Congenital malformations, deformations and chromosomal abnormalities",7210,,,,,ICD-10 -P77 Necrotizing enterocolitis of fetus and newborn,7211,P77,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P77,ORPHAcode: 391673 Necrotizing enterocolitis +P77 Necrotizing enterocolitis of fetus and newborn,7211,P77,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P77,ORPHAcode: 391673 Necrotizing enterocolitis,ICD-10 P78 Other perinatal digestive system disorders,7212,P78,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78,,ICD-10 P78.0 Perinatal intestinal perforation,7213,P78.0,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78.0,,ICD-10 P78.1 Other neonatal peritonitis,7214,P78.1,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78.1,,ICD-10 P78.2 Other perinatal digestive system disorders - Neonatal haematemesis and melaena due to swallowed maternal blood,7215,P78.2,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78.2,,ICD-10 -P78.3 Other perinatal digestive system disorders - Noninfective neonatal diarrhoea,7216,P78.3,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78.3,ORPHAcode: 2290 Microvillus inclusion disease +P78.3 Other perinatal digestive system disorders - Noninfective neonatal diarrhoea,7216,P78.3,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78.3,ORPHAcode: 2290 Microvillus inclusion disease,ICD-10 P78.8 Other specified perinatal digestive system disorders,7217,P78.8,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78.8,,ICD-10 "P78.9 Perinatal digestive system disorder, unspecified",7218,P78.9,P75-P78 Digestive system disorders of fetus and newborn,http://identifiers.org/icd/P78.9,,ICD-10 P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,7219,,XVI Certain conditions originating in the perinatal period,,,ICD-10 @@ -7236,23 +7236,23 @@ P81.8 Other specified disturbances of temperature regulation of newborn,7228,P81 P83 Other conditions of integument specific to fetus and newborn,7230,P83,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83,,ICD-10 P83.0 Sclerema neonatorum,7231,P83.0,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.0,,ICD-10 P83.1 Neonatal erythema toxicum,7232,P83.1,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.1,,ICD-10 -P83.2 Hydrops fetalis not due to haemolytic disease,7233,P83.2,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.2,ORPHAcode: 1041 Hydrops fetalis +P83.2 Hydrops fetalis not due to haemolytic disease,7233,P83.2,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.2,ORPHAcode: 1041 Hydrops fetalis,ICD-10 P83.3 Other and unspecified oedema specific to fetus and newborn,7234,P83.3,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.3,,ICD-10 P83.4 Breast engorgement of newborn,7235,P83.4,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.4,,ICD-10 P83.5 Other conditions of integument specific to fetus and newborn - Congenital hydrocele,7236,P83.5,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.5,,ICD-10 P83.6 Umbilical polyp of newborn,7237,P83.6,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.6,,ICD-10 S14.3 Injury of brachial plexus,7238,S14.3,S10-S19 Injuries to the neck,http://identifiers.org/icd/S14.3,,ICD-10 -P83.8 Other specified conditions of integument specific to fetus and newborn,7239,P83.8,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.8,ORPHAcode: 398127 Neonatal scleroderma +P83.8 Other specified conditions of integument specific to fetus and newborn,7239,P83.8,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.8,ORPHAcode: 398127 Neonatal scleroderma,ICD-10 "P83.9 Condition of integument specific to fetus and newborn, unspecified",7240,P83.9,P80-P83 Conditions involving the integument and temperature regulation of fetus and newborn,http://identifiers.org/icd/P83.9,,ICD-10 P90-P96 Other disorders originating in the perinatal period,7241,,XVI Certain conditions originating in the perinatal period,,,ICD-10 P90 Convulsions of newborn,7242,P90,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P90,,ICD-10 P91 Other disturbances of cerebral status of newborn,7243,P91,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91,,ICD-10 P91.1 Acquired periventricular cysts of newborn,7244,P91.1,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.1,,ICD-10 -P91.2 Neonatal cerebral leukomalacia,7245,P91.2,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.2,ORPHAcode: 171676 Periventricular leukomalacia +P91.2 Neonatal cerebral leukomalacia,7245,P91.2,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.2,ORPHAcode: 171676 Periventricular leukomalacia,ICD-10 P91.3 Neonatal cerebral irritability,7246,P91.3,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.3,,ICD-10 P91.4 Neonatal cerebral depression,7247,P91.4,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.4,,ICD-10 P91.5 Other disturbances of cerebral status of newborn - Neonatal coma,7248,P91.5,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.5,,ICD-10 -P91.6 Hypoxic ischaemic encephalopathy of newborn,7249,P91.6,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.6,ORPHAcode: 137577 Neonatal hypoxic and ischemic brain injury +P91.6 Hypoxic ischaemic encephalopathy of newborn,7249,P91.6,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.6,ORPHAcode: 137577 Neonatal hypoxic and ischemic brain injury,ICD-10 P91.7 Acquired hydrocephalus of newborn,7250,P91.7,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.7,,ICD-10 P91.8 Other specified disturbances of cerebral status of newborn,7251,P91.8,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.8,,ICD-10 "P91.9 Disturbance of cerebral status of newborn, unspecified",7252,P91.9,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P91.9,,ICD-10 @@ -7273,7 +7273,7 @@ P94.8 Other disorders of muscle tone of newborn,7266,P94.8,P90-P96 Other disorde "P94.9 Disorder of muscle tone of newborn, unspecified",7267,P94.9,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P94.9,,ICD-10 P95 Fetal death of unspecified cause,7268,P95,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P95,,ICD-10 P96 Other conditions originating in the perinatal period,7269,P96,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P96,,ICD-10 -P96.0 Other conditions originating in the perinatal period - Congenital renal failure,7270,P96.0,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P96.0,ORPHAcode: 69063 Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization +P96.0 Other conditions originating in the perinatal period - Congenital renal failure,7270,P96.0,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P96.0,ORPHAcode: 69063 Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization,ICD-10 P96.1 Other conditions originating in the perinatal period - Neonatal withdrawal symptoms from maternal use of drugs of addiction,7271,P96.1,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P96.1,,ICD-10 P96.2 Withdrawal symptoms from therapeutic use of drugs in newborn,7272,P96.2,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P96.2,,ICD-10 P96.3 Other conditions originating in the perinatal period - Wide cranial sutures of newborn,7273,P96.3,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P96.3,,ICD-10 @@ -7283,31 +7283,31 @@ P96.8 Other specified conditions originating in the perinatal period,7276,P96.8, "P96.9 Condition originating in the perinatal period, unspecified",7277,P96.9,P90-P96 Other disorders originating in the perinatal period,http://identifiers.org/icd/P96.9,,ICD-10 Q00-Q07 Congenital malformations of the nervous system,7278,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 Q00 Anencephaly and similar malformations,7279,Q00,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q00,,ICD-10 -Q00.0 Anencephaly,7280,Q00.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q00.0,ORPHAcode: 945 Acalvaria -Q00.1 Anencephaly and similar malformations - Craniorachischisis,7281,Q00.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q00.1,ORPHAcode: 63260 Craniorachischisis -Q00.2 Anencephaly and similar malformations - Iniencephaly,7282,Q00.2,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q00.2,ORPHAcode: 63259 Iniencephaly +Q00.0 Anencephaly,7280,Q00.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q00.0,ORPHAcode: 945 Acalvaria,ICD-10 +Q00.1 Anencephaly and similar malformations - Craniorachischisis,7281,Q00.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q00.1,ORPHAcode: 63260 Craniorachischisis,ICD-10 +Q00.2 Anencephaly and similar malformations - Iniencephaly,7282,Q00.2,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q00.2,ORPHAcode: 63259 Iniencephaly,ICD-10 Q01 Encephalocele,7283,Q01,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01,,ICD-10 -Q01.0 Frontal encephalocele,7284,Q01.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01.0,ORPHAcode: 199647 Isolated encephalocele -Q01.1 Nasofrontal encephalocele,7285,Q01.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01.1,ORPHAcode: 268820 Cranial meningocele +Q01.0 Frontal encephalocele,7284,Q01.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01.0,ORPHAcode: 199647 Isolated encephalocele,ICD-10 +Q01.1 Nasofrontal encephalocele,7285,Q01.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01.1,ORPHAcode: 268820 Cranial meningocele,ICD-10 Q01.2 Occipital encephalocele,7286,Q01.2,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01.2,,ICD-10 Q01.8 Encephalocele of other sites,7287,Q01.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01.8,,ICD-10 "Q01.9 Encephalocele, unspecified",7288,Q01.9,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q01.9,,ICD-10 -Q02 Microcephaly,7289,Q02,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q02,ORPHAcode: 1665 Sporadic fetal brain disruption sequence +Q02 Microcephaly,7289,Q02,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q02,ORPHAcode: 1665 Sporadic fetal brain disruption sequence,ICD-10 Q03 Congenital hydrocephalus,7290,Q03,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q03,,ICD-10 Q03.0 Congenital hydrocephalus - Malformations of aqueduct of Sylvius,7291,Q03.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q03.0,,ICD-10 -Q03.1 Congenital hydrocephalus - Atresia of foramina of Magendie and Luschka,7292,Q03.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q03.1,ORPHAcode: 217 Isolated Dandy-Walker malformation +Q03.1 Congenital hydrocephalus - Atresia of foramina of Magendie and Luschka,7292,Q03.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q03.1,ORPHAcode: 217 Isolated Dandy-Walker malformation,ICD-10 Q03.8 Other congenital hydrocephalus,7293,Q03.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q03.8,,ICD-10 "Q03.9 Congenital hydrocephalus, unspecified",7294,Q03.9,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q03.9,,ICD-10 Q04 Other congenital malformations of brain,7295,Q04,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04,,ICD-10 -Q04.0 Congenital malformations of corpus callosum,7296,Q04.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.0,ORPHAcode: 36 Acrocallosal syndrome -Q04.1 Other congenital malformations of brain - Arhinencephaly,7297,Q04.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.1,ORPHAcode: 268936 Isolated arhinencephaly -Q04.2 Other congenital malformations of brain - Holoprosencephaly,7298,Q04.2,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.2,ORPHAcode: 2162 Holoprosencephaly -Q04.3 Other reduction deformities of brain,7299,Q04.3,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.3,ORPHAcode: 452 X-linked lissencephaly with abnormal genitalia -Q04.4 Other congenital malformations of brain - Septo-optic dysplasia,7300,Q04.4,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.4,ORPHAcode: 3157 Septo-optic dysplasia spectrum -Q04.5 Other congenital malformations of brain - Megalencephaly,7301,Q04.5,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.5,ORPHAcode: 2477 Megalencephaly -Q04.6 Congenital cerebral cysts,7302,Q04.6,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.6,ORPHAcode: 799 Schizencephaly +Q04.0 Congenital malformations of corpus callosum,7296,Q04.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.0,ORPHAcode: 36 Acrocallosal syndrome,ICD-10 +Q04.1 Other congenital malformations of brain - Arhinencephaly,7297,Q04.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.1,ORPHAcode: 268936 Isolated arhinencephaly,ICD-10 +Q04.2 Other congenital malformations of brain - Holoprosencephaly,7298,Q04.2,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.2,ORPHAcode: 2162 Holoprosencephaly,ICD-10 +Q04.3 Other reduction deformities of brain,7299,Q04.3,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.3,ORPHAcode: 452 X-linked lissencephaly with abnormal genitalia,ICD-10 +Q04.4 Other congenital malformations of brain - Septo-optic dysplasia,7300,Q04.4,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.4,ORPHAcode: 3157 Septo-optic dysplasia spectrum,ICD-10 +Q04.5 Other congenital malformations of brain - Megalencephaly,7301,Q04.5,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.5,ORPHAcode: 2477 Megalencephaly,ICD-10 +Q04.6 Congenital cerebral cysts,7302,Q04.6,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.6,ORPHAcode: 799 Schizencephaly,ICD-10 Q33.5 Ectopic tissue in lung,7303,Q33.5,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.5,,ICD-10 -Q04.8 Other specified congenital malformations of brain,7304,Q04.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.8,ORPHAcode: 1261 Bonnemann-Meinecke-Reich syndrome +Q04.8 Other specified congenital malformations of brain,7304,Q04.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.8,ORPHAcode: 1261 Bonnemann-Meinecke-Reich syndrome,ICD-10 "Q04.9 Congenital malformation of brain, unspecified",7305,Q04.9,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q04.9,,ICD-10 Q05 Spina bifida,7306,Q05,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05,,ICD-10 Q05.0 Cervical spina bifida with hydrocephalus,7307,Q05.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.0,,ICD-10 @@ -7317,229 +7317,229 @@ Q05.3 Sacral spina bifida with hydrocephalus,7310,Q05.3,Q00-Q07 Congenital malfo Q05.4 Unspecified spina bifida with hydrocephalus,7311,Q05.4,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.4,,ICD-10 Q05.5 Cervical spina bifida without hydrocephalus,7312,Q05.5,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.5,,ICD-10 Q05.6 Thoracic spina bifida without hydrocephalus,7313,Q05.6,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.6,,ICD-10 -Q05.7 Lumbar spina bifida without hydrocephalus,7314,Q05.7,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.7,ORPHAcode: 93969 Myelomeningocele -Q05.8 Sacral spina bifida without hydrocephalus,7315,Q05.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.8,ORPHAcode: 268369 Spina bifida aperta -"Q05.9 Spina bifida, unspecified",7316,Q05.9,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.9,ORPHAcode: 3176 Spina bifida-hypospadias syndrome +Q05.7 Lumbar spina bifida without hydrocephalus,7314,Q05.7,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.7,ORPHAcode: 93969 Myelomeningocele,ICD-10 +Q05.8 Sacral spina bifida without hydrocephalus,7315,Q05.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.8,ORPHAcode: 268369 Spina bifida aperta,ICD-10 +"Q05.9 Spina bifida, unspecified",7316,Q05.9,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q05.9,ORPHAcode: 3176 Spina bifida-hypospadias syndrome,ICD-10 Q06 Other congenital malformations of spinal cord,7317,Q06,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06,,ICD-10 -Q06.0 Other congenital malformations of spinal cord - Amyelia,7318,Q06.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.0,ORPHAcode: 268868 Isolated amyelia +Q06.0 Other congenital malformations of spinal cord - Amyelia,7318,Q06.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.0,ORPHAcode: 268868 Isolated amyelia,ICD-10 Q06.1 Hypoplasia and dysplasia of spinal cord,7319,Q06.1,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.1,,ICD-10 Q06.2 Other congenital malformations of spinal cord - Diastematomyelia,7320,Q06.2,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.2,,ICD-10 Q37 Cleft palate with cleft lip,7321,Q37,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q37,,ICD-10 Q06.3 Other congenital cauda equina malformations,7322,Q06.3,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.3,,ICD-10 -Q06.4 Other congenital malformations of spinal cord - Hydromyelia,7323,Q06.4,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.4,ORPHAcode: 99856 Primary syringomyelia -Q06.8 Other specified congenital malformations of spinal cord,7324,Q06.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.8,ORPHAcode: 831 Congenital cervical spinal stenosis +Q06.4 Other congenital malformations of spinal cord - Hydromyelia,7323,Q06.4,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.4,ORPHAcode: 99856 Primary syringomyelia,ICD-10 +Q06.8 Other specified congenital malformations of spinal cord,7324,Q06.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.8,ORPHAcode: 831 Congenital cervical spinal stenosis,ICD-10 "Q06.9 Congenital malformation of spinal cord, unspecified",7325,Q06.9,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q06.9,,ICD-10 Q07 Other congenital malformations of nervous system,7326,Q07,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q07,,ICD-10 -Q07.0 Other congenital malformations of nervous system - Arnold-Chiari syndrome,7327,Q07.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q07.0,ORPHAcode: 1136 Arnold-Chiari malformation type II -Q07.8 Other specified congenital malformations of nervous system,7328,Q07.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q07.8,ORPHAcode: 1532 G mez-L pez-Hern +Q07.0 Other congenital malformations of nervous system - Arnold-Chiari syndrome,7327,Q07.0,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q07.0,ORPHAcode: 1136 Arnold-Chiari malformation type II,ICD-10 +Q07.8 Other specified congenital malformations of nervous system,7328,Q07.8,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q07.8,ORPHAcode: 1532 G mez-L pez-Hern,ICD-10 "Q07.9 Congenital malformation of nervous system, unspecified",7329,Q07.9,Q00-Q07 Congenital malformations of the nervous system,http://identifiers.org/icd/Q07.9,,ICD-10 "Q10-Q18 Congenital malformations of eye, ear, face and neck",7330,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 "Q10 Congenital malformations of eyelid, lacrimal apparatus and orbit",7331,Q10,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10,,ICD-10 -Q10.0 Congenital ptosis,7332,Q10.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.0,ORPHAcode: 91411 Congenital ptosis -Q10.1 Congenital ectropion,7333,Q10.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.1,ORPHAcode: 99171 Isolated congenital ectropion +Q10.0 Congenital ptosis,7332,Q10.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.0,ORPHAcode: 91411 Congenital ptosis,ICD-10 +Q10.1 Congenital ectropion,7333,Q10.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.1,ORPHAcode: 99171 Isolated congenital ectropion,ICD-10 Q10.2 Congenital entropion,7334,Q10.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.2,,ICD-10 -Q10.3 Other congenital malformations of eyelid,7335,Q10.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.3,ORPHAcode: 126 Blepharophimosis-ptosis-epicanthus inversus syndrome -Q10.4 Absence and agenesis of lacrimal apparatus,7336,Q10.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.4,ORPHAcode: 86815 Aplasia of lacrimal and salivary glands -Q10.5 Congenital stenosis and stricture of lacrimal duct,7337,Q10.5,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.5,ORPHAcode: 451612 Familial congenital nasolacrimal duct obstruction +Q10.3 Other congenital malformations of eyelid,7335,Q10.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.3,ORPHAcode: 126 Blepharophimosis-ptosis-epicanthus inversus syndrome,ICD-10 +Q10.4 Absence and agenesis of lacrimal apparatus,7336,Q10.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.4,ORPHAcode: 86815 Aplasia of lacrimal and salivary glands,ICD-10 +Q10.5 Congenital stenosis and stricture of lacrimal duct,7337,Q10.5,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.5,ORPHAcode: 451612 Familial congenital nasolacrimal duct obstruction,ICD-10 Q17.8 Other specified congenital malformations of ear,7338,Q17.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.8,,ICD-10 -Q10.6 Other congenital malformations of lacrimal apparatus,7339,Q10.6,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.6,ORPHAcode: 91416 Isolated congenital alacrima +Q10.6 Other congenital malformations of lacrimal apparatus,7339,Q10.6,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.6,ORPHAcode: 91416 Isolated congenital alacrima,ICD-10 Q10.7 Congenital malformation of orbit,7340,Q10.7,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q10.7,,ICD-10 "Q11 Anophthalmos, microphthalmos and macrophthalmos",7341,Q11,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q11,,ICD-10 "Q11.0 Anophthalmos, microphthalmos and macrophthalmos - Cystic eyeball",7342,Q11.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q11.0,,ICD-10 Q11.1 Other anophthalmos,7343,Q11.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q11.1,,ICD-10 -Q11.2 Microphthalmos,7344,Q11.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q11.2,"ORPHAcode: 568 Microphthalmia, Lenz type" +Q11.2 Microphthalmos,7344,Q11.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q11.2,"ORPHAcode: 568 Microphthalmia, Lenz type",ICD-10 Q11.3 Macrophthalmos,7345,Q11.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q11.3,,ICD-10 Q12 Congenital lens malformations,7346,Q12,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12,,ICD-10 -Q12.0 Congenital cataract,7347,Q12.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.0,ORPHAcode: 162 Cataract-glaucoma syndrome -Q12.1 Congenital displaced lens,7348,Q12.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.1,ORPHAcode: 1885 Isolated ectopia lentis -Q12.2 Coloboma of lens,7349,Q12.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.2,ORPHAcode: 98943 Coloboma of eye lens -Q12.3 Congenital aphakia,7350,Q12.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.3,ORPHAcode: 83461 Congenital primary aphakia +Q12.0 Congenital cataract,7347,Q12.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.0,ORPHAcode: 162 Cataract-glaucoma syndrome,ICD-10 +Q12.1 Congenital displaced lens,7348,Q12.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.1,ORPHAcode: 1885 Isolated ectopia lentis,ICD-10 +Q12.2 Coloboma of lens,7349,Q12.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.2,ORPHAcode: 98943 Coloboma of eye lens,ICD-10 +Q12.3 Congenital aphakia,7350,Q12.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.3,ORPHAcode: 83461 Congenital primary aphakia,ICD-10 Q12.4 Congenital lens malformations - Spherophakia,7351,Q12.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.4,,ICD-10 Q12.8 Other congenital lens malformations,7352,Q12.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.8,,ICD-10 "Q12.9 Congenital lens malformation, unspecified",7353,Q12.9,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q12.9,,ICD-10 Q13 Congenital malformations of anterior segment of eye,7354,Q13,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13,,ICD-10 -Q13.0 Coloboma of iris,7355,Q13.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.0,ORPHAcode: 98944 Coloboma of iris +Q13.0 Coloboma of iris,7355,Q13.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.0,ORPHAcode: 98944 Coloboma of iris,ICD-10 R13 Dysphagia,7356,R13,R10-R19 Symptoms and signs involving the digestive system and abdomen,http://identifiers.org/icd/R13,,ICD-10 -Q13.1 Absence of iris,7357,Q13.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.1,ORPHAcode: 1067 Aniridia-ptosis-intellectual disability-familial obesity syndrome +Q13.1 Absence of iris,7357,Q13.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.1,ORPHAcode: 1067 Aniridia-ptosis-intellectual disability-familial obesity syndrome,ICD-10 Q13.2 Other congenital malformations of iris,7358,Q13.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.2,,ICD-10 -Q13.3 Congenital corneal opacity,7359,Q13.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.3,ORPHAcode: 91490 Isolated congenital sclerocornea -Q13.4 Other congenital corneal malformations,7360,Q13.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.4,ORPHAcode: 708 Peters anomaly +Q13.3 Congenital corneal opacity,7359,Q13.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.3,ORPHAcode: 91490 Isolated congenital sclerocornea,ICD-10 +Q13.4 Other congenital corneal malformations,7360,Q13.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.4,ORPHAcode: 708 Peters anomaly,ICD-10 Q13.5 Congenital malformations of anterior segment of eye - Blue sclera,7361,Q13.5,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.5,,ICD-10 -Q13.8 Other congenital malformations of anterior segment of eye,7362,Q13.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.8,ORPHAcode: 566 Congenital microcoria +Q13.8 Other congenital malformations of anterior segment of eye,7362,Q13.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.8,ORPHAcode: 566 Congenital microcoria,ICD-10 "Q13.9 Congenital malformation of anterior segment of eye, unspecified",7363,Q13.9,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q13.9,,ICD-10 Q14 Congenital malformations of posterior segment of eye,7364,Q14,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14,,ICD-10 -Q14.0 Congenital malformation of vitreous humour,7365,Q14.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.0,ORPHAcode: 91495 Persistent hyperplastic primary vitreous -Q14.1 Congenital malformation of retina,7366,Q14.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.1,ORPHAcode: 792 X-linked retinoschisis -Q14.2 Congenital malformation of optic disc,7367,Q14.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.2,ORPHAcode: 35737 Morning glory disc anomaly +Q14.0 Congenital malformation of vitreous humour,7365,Q14.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.0,ORPHAcode: 91495 Persistent hyperplastic primary vitreous,ICD-10 +Q14.1 Congenital malformation of retina,7366,Q14.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.1,ORPHAcode: 792 X-linked retinoschisis,ICD-10 +Q14.2 Congenital malformation of optic disc,7367,Q14.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.2,ORPHAcode: 35737 Morning glory disc anomaly,ICD-10 Q14.3 Congenital malformation of choroid,7368,Q14.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.3,,ICD-10 -Q14.8 Other congenital malformations of posterior segment of eye,7369,Q14.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.8,ORPHAcode: 98942 Coloboma of choroid and retina +Q14.8 Other congenital malformations of posterior segment of eye,7369,Q14.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.8,ORPHAcode: 98942 Coloboma of choroid and retina,ICD-10 "Q14.9 Congenital malformation of posterior segment of eye, unspecified",7370,Q14.9,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q14.9,,ICD-10 Q15 Other congenital malformations of eye,7371,Q15,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q15,,ICD-10 -Q15.0 Congenital glaucoma,7372,Q15.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q15.0,ORPHAcode: 98976 Congenital glaucoma -Q15.8 Other specified congenital malformations of eye,7373,Q15.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q15.8,ORPHAcode: 1259 Blepharoptosis-myopia-ectopia lentis syndrome +Q15.0 Congenital glaucoma,7372,Q15.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q15.0,ORPHAcode: 98976 Congenital glaucoma,ICD-10 +Q15.8 Other specified congenital malformations of eye,7373,Q15.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q15.8,ORPHAcode: 1259 Blepharoptosis-myopia-ectopia lentis syndrome,ICD-10 "Q15.9 Congenital malformation of eye, unspecified",7374,Q15.9,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q15.9,,ICD-10 Q16 Congenital malformations of ear causing impairment of hearing,7375,Q16,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16,,ICD-10 Q16.0 Congenital absence of (ear) auricle,7376,Q16.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.0,,ICD-10 -"Q16.1 Congenital absence, atresia and stricture of auditory canal (external)",7377,Q16.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.1,ORPHAcode: 93976 Anotia +"Q16.1 Congenital absence, atresia and stricture of auditory canal (external)",7377,Q16.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.1,ORPHAcode: 93976 Anotia,ICD-10 Q16.2 Absence of eustachian tube,7378,Q16.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.2,,ICD-10 -Q16.3 Congenital malformation of ear ossicles,7379,Q16.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.3,ORPHAcode: 162526 Isolated congenital auditory ossicle malformation +Q16.3 Congenital malformation of ear ossicles,7379,Q16.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.3,ORPHAcode: 162526 Isolated congenital auditory ossicle malformation,ICD-10 Q16.4 Other congenital malformations of middle ear,7380,Q16.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.4,,ICD-10 -Q16.5 Congenital malformation of inner ear,7381,Q16.5,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.5,"ORPHAcode: 90024 Deafness with labyrinthine aplasia, microtia, and microdontia" +Q16.5 Congenital malformation of inner ear,7381,Q16.5,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.5,"ORPHAcode: 90024 Deafness with labyrinthine aplasia, microtia, and microdontia",ICD-10 "Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified",7382,Q16.9,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q16.9,,ICD-10 Q17 Other congenital malformations of ear,7383,Q17,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17,,ICD-10 Q17.0 Other congenital malformations of ear - Accessory auricle,7384,Q17.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.0,,ICD-10 Q17.1 Other congenital malformations of ear - Macrotia,7385,Q17.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.1,,ICD-10 -Q17.2 Other congenital malformations of ear - Microtia,7386,Q17.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.2,ORPHAcode: 83463 Microtia +Q17.2 Other congenital malformations of ear - Microtia,7386,Q17.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.2,ORPHAcode: 83463 Microtia,ICD-10 Q17.3 Other misshapen ear,7387,Q17.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.3,,ICD-10 Q17.4 Misplaced ear,7388,Q17.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.4,,ICD-10 Q17.5 Prominent ear,7389,Q17.5,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.5,,ICD-10 "Q17.9 Congenital malformation of ear, unspecified",7390,Q17.9,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q17.9,,ICD-10 Q18 Other congenital malformations of face and neck,7391,Q18,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18,,ICD-10 -"Q18.0 Sinus, fistula and cyst of branchial cleft",7392,Q18.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.0,ORPHAcode: 141013 First branchial cleft anomaly +"Q18.0 Sinus, fistula and cyst of branchial cleft",7392,Q18.0,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.0,ORPHAcode: 141013 First branchial cleft anomaly,ICD-10 Q18.1 Preauricular sinus and cyst,7393,Q18.1,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.1,,ICD-10 Q18.2 Other branchial cleft malformations,7394,Q18.2,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.2,,ICD-10 Q18.3 Webbing of neck,7395,Q18.3,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.3,,ICD-10 -Q18.4 Other congenital malformations of face and neck - Macrostomia,7396,Q18.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.4,ORPHAcode: 141276 Tessier number 7 facial cleft +Q18.4 Other congenital malformations of face and neck - Macrostomia,7396,Q18.4,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.4,ORPHAcode: 141276 Tessier number 7 facial cleft,ICD-10 Q18.5 Other congenital malformations of face and neck - Microstomia,7397,Q18.5,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.5,,ICD-10 Q18.6 Other congenital malformations of face and neck - Macrocheilia,7398,Q18.6,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.6,,ICD-10 Q18.7 Other congenital malformations of face and neck - Microcheilia,7399,Q18.7,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.7,,ICD-10 -Q18.8 Other specified congenital malformations of face and neck,7400,Q18.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.8,ORPHAcode: 1297 Branchio-oculo-facial syndrome +Q18.8 Other specified congenital malformations of face and neck,7400,Q18.8,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.8,ORPHAcode: 1297 Branchio-oculo-facial syndrome,ICD-10 "Q18.9 Congenital malformation of face and neck, unspecified",7401,Q18.9,"Q10-Q18 Congenital malformations of eye, ear, face and neck",http://identifiers.org/icd/Q18.9,,ICD-10 Q20-Q28 Congenital malformations of the circulatory system,7402,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 Q20 Congenital malformations of cardiac chambers and connections,7403,Q20,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20,,ICD-10 -Q20.0 Congenital malformations of cardiac chambers and connections - Common arterial trunk,7404,Q20.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.0,ORPHAcode: 3384 Truncus arteriosus +Q20.0 Congenital malformations of cardiac chambers and connections - Common arterial trunk,7404,Q20.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.0,ORPHAcode: 3384 Truncus arteriosus,ICD-10 Q54.4 Hypospadias - Congenital chordee,7405,Q54.4,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.4,,ICD-10 Q21.8 Other congenital malformations of cardiac septa,7406,Q21.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.8,,ICD-10 -Q20.1 Congenital malformations of cardiac chambers and connections - Double outlet right ventricle,7407,Q20.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.1,ORPHAcode: 3426 Double outlet right ventricle -Q20.2 Congenital malformations of cardiac chambers and connections - Double outlet left ventricle,7408,Q20.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.2,ORPHAcode: 3427 Double outlet left ventricle -Q20.3 Congenital malformations of cardiac chambers and connections - Discordant ventriculoarterial connection,7409,Q20.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.3,ORPHAcode: 860 Congenitally uncorrected transposition of the great arteries -Q20.4 Congenital malformations of cardiac chambers and connections - Double inlet ventricle,7410,Q20.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.4,ORPHAcode: 1464 Univentricular heart -Q20.5 Congenital malformations of cardiac chambers and connections - Discordant atrioventricular connection,7411,Q20.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.5,ORPHAcode: 216694 Congenitally corrected transposition of the great arteries -Q20.6 Isomerism of atrial appendages,7412,Q20.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.6,ORPHAcode: 97548 Right sided atrial isomerism -Q20.8 Other congenital malformations of cardiac chambers and connections,7413,Q20.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.8,ORPHAcode: 1677 Familial idiopathic dilatation of the right atrium +Q20.1 Congenital malformations of cardiac chambers and connections - Double outlet right ventricle,7407,Q20.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.1,ORPHAcode: 3426 Double outlet right ventricle,ICD-10 +Q20.2 Congenital malformations of cardiac chambers and connections - Double outlet left ventricle,7408,Q20.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.2,ORPHAcode: 3427 Double outlet left ventricle,ICD-10 +Q20.3 Congenital malformations of cardiac chambers and connections - Discordant ventriculoarterial connection,7409,Q20.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.3,ORPHAcode: 860 Congenitally uncorrected transposition of the great arteries,ICD-10 +Q20.4 Congenital malformations of cardiac chambers and connections - Double inlet ventricle,7410,Q20.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.4,ORPHAcode: 1464 Univentricular heart,ICD-10 +Q20.5 Congenital malformations of cardiac chambers and connections - Discordant atrioventricular connection,7411,Q20.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.5,ORPHAcode: 216694 Congenitally corrected transposition of the great arteries,ICD-10 +Q20.6 Isomerism of atrial appendages,7412,Q20.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.6,ORPHAcode: 97548 Right sided atrial isomerism,ICD-10 +Q20.8 Other congenital malformations of cardiac chambers and connections,7413,Q20.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.8,ORPHAcode: 1677 Familial idiopathic dilatation of the right atrium,ICD-10 "Q20.9 Congenital malformation of cardiac chambers and connections, unspecified",7414,Q20.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q20.9,,ICD-10 Q21 Congenital malformations of cardiac septa,7415,Q21,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21,,ICD-10 -Q21.0 Ventricular septal defect,7416,Q21.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.0,ORPHAcode: 49827 Thiamine-responsive megaloblastic anemia syndrome -Q21.1 Atrial septal defect,7417,Q21.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.1,ORPHAcode: 1478 Interatrial communication -Q21.2 Atrioventricular septal defect,7418,Q21.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.2,ORPHAcode: 1329 Complete atrioventricular septal defect -Q21.3 Tetralogy of Fallot,7419,Q21.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.3,ORPHAcode: 3303 Tetralogy of Fallot -Q21.4 Aortopulmonary septal defect,7420,Q21.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.4,ORPHAcode: 2037 Congenital aortopulmonary window +Q21.0 Ventricular septal defect,7416,Q21.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.0,ORPHAcode: 49827 Thiamine-responsive megaloblastic anemia syndrome,ICD-10 +Q21.1 Atrial septal defect,7417,Q21.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.1,ORPHAcode: 1478 Interatrial communication,ICD-10 +Q21.2 Atrioventricular septal defect,7418,Q21.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.2,ORPHAcode: 1329 Complete atrioventricular septal defect,ICD-10 +Q21.3 Tetralogy of Fallot,7419,Q21.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.3,ORPHAcode: 3303 Tetralogy of Fallot,ICD-10 +Q21.4 Aortopulmonary septal defect,7420,Q21.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.4,ORPHAcode: 2037 Congenital aortopulmonary window,ICD-10 "Q21.9 Congenital malformation of cardiac septum, unspecified",7421,Q21.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q21.9,,ICD-10 Q22 Congenital malformations of pulmonary and tricuspid valves,7422,Q22,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22,,ICD-10 Q22.0 Pulmonary valve atresia,7423,Q22.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.0,,ICD-10 -Q22.1 Congenital pulmonary valve stenosis,7424,Q22.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.1,ORPHAcode: 3189 Congenital pulmonary valvar stenosis -Q22.2 Congenital pulmonary valve insufficiency,7425,Q22.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.2,ORPHAcode: 99048 Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome +Q22.1 Congenital pulmonary valve stenosis,7424,Q22.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.1,ORPHAcode: 3189 Congenital pulmonary valvar stenosis,ICD-10 +Q22.2 Congenital pulmonary valve insufficiency,7425,Q22.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.2,ORPHAcode: 99048 Pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome,ICD-10 Q22.3 Other congenital malformations of pulmonary valve,7426,Q22.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.3,,ICD-10 -Q22.4 Congenital tricuspid stenosis,7427,Q22.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.4,ORPHAcode: 1209 Tricuspid atresia -Q22.5 Congenital malformations of pulmonary and tricuspid valves - Ebstein anomaly,7428,Q22.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.5,ORPHAcode: 1880 Ebstein malformation of the tricuspid valve -Q22.6 Congenital malformations of pulmonary and tricuspid valves - Hypoplastic right heart syndrome,7429,Q22.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.6,ORPHAcode: 439 Isolated right ventricular hypoplasia -Q22.8 Other congenital malformations of tricuspid valve,7430,Q22.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.8,ORPHAcode: 95461 Straddling or overriding tricuspid valve +Q22.4 Congenital tricuspid stenosis,7427,Q22.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.4,ORPHAcode: 1209 Tricuspid atresia,ICD-10 +Q22.5 Congenital malformations of pulmonary and tricuspid valves - Ebstein anomaly,7428,Q22.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.5,ORPHAcode: 1880 Ebstein malformation of the tricuspid valve,ICD-10 +Q22.6 Congenital malformations of pulmonary and tricuspid valves - Hypoplastic right heart syndrome,7429,Q22.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.6,ORPHAcode: 439 Isolated right ventricular hypoplasia,ICD-10 +Q22.8 Other congenital malformations of tricuspid valve,7430,Q22.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.8,ORPHAcode: 95461 Straddling or overriding tricuspid valve,ICD-10 "Q22.9 Congenital malformation of tricuspid valve, unspecified",7431,Q22.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q22.9,,ICD-10 Q23 Congenital malformations of aortic and mitral valves,7432,Q23,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23,,ICD-10 -Q23.0 Congenital stenosis of aortic valve,7433,Q23.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.0,ORPHAcode: 3093 Congenital aortic valve stenosis -Q23.1 Congenital insufficiency of aortic valve,7434,Q23.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.1,ORPHAcode: 402075 Familial bicuspid aortic valve +Q23.0 Congenital stenosis of aortic valve,7433,Q23.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.0,ORPHAcode: 3093 Congenital aortic valve stenosis,ICD-10 +Q23.1 Congenital insufficiency of aortic valve,7434,Q23.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.1,ORPHAcode: 402075 Familial bicuspid aortic valve,ICD-10 S20 Superficial injury of thorax,7435,S20,S20-S29 Injuries to the thorax,http://identifiers.org/icd/S20,,ICD-10 -Q23.2 Congenital mitral stenosis,7436,Q23.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.2,ORPHAcode: 1205 Mitral atresia -Q23.3 Congenital mitral insufficiency,7437,Q23.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.3,ORPHAcode: 95465 Cleft mitral valve -Q23.4 Congenital malformations of aortic and mitral valves - Hypoplastic left heart syndrome,7438,Q23.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.4,ORPHAcode: 2248 Hypoplastic left heart syndrome -Q23.8 Other congenital malformations of aortic and mitral valves,7439,Q23.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.8,ORPHAcode: 1568 X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome +Q23.2 Congenital mitral stenosis,7436,Q23.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.2,ORPHAcode: 1205 Mitral atresia,ICD-10 +Q23.3 Congenital mitral insufficiency,7437,Q23.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.3,ORPHAcode: 95465 Cleft mitral valve,ICD-10 +Q23.4 Congenital malformations of aortic and mitral valves - Hypoplastic left heart syndrome,7438,Q23.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.4,ORPHAcode: 2248 Hypoplastic left heart syndrome,ICD-10 +Q23.8 Other congenital malformations of aortic and mitral valves,7439,Q23.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.8,ORPHAcode: 1568 X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome,ICD-10 "Q23.9 Congenital malformation of aortic and mitral valves, unspecified",7440,Q23.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q23.9,,ICD-10 Q24 Other congenital malformations of heart,7441,Q24,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24,,ICD-10 -Q24.0 Other congenital malformations of heart - Dextrocardia,7442,Q24.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.0,ORPHAcode: 1666 Dextrocardia -Q24.1 Other congenital malformations of heart - Laevocardia,7443,Q24.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.1,ORPHAcode: 95854 Levocardia -Q24.2 Other congenital malformations of heart - Cor triatriatum,7444,Q24.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.2,ORPHAcode: 99098 Cor triatriatum dexter +Q24.0 Other congenital malformations of heart - Dextrocardia,7442,Q24.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.0,ORPHAcode: 1666 Dextrocardia,ICD-10 +Q24.1 Other congenital malformations of heart - Laevocardia,7443,Q24.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.1,ORPHAcode: 95854 Levocardia,ICD-10 +Q24.2 Other congenital malformations of heart - Cor triatriatum,7444,Q24.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.2,ORPHAcode: 99098 Cor triatriatum dexter,ICD-10 Q24.3 Other congenital malformations of heart - Pulmonary infundibular stenosis,7445,Q24.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.3,,ICD-10 -Q24.4 Congenital subaortic stenosis,7446,Q24.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.4,ORPHAcode: 3092 Fixed subaortic stenosis -Q24.5 Malformation of coronary vessels,7447,Q24.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.5,ORPHAcode: 2041 Coronary arterial fistula -Q24.6 Congenital heart block,7448,Q24.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.6,ORPHAcode: 60041 Congenital heart block -Q24.8 Other specified congenital malformations of heart,7449,Q24.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.8,ORPHAcode: 1055 Congenital left ventricular aneurysm +Q24.4 Congenital subaortic stenosis,7446,Q24.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.4,ORPHAcode: 3092 Fixed subaortic stenosis,ICD-10 +Q24.5 Malformation of coronary vessels,7447,Q24.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.5,ORPHAcode: 2041 Coronary arterial fistula,ICD-10 +Q24.6 Congenital heart block,7448,Q24.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.6,ORPHAcode: 60041 Congenital heart block,ICD-10 +Q24.8 Other specified congenital malformations of heart,7449,Q24.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.8,ORPHAcode: 1055 Congenital left ventricular aneurysm,ICD-10 "Q24.9 Congenital malformation of heart, unspecified",7450,Q24.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q24.9,,ICD-10 Q25 Congenital malformations of great arteries,7451,Q25,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25,,ICD-10 Q25.0 Congenital malformations of great arteries - Patent ductus arteriosus,7452,Q25.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.0,,ICD-10 -Q25.1 Coarctation of aorta,7453,Q25.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.1,ORPHAcode: 1457 Aorta coarctation +Q25.1 Coarctation of aorta,7453,Q25.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.1,ORPHAcode: 1457 Aorta coarctation,ICD-10 Q25.2 Atresia of aorta,7454,Q25.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.2,,ICD-10 -Q25.3 Stenosis of aorta,7455,Q25.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.3,ORPHAcode: 3193 Supravalvular aortic stenosis -Q25.4 Other congenital malformations of aorta,7456,Q25.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.4,ORPHAcode: 1054 Aneurysm of sinus of Valsalva -Q25.5 Atresia of pulmonary artery,7457,Q25.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.5,ORPHAcode: 1207 Pulmonary atresia with ventricular septal defect -Q25.6 Stenosis of pulmonary artery,7458,Q25.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.6,ORPHAcode: 99084 Peripheral pulmonary stenosis -Q25.7 Other congenital malformations of pulmonary artery,7459,Q25.7,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.7,ORPHAcode: 980 Absence of the pulmonary artery -Q25.8 Other congenital malformations of great arteries,7460,Q25.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.8,ORPHAcode: 95486 Premature closure of the arterial duct +Q25.3 Stenosis of aorta,7455,Q25.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.3,ORPHAcode: 3193 Supravalvular aortic stenosis,ICD-10 +Q25.4 Other congenital malformations of aorta,7456,Q25.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.4,ORPHAcode: 1054 Aneurysm of sinus of Valsalva,ICD-10 +Q25.5 Atresia of pulmonary artery,7457,Q25.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.5,ORPHAcode: 1207 Pulmonary atresia with ventricular septal defect,ICD-10 +Q25.6 Stenosis of pulmonary artery,7458,Q25.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.6,ORPHAcode: 99084 Peripheral pulmonary stenosis,ICD-10 +Q25.7 Other congenital malformations of pulmonary artery,7459,Q25.7,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.7,ORPHAcode: 980 Absence of the pulmonary artery,ICD-10 +Q25.8 Other congenital malformations of great arteries,7460,Q25.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.8,ORPHAcode: 95486 Premature closure of the arterial duct,ICD-10 "Q25.9 Congenital malformation of great arteries, unspecified",7461,Q25.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q25.9,,ICD-10 Q26 Congenital malformations of great veins,7462,Q26,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26,,ICD-10 -Q26.0 Congenital stenosis of vena cava,7463,Q26.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.0,ORPHAcode: 99122 Congenital stenosis of the inferior vena cava -Q26.1 Congenital malformations of great veins - Persistent left superior vena cava,7464,Q26.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.1,ORPHAcode: 99109 Persistent left superior vena cava connecting through coronary sinus to left-sided atrium -Q26.2 Congenital malformations of great veins - Total anomalous pulmonary venous connection,7465,Q26.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.2,ORPHAcode: 99125 Congenital total pulmonary venous return anomaly +Q26.0 Congenital stenosis of vena cava,7463,Q26.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.0,ORPHAcode: 99122 Congenital stenosis of the inferior vena cava,ICD-10 +Q26.1 Congenital malformations of great veins - Persistent left superior vena cava,7464,Q26.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.1,ORPHAcode: 99109 Persistent left superior vena cava connecting through coronary sinus to left-sided atrium,ICD-10 +Q26.2 Congenital malformations of great veins - Total anomalous pulmonary venous connection,7465,Q26.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.2,ORPHAcode: 99125 Congenital total pulmonary venous return anomaly,ICD-10 Q43 Other congenital malformations of intestine,7466,Q43,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43,,ICD-10 -Q26.3 Congenital malformations of great veins - Partial anomalous pulmonary venous connection,7467,Q26.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.3,ORPHAcode: 3188 Congenital pulmonary veins atresia or stenosis +Q26.3 Congenital malformations of great veins - Partial anomalous pulmonary venous connection,7467,Q26.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.3,ORPHAcode: 3188 Congenital pulmonary veins atresia or stenosis,ICD-10 "Q26.4 Congenital malformations of great veins - Anomalous pulmonary venous connection, unspecified",7468,Q26.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.4,,ICD-10 Q26.5 Congenital malformations of great veins - Anomalous portal venous connection,7469,Q26.5,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.5,,ICD-10 Q26.6 Congenital malformations of great veins - Portal vein-hepatic artery fistula,7470,Q26.6,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.6,,ICD-10 -Q26.8 Other congenital malformations of great veins,7471,Q26.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.8,ORPHAcode: 185 Scimitar syndrome +Q26.8 Other congenital malformations of great veins,7471,Q26.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.8,ORPHAcode: 185 Scimitar syndrome,ICD-10 "Q26.9 Congenital malformation of great vein, unspecified",7472,Q26.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q26.9,,ICD-10 Q27 Other congenital malformations of peripheral vascular system,7473,Q27,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27,,ICD-10 Q27.0 Congenital absence and hypoplasia of umbilical artery,7474,Q27.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.0,,ICD-10 -Q27.1 Congenital renal artery stenosis,7475,Q27.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.1,ORPHAcode: 97598 Congenital renal artery stenosis +Q27.1 Congenital renal artery stenosis,7475,Q27.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.1,ORPHAcode: 97598 Congenital renal artery stenosis,ICD-10 Q27.2 Other congenital malformations of renal artery,7476,Q27.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.2,,ICD-10 -Q27.3 Peripheral arteriovenous malformation,7477,Q27.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.3,ORPHAcode: 2039 Congenital systemic arteriovenous fistula -Q27.4 Congenital phlebectasia,7478,Q27.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.4,ORPHAcode: 217008 Bockenheimer syndrome -Q27.8 Other specified congenital malformations of peripheral vascular system,7479,Q27.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.8,ORPHAcode: 1059 Blue rubber bleb nevus +Q27.3 Peripheral arteriovenous malformation,7477,Q27.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.3,ORPHAcode: 2039 Congenital systemic arteriovenous fistula,ICD-10 +Q27.4 Congenital phlebectasia,7478,Q27.4,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.4,ORPHAcode: 217008 Bockenheimer syndrome,ICD-10 +Q27.8 Other specified congenital malformations of peripheral vascular system,7479,Q27.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.8,ORPHAcode: 1059 Blue rubber bleb nevus,ICD-10 "Q27.9 Congenital malformation of peripheral vascular system, unspecified",7480,Q27.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q27.9,,ICD-10 Q28 Other congenital malformations of circulatory system,7481,Q28,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28,,ICD-10 Q28.0 Arteriovenous malformation of precerebral vessels,7482,Q28.0,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.0,,ICD-10 -Q28.1 Other malformations of precerebral vessels,7483,Q28.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.1,ORPHAcode: 981 Internal carotid absence -Q28.2 Arteriovenous malformation of cerebral vessels,7484,Q28.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.2,ORPHAcode: 1053 Vein of Galen aneurysmal malformation -Q28.3 Other malformations of cerebral vessels,7485,Q28.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.3,ORPHAcode: 97339 Dural sinus malformation -Q28.8 Other specified congenital malformations of circulatory system,7486,Q28.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.8,ORPHAcode: 42775 PHACE syndrome +Q28.1 Other malformations of precerebral vessels,7483,Q28.1,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.1,ORPHAcode: 981 Internal carotid absence,ICD-10 +Q28.2 Arteriovenous malformation of cerebral vessels,7484,Q28.2,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.2,ORPHAcode: 1053 Vein of Galen aneurysmal malformation,ICD-10 +Q28.3 Other malformations of cerebral vessels,7485,Q28.3,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.3,ORPHAcode: 97339 Dural sinus malformation,ICD-10 +Q28.8 Other specified congenital malformations of circulatory system,7486,Q28.8,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.8,ORPHAcode: 42775 PHACE syndrome,ICD-10 "Q28.9 Congenital malformation of circulatory system, unspecified",7487,Q28.9,Q20-Q28 Congenital malformations of the circulatory system,http://identifiers.org/icd/Q28.9,,ICD-10 Q30-Q34 Congenital malformations of the respiratory system,7488,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 Q30 Congenital malformations of nose,7489,Q30,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30,,ICD-10 -Q30.0 Congenital malformations of nose - Choanal atresia,7490,Q30.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.0,ORPHAcode: 137914 Choanal atresia -Q30.1 Agenesis and underdevelopment of nose,7491,Q30.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.1,ORPHAcode: 1134 Isolated arrhinia -"Q30.2 Fissured, notched and cleft nose",7492,Q30.2,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.2,ORPHAcode: 2695 Bifid nose +Q30.0 Congenital malformations of nose - Choanal atresia,7490,Q30.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.0,ORPHAcode: 137914 Choanal atresia,ICD-10 +Q30.1 Agenesis and underdevelopment of nose,7491,Q30.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.1,ORPHAcode: 1134 Isolated arrhinia,ICD-10 +"Q30.2 Fissured, notched and cleft nose",7492,Q30.2,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.2,ORPHAcode: 2695 Bifid nose,ICD-10 Q30.3 Congenital perforated nasal septum,7493,Q30.3,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.3,,ICD-10 -Q30.8 Other congenital malformations of nose,7494,Q30.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.8,ORPHAcode: 922 Familial nasal acilia +Q30.8 Other congenital malformations of nose,7494,Q30.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.8,ORPHAcode: 922 Familial nasal acilia,ICD-10 "Q30.9 Congenital malformation of nose, unspecified",7495,Q30.9,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q30.9,,ICD-10 Q31 Congenital malformations of larynx,7496,Q31,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31,,ICD-10 -Q31.0 Web of larynx,7497,Q31.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.0,ORPHAcode: 2374 Congenital laryngeal web -Q31.1 Congenital subglottic stenosis,7498,Q31.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.1,ORPHAcode: 141121 Congenital subglottic stenosis +Q31.0 Web of larynx,7497,Q31.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.0,ORPHAcode: 2374 Congenital laryngeal web,ICD-10 +Q31.1 Congenital subglottic stenosis,7498,Q31.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.1,ORPHAcode: 141121 Congenital subglottic stenosis,ICD-10 Q54.8 Other hypospadias,7499,Q54.8,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.8,,ICD-10 Q31.2 Congenital malformations of larynx - Laryngeal hypoplasia,7500,Q31.2,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.2,,ICD-10 -Q31.3 Congenital malformations of larynx - Laryngocele,7501,Q31.3,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.3,ORPHAcode: 2372 Laryngocele -Q31.5 Congenital laryngomalacia,7502,Q31.5,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.5,ORPHAcode: 2373 Congenital laryngomalacia -Q31.8 Other congenital malformations of larynx,7503,Q31.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.8,ORPHAcode: 1202 Larynx atresia +Q31.3 Congenital malformations of larynx - Laryngocele,7501,Q31.3,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.3,ORPHAcode: 2372 Laryngocele,ICD-10 +Q31.5 Congenital laryngomalacia,7502,Q31.5,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.5,ORPHAcode: 2373 Congenital laryngomalacia,ICD-10 +Q31.8 Other congenital malformations of larynx,7503,Q31.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.8,ORPHAcode: 1202 Larynx atresia,ICD-10 "Q31.9 Congenital malformation of larynx, unspecified",7504,Q31.9,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q31.9,,ICD-10 Q32 Congenital malformations of trachea and bronchus,7505,Q32,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32,,ICD-10 -Q32.0 Congenital tracheomalacia,7506,Q32.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.0,ORPHAcode: 95430 Congenital tracheomalacia -Q32.1 Other congenital malformations of trachea,7507,Q32.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.1,ORPHAcode: 2004 Laryngotracheoesophageal cleft +Q32.0 Congenital tracheomalacia,7506,Q32.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.0,ORPHAcode: 95430 Congenital tracheomalacia,ICD-10 +Q32.1 Other congenital malformations of trachea,7507,Q32.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.1,ORPHAcode: 2004 Laryngotracheoesophageal cleft,ICD-10 Q32.2 Congenital bronchomalacia,7508,Q32.2,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.2,,ICD-10 Q32.3 Congenital stenosis of bronchus,7509,Q32.3,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.3,,ICD-10 -Q32.4 Other congenital malformations of bronchus,7510,Q32.4,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.4,ORPHAcode: 2040 Congenital respiratory-biliary fistula +Q32.4 Other congenital malformations of bronchus,7510,Q32.4,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q32.4,ORPHAcode: 2040 Congenital respiratory-biliary fistula,ICD-10 Q33 Congenital malformations of lung,7511,Q33,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33,,ICD-10 -Q33.0 Congenital cystic lung,7512,Q33.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.0,ORPHAcode: 2444 Congenital pulmonary airway malformation +Q33.0 Congenital cystic lung,7512,Q33.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.0,ORPHAcode: 2444 Congenital pulmonary airway malformation,ICD-10 Q33.1 Accessory lobe of lung,7513,Q33.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.1,,ICD-10 -Q33.2 Sequestration of lung,7514,Q33.2,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.2,ORPHAcode: 3161 Congenital pulmonary sequestration -Q33.3 Agenesis of lung,7515,Q33.3,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.3,ORPHAcode: 984 Pulmonary agenesis -Q33.4 Congenital bronchiectasis,7516,Q33.4,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.4,ORPHAcode: 411501 Williams-Campbell syndrome -Q33.6 Hypoplasia and dysplasia of lung,7517,Q33.6,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.6,ORPHAcode: 2257 Primary pulmonary hypoplasia -Q33.8 Other congenital malformations of lung,7518,Q33.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.8,ORPHAcode: 1928 Congenital lobar emphysema +Q33.2 Sequestration of lung,7514,Q33.2,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.2,ORPHAcode: 3161 Congenital pulmonary sequestration,ICD-10 +Q33.3 Agenesis of lung,7515,Q33.3,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.3,ORPHAcode: 984 Pulmonary agenesis,ICD-10 +Q33.4 Congenital bronchiectasis,7516,Q33.4,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.4,ORPHAcode: 411501 Williams-Campbell syndrome,ICD-10 +Q33.6 Hypoplasia and dysplasia of lung,7517,Q33.6,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.6,ORPHAcode: 2257 Primary pulmonary hypoplasia,ICD-10 +Q33.8 Other congenital malformations of lung,7518,Q33.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.8,ORPHAcode: 1928 Congenital lobar emphysema,ICD-10 "Q33.9 Congenital malformation of lung, unspecified",7519,Q33.9,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q33.9,,ICD-10 Q34 Other congenital malformations of respiratory system,7520,Q34,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q34,,ICD-10 Q34.0 Anomaly of pleura,7521,Q34.0,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q34.0,,ICD-10 Q34.1 Congenital cyst of mediastinum,7522,Q34.1,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q34.1,,ICD-10 -Q34.8 Other specified congenital malformations of respiratory system,7523,Q34.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q34.8,ORPHAcode: 244 Primary ciliary dyskinesia +Q34.8 Other specified congenital malformations of respiratory system,7523,Q34.8,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q34.8,ORPHAcode: 244 Primary ciliary dyskinesia,ICD-10 "Q34.9 Congenital malformation of respiratory system, unspecified",7524,Q34.9,Q30-Q34 Congenital malformations of the respiratory system,http://identifiers.org/icd/Q34.9,,ICD-10 Q35-Q37 Cleft lip and cleft palate,7525,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 Q35 Cleft palate,7526,Q35,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35,,ICD-10 -Q35.1 Cleft hard palate,7527,Q35.1,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.1,ORPHAcode: 101023 Cleft hard palate -Q35.3 Cleft soft palate,7528,Q35.3,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.3,ORPHAcode: 99772 Cleft velum +Q35.1 Cleft hard palate,7527,Q35.1,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.1,ORPHAcode: 101023 Cleft hard palate,ICD-10 +Q35.3 Cleft soft palate,7528,Q35.3,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.3,ORPHAcode: 99772 Cleft velum,ICD-10 Q35.5 Cleft hard palate with cleft soft palate,7529,Q35.5,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.5,,ICD-10 -Q35.7 Cleft uvula,7530,Q35.7,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.7,ORPHAcode: 99771 Bifid uvula -"Q35.9 Cleft palate, unspecified",7531,Q35.9,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.9,ORPHAcode: 155878 Submucosal cleft palate +Q35.7 Cleft uvula,7530,Q35.7,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.7,ORPHAcode: 99771 Bifid uvula,ICD-10 +"Q35.9 Cleft palate, unspecified",7531,Q35.9,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q35.9,ORPHAcode: 155878 Submucosal cleft palate,ICD-10 Q36 Cleft lip,7532,Q36,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q36,,ICD-10 -"Q36.0 Cleft lip, bilateral",7533,Q36.0,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q36.0,ORPHAcode: 141291 Cleft lip and alveolus -"Q36.1 Cleft lip, median",7534,Q36.1,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q36.1,ORPHAcode: 2006 Median cleft lip/mandibule +"Q36.0 Cleft lip, bilateral",7533,Q36.0,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q36.0,ORPHAcode: 141291 Cleft lip and alveolus,ICD-10 +"Q36.1 Cleft lip, median",7534,Q36.1,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q36.1,ORPHAcode: 2006 Median cleft lip/mandibule,ICD-10 "Q36.9 Cleft lip, unilateral",7535,Q36.9,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q36.9,,ICD-10 -Q37.0 Cleft hard palate with bilateral cleft lip,7536,Q37.0,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q37.0,ORPHAcode: 199306 Cleft lip/palate +Q37.0 Cleft hard palate with bilateral cleft lip,7536,Q37.0,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q37.0,ORPHAcode: 199306 Cleft lip/palate,ICD-10 Q37.1 Cleft hard palate with unilateral cleft lip,7537,Q37.1,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q37.1,,ICD-10 Q37.2 Cleft soft palate with bilateral cleft lip,7538,Q37.2,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q37.2,,ICD-10 Q37.3 Cleft soft palate with unilateral cleft lip,7539,Q37.3,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q37.3,,ICD-10 @@ -7549,35 +7549,35 @@ Q37.8 Unspecified cleft palate with bilateral cleft lip,7542,Q37.8,Q35-Q37 Cleft Q37.9 Unspecified cleft palate with unilateral cleft lip,7543,Q37.9,Q35-Q37 Cleft lip and cleft palate,http://identifiers.org/icd/Q37.9,,ICD-10 Q38-Q45 Other congenital malformations of the digestive system,7544,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 "Q38 Other congenital malformations of tongue, mouth and pharynx",7545,Q38,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38,,ICD-10 -"Q38.0 Congenital malformations of lips, not elsewhere classified",7546,Q38.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.0,ORPHAcode: 888 Van der Woude syndrome +"Q38.0 Congenital malformations of lips, not elsewhere classified",7546,Q38.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.0,ORPHAcode: 888 Van der Woude syndrome,ICD-10 "Q38.1 Other congenital malformations of tongue, mouth and pharynx - Ankyloglossia",7547,Q38.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.1,,ICD-10 -"Q38.2 Other congenital malformations of tongue, mouth and pharynx - Macroglossia",7548,Q38.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.2,ORPHAcode: 2430 Congenital macroglossia -Q38.3 Other congenital malformations of tongue,7549,Q38.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.3,ORPHAcode: 141071 Digestive duplication cyst of the tongue +"Q38.2 Other congenital malformations of tongue, mouth and pharynx - Macroglossia",7548,Q38.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.2,ORPHAcode: 2430 Congenital macroglossia,ICD-10 +Q38.3 Other congenital malformations of tongue,7549,Q38.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.3,ORPHAcode: 141071 Digestive duplication cyst of the tongue,ICD-10 Q38.4 Congenital malformations of salivary glands and ducts,7550,Q38.4,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.4,,ICD-10 "Q38.5 Congenital malformations of palate, not elsewhere classified",7551,Q38.5,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.5,,ICD-10 -Q38.6 Other congenital malformations of mouth,7552,Q38.6,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.6,ORPHAcode: 171723 White sponge nevus +Q38.6 Other congenital malformations of mouth,7552,Q38.6,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.6,ORPHAcode: 171723 White sponge nevus,ICD-10 "Q38.7 Other congenital malformations of tongue, mouth and pharynx - Pharyngeal pouch",7553,Q38.7,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.7,,ICD-10 Q38.8 Other congenital malformations of pharynx,7554,Q38.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q38.8,,ICD-10 Q39 Congenital malformations of oesophagus,7555,Q39,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39,,ICD-10 Q55.1 Hypoplasia of testis and scrotum,7556,Q55.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.1,,ICD-10 -Q39.0 Atresia of oesophagus without fistula,7557,Q39.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.0,ORPHAcode: 1199 Esophageal atresia +Q39.0 Atresia of oesophagus without fistula,7557,Q39.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.0,ORPHAcode: 1199 Esophageal atresia,ICD-10 Q39.1 Atresia of oesophagus with tracheo-oesophageal fistula,7558,Q39.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.1,,ICD-10 -Q39.2 Congenital tracheo-oesophageal fistula without atresia,7559,Q39.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.2,ORPHAcode: 454750 Isolated tracheoesophageal fistula +Q39.2 Congenital tracheo-oesophageal fistula without atresia,7559,Q39.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.2,ORPHAcode: 454750 Isolated tracheoesophageal fistula,ICD-10 Q39.3 Congenital stenosis and stricture of oesophagus,7560,Q39.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.3,,ICD-10 Q39.4 Congenital malformations of oesophagus - Oesophageal web,7561,Q39.4,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.4,,ICD-10 -Q39.5 Congenital dilatation of oesophagus,7562,Q39.5,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.5,ORPHAcode: 929 Achalasia-microcephaly syndrome -Q39.6 Diverticulum of oesophagus,7563,Q39.6,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.6,ORPHAcode: 91358 Congenital esophageal diverticulum -Q39.8 Other congenital malformations of oesophagus,7564,Q39.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.8,ORPHAcode: 100047 Esophageal duplication cyst +Q39.5 Congenital dilatation of oesophagus,7562,Q39.5,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.5,ORPHAcode: 929 Achalasia-microcephaly syndrome,ICD-10 +Q39.6 Diverticulum of oesophagus,7563,Q39.6,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.6,ORPHAcode: 91358 Congenital esophageal diverticulum,ICD-10 +Q39.8 Other congenital malformations of oesophagus,7564,Q39.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.8,ORPHAcode: 100047 Esophageal duplication cyst,ICD-10 "Q39.9 Congenital malformation of oesophagus, unspecified",7565,Q39.9,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q39.9,,ICD-10 Q40 Other congenital malformations of upper alimentary tract,7566,Q40,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40,,ICD-10 Q40.0 Congenital hypertrophic pyloric stenosis,7567,Q40.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40.0,,ICD-10 Q40.1 Congenital hiatus hernia,7568,Q40.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40.1,,ICD-10 -Q40.2 Other specified congenital malformations of stomach,7569,Q40.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40.2,ORPHAcode: 199293 Congenital microgastria +Q40.2 Other specified congenital malformations of stomach,7569,Q40.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40.2,ORPHAcode: 199293 Congenital microgastria,ICD-10 "Q40.3 Congenital malformation of stomach, unspecified",7570,Q40.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40.3,,ICD-10 Q40.8 Other specified congenital malformations of upper alimentary tract,7571,Q40.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40.8,,ICD-10 "Q40.9 Congenital malformation of upper alimentary tract, unspecified",7572,Q40.9,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q40.9,,ICD-10 "Q41 Congenital absence, atresia and stenosis of small intestine",7573,Q41,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q41,,ICD-10 -"Q41.0 Congenital absence, atresia and stenosis of duodenum",7574,Q41.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q41.0,ORPHAcode: 1201 Atresia of small intestine +"Q41.0 Congenital absence, atresia and stenosis of duodenum",7574,Q41.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q41.0,ORPHAcode: 1201 Atresia of small intestine,ICD-10 "Q41.1 Congenital absence, atresia and stenosis of jejunum",7575,Q41.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q41.1,,ICD-10 "Q41.2 Congenital absence, atresia and stenosis of ileum",7576,Q41.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q41.2,,ICD-10 "Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine",7577,Q41.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q41.8,,ICD-10 @@ -7588,34 +7588,34 @@ Q40.8 Other specified congenital malformations of upper alimentary tract,7571,Q4 "Q42.2 Congenital absence, atresia and stenosis of anus with fistula",7582,Q42.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q42.2,,ICD-10 "Q42.3 Congenital absence, atresia and stenosis of anus without fistula",7583,Q42.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q42.3,,ICD-10 "Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine",7584,Q42.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q42.8,,ICD-10 -"Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified",7585,Q42.9,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q42.9,ORPHAcode: 1198 Colonic atresia -Q43.0 Other congenital malformations of intestine - Meckel diverticulum,7586,Q43.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.0,ORPHAcode: 490 Omphalomesenteric cyst -Q43.1 Other congenital malformations of intestine - Hirschsprung disease,7587,Q43.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.1,ORPHAcode: 388 Hirschsprung disease +"Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified",7585,Q42.9,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q42.9,ORPHAcode: 1198 Colonic atresia,ICD-10 +Q43.0 Other congenital malformations of intestine - Meckel diverticulum,7586,Q43.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.0,ORPHAcode: 490 Omphalomesenteric cyst,ICD-10 +Q43.1 Other congenital malformations of intestine - Hirschsprung disease,7587,Q43.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.1,ORPHAcode: 388 Hirschsprung disease,ICD-10 R57.2 Septic shock,7588,R57.2,R50-R69 General symptoms and signs,http://identifiers.org/icd/R57.2,,ICD-10 Q43.2 Other congenital functional disorders of colon,7589,Q43.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.2,,ICD-10 -Q43.3 Congenital malformations of intestinal fixation,7590,Q43.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.3,ORPHAcode: 620 Common mesentery -Q43.4 Duplication of intestine,7591,Q43.4,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.4,ORPHAcode: 1759 Thoraco-abdominal enteric duplication +Q43.3 Congenital malformations of intestinal fixation,7590,Q43.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.3,ORPHAcode: 620 Common mesentery,ICD-10 +Q43.4 Duplication of intestine,7591,Q43.4,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.4,ORPHAcode: 1759 Thoraco-abdominal enteric duplication,ICD-10 Q43.5 Other congenital malformations of intestine - Ectopic anus,7592,Q43.5,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.5,,ICD-10 Q43.6 Congenital fistula of rectum and anus,7593,Q43.6,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.6,,ICD-10 Q43.7 Other congenital malformations of intestine - Persistent cloaca,7594,Q43.7,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.7,,ICD-10 -Q43.8 Other specified congenital malformations of intestine,7595,Q43.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.8,ORPHAcode: 2241 Megacystis-microcolon-intestinal hypoperistalsis syndrome +Q43.8 Other specified congenital malformations of intestine,7595,Q43.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.8,ORPHAcode: 2241 Megacystis-microcolon-intestinal hypoperistalsis syndrome,ICD-10 "Q43.9 Congenital malformation of intestine, unspecified",7596,Q43.9,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q43.9,,ICD-10 "Q44 Congenital malformations of gallbladder, bile ducts and liver",7597,Q44,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44,,ICD-10 -"Q44.0 Agenesis, aplasia and hypoplasia of gallbladder",7598,Q44.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.0,ORPHAcode: 440987 Isolated agenesis of gallbladder +"Q44.0 Agenesis, aplasia and hypoplasia of gallbladder",7598,Q44.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.0,ORPHAcode: 440987 Isolated agenesis of gallbladder,ICD-10 Q44.1 Other congenital malformations of gallbladder,7599,Q44.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.1,,ICD-10 -Q44.2 Atresia of bile ducts,7600,Q44.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.2,ORPHAcode: 30391 Isolated biliary atresia +Q44.2 Atresia of bile ducts,7600,Q44.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.2,ORPHAcode: 30391 Isolated biliary atresia,ICD-10 Q44.3 Congenital stenosis and stricture of bile ducts,7601,Q44.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.3,,ICD-10 Q50.3 Other congenital malformations of ovary,7602,Q50.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q50.3,,ICD-10 -"Q44.4 Congenital malformations of gallbladder, bile ducts and liver - Choledochal cyst",7603,Q44.4,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.4,ORPHAcode: 480501 Choledochal cyst +"Q44.4 Congenital malformations of gallbladder, bile ducts and liver - Choledochal cyst",7603,Q44.4,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.4,ORPHAcode: 480501 Choledochal cyst,ICD-10 Q44.5 Other congenital malformations of bile ducts,7604,Q44.5,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.5,,ICD-10 -Q44.6 Cystic disease of liver,7605,Q44.6,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.6,ORPHAcode: 2924 Isolated polycystic liver disease -Q44.7 Other congenital malformations of liver,7606,Q44.7,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.7,ORPHAcode: 52 Alagille syndrome +Q44.6 Cystic disease of liver,7605,Q44.6,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.6,ORPHAcode: 2924 Isolated polycystic liver disease,ICD-10 +Q44.7 Other congenital malformations of liver,7606,Q44.7,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q44.7,ORPHAcode: 52 Alagille syndrome,ICD-10 Q45 Other congenital malformations of digestive system,7607,Q45,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45,,ICD-10 -"Q45.0 Agenesis, aplasia and hypoplasia of pancreas",7608,Q45.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.0,ORPHAcode: 2805 Partial pancreatic agenesis -Q45.1 Other congenital malformations of digestive system - Annular pancreas,7609,Q45.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.1,ORPHAcode: 675 Annular pancreas -Q45.2 Congenital pancreatic cyst,7610,Q45.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.2,ORPHAcode: 313906 Congenital pancreatic cyst -Q45.3 Other congenital malformations of pancreas and pancreatic duct,7611,Q45.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.3,ORPHAcode: 674 Accessory pancreas -Q45.8 Other specified congenital malformations of digestive system,7612,Q45.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.8,ORPHAcode: 238 Digestive duplication +"Q45.0 Agenesis, aplasia and hypoplasia of pancreas",7608,Q45.0,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.0,ORPHAcode: 2805 Partial pancreatic agenesis,ICD-10 +Q45.1 Other congenital malformations of digestive system - Annular pancreas,7609,Q45.1,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.1,ORPHAcode: 675 Annular pancreas,ICD-10 +Q45.2 Congenital pancreatic cyst,7610,Q45.2,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.2,ORPHAcode: 313906 Congenital pancreatic cyst,ICD-10 +Q45.3 Other congenital malformations of pancreas and pancreatic duct,7611,Q45.3,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.3,ORPHAcode: 674 Accessory pancreas,ICD-10 +Q45.8 Other specified congenital malformations of digestive system,7612,Q45.8,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.8,ORPHAcode: 238 Digestive duplication,ICD-10 "Q45.9 Congenital malformation of digestive system, unspecified",7613,Q45.9,Q38-Q45 Other congenital malformations of the digestive system,http://identifiers.org/icd/Q45.9,,ICD-10 Q50-Q56 Congenital malformations of genital organs,7614,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 "Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments",7615,Q50,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q50,,ICD-10 @@ -7627,19 +7627,19 @@ Q50.5 Embryonic cyst of broad ligament,7620,Q50.5,Q50-Q56 Congenital malformatio R57.8 Other shock,7621,R57.8,R50-R69 General symptoms and signs,http://identifiers.org/icd/R57.8,,ICD-10 Q50.6 Other congenital malformations of fallopian tube and broad ligament,7622,Q50.6,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q50.6,,ICD-10 Q51 Congenital malformations of uterus and cervix,7623,Q51,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51,,ICD-10 -Q51.0 Agenesis and aplasia of uterus,7624,Q51.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.0,ORPHAcode: 180142 Absence of uterine body -Q51.1 Doubling of uterus with doubling of cervix and vagina,7625,Q51.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.1,ORPHAcode: 180086 Didelphys uterus -Q51.2 Other doubling of uterus,7626,Q51.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.2,ORPHAcode: 2438 Hand-foot-genital syndrome -Q51.3 Bicornate uterus,7627,Q51.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.3,ORPHAcode: 180114 Unicervical bicornuate uterus -Q51.4 Unicornate uterus,7628,Q51.4,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.4,ORPHAcode: 180074 True unicornuate uterus -Q51.5 Agenesis and aplasia of cervix,7629,Q51.5,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.5,ORPHAcode: 180145 Uterine cervical aplasia and agenesis +Q51.0 Agenesis and aplasia of uterus,7624,Q51.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.0,ORPHAcode: 180142 Absence of uterine body,ICD-10 +Q51.1 Doubling of uterus with doubling of cervix and vagina,7625,Q51.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.1,ORPHAcode: 180086 Didelphys uterus,ICD-10 +Q51.2 Other doubling of uterus,7626,Q51.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.2,ORPHAcode: 2438 Hand-foot-genital syndrome,ICD-10 +Q51.3 Bicornate uterus,7627,Q51.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.3,ORPHAcode: 180114 Unicervical bicornuate uterus,ICD-10 +Q51.4 Unicornate uterus,7628,Q51.4,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.4,ORPHAcode: 180074 True unicornuate uterus,ICD-10 +Q51.5 Agenesis and aplasia of cervix,7629,Q51.5,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.5,ORPHAcode: 180145 Uterine cervical aplasia and agenesis,ICD-10 Q51.6 Embryonic cyst of cervix,7630,Q51.6,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.6,,ICD-10 Q51.7 Congenital fistulae between uterus and digestive and urinary tracts,7631,Q51.7,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.7,,ICD-10 -Q51.8 Other congenital malformations of uterus and cervix,7632,Q51.8,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.8,ORPHAcode: 3109 Mayer-Rokitansky-Kuster-Hauser syndro +Q51.8 Other congenital malformations of uterus and cervix,7632,Q51.8,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.8,ORPHAcode: 3109 Mayer-Rokitansky-Kuster-Hauser syndro,ICD-10 "Q51.9 Congenital malformation of uterus and cervix, unspecified",7633,Q51.9,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q51.9,,ICD-10 Q52 Other congenital malformations of female genitalia,7634,Q52,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52,,ICD-10 -Q52.0 Congenital absence of vagina,7635,Q52.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52.0,ORPHAcode: 65681 Vaginal atresia -Q52.1 Doubling of vagina,7636,Q52.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52.1,ORPHAcode: 180154 Septate vagina +Q52.0 Congenital absence of vagina,7635,Q52.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52.0,ORPHAcode: 65681 Vaginal atresia,ICD-10 +Q52.1 Doubling of vagina,7636,Q52.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52.1,ORPHAcode: 180154 Septate vagina,ICD-10 Q52.2 Congenital rectovaginal fistula,7637,Q52.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52.2,,ICD-10 Q52.3 Other congenital malformations of female genitalia - Imperforate hymen,7638,Q52.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52.3,,ICD-10 Q52.4 Other congenital malformations of vagina,7639,Q52.4,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q52.4,,ICD-10 @@ -7656,71 +7656,71 @@ Q53.0 Undescended testicle - Ectopic testis,7646,Q53.0,Q50-Q56 Congenital malfor Q54 Hypospadias,7650,Q54,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54,,ICD-10 "Q54.0 Hypospadias, balanic",7651,Q54.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.0,,ICD-10 "Q54.1 Hypospadias, penile",7652,Q54.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.1,,ICD-10 -"Q54.2 Hypospadias, penoscrotal",7653,Q54.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.2,ORPHAcode: 95706 Posterior hypospadias +"Q54.2 Hypospadias, penoscrotal",7653,Q54.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.2,ORPHAcode: 95706 Posterior hypospadias,ICD-10 "Q54.3 Hypospadias, perineal",7654,Q54.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.3,,ICD-10 "Q54.9 Hypospadias, unspecified",7655,Q54.9,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q54.9,,ICD-10 Q55 Other congenital malformations of male genital organs,7656,Q55,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55,,ICD-10 -Q55.0 Absence and aplasia of testis,7657,Q55.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.0,ORPHAcode: 983 Testicular regression syndrome +Q55.0 Absence and aplasia of testis,7657,Q55.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.0,ORPHAcode: 983 Testicular regression syndrome,ICD-10 Q55.2 Other congenital malformations of testis and scrotum,7658,Q55.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.2,,ICD-10 Q55.3 Atresia of vas deferens,7659,Q55.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.3,,ICD-10 -"Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate",7660,Q55.4,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.4,ORPHAcode: 48 Congenital bilateral absence of vas deferens -Q55.5 Congenital absence and aplasia of penis,7661,Q55.5,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.5,ORPHAcode: 49 Penile agenesis -Q55.6 Other congenital malformations of penis,7662,Q55.6,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.6,ORPHAcode: 227 Diphallia -Q55.8 Other specified congenital malformations of male genital organs,7663,Q55.8,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.8,ORPHAcode: 2842 Penoscrotal transposition +"Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate",7660,Q55.4,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.4,ORPHAcode: 48 Congenital bilateral absence of vas deferens,ICD-10 +Q55.5 Congenital absence and aplasia of penis,7661,Q55.5,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.5,ORPHAcode: 49 Penile agenesis,ICD-10 +Q55.6 Other congenital malformations of penis,7662,Q55.6,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.6,ORPHAcode: 227 Diphallia,ICD-10 +Q55.8 Other specified congenital malformations of male genital organs,7663,Q55.8,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.8,ORPHAcode: 2842 Penoscrotal transposition,ICD-10 "Q55.9 Congenital malformation of male genital organ, unspecified",7664,Q55.9,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q55.9,,ICD-10 Q56 Indeterminate sex and pseudohermaphroditism,7665,Q56,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56,,ICD-10 -"Q56.0 Indeterminate sex and pseudohermaphroditism - Hermaphroditism, not elsewhere classified",7666,Q56.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.0,"ORPHAcode: 2138 46,XX ovotesticular disorder of sex development" -"Q56.1 Male pseudohermaphroditism, not elsewhere classified",7667,Q56.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.1,ORPHAcode: 755 Leydig cell hypoplasia -"Q56.2 Female pseudohermaphroditism, not elsewhere classified",7668,Q56.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.2,"ORPHAcode: 2973 46,XX disorder of sex development-anorectal anomalies syndrome" -"Q56.3 Pseudohermaphroditism, unspecified",7669,Q56.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.3,ORPHAcode: 2983 Disorder of sex development-intellectual disability syndrome +"Q56.0 Indeterminate sex and pseudohermaphroditism - Hermaphroditism, not elsewhere classified",7666,Q56.0,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.0,"ORPHAcode: 2138 46,XX ovotesticular disorder of sex development",ICD-10 +"Q56.1 Male pseudohermaphroditism, not elsewhere classified",7667,Q56.1,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.1,ORPHAcode: 755 Leydig cell hypoplasia,ICD-10 +"Q56.2 Female pseudohermaphroditism, not elsewhere classified",7668,Q56.2,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.2,"ORPHAcode: 2973 46,XX disorder of sex development-anorectal anomalies syndrome",ICD-10 +"Q56.3 Pseudohermaphroditism, unspecified",7669,Q56.3,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.3,ORPHAcode: 2983 Disorder of sex development-intellectual disability syndrome,ICD-10 "Q56.4 Indeterminate sex, unspecified",7670,Q56.4,Q50-Q56 Congenital malformations of genital organs,http://identifiers.org/icd/Q56.4,,ICD-10 Q60-Q64 Congenital malformations of the urinary system,7671,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 Q60 Renal agenesis and other reduction defects of kidney,7672,Q60,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60,,ICD-10 "Q60.0 Renal agenesis, unilateral",7673,Q60.0,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.0,,ICD-10 "Q60.1 Renal agenesis, bilateral",7674,Q60.1,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.1,,ICD-10 -"Q60.2 Renal agenesis, unspecified",7675,Q60.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.2,ORPHAcode: 411709 Renal agenesis -"Q60.3 Renal hypoplasia, unilateral",7676,Q60.3,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.3,ORPHAcode: 93101 Renal hypoplasia -"Q60.4 Renal hypoplasia, bilateral",7677,Q60.4,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.4,ORPHAcode: 1475 Renal coloboma syndrome +"Q60.2 Renal agenesis, unspecified",7675,Q60.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.2,ORPHAcode: 411709 Renal agenesis,ICD-10 +"Q60.3 Renal hypoplasia, unilateral",7676,Q60.3,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.3,ORPHAcode: 93101 Renal hypoplasia,ICD-10 +"Q60.4 Renal hypoplasia, bilateral",7677,Q60.4,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.4,ORPHAcode: 1475 Renal coloboma syndrome,ICD-10 "Q60.5 Renal hypoplasia, unspecified",7678,Q60.5,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.5,,ICD-10 Q60.6 Renal agenesis and other reduction defects of kidney - Potter syndrome,7679,Q60.6,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q60.6,,ICD-10 Q61 Cystic kidney disease,7680,Q61,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61,,ICD-10 Q61.0 Cystic kidney disease - Congenital single renal cyst,7681,Q61.0,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.0,,ICD-10 -"Q61.1 Polycystic kidney, autosomal recessive",7682,Q61.1,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.1,ORPHAcode: 731 Autosomal recessive polycystic kidney disease -"Q61.2 Polycystic kidney, autosomal dominant",7683,Q61.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.2,ORPHAcode: 730 Autosomal dominant polycystic kidney disease +"Q61.1 Polycystic kidney, autosomal recessive",7682,Q61.1,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.1,ORPHAcode: 731 Autosomal recessive polycystic kidney disease,ICD-10 +"Q61.2 Polycystic kidney, autosomal dominant",7683,Q61.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.2,ORPHAcode: 730 Autosomal dominant polycystic kidney disease,ICD-10 "Q61.3 Polycystic kidney, unspecified",7684,Q61.3,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.3,,ICD-10 -Q61.4 Cystic kidney disease - Renal dysplasia,7685,Q61.4,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.4,ORPHAcode: 1851 Multicystic dysplastic kidney -Q61.5 Medullary cystic kidney,7686,Q61.5,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.5,ORPHAcode: 655 Nephronophthisis +Q61.4 Cystic kidney disease - Renal dysplasia,7685,Q61.4,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.4,ORPHAcode: 1851 Multicystic dysplastic kidney,ICD-10 +Q61.5 Medullary cystic kidney,7686,Q61.5,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.5,ORPHAcode: 655 Nephronophthisis,ICD-10 "Q89.9 Congenital malformation, unspecified",7687,Q89.9,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.9,,ICD-10 R23.3 Other skin changes - Spontaneous ecchymoses,7688,R23.3,R20 Disturbances of skin sensation,http://identifiers.org/icd/R23.3,,ICD-10 -Q61.8 Other cystic kidney diseases,7689,Q61.8,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.8,ORPHAcode: 2666 Adult familial nephronophthisis-spastic quadriparesia syndrome -"Q61.9 Cystic kidney disease, unspecified",7690,Q61.9,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.9,ORPHAcode: 564 Meckel syndrome +Q61.8 Other cystic kidney diseases,7689,Q61.8,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.8,ORPHAcode: 2666 Adult familial nephronophthisis-spastic quadriparesia syndrome,ICD-10 +"Q61.9 Cystic kidney disease, unspecified",7690,Q61.9,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q61.9,ORPHAcode: 564 Meckel syndrome,ICD-10 Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter,7691,Q62,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62,,ICD-10 Q62.0 Congenital hydronephrosis,7692,Q62.0,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.0,,ICD-10 Q62.1 Atresia and stenosis of ureter,7693,Q62.1,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.1,,ICD-10 -Q62.2 Congenital megaloureter,7694,Q62.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.2,ORPHAcode: 617 Congenital primary megaureter +Q62.2 Congenital megaloureter,7694,Q62.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.2,ORPHAcode: 617 Congenital primary megaureter,ICD-10 Q62.3 Other obstructive defects of renal pelvis and ureter,7695,Q62.3,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.3,,ICD-10 Q62.4 Agenesis of ureter,7696,Q62.4,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.4,,ICD-10 Q62.5 Duplication of ureter,7697,Q62.5,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.5,,ICD-10 Q62.6 Malposition of ureter,7698,Q62.6,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.6,,ICD-10 -Q62.7 Congenital vesico-uretero-renal reflux,7699,Q62.7,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.7,ORPHAcode: 238637 Megacystis-megaureter syndrome +Q62.7 Congenital vesico-uretero-renal reflux,7699,Q62.7,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.7,ORPHAcode: 238637 Megacystis-megaureter syndrome,ICD-10 Q62.8 Other congenital malformations of ureter,7700,Q62.8,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q62.8,,ICD-10 Q63 Other congenital malformations of kidney,7701,Q63,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63,,ICD-10 Q63.0 Accessory kidney,7702,Q63.0,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63.0,,ICD-10 "Q63.1 Lobulated, fused and horseshoe kidney",7703,Q63.1,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63.1,,ICD-10 Q63.2 Ectopic kidney,7704,Q63.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63.2,,ICD-10 Q63.3 Hyperplastic and giant kidney,7705,Q63.3,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63.3,,ICD-10 -Q63.8 Other specified congenital malformations of kidney,7706,Q63.8,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63.8,ORPHAcode: 3033 Renal tubular dysgenesis +Q63.8 Other specified congenital malformations of kidney,7706,Q63.8,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63.8,ORPHAcode: 3033 Renal tubular dysgenesis,ICD-10 "Q63.9 Congenital malformation of kidney, unspecified",7707,Q63.9,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q63.9,,ICD-10 Q64 Other congenital malformations of urinary system,7708,Q64,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64,,ICD-10 Q64.0 Other congenital malformations of urinary system - Epispadias,7709,Q64.0,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.0,,ICD-10 -Q64.1 Exstrophy of urinary bladder,7710,Q64.1,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.1,ORPHAcode: 322 Exstrophy-epispadias complex -Q64.2 Congenital posterior urethral valves,7711,Q64.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.2,ORPHAcode: 93110 Posterior urethral valve -Q64.3 Other atresia and stenosis of urethra and bladder neck,7712,Q64.3,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.3,ORPHAcode: 105 Atresia of urethra -Q64.4 Malformation of urachus,7713,Q64.4,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.4,ORPHAcode: 488 Urachal cyst +Q64.1 Exstrophy of urinary bladder,7710,Q64.1,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.1,ORPHAcode: 322 Exstrophy-epispadias complex,ICD-10 +Q64.2 Congenital posterior urethral valves,7711,Q64.2,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.2,ORPHAcode: 93110 Posterior urethral valve,ICD-10 +Q64.3 Other atresia and stenosis of urethra and bladder neck,7712,Q64.3,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.3,ORPHAcode: 105 Atresia of urethra,ICD-10 +Q64.4 Malformation of urachus,7713,Q64.4,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.4,ORPHAcode: 488 Urachal cyst,ICD-10 Q64.5 Congenital absence of bladder and urethra,7714,Q64.5,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.5,,ICD-10 Q64.6 Congenital diverticulum of bladder,7715,Q64.6,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.6,,ICD-10 -Q64.7 Other congenital malformations of bladder and urethra,7716,Q64.7,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.7,ORPHAcode: 237 Duplication of urethra -Q64.8 Other specified congenital malformations of urinary system,7717,Q64.8,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.8,ORPHAcode: 71273 Renal nutcracker syndrome +Q64.7 Other congenital malformations of bladder and urethra,7716,Q64.7,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.7,ORPHAcode: 237 Duplication of urethra,ICD-10 +Q64.8 Other specified congenital malformations of urinary system,7717,Q64.8,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.8,ORPHAcode: 71273 Renal nutcracker syndrome,ICD-10 "Q64.9 Congenital malformation of urinary system, unspecified",7718,Q64.9,Q60-Q64 Congenital malformations of the urinary system,http://identifiers.org/icd/Q64.9,,ICD-10 Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,7719,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 Q65 Congenital deformities of hip,7720,Q65,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q65,,ICD-10 @@ -7732,7 +7732,7 @@ R15 Faecal incontinence,7725,R15,R10-R19 Symptoms and signs involving the digest "Q65.4 Congenital subluxation of hip, bilateral",7726,Q65.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q65.4,,ICD-10 "Q65.5 Congenital subluxation of hip, unspecified",7727,Q65.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q65.5,,ICD-10 Q65.6 Unstable hip,7728,Q65.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q65.6,,ICD-10 -Q65.8 Other congenital deformities of hip,7729,Q65.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q65.8,"ORPHAcode: 2114 Hip dysplasia, Beukes type" +Q65.8 Other congenital deformities of hip,7729,Q65.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q65.8,"ORPHAcode: 2114 Hip dysplasia, Beukes type",ICD-10 "Q65.9 Congenital deformity of hip, unspecified",7730,Q65.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q65.9,,ICD-10 Q66 Congenital deformities of feet,7731,Q66,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66,,ICD-10 Q66.0 Congenital deformities of feet - Talipes equinovarus,7732,Q66.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66.0,,ICD-10 @@ -7743,264 +7743,264 @@ Q66.4 Congenital deformities of feet - Talipes calcaneovalgus,7736,Q66.4,Q65-Q79 Q66.5 Congenital pes planus,7737,Q66.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66.5,,ICD-10 Q66.6 Other congenital valgus deformities of feet,7738,Q66.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66.6,,ICD-10 Q66.7 Congenital deformities of feet - Pes cavus,7739,Q66.7,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66.7,,ICD-10 -Q66.8 Other congenital deformities of feet,7740,Q66.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66.8,ORPHAcode: 178382 Congenital vertical talus +Q66.8 Other congenital deformities of feet,7740,Q66.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66.8,ORPHAcode: 178382 Congenital vertical talus,ICD-10 "Q66.9 Congenital deformity of feet, unspecified",7741,Q66.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q66.9,,ICD-10 "Q67 Congenital musculoskeletal deformities of head, face, spine and chest",7742,Q67,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67,,ICD-10 "Q67.0 Congenital musculoskeletal deformities of head, face, spine and chest - Facial asymmetry",7743,Q67.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.0,,ICD-10 "Q67.1 Congenital musculoskeletal deformities of head, face, spine and chest - Compression facies",7744,Q67.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.1,,ICD-10 "Q67.2 Congenital musculoskeletal deformities of head, face, spine and chest - Dolichocephaly",7745,Q67.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.2,,ICD-10 -"Q67.3 Congenital musculoskeletal deformities of head, face, spine and chest - Plagiocephaly",7746,Q67.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.3,ORPHAcode: 35098 Isolated plagiocephaly -"Q67.4 Other congenital deformities of skull, face and jaw",7747,Q67.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.4,ORPHAcode: 1241 Bencze syndrome +"Q67.3 Congenital musculoskeletal deformities of head, face, spine and chest - Plagiocephaly",7746,Q67.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.3,ORPHAcode: 35098 Isolated plagiocephaly,ICD-10 +"Q67.4 Other congenital deformities of skull, face and jaw",7747,Q67.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.4,ORPHAcode: 1241 Bencze syndrome,ICD-10 Q67.5 Congenital deformity of spine,7748,Q67.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.5,,ICD-10 "Q67.6 Congenital musculoskeletal deformities of head, face, spine and chest - Pectus excavatum",7749,Q67.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.6,,ICD-10 "Q67.7 Congenital musculoskeletal deformities of head, face, spine and chest - Pectus carinatum",7750,Q67.7,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.7,,ICD-10 Q67.8 Other congenital deformities of chest,7751,Q67.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q67.8,,ICD-10 Q68 Other congenital musculoskeletal deformities,7752,Q68,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68,,ICD-10 Q68.0 Congenital deformity of sternocleidomastoid muscle,7753,Q68.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.0,,ICD-10 -Q68.1 Congenital deformity of hand,7754,Q68.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.1,ORPHAcode: 1228 Banki syndrome -Q68.2 Congenital deformity of knee,7755,Q68.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.2,ORPHAcode: 295034 Congenital knee dislocation +Q68.1 Congenital deformity of hand,7754,Q68.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.1,ORPHAcode: 1228 Banki syndrome,ICD-10 +Q68.2 Congenital deformity of knee,7755,Q68.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.2,ORPHAcode: 295034 Congenital knee dislocation,ICD-10 Q68.3 Congenital bowing of femur,7756,Q68.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.3,,ICD-10 -Q68.4 Congenital bowing of tibia and fibula,7757,Q68.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.4,ORPHAcode: 324307 Severe lateral tibial bowing with short stature +Q68.4 Congenital bowing of tibia and fibula,7757,Q68.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.4,ORPHAcode: 324307 Severe lateral tibial bowing with short stature,ICD-10 "Q68.5 Congenital bowing of long bones of leg, unspecified",7758,Q68.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.5,,ICD-10 -Q68.8 Other specified congenital musculoskeletal deformities,7759,Q68.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.8,ORPHAcode: 115 Congenital contractural arachnodactyly +Q68.8 Other specified congenital musculoskeletal deformities,7759,Q68.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q68.8,ORPHAcode: 115 Congenital contractural arachnodactyly,ICD-10 Q69 Polydactyly,7760,Q69,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69,,ICD-10 -Q69.0 Polydactyly - Accessory finger(s),7761,Q69.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69.0,ORPHAcode: 93334 Postaxial polydactyly type A -Q69.1 Polydactyly - Accessory thumb(s),7762,Q69.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69.1,ORPHAcode: 93336 Polydactyly of a triphalangeal thumb +Q69.0 Polydactyly - Accessory finger(s),7761,Q69.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69.0,ORPHAcode: 93334 Postaxial polydactyly type A,ICD-10 +Q69.1 Polydactyly - Accessory thumb(s),7762,Q69.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69.1,ORPHAcode: 93336 Polydactyly of a triphalangeal thumb,ICD-10 Q69.2 Polydactyly - Accessory toe(s),7763,Q69.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69.2,,ICD-10 -"Q69.9 Polydactyly, unspecified",7764,Q69.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69.9,ORPHAcode: 1892 Ectrodactyly-polydactyly syndrome +"Q69.9 Polydactyly, unspecified",7764,Q69.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q69.9,ORPHAcode: 1892 Ectrodactyly-polydactyly syndrome,ICD-10 Q70 Syndactyly,7765,Q70,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70,,ICD-10 -Q70.0 Syndactyly - Fused fingers,7766,Q70.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.0,ORPHAcode: 2498 Syndactyly type 8 -Q70.1 Syndactyly - Webbed fingers,7767,Q70.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.1,ORPHAcode: 93404 Syndactyly type 3 +Q70.0 Syndactyly - Fused fingers,7766,Q70.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.0,ORPHAcode: 2498 Syndactyly type 8,ICD-10 +Q70.1 Syndactyly - Webbed fingers,7767,Q70.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.1,ORPHAcode: 93404 Syndactyly type 3,ICD-10 Q70.2 Syndactyly - Fused toes,7768,Q70.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.2,,ICD-10 -Q70.3 Syndactyly - Webbed toes,7769,Q70.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.3,ORPHAcode: 93402 Syndactyly type 1 -Q70.4 Polysyndactyly,7770,Q70.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.4,ORPHAcode: 2935 Crossed polysyndactyly +Q70.3 Syndactyly - Webbed toes,7769,Q70.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.3,ORPHAcode: 93402 Syndactyly type 1,ICD-10 +Q70.4 Polysyndactyly,7770,Q70.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.4,ORPHAcode: 2935 Crossed polysyndactyly,ICD-10 "Q90-Q99 Chromosomal abnormalities, not elsewhere classified",7771,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 -Q84.2 Other congenital malformations of hair,7772,Q84.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.2,ORPHAcode: 2220 Hypertrichosis cubiti -"Q70.9 Syndactyly, unspecified",7773,Q70.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.9,ORPHAcode: 3248 Distal symphalangism +Q84.2 Other congenital malformations of hair,7772,Q84.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.2,ORPHAcode: 2220 Hypertrichosis cubiti,ICD-10 +"Q70.9 Syndactyly, unspecified",7773,Q70.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q70.9,ORPHAcode: 3248 Distal symphalangism,ICD-10 Q71 Reduction defects of upper limb,7774,Q71,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71,,ICD-10 -Q71.0 Congenital complete absence of upper limb(s),7775,Q71.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.0,ORPHAcode: 294967 Amelia of upper limb -Q71.1 Congenital absence of upper arm and forearm with hand present,7776,Q71.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.1,ORPHAcode: 294975 Congenital absence of upper arm and forearm with hand present -Q71.2 Congenital absence of both forearm and hand,7777,Q71.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.2,ORPHAcode: 294979 Congenital absence of both forearm and hand -Q71.3 Congenital absence of hand and finger(s),7778,Q71.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.3,"ORPHAcode: 973 Congenital absence/hypoplasia of fingers excluding thumb, unilateral" -Q71.4 Longitudinal reduction defect of radius,7779,Q71.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.4,ORPHAcode: 93321 Radial hemimelia -Q71.5 Longitudinal reduction defect of ulna,7780,Q71.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.5,ORPHAcode: 93320 Ulnar hemimelia -Q71.6 Reduction defects of upper limb - Lobster-claw hand,7781,Q71.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.6,ORPHAcode: 2440 Isolated split hand-split foot malformation -Q71.8 Other reduction defects of upper limb(s),7782,Q71.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.8,ORPHAcode: 2307 IVIC syndrome +Q71.0 Congenital complete absence of upper limb(s),7775,Q71.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.0,ORPHAcode: 294967 Amelia of upper limb,ICD-10 +Q71.1 Congenital absence of upper arm and forearm with hand present,7776,Q71.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.1,ORPHAcode: 294975 Congenital absence of upper arm and forearm with hand present,ICD-10 +Q71.2 Congenital absence of both forearm and hand,7777,Q71.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.2,ORPHAcode: 294979 Congenital absence of both forearm and hand,ICD-10 +Q71.3 Congenital absence of hand and finger(s),7778,Q71.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.3,"ORPHAcode: 973 Congenital absence/hypoplasia of fingers excluding thumb, unilateral",ICD-10 +Q71.4 Longitudinal reduction defect of radius,7779,Q71.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.4,ORPHAcode: 93321 Radial hemimelia,ICD-10 +Q71.5 Longitudinal reduction defect of ulna,7780,Q71.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.5,ORPHAcode: 93320 Ulnar hemimelia,ICD-10 +Q71.6 Reduction defects of upper limb - Lobster-claw hand,7781,Q71.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.6,ORPHAcode: 2440 Isolated split hand-split foot malformation,ICD-10 +Q71.8 Other reduction defects of upper limb(s),7782,Q71.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.8,ORPHAcode: 2307 IVIC syndrome,ICD-10 "Q71.9 Reduction defect of upper limb, unspecified",7783,Q71.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q71.9,,ICD-10 Q72 Reduction defects of lower limb,7784,Q72,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72,,ICD-10 -Q72.0 Congenital complete absence of lower limb(s),7785,Q72.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.0,ORPHAcode: 294969 Amelia of lower limb -Q72.1 Congenital absence of thigh and lower leg with foot present,7786,Q72.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.1,ORPHAcode: 294977 Congenital absence of thigh and lower leg with foot present -Q72.2 Congenital absence of both lower leg and foot,7787,Q72.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.2,ORPHAcode: 294981 Congenital absence of both lower leg and foot -Q72.3 Congenital absence of foot and toe(s),7788,Q72.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.3,ORPHAcode: 294986 Apodia -Q72.4 Longitudinal reduction defect of femur,7789,Q72.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.4,ORPHAcode: 1987 Femoral agenesis/hypoplasia -Q72.5 Longitudinal reduction defect of tibia,7790,Q72.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.5,ORPHAcode: 93322 Tibial hemimelia -Q72.6 Longitudinal reduction defect of fibula,7791,Q72.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.6,ORPHAcode: 93323 Fibular hemimelia +Q72.0 Congenital complete absence of lower limb(s),7785,Q72.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.0,ORPHAcode: 294969 Amelia of lower limb,ICD-10 +Q72.1 Congenital absence of thigh and lower leg with foot present,7786,Q72.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.1,ORPHAcode: 294977 Congenital absence of thigh and lower leg with foot present,ICD-10 +Q72.2 Congenital absence of both lower leg and foot,7787,Q72.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.2,ORPHAcode: 294981 Congenital absence of both lower leg and foot,ICD-10 +Q72.3 Congenital absence of foot and toe(s),7788,Q72.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.3,ORPHAcode: 294986 Apodia,ICD-10 +Q72.4 Longitudinal reduction defect of femur,7789,Q72.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.4,ORPHAcode: 1987 Femoral agenesis/hypoplasia,ICD-10 +Q72.5 Longitudinal reduction defect of tibia,7790,Q72.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.5,ORPHAcode: 93322 Tibial hemimelia,ICD-10 +Q72.6 Longitudinal reduction defect of fibula,7791,Q72.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.6,ORPHAcode: 93323 Fibular hemimelia,ICD-10 Q72.7 Reduction defects of lower limb - Split foot,7792,Q72.7,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.7,,ICD-10 Q72.8 Other reduction defects of lower limb(s),7793,Q72.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.8,,ICD-10 "Q72.9 Reduction defect of lower limb, unspecified",7794,Q72.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q72.9,,ICD-10 Q73 Reduction defects of unspecified limb,7795,Q73,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q73,,ICD-10 -Q73.0 Congenital absence of unspecified limb(s),7796,Q73.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q73.0,ORPHAcode: 1027 Autosomal recessive amelia +Q73.0 Congenital absence of unspecified limb(s),7796,Q73.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q73.0,ORPHAcode: 1027 Autosomal recessive amelia,ICD-10 "Q73.1 Phocomelia, unspecified limb(s)",7797,Q73.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q73.1,,ICD-10 -Q73.8 Other reduction defects of unspecified limb(s),7798,Q73.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q73.8,ORPHAcode: 1118 Fibular aplasia-ectrodactyly syndrome +Q73.8 Other reduction defects of unspecified limb(s),7798,Q73.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q73.8,ORPHAcode: 1118 Fibular aplasia-ectrodactyly syndrome,ICD-10 Q74 Other congenital malformations of limb(s),7799,Q74,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74,,ICD-10 -"Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle",7800,Q74.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.0,ORPHAcode: 1452 Cleidocranial dysplasia -Q74.1 Congenital malformation of knee,7801,Q74.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.1,ORPHAcode: 1509 Coxopodopatellar syndrome -"Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle",7802,Q74.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.2,ORPHAcode: 2110 Hallux varus-preaxial polysyndactyly syndrome -Q74.3 Other congenital malformations of limb(s) - Arthrogryposis multiplex congenita,7803,Q74.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.3,ORPHAcode: 1143 Neurogenic arthrogryposis multiplex congenita -Q74.8 Other specified congenital malformations of limb(s),7804,Q74.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.8,ORPHAcode: 503 Larsen syndrome +"Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle",7800,Q74.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.0,ORPHAcode: 1452 Cleidocranial dysplasia,ICD-10 +Q74.1 Congenital malformation of knee,7801,Q74.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.1,ORPHAcode: 1509 Coxopodopatellar syndrome,ICD-10 +"Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle",7802,Q74.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.2,ORPHAcode: 2110 Hallux varus-preaxial polysyndactyly syndrome,ICD-10 +Q74.3 Other congenital malformations of limb(s) - Arthrogryposis multiplex congenita,7803,Q74.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.3,ORPHAcode: 1143 Neurogenic arthrogryposis multiplex congenita,ICD-10 +Q74.8 Other specified congenital malformations of limb(s),7804,Q74.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.8,ORPHAcode: 503 Larsen syndrome,ICD-10 Q74.9 Unspecified congenital malformation of limb(s),7805,Q74.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q74.9,,ICD-10 Q75 Other congenital malformations of skull and face bones,7806,Q75,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75,,ICD-10 -Q75.0 Other congenital malformations of skull and face bones - Craniosynostosis,7807,Q75.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.0,ORPHAcode: 1225 Baller-Gerold syndrome -Q75.1 Craniofacial dysostosis,7808,Q75.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.1,ORPHAcode: 207 Crouzon disease +Q75.0 Other congenital malformations of skull and face bones - Craniosynostosis,7807,Q75.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.0,ORPHAcode: 1225 Baller-Gerold syndrome,ICD-10 +Q75.1 Craniofacial dysostosis,7808,Q75.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.1,ORPHAcode: 207 Crouzon disease,ICD-10 Q75.2 Other congenital malformations of skull and face bones - Hypertelorism,7809,Q75.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.2,,ICD-10 -Q75.3 Other congenital malformations of skull and face bones - Macrocephaly,7810,Q75.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.3,ORPHAcode: 397612 Macrocephaly-developmental delay syndrome -Q75.4 Mandibulofacial dysostosis,7811,Q75.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.4,ORPHAcode: 245 Nager syndrome +Q75.3 Other congenital malformations of skull and face bones - Macrocephaly,7810,Q75.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.3,ORPHAcode: 397612 Macrocephaly-developmental delay syndrome,ICD-10 +Q75.4 Mandibulofacial dysostosis,7811,Q75.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.4,ORPHAcode: 245 Nager syndrome,ICD-10 Q75.5 Oculomandibular dysostosis,7812,Q75.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.5,,ICD-10 -Q75.8 Other specified congenital malformations of skull and face bones,7813,Q75.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.8,ORPHAcode: 1248 Maxillonasal dysplasia +Q75.8 Other specified congenital malformations of skull and face bones,7813,Q75.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.8,ORPHAcode: 1248 Maxillonasal dysplasia,ICD-10 "Q75.9 Congenital malformation of skull and face bones, unspecified",7814,Q75.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q75.9,,ICD-10 Q76 Congenital malformations of spine and bony thorax,7815,Q76,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76,,ICD-10 -Q76.0 Congenital malformations of spine and bony thorax - Spina bifida occulta,7816,Q76.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.0,ORPHAcode: 3027 Caudal regression sequence -Q76.1 Congenital malformations of spine and bony thorax - Klippel-Feil syndrome,7817,Q76.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.1,ORPHAcode: 2345 Isolated Klippel-Feil syndrome +Q76.0 Congenital malformations of spine and bony thorax - Spina bifida occulta,7816,Q76.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.0,ORPHAcode: 3027 Caudal regression sequence,ICD-10 +Q76.1 Congenital malformations of spine and bony thorax - Klippel-Feil syndrome,7817,Q76.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.1,ORPHAcode: 2345 Isolated Klippel-Feil syndrome,ICD-10 Q76.2 Congenital spondylolisthesis,7818,Q76.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.2,,ICD-10 -Q76.3 Congenital scoliosis due to congenital bony malformation,7819,Q76.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.3,ORPHAcode: 2899 Brachyolmia-amelogenesis imperfecta syndrome -"Q76.4 Other congenital malformations of spine, not associated with scoliosis",7820,Q76.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.4,ORPHAcode: 1797 Autosomal dominant spondylocostal dysostosis +Q76.3 Congenital scoliosis due to congenital bony malformation,7819,Q76.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.3,ORPHAcode: 2899 Brachyolmia-amelogenesis imperfecta syndrome,ICD-10 +"Q76.4 Other congenital malformations of spine, not associated with scoliosis",7820,Q76.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.4,ORPHAcode: 1797 Autosomal dominant spondylocostal dysostosis,ICD-10 Q76.5 Congenital malformations of spine and bony thorax - Cervical rib,7821,Q76.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.5,,ICD-10 Q76.6 Other congenital malformations of ribs,7822,Q76.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.6,,ICD-10 -Q76.7 Congenital malformation of sternum,7823,Q76.7,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.7,ORPHAcode: 2017 Sternal cleft -Q76.8 Other congenital malformations of bony thorax,7824,Q76.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.8,ORPHAcode: 2311 Autosomal recessive spondylocostal dysostosis +Q76.7 Congenital malformation of sternum,7823,Q76.7,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.7,ORPHAcode: 2017 Sternal cleft,ICD-10 +Q76.8 Other congenital malformations of bony thorax,7824,Q76.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.8,ORPHAcode: 2311 Autosomal recessive spondylocostal dysostosis,ICD-10 "Q76.9 Congenital malformation of bony thorax, unspecified",7825,Q76.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q76.9,,ICD-10 Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine,7826,Q77,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77,,ICD-10 -Q77.0 Osteochondrodysplasia with defects of growth of tubular bones and spine - Achondrogenesis,7827,Q77.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.0,ORPHAcode: 932 Achondrogenesis -Q77.1 Osteochondrodysplasia with defects of growth of tubular bones and spine - Thanatophoric short stature,7828,Q77.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.1,ORPHAcode: 2655 Thanatophoric dysplasia -Q78.4 Other osteochondrodysplasias - Enchondromatosis,7829,Q78.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.4,ORPHAcode: 296 Ollier disease -Q77.2 Osteochondrodysplasia with defects of growth of tubular bones and spine - Short rib syndrome,7830,Q77.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.2,ORPHAcode: 474 Jeune syndrome -Q77.3 Osteochondrodysplasia with defects of growth of tubular bones and spine - Chondrodysplasia punctata,7831,Q77.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.3,ORPHAcode: 177 Rhizomelic chondrodysplasia punctata -Q77.4 Osteochondrodysplasia with defects of growth of tubular bones and spine - Achondroplasia,7832,Q77.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.4,ORPHAcode: 15 Achondroplasia -Q77.5 Osteochondrodysplasia with defects of growth of tubular bones and spine - Dystrophic dysplasia,7833,Q77.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.5,ORPHAcode: 628 Diastrophic dwarfism -Q77.6 Osteochondrodysplasia with defects of growth of tubular bones and spine - Chondroectodermal dysplasia,7834,Q77.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.6,ORPHAcode: 289 Ellis Van Creveld syndrome -Q77.7 Osteochondrodysplasia with defects of growth of tubular bones and spine - Spondyloepiphyseal dysplasia,7835,Q77.7,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.7,ORPHAcode: 239 Dyggve-Melchior-Clausen disease -Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine,7836,Q77.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.8,"ORPHAcode: 40 Acromesomelic dysplasia, Maroteaux type" +Q77.0 Osteochondrodysplasia with defects of growth of tubular bones and spine - Achondrogenesis,7827,Q77.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.0,ORPHAcode: 932 Achondrogenesis,ICD-10 +Q77.1 Osteochondrodysplasia with defects of growth of tubular bones and spine - Thanatophoric short stature,7828,Q77.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.1,ORPHAcode: 2655 Thanatophoric dysplasia,ICD-10 +Q78.4 Other osteochondrodysplasias - Enchondromatosis,7829,Q78.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.4,ORPHAcode: 296 Ollier disease,ICD-10 +Q77.2 Osteochondrodysplasia with defects of growth of tubular bones and spine - Short rib syndrome,7830,Q77.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.2,ORPHAcode: 474 Jeune syndrome,ICD-10 +Q77.3 Osteochondrodysplasia with defects of growth of tubular bones and spine - Chondrodysplasia punctata,7831,Q77.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.3,ORPHAcode: 177 Rhizomelic chondrodysplasia punctata,ICD-10 +Q77.4 Osteochondrodysplasia with defects of growth of tubular bones and spine - Achondroplasia,7832,Q77.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.4,ORPHAcode: 15 Achondroplasia,ICD-10 +Q77.5 Osteochondrodysplasia with defects of growth of tubular bones and spine - Dystrophic dysplasia,7833,Q77.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.5,ORPHAcode: 628 Diastrophic dwarfism,ICD-10 +Q77.6 Osteochondrodysplasia with defects of growth of tubular bones and spine - Chondroectodermal dysplasia,7834,Q77.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.6,ORPHAcode: 289 Ellis Van Creveld syndrome,ICD-10 +Q77.7 Osteochondrodysplasia with defects of growth of tubular bones and spine - Spondyloepiphyseal dysplasia,7835,Q77.7,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.7,ORPHAcode: 239 Dyggve-Melchior-Clausen disease,ICD-10 +Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine,7836,Q77.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.8,"ORPHAcode: 40 Acromesomelic dysplasia, Maroteaux type",ICD-10 "Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified",7837,Q77.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q77.9,,ICD-10 Q78 Other osteochondrodysplasias,7838,Q78,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78,,ICD-10 -Q78.0 Other osteochondrodysplasias - Osteogenesis imperfecta,7839,Q78.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.0,ORPHAcode: 666 Osteogenesis imperfecta -Q78.1 Other osteochondrodysplasias - Polyostotic fibrous dysplasia,7840,Q78.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.1,ORPHAcode: 249 Fibrous dysplasia of bone -Q78.2 Other osteochondrodysplasias - Osteopetrosis,7841,Q78.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.2,ORPHAcode: 53 Albers-Sch nberg osteope -Q78.3 Other osteochondrodysplasias - Progressive diaphyseal dysplasia,7842,Q78.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.3,ORPHAcode: 1328 Camurati-Engelmann disease -Q78.5 Other osteochondrodysplasias - Metaphyseal dysplasia,7843,Q78.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.5,"ORPHAcode: 174 Metaphyseal chondrodysplasia, Schmid type" -Q78.6 Other osteochondrodysplasias - Multiple congenital exostoses,7844,Q78.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.6,ORPHAcode: 321 Multiple osteochondromas -Q78.8 Other specified osteochondrodysplasias,7845,Q78.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.8,ORPHAcode: 175 Cartilage-hair hypoplasia +Q78.0 Other osteochondrodysplasias - Osteogenesis imperfecta,7839,Q78.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.0,ORPHAcode: 666 Osteogenesis imperfecta,ICD-10 +Q78.1 Other osteochondrodysplasias - Polyostotic fibrous dysplasia,7840,Q78.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.1,ORPHAcode: 249 Fibrous dysplasia of bone,ICD-10 +Q78.2 Other osteochondrodysplasias - Osteopetrosis,7841,Q78.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.2,ORPHAcode: 53 Albers-Sch nberg osteope,ICD-10 +Q78.3 Other osteochondrodysplasias - Progressive diaphyseal dysplasia,7842,Q78.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.3,ORPHAcode: 1328 Camurati-Engelmann disease,ICD-10 +Q78.5 Other osteochondrodysplasias - Metaphyseal dysplasia,7843,Q78.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.5,"ORPHAcode: 174 Metaphyseal chondrodysplasia, Schmid type",ICD-10 +Q78.6 Other osteochondrodysplasias - Multiple congenital exostoses,7844,Q78.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.6,ORPHAcode: 321 Multiple osteochondromas,ICD-10 +Q78.8 Other specified osteochondrodysplasias,7845,Q78.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.8,ORPHAcode: 175 Cartilage-hair hypoplasia,ICD-10 "Q78.9 Other osteochondrodysplasias - Osteochondrodysplasia, unspecified",7846,Q78.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q78.9,,ICD-10 "Q79 Congenital malformations of the musculoskeletal system, not elsewhere classified",7847,Q79,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79,,ICD-10 -Q79.0 Congenital diaphragmatic hernia,7848,Q79.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.0,ORPHAcode: 2140 Congenital diaphragmatic hernia +Q79.0 Congenital diaphragmatic hernia,7848,Q79.0,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.0,ORPHAcode: 2140 Congenital diaphragmatic hernia,ICD-10 Q79.1 Other congenital malformations of diaphragm,7849,Q79.1,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.1,,ICD-10 -"Q79.2 Congenital malformations of the musculoskeletal system, not elsewhere classified - Exomphalos",7850,Q79.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.2,ORPHAcode: 660 Omphalocele -"Q79.3 Congenital malformations of the musculoskeletal system, not elsewhere classified - Gastroschisis",7851,Q79.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.3,ORPHAcode: 2368 Gastroschisis -"Q79.4 Congenital malformations of the musculoskeletal system, not elsewhere classified - Prune belly syndrome",7852,Q79.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.4,ORPHAcode: 2970 Prune belly syndrome +"Q79.2 Congenital malformations of the musculoskeletal system, not elsewhere classified - Exomphalos",7850,Q79.2,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.2,ORPHAcode: 660 Omphalocele,ICD-10 +"Q79.3 Congenital malformations of the musculoskeletal system, not elsewhere classified - Gastroschisis",7851,Q79.3,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.3,ORPHAcode: 2368 Gastroschisis,ICD-10 +"Q79.4 Congenital malformations of the musculoskeletal system, not elsewhere classified - Prune belly syndrome",7852,Q79.4,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.4,ORPHAcode: 2970 Prune belly syndrome,ICD-10 Q79.5 Other congenital malformations of abdominal wall,7853,Q79.5,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.5,,ICD-10 -"Q79.6 Congenital malformations of the musculoskeletal system, not elsewhere classified - Ehlers-Danlos syndrome",7854,Q79.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.6,ORPHAcode: 285 Hypermobile Ehlers-Danlos syndrome -Q79.8 Other congenital malformations of musculoskeletal system,7855,Q79.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.8,ORPHAcode: 1801 Kyphomelic dysplasia +"Q79.6 Congenital malformations of the musculoskeletal system, not elsewhere classified - Ehlers-Danlos syndrome",7854,Q79.6,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.6,ORPHAcode: 285 Hypermobile Ehlers-Danlos syndrome,ICD-10 +Q79.8 Other congenital malformations of musculoskeletal system,7855,Q79.8,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.8,ORPHAcode: 1801 Kyphomelic dysplasia,ICD-10 Q89.8 Other specified congenital malformations,7856,Q89.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.8,,ICD-10 "Q79.9 Congenital malformation of musculoskeletal system, unspecified",7857,Q79.9,Q65-Q79 Congenital malformations and deformations of the musculoskeletal system,http://identifiers.org/icd/Q79.9,,ICD-10 Q80-Q89 Other congenital malformations,7858,,"XVII Congenital malformations, deformations and chromosomal abnormalities",,,ICD-10 Q80 Congenital ichthyosis,7859,Q80,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80,,ICD-10 Q80.0 Ichthyosis vulgaris,7860,Q80.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.0,,ICD-10 -Q80.1 X-linked ichthyosis,7861,Q80.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.1,ORPHAcode: 461 Recessive X-linked ichthyosis -Q80.2 Lamellar ichthyosis,7862,Q80.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.2,ORPHAcode: 313 Lamellar ichthyosis -Q80.3 Congenital bullous ichthyosiform erythroderma,7863,Q80.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.3,ORPHAcode: 312 Autosomal dominant epidermolytic ichthyosis -Q80.4 Congenital ichthyosis - Harlequin fetus,7864,Q80.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.4,ORPHAcode: 457 Harlequin ichthyosis -Q80.8 Other congenital ichthyosis,7865,Q80.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.8,ORPHAcode: 455 Superficial epidermolytic ichthyosis +Q80.1 X-linked ichthyosis,7861,Q80.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.1,ORPHAcode: 461 Recessive X-linked ichthyosis,ICD-10 +Q80.2 Lamellar ichthyosis,7862,Q80.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.2,ORPHAcode: 313 Lamellar ichthyosis,ICD-10 +Q80.3 Congenital bullous ichthyosiform erythroderma,7863,Q80.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.3,ORPHAcode: 312 Autosomal dominant epidermolytic ichthyosis,ICD-10 +Q80.4 Congenital ichthyosis - Harlequin fetus,7864,Q80.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.4,ORPHAcode: 457 Harlequin ichthyosis,ICD-10 +Q80.8 Other congenital ichthyosis,7865,Q80.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.8,ORPHAcode: 455 Superficial epidermolytic ichthyosis,ICD-10 "Q80.9 Congenital ichthyosis, unspecified",7866,Q80.9,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q80.9,,ICD-10 Q81 Epidermolysis bullosa,7867,Q81,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81,,ICD-10 -Q81.0 Epidermolysis bullosa simplex,7868,Q81.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.0,ORPHAcode: 257 Epidermolysis bullosa simplex with muscular dystrophy -Q81.1 Epidermolysis bullosa letalis,7869,Q81.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.1,ORPHAcode: 79404 Severe generalized junctional epidermolysis bullosa -Q81.2 Epidermolysis bullosa dystrophica,7870,Q81.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.2,"ORPHAcode: 79408 Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form" -Q81.8 Other epidermolysis bullosa,7871,Q81.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.8,"ORPHAcode: 1867 Hereditary bullous dystrophy, macular type" +Q81.0 Epidermolysis bullosa simplex,7868,Q81.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.0,ORPHAcode: 257 Epidermolysis bullosa simplex with muscular dystrophy,ICD-10 +Q81.1 Epidermolysis bullosa letalis,7869,Q81.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.1,ORPHAcode: 79404 Severe generalized junctional epidermolysis bullosa,ICD-10 +Q81.2 Epidermolysis bullosa dystrophica,7870,Q81.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.2,"ORPHAcode: 79408 Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form",ICD-10 +Q81.8 Other epidermolysis bullosa,7871,Q81.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.8,"ORPHAcode: 1867 Hereditary bullous dystrophy, macular type",ICD-10 "Q81.9 Epidermolysis bullosa, unspecified",7872,Q81.9,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q81.9,,ICD-10 Q82 Other congenital malformations of skin,7873,Q82,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82,,ICD-10 -Q82.0 Other congenital malformations of skin - Hereditary lymphoedema,7874,Q82.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.0,ORPHAcode: 1414 Cholestasis-lymphedema syndrome -Q82.1 Other congenital malformations of skin - Xeroderma pigmentosum,7875,Q82.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.1,ORPHAcode: 910 Xeroderma pigmentosum -Q82.2 Other congenital malformations of skin - Mastocytosis,7876,Q82.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.2,ORPHAcode: 125 Bloom syndrome -Q82.3 Other congenital malformations of skin - Incontinentia pigmenti,7877,Q82.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.3,ORPHAcode: 464 Incontinentia pigmenti -Q82.4 Other congenital malformations of skin - Ectodermal dysplasia (anhidrotic),7878,Q82.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.4,ORPHAcode: 1028 Amelo-onycho-hypohidrotic syndrome -Q82.5 Congenital non-neoplastic naevus,7879,Q82.5,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.5,ORPHAcode: 624 Familial multiple nevi flammei -Q82.8 Other specified congenital malformations of skin,7880,Q82.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.8,ORPHAcode: 38 Acrokeratoelastoidosis of Costa +Q82.0 Other congenital malformations of skin - Hereditary lymphoedema,7874,Q82.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.0,ORPHAcode: 1414 Cholestasis-lymphedema syndrome,ICD-10 +Q82.1 Other congenital malformations of skin - Xeroderma pigmentosum,7875,Q82.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.1,ORPHAcode: 910 Xeroderma pigmentosum,ICD-10 +Q82.2 Other congenital malformations of skin - Mastocytosis,7876,Q82.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.2,ORPHAcode: 125 Bloom syndrome,ICD-10 +Q82.3 Other congenital malformations of skin - Incontinentia pigmenti,7877,Q82.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.3,ORPHAcode: 464 Incontinentia pigmenti,ICD-10 +Q82.4 Other congenital malformations of skin - Ectodermal dysplasia (anhidrotic),7878,Q82.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.4,ORPHAcode: 1028 Amelo-onycho-hypohidrotic syndrome,ICD-10 +Q82.5 Congenital non-neoplastic naevus,7879,Q82.5,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.5,ORPHAcode: 624 Familial multiple nevi flammei,ICD-10 +Q82.8 Other specified congenital malformations of skin,7880,Q82.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.8,ORPHAcode: 38 Acrokeratoelastoidosis of Costa,ICD-10 "Q82.9 Congenital malformation of skin, unspecified",7881,Q82.9,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q82.9,,ICD-10 Q83 Congenital malformations of breast,7882,Q83,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83,,ICD-10 -Q83.0 Congenital absence of breast with absent nipple,7883,Q83.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.0,ORPHAcode: 180188 Isolated congenital breast hypoplasia/aplasia -Q83.1 Accessory breast,7884,Q83.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.1,ORPHAcode: 180182 Supernumerary breasts +Q83.0 Congenital absence of breast with absent nipple,7883,Q83.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.0,ORPHAcode: 180188 Isolated congenital breast hypoplasia/aplasia,ICD-10 +Q83.1 Accessory breast,7884,Q83.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.1,ORPHAcode: 180182 Supernumerary breasts,ICD-10 Q83.2 Congenital malformations of breast - Absent nipple,7885,Q83.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.2,,ICD-10 -Q83.3 Congenital malformations of breast - Accessory nipple,7886,Q83.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.3,ORPHAcode: 2456 Familial supernumerary nipples +Q83.3 Congenital malformations of breast - Accessory nipple,7886,Q83.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.3,ORPHAcode: 2456 Familial supernumerary nipples,ICD-10 Q83.8 Other congenital malformations of breast,7887,Q83.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.8,,ICD-10 "Q83.9 Congenital malformation of breast, unspecified",7888,Q83.9,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q83.9,,ICD-10 Q84 Other congenital malformations of integument,7889,Q84,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84,,ICD-10 -Q84.0 Congenital alopecia,7890,Q84.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.0,ORPHAcode: 444 Marie Unna hereditary hypotrichosis -"Q84.1 Congenital morphological disturbances of hair, not elsewhere classified",7891,Q84.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.1,ORPHAcode: 169 Ringed hair disease -Q84.3 Other congenital malformations of integument - Anonychia,7892,Q84.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.3,ORPHAcode: 79143 Isolated congenital anonychia -Q84.4 Congenital leukonychia,7893,Q84.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.4,ORPHAcode: 2387 Leukonychia totalis -Q84.5 Other congenital malformations of integument - Enlarged and hypertrophic nails,7894,Q84.5,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.5,ORPHAcode: 2309 Pachyonychia congenita -Q84.6 Other congenital malformations of nails,7895,Q84.6,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.6,ORPHAcode: 1487 Cooks syndrome -Q84.8 Other specified congenital malformations of integument,7896,Q84.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.8,ORPHAcode: 1114 Aplasia cutis congenita +Q84.0 Congenital alopecia,7890,Q84.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.0,ORPHAcode: 444 Marie Unna hereditary hypotrichosis,ICD-10 +"Q84.1 Congenital morphological disturbances of hair, not elsewhere classified",7891,Q84.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.1,ORPHAcode: 169 Ringed hair disease,ICD-10 +Q84.3 Other congenital malformations of integument - Anonychia,7892,Q84.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.3,ORPHAcode: 79143 Isolated congenital anonychia,ICD-10 +Q84.4 Congenital leukonychia,7893,Q84.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.4,ORPHAcode: 2387 Leukonychia totalis,ICD-10 +Q84.5 Other congenital malformations of integument - Enlarged and hypertrophic nails,7894,Q84.5,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.5,ORPHAcode: 2309 Pachyonychia congenita,ICD-10 +Q84.6 Other congenital malformations of nails,7895,Q84.6,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.6,ORPHAcode: 1487 Cooks syndrome,ICD-10 +Q84.8 Other specified congenital malformations of integument,7896,Q84.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.8,ORPHAcode: 1114 Aplasia cutis congenita,ICD-10 "Q84.9 Congenital malformation of integument, unspecified",7897,Q84.9,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q84.9,,ICD-10 "Q85 Phakomatoses, not elsewhere classified",7898,Q85,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85,,ICD-10 -"Q85.0 Phakomatoses, not elsewhere classified - Neurofibromatosis (nonmalignant)",7899,Q85.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85.0,ORPHAcode: 636 Neurofibromatosis type 1 -"Q85.1 Phakomatoses, not elsewhere classified - Tuberous sclerosis",7900,Q85.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85.1,ORPHAcode: 805 Tuberous sclerosis complex -"Q85.8 Other phakomatoses, not elsewhere classified",7901,Q85.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85.8,ORPHAcode: 201 Cowden syndrome +"Q85.0 Phakomatoses, not elsewhere classified - Neurofibromatosis (nonmalignant)",7899,Q85.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85.0,ORPHAcode: 636 Neurofibromatosis type 1,ICD-10 +"Q85.1 Phakomatoses, not elsewhere classified - Tuberous sclerosis",7900,Q85.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85.1,ORPHAcode: 805 Tuberous sclerosis complex,ICD-10 +"Q85.8 Other phakomatoses, not elsewhere classified",7901,Q85.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85.8,ORPHAcode: 201 Cowden syndrome,ICD-10 "Q85.9 Phakomatoses, not elsewhere classified - Phakomatosis, unspecified",7902,Q85.9,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q85.9,,ICD-10 "Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified",7903,Q86,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86,,ICD-10 -"Q86.0 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified - Fetal alcohol syndrome (dysmorphic)",7904,Q86.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.0,ORPHAcode: 1915 Fetal alcohol syndrome -Q86.1 Fetal hydantoin syndrome,7905,Q86.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.1,ORPHAcode: 1912 Fetal hydantoin syndrome -Q86.2 Dysmorphism due to warfarin,7906,Q86.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.2,ORPHAcode: 1914 Vitamin K antagonist embryofetopathy -Q86.8 Other congenital malformation syndromes due to known exogenous causes,7907,Q86.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.8,ORPHAcode: 1906 Fetal valproate spectrum disorder +"Q86.0 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified - Fetal alcohol syndrome (dysmorphic)",7904,Q86.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.0,ORPHAcode: 1915 Fetal alcohol syndrome,ICD-10 +Q86.1 Fetal hydantoin syndrome,7905,Q86.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.1,ORPHAcode: 1912 Fetal hydantoin syndrome,ICD-10 +Q86.2 Dysmorphism due to warfarin,7906,Q86.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.2,ORPHAcode: 1914 Vitamin K antagonist embryofetopathy,ICD-10 +Q86.8 Other congenital malformation syndromes due to known exogenous causes,7907,Q86.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q86.8,ORPHAcode: 1906 Fetal valproate spectrum disorder,ICD-10 Q87 Other specified congenital malformation syndromes affecting multiple systems,7908,Q87,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87,,ICD-10 -Q87.0 Congenital malformation syndromes predominantly affecting facial appearance,7909,Q87.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.0,ORPHAcode: 83 Antley-Bixler syndrome -Q87.1 Congenital malformation syndromes predominantly associated with short stature,7910,Q87.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.1,ORPHAcode: 140 Campomelic dysplasia -Q87.2 Congenital malformation syndromes predominantly involving limbs,7911,Q87.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.2,ORPHAcode: 392 Holt-Oram syndrome -Q87.3 Congenital malformation syndromes involving early overgrowth,7912,Q87.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.3,ORPHAcode: 116 Beckwith-Wiedemann syndrome -Q87.4 Other specified congenital malformation syndromes affecting multiple systems - Marfan syndrome,7913,Q87.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.4,ORPHAcode: 558 Marfan syndrome -Q87.5 Other congenital malformation syndromes with other skeletal changes,7914,Q87.5,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.5,ORPHAcode: 114 Auriculoosteodysplasia -"Q87.8 Other specified congenital malformation syndromes, not elsewhere classified",7915,Q87.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.8,ORPHAcode: 7 3C syndrome +Q87.0 Congenital malformation syndromes predominantly affecting facial appearance,7909,Q87.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.0,ORPHAcode: 83 Antley-Bixler syndrome,ICD-10 +Q87.1 Congenital malformation syndromes predominantly associated with short stature,7910,Q87.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.1,ORPHAcode: 140 Campomelic dysplasia,ICD-10 +Q87.2 Congenital malformation syndromes predominantly involving limbs,7911,Q87.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.2,ORPHAcode: 392 Holt-Oram syndrome,ICD-10 +Q87.3 Congenital malformation syndromes involving early overgrowth,7912,Q87.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.3,ORPHAcode: 116 Beckwith-Wiedemann syndrome,ICD-10 +Q87.4 Other specified congenital malformation syndromes affecting multiple systems - Marfan syndrome,7913,Q87.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.4,ORPHAcode: 558 Marfan syndrome,ICD-10 +Q87.5 Other congenital malformation syndromes with other skeletal changes,7914,Q87.5,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.5,ORPHAcode: 114 Auriculoosteodysplasia,ICD-10 +"Q87.8 Other specified congenital malformation syndromes, not elsewhere classified",7915,Q87.8,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q87.8,ORPHAcode: 7 3C syndrome,ICD-10 "Q89 Other congenital malformations, not elsewhere classified",7916,Q89,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89,,ICD-10 -Q89.0 Congenital malformations of spleen,7917,Q89.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.0,ORPHAcode: 101351 Familial isolated congenital asplenia +Q89.0 Congenital malformations of spleen,7917,Q89.0,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.0,ORPHAcode: 101351 Familial isolated congenital asplenia,ICD-10 Q89.1 Congenital malformations of adrenal gland,7918,Q89.1,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.1,,ICD-10 -Q89.2 Congenital malformations of other endocrine glands,7919,Q89.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.2,ORPHAcode: 93953 Familial thyroglossal duct cyst -"Q89.3 Other congenital malformations, not elsewhere classified - Situs inversus",7920,Q89.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.3,ORPHAcode: 101063 Situs inversus totalis +Q89.2 Congenital malformations of other endocrine glands,7919,Q89.2,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.2,ORPHAcode: 93953 Familial thyroglossal duct cyst,ICD-10 +"Q89.3 Other congenital malformations, not elsewhere classified - Situs inversus",7920,Q89.3,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.3,ORPHAcode: 101063 Situs inversus totalis,ICD-10 "Q89.4 Other congenital malformations, not elsewhere classified - Conjoined twins",7921,Q89.4,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.4,,ICD-10 -"Q89.7 Multiple congenital malformations, not elsewhere classified",7922,Q89.7,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.7,ORPHAcode: 1335 Pentalogy of Cantrell -"Q90.0 Down syndrome - Trisomy 21, meiotic nondisjunction",7923,Q90.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q90.0,ORPHAcode: 870 Down syndrome +"Q89.7 Multiple congenital malformations, not elsewhere classified",7922,Q89.7,Q80-Q89 Other congenital malformations,http://identifiers.org/icd/Q89.7,ORPHAcode: 1335 Pentalogy of Cantrell,ICD-10 +"Q90.0 Down syndrome - Trisomy 21, meiotic nondisjunction",7923,Q90.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q90.0,ORPHAcode: 870 Down syndrome,ICD-10 "Q90.1 Down syndrome - Trisomy 21, mosaicism (mitotic nondisjunction)",7924,Q90.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q90.1,,ICD-10 "Q90.2 Down syndrome - Trisomy 21, translocation",7925,Q90.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q90.2,,ICD-10 "Q90.9 Down syndrome, unspecified",7926,Q90.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q90.9,,ICD-10 Q91 Edwards syndrome and Patau syndrome,7927,Q91,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91,,ICD-10 -"Q91.0 Edwards syndrome and Patau syndrome - Trisomy 18, meiotic nondisjunction",7928,Q91.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.0,ORPHAcode: 3380 Trisomy 18 +"Q91.0 Edwards syndrome and Patau syndrome - Trisomy 18, meiotic nondisjunction",7928,Q91.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.0,ORPHAcode: 3380 Trisomy 18,ICD-10 "Q91.1 Edwards syndrome and Patau syndrome - Trisomy 18, mosaicism (mitotic nondisjunction)",7929,Q91.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.1,,ICD-10 "Q91.2 Edwards syndrome and Patau syndrome - Trisomy 18, translocation",7930,Q91.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.2,,ICD-10 "Q91.3 Edwards syndrome, unspecified",7931,Q91.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.3,,ICD-10 -"Q91.4 Edwards syndrome and Patau syndrome - Trisomy 13, meiotic nondisjunction",7932,Q91.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.4,ORPHAcode: 3378 Trisomy 13 +"Q91.4 Edwards syndrome and Patau syndrome - Trisomy 13, meiotic nondisjunction",7932,Q91.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.4,ORPHAcode: 3378 Trisomy 13,ICD-10 "Q91.5 Edwards syndrome and Patau syndrome - Trisomy 13, mosaicism (mitotic nondisjunction)",7933,Q91.5,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.5,,ICD-10 "Q91.6 Edwards syndrome and Patau syndrome - Trisomy 13, translocation",7934,Q91.6,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.6,,ICD-10 "Q91.7 Patau syndrome, unspecified",7935,Q91.7,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q91.7,,ICD-10 "Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified",7936,Q92,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92,,ICD-10 "Q92.0 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Whole chromosome trisomy, meiotic nondisjunction",7937,Q92.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.0,,ICD-10 -"Q93.4 Monosomies and deletions from the autosomes, not elsewhere classified - Deletion of short arm of chromosome 5",7938,Q93.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.4,ORPHAcode: 281 Monosomy 5p -Q93.5 Other deletions of part of a chromosome,7939,Q93.5,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.5,ORPHAcode: 72 Angelman syndrome -"Q92.1 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Whole chromosome trisomy, mosaicism (mitotic nondisjunction)",7940,Q92.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.1,ORPHAcode: 1692 Mosaic trisomy 1 -Q92.2 Major partial trisomy,7941,Q92.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.2,ORPHAcode: 236 Trisomy 9p -Q92.3 Minor partial trisomy,7942,Q92.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.3,ORPHAcode: 1307 Distal limb deficiencies-micrognathia syndrome +"Q93.4 Monosomies and deletions from the autosomes, not elsewhere classified - Deletion of short arm of chromosome 5",7938,Q93.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.4,ORPHAcode: 281 Monosomy 5p,ICD-10 +Q93.5 Other deletions of part of a chromosome,7939,Q93.5,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.5,ORPHAcode: 72 Angelman syndrome,ICD-10 +"Q92.1 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Whole chromosome trisomy, mosaicism (mitotic nondisjunction)",7940,Q92.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.1,ORPHAcode: 1692 Mosaic trisomy 1,ICD-10 +Q92.2 Major partial trisomy,7941,Q92.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.2,ORPHAcode: 236 Trisomy 9p,ICD-10 +Q92.3 Minor partial trisomy,7942,Q92.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.3,ORPHAcode: 1307 Distal limb deficiencies-micrognathia syndrome,ICD-10 "Q92.4 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Duplications seen only at prometaphase",7943,Q92.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.4,,ICD-10 Q92.5 Duplications with other complex rearrangements,7944,Q92.5,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.5,,ICD-10 -"Q92.6 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Extra marker chromosomes",7945,Q92.6,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.6,ORPHAcode: 96170 Emanuel syndrome -Q92.7 Triploidy and polyploidy,7946,Q92.7,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.7,ORPHAcode: 3305 Tetraploidy -Q92.8 Other specified trisomies and partial trisomies of autosomes,7947,Q92.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.8,ORPHAcode: 195 Cat-eye syndrome +"Q92.6 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Extra marker chromosomes",7945,Q92.6,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.6,ORPHAcode: 96170 Emanuel syndrome,ICD-10 +Q92.7 Triploidy and polyploidy,7946,Q92.7,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.7,ORPHAcode: 3305 Tetraploidy,ICD-10 +Q92.8 Other specified trisomies and partial trisomies of autosomes,7947,Q92.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.8,ORPHAcode: 195 Cat-eye syndrome,ICD-10 "Q92.9 Trisomy and partial trisomy of autosomes, unspecified",7948,Q92.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q92.9,,ICD-10 "Q93 Monosomies and deletions from the autosomes, not elsewhere classified",7949,Q93,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93,,ICD-10 -"Q93.0 Monosomies and deletions from the autosomes, not elsewhere classified - Whole chromosome monosomy, meiotic nondisjunction",7950,Q93.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.0,ORPHAcode: 574 Monosomy 21 +"Q93.0 Monosomies and deletions from the autosomes, not elsewhere classified - Whole chromosome monosomy, meiotic nondisjunction",7950,Q93.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.0,ORPHAcode: 574 Monosomy 21,ICD-10 "Q93.1 Monosomies and deletions from the autosomes, not elsewhere classified - Whole chromosome monosomy, mosaicism (mitotic nondisjunction)",7951,Q93.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.1,,ICD-10 -"Q93.2 Monosomies and deletions from the autosomes, not elsewhere classified - Chromosome replaced with ring or dicentric",7952,Q93.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.2,ORPHAcode: 1437 Ring chromosome 1 syndrome -"Q93.3 Monosomies and deletions from the autosomes, not elsewhere classified - Deletion of short arm of chromosome 4",7953,Q93.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.3,ORPHAcode: 280 Wolf-Hirschhorn syndrome +"Q93.2 Monosomies and deletions from the autosomes, not elsewhere classified - Chromosome replaced with ring or dicentric",7952,Q93.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.2,ORPHAcode: 1437 Ring chromosome 1 syndrome,ICD-10 +"Q93.3 Monosomies and deletions from the autosomes, not elsewhere classified - Deletion of short arm of chromosome 4",7953,Q93.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.3,ORPHAcode: 280 Wolf-Hirschhorn syndrome,ICD-10 Q93.6 Deletions seen only at prometaphase,7954,Q93.6,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.6,,ICD-10 Q93.7 Deletions with other complex rearrangements,7955,Q93.7,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.7,,ICD-10 -Q93.8 Other deletions from the autosomes,7956,Q93.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.8,ORPHAcode: 904 Williams syndrome +Q93.8 Other deletions from the autosomes,7956,Q93.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.8,ORPHAcode: 904 Williams syndrome,ICD-10 "Q93.9 Deletion from autosomes, unspecified",7957,Q93.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q93.9,,ICD-10 "Q95 Balanced rearrangements and structural markers, not elsewhere classified",7958,Q95,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95,,ICD-10 Q95.0 Balanced translocation and insertion in normal individual,7959,Q95.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.0,,ICD-10 "Q95.1 Balanced rearrangements and structural markers, not elsewhere classified - Chromosome inversion in normal individual",7960,Q95.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.1,,ICD-10 -Q95.2 Balanced autosomal rearrangement in abnormal individual,7961,Q95.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.2,ORPHAcode: 1895 Edinburgh malformation syndrome +Q95.2 Balanced autosomal rearrangement in abnormal individual,7961,Q95.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.2,ORPHAcode: 1895 Edinburgh malformation syndrome,ICD-10 Q95.3 Balanced sex/autosomal rearrangement in abnormal individual,7962,Q95.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.3,,ICD-10 "Q95.4 Balanced rearrangements and structural markers, not elsewhere classified - Individuals with marker heterochromatin",7963,Q95.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.4,,ICD-10 "Q95.5 Balanced rearrangements and structural markers, not elsewhere classified - Individuals with autosomal fragile site",7964,Q95.5,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.5,,ICD-10 Q95.8 Other balanced rearrangements and structural markers,7965,Q95.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.8,,ICD-10 "Q95.9 Balanced rearrangement and structural marker, unspecified",7966,Q95.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q95.9,,ICD-10 Q96 Turner syndrome,7967,Q96,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96,,ICD-10 -"Q96.0 Turner syndrome - Karyotype 45,X",7968,Q96.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.0,ORPHAcode: 881 Turner syndrome +"Q96.0 Turner syndrome - Karyotype 45,X",7968,Q96.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.0,ORPHAcode: 881 Turner syndrome,ICD-10 "Q96.1 Turner syndrome - Karyotype 46,X iso (Xq)",7969,Q96.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.1,,ICD-10 "Q96.2 Turner syndrome - Karyotype 46,X with abnormal sex chromosome, except iso (Xq)",7970,Q96.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.2,,ICD-10 "Q96.3 Turner syndrome - Mosaicism, 45,X/46,XX or XY",7971,Q96.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.3,,ICD-10 "Q96.4 Turner syndrome - Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome",7972,Q96.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.4,,ICD-10 -Q96.8 Other variants of Turner syndrome,7973,Q96.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.8,"ORPHAcode: 444048 46,XX ovarian dysgenesis-short stature syndrome" +Q96.8 Other variants of Turner syndrome,7973,Q96.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.8,"ORPHAcode: 444048 46,XX ovarian dysgenesis-short stature syndrome",ICD-10 "Q96.9 Turner syndrome, unspecified",7974,Q96.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q96.9,,ICD-10 "Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified",7975,Q97,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97,,ICD-10 -"Q97.0 Other sex chromosome abnormalities, female phenotype, not elsewhere classified - Karyotype 47,XXX",7976,Q97.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.0,ORPHAcode: 3375 Trisomy X -Q97.1 Female with more than three X chromosomes,7977,Q97.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.1,ORPHAcode: 9 Tetrasomy X +"Q97.0 Other sex chromosome abnormalities, female phenotype, not elsewhere classified - Karyotype 47,XXX",7976,Q97.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.0,ORPHAcode: 3375 Trisomy X,ICD-10 +Q97.1 Female with more than three X chromosomes,7977,Q97.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.1,ORPHAcode: 9 Tetrasomy X,ICD-10 "Q97.2 Mosaicism, lines with various numbers of X chromosomes",7978,Q97.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.2,,ICD-10 "Q97.3 Female with 46,XY karyotype",7979,Q97.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.3,,ICD-10 "Q97.8 Other specified sex chromosome abnormalities, female phenotype",7980,Q97.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.8,,ICD-10 "Q97.9 Sex chromosome abnormality, female phenotype, unspecified",7981,Q97.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q97.9,,ICD-10 "Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified",7982,Q98,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98,,ICD-10 "Q98.0 Other sex chromosome abnormalities, male phenotype, not elsewhere classified - Klinefelter syndrome karyotype 47,XXY",7983,Q98.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.0,,ICD-10 -"Q98.1 Klinefelter syndrome, male with more than two X chromosomes",7984,Q98.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.1,"ORPHAcode: 96263 48,XXXY syndrome" +"Q98.1 Klinefelter syndrome, male with more than two X chromosomes",7984,Q98.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.1,"ORPHAcode: 96263 48,XXXY syndrome",ICD-10 "Q98.2 Klinefelter syndrome, male with 46,XX karyotype",7985,Q98.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.2,,ICD-10 "Q98.3 Other male with 46,XX karyotype",7986,Q98.3,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.3,,ICD-10 "Q98.4 Other sex chromosome abnormalities, male phenotype, not elsewhere classified - Klinefelter syndrome, unspecified",7987,Q98.4,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.4,,ICD-10 -"Q98.5 Other sex chromosome abnormalities, male phenotype, not elsewhere classified - Karyotype 47,XYY",7988,Q98.5,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.5,"ORPHAcode: 8 47,XYY syndrome" -Q98.6 Male with structurally abnormal sex chromosome,7989,Q98.6,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.6,ORPHAcode: 1646 Partial chromosome Y deletion -Q98.7 Male with sex chromosome mosaicism,7990,Q98.7,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.7,"ORPHAcode: 1772 45,X/46,XY mixed gonadal dysgenesis" -"Q98.8 Other specified sex chromosome abnormalities, male phenotype",7991,Q98.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.8,"ORPHAcode: 10 48,XXYY syndrome" +"Q98.5 Other sex chromosome abnormalities, male phenotype, not elsewhere classified - Karyotype 47,XYY",7988,Q98.5,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.5,"ORPHAcode: 8 47,XYY syndrome",ICD-10 +Q98.6 Male with structurally abnormal sex chromosome,7989,Q98.6,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.6,ORPHAcode: 1646 Partial chromosome Y deletion,ICD-10 +Q98.7 Male with sex chromosome mosaicism,7990,Q98.7,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.7,"ORPHAcode: 1772 45,X/46,XY mixed gonadal dysgenesis",ICD-10 +"Q98.8 Other specified sex chromosome abnormalities, male phenotype",7991,Q98.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.8,"ORPHAcode: 10 48,XXYY syndrome",ICD-10 "Q98.9 Sex chromosome abnormality, male phenotype, unspecified",7992,Q98.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q98.9,,ICD-10 "Q99 Other chromosome abnormalities, not elsewhere classified",7993,Q99,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99,,ICD-10 -"Q99.0 Other chromosome abnormalities, not elsewhere classified - Chimera 46,XX/46,XY",7994,Q99.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.0,ORPHAcode: 199310 Tetragametic chimerism -"Q99.1 Other chromosome abnormalities, not elsewhere classified - 46,XX true hermaphrodite",7995,Q99.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.1,"ORPHAcode: 242 46,XY complete gonadal dysgenesis" -Q99.2 Fragile X chromosome,7996,Q99.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.2,ORPHAcode: 908 Fragile X syndrome -Q99.8 Other specified chromosome abnormalities,7997,Q99.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.8,ORPHAcode: 884 Tetrasomy 12p +"Q99.0 Other chromosome abnormalities, not elsewhere classified - Chimera 46,XX/46,XY",7994,Q99.0,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.0,ORPHAcode: 199310 Tetragametic chimerism,ICD-10 +"Q99.1 Other chromosome abnormalities, not elsewhere classified - 46,XX true hermaphrodite",7995,Q99.1,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.1,"ORPHAcode: 242 46,XY complete gonadal dysgenesis",ICD-10 +Q99.2 Fragile X chromosome,7996,Q99.2,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.2,ORPHAcode: 908 Fragile X syndrome,ICD-10 +Q99.8 Other specified chromosome abnormalities,7997,Q99.8,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.8,ORPHAcode: 884 Tetrasomy 12p,ICD-10 "Q99.9 Other chromosome abnormalities, not elsewhere classified - Chromosomal abnormality, unspecified",7998,Q99.9,"Q90-Q99 Chromosomal abnormalities, not elsewhere classified",http://identifiers.org/icd/Q99.9,,ICD-10 "XVIII Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified",7999,,,,,ICD-10 R12 Heartburn,8000,R12,R10-R19 Symptoms and signs involving the digestive system and abdomen,http://identifiers.org/icd/R12,,ICD-10 @@ -8208,7 +8208,7 @@ R55 Syncope and collapse,8200,R55,R50-R69 General symptoms and signs,http://iden R56.0 Febrile convulsions,8202,R56.0,R50-R69 General symptoms and signs,http://identifiers.org/icd/R56.0,,ICD-10 R56.8 Other and unspecified convulsions,8203,R56.8,R50-R69 General symptoms and signs,http://identifiers.org/icd/R56.8,,ICD-10 "R57 Shock, not elsewhere classified",8204,R57,R50-R69 General symptoms and signs,http://identifiers.org/icd/R57,,ICD-10 -R57.0 Cardiogenic shock,8205,R57.0,R50-R69 General symptoms and signs,http://identifiers.org/icd/R57.0,ORPHAcode: 97292 Cardiogenic shock +R57.0 Cardiogenic shock,8205,R57.0,R50-R69 General symptoms and signs,http://identifiers.org/icd/R57.0,ORPHAcode: 97292 Cardiogenic shock,ICD-10 R57.1 Hypovolaemic shock,8206,R57.1,R50-R69 General symptoms and signs,http://identifiers.org/icd/R57.1,,ICD-10 "R57.9 Shock, unspecified",8207,R57.9,R50-R69 General symptoms and signs,http://identifiers.org/icd/R57.9,,ICD-10 "R58 Haemorrhage, not elsewhere classified",8208,R58,R50-R69 General symptoms and signs,http://identifiers.org/icd/R58,,ICD-10 @@ -8242,7 +8242,7 @@ R64 Cachexia,8235,R64,R50-R69 General symptoms and signs,http://identifiers.org/ R65 Systemic Inflammatory Response Syndrome [SIRS],8236,R65,R50-R69 General symptoms and signs,http://identifiers.org/icd/R65,,ICD-10 R65.0 Systemic Inflammatory Response Syndrome of infectious origin without organ failure,8237,R65.0,R50-R69 General symptoms and signs,http://identifiers.org/icd/R65.0,,ICD-10 R65.1 Systemic Inflammatory Response Syndrome of infectious origin with organ failure,8238,R65.1,R50-R69 General symptoms and signs,http://identifiers.org/icd/R65.1,,ICD-10 -R65.2 Systemic Inflammatory Response Syndrome of non-infectious origin without organ failure,8239,R65.2,R50-R69 General symptoms and signs,http://identifiers.org/icd/R65.2,ORPHAcode: 251332 Unexplained long-lasting fever/inflammatory syndrome +R65.2 Systemic Inflammatory Response Syndrome of non-infectious origin without organ failure,8239,R65.2,R50-R69 General symptoms and signs,http://identifiers.org/icd/R65.2,ORPHAcode: 251332 Unexplained long-lasting fever/inflammatory syndrome,ICD-10 R65.3 Systemic Inflammatory Response Syndrome of non-infectious origin with organ failure,8240,R65.3,R50-R69 General symptoms and signs,http://identifiers.org/icd/R65.3,,ICD-10 "R65.9 Systemic Inflammatory Response Syndrome, unspecified",8241,R65.9,R50-R69 General symptoms and signs,http://identifiers.org/icd/R65.9,,ICD-10 R68 Other general symptoms and signs,8242,R68,R50-R69 General symptoms and signs,http://identifiers.org/icd/R68,,ICD-10 @@ -8264,7 +8264,7 @@ R73.0 Abnormal glucose tolerance test,8256,R73.0,"R70-R79 Abnormal findings on e R74 Abnormal serum enzyme levels,8258,R74,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R74,,ICD-10 R74.0 Elevation of levels of transaminase and lactic acid dehydrogenase [LDH],8259,R74.0,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R74.0,,ICD-10 R78.0 Finding of alcohol in blood,8260,R78.0,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R78.0,,ICD-10 -R74.8 Abnormal levels of other serum enzymes,8261,R74.8,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R74.8,ORPHAcode: 206599 Isolated asymptomatic elevation of creatine phosphokinase +R74.8 Abnormal levels of other serum enzymes,8261,R74.8,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R74.8,ORPHAcode: 206599 Isolated asymptomatic elevation of creatine phosphokinase,ICD-10 R74.9 Abnormal level of unspecified serum enzyme,8262,R74.9,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R74.9,,ICD-10 R75 Laboratory evidence of human immunodeficiency virus [HIV],8263,R75,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R75,,ICD-10 R76 Other abnormal immunological findings in serum,8264,R76,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R76,,ICD-10 @@ -8274,10 +8274,10 @@ R76.2 Other abnormal immunological findings in serum - False-positive serologica R76.8 Other specified abnormal immunological findings in serum,8268,R76.8,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R76.8,,ICD-10 "R76.9 Abnormal immunological finding in serum, unspecified",8269,R76.9,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R76.9,,ICD-10 R77 Other abnormalities of plasma proteins,8270,R77,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77,,ICD-10 -R77.0 Abnormality of albumin,8271,R77.0,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.0,ORPHAcode: 86816 Congenital analbuminemia +R77.0 Abnormality of albumin,8271,R77.0,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.0,ORPHAcode: 86816 Congenital analbuminemia,ICD-10 R77.1 Abnormality of globulin,8272,R77.1,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.1,,ICD-10 -R77.2 Abnormality of alphafetoprotein,8273,R77.2,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.2,ORPHAcode: 168612 Congenital deficiency in alpha-fetoprotein -R77.8 Other specified abnormalities of plasma proteins,8274,R77.8,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.8,ORPHAcode: 254704 Genetic hyperferritinemia without iron overload +R77.2 Abnormality of alphafetoprotein,8273,R77.2,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.2,ORPHAcode: 168612 Congenital deficiency in alpha-fetoprotein,ICD-10 +R77.8 Other specified abnormalities of plasma proteins,8274,R77.8,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.8,ORPHAcode: 254704 Genetic hyperferritinemia without iron overload,ICD-10 "R77.9 Abnormality of plasma protein, unspecified",8275,R77.9,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R77.9,,ICD-10 "R78 Findings of drugs and other substances, not normally found in blood",8276,R78,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R78,,ICD-10 R78.1 Finding of opiate drug in blood,8277,R78.1,"R70-R79 Abnormal findings on examination of blood, without diagnosis",http://identifiers.org/icd/R78.1,,ICD-10 @@ -8300,7 +8300,7 @@ R82 Other abnormal findings in urine,8293,R82,"R80-R82 Abnormal findings on exam X34 Victim of earthquake,8294,X34,X30-X39 Exposure to forces of nature,http://identifiers.org/icd/X34,,ICD-10 R82.0 Other abnormal findings in urine - Chyluria,8295,R82.0,"R80-R82 Abnormal findings on examination of urine, without diagnosis",http://identifiers.org/icd/R82.0,,ICD-10 "R96 Other sudden death, cause unknown",8296,R96,R95-R99 Ill-defined and unknown causes of mortality,http://identifiers.org/icd/R96,,ICD-10 -R82.1 Myoglobinuria,8297,R82.1,"R80-R82 Abnormal findings on examination of urine, without diagnosis",http://identifiers.org/icd/R82.1,ORPHAcode: 99845 Genetic recurrent myoglobinuria +R82.1 Myoglobinuria,8297,R82.1,"R80-R82 Abnormal findings on examination of urine, without diagnosis",http://identifiers.org/icd/R82.1,ORPHAcode: 99845 Genetic recurrent myoglobinuria,ICD-10 R82.2 Other abnormal findings in urine - Biliuria,8298,R82.2,"R80-R82 Abnormal findings on examination of urine, without diagnosis",http://identifiers.org/icd/R82.2,,ICD-10 R82.3 Haemoglobinuria,8299,R82.3,"R80-R82 Abnormal findings on examination of urine, without diagnosis",http://identifiers.org/icd/R82.3,,ICD-10 R82.4 Other abnormal findings in urine - Acetonuria,8300,R82.4,"R80-R82 Abnormal findings on examination of urine, without diagnosis",http://identifiers.org/icd/R82.4,,ICD-10 @@ -8414,7 +8414,7 @@ S06.0 Intracranial injury - Concussion,8407,S06.0,S00-S09 Injuries to the head,h S06.1 Intracranial injury - Traumatic cerebral oedema,8408,S06.1,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.1,,ICD-10 S06.2 Diffuse brain injury,8409,S06.2,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.2,,ICD-10 S06.3 Focal brain injury,8410,S06.3,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.3,,ICD-10 -S06.4 Intracranial injury - Epidural haemorrhage,8411,S06.4,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.4,ORPHAcode: 90056 Moderate and severe traumatic brain injury +S06.4 Intracranial injury - Epidural haemorrhage,8411,S06.4,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.4,ORPHAcode: 90056 Moderate and severe traumatic brain injury,ICD-10 S06.5 Intracranial injury - Traumatic subdural haemorrhage,8412,S06.5,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.5,,ICD-10 S06.6 Intracranial injury - Traumatic subarachnoid haemorrhage,8413,S06.6,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.6,,ICD-10 S06.7 Intracranial injury with prolonged coma,8414,S06.7,S00-S09 Injuries to the head,http://identifiers.org/icd/S06.7,,ICD-10 @@ -9122,7 +9122,7 @@ T07 Unspecified multiple injuries,9112,T07,T00-T07 Injuries involving multiple b "T09.0 Superficial injury of trunk, level unspecified",9116,T09.0,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.0,,ICD-10 "T09.1 Open wound of trunk, level unspecified",9117,T09.1,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.1,,ICD-10 "T09.2 Dislocation, sprain and strain of unspecified joint and ligament of trunk",9118,T09.2,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.2,,ICD-10 -"T09.3 Injury of spinal cord, level unspecified",9119,T09.3,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.3,ORPHAcode: 90058 Spinal cord injury +"T09.3 Injury of spinal cord, level unspecified",9119,T09.3,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.3,ORPHAcode: 90058 Spinal cord injury,ICD-10 "T09.4 Injury of unspecified nerve, spinal nerve root and plexus of trunk",9120,T09.4,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.4,,ICD-10 T09.5 Injury of unspecified muscle and tendon of trunk,9121,T09.5,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.5,,ICD-10 "T09.6 Traumatic amputation of trunk, level unspecified",9122,T09.6,"T08-T14 Injuries to unspecified part of trunk, limb or body region",http://identifiers.org/icd/T09.6,,ICD-10 @@ -9295,7 +9295,7 @@ T29 Burns and corrosions of multiple body regions,9278,T29,T29-T32 Burns and cor "T30.1 Burn of first degree, body region unspecified",9289,T30.1,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T30.1,,ICD-10 "T30.2 Burn of second degree, body region unspecified",9290,T30.2,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T30.2,,ICD-10 T32 Corrosions classified according to extent of body surface involved,9291,T32,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T32,,ICD-10 -"T30.3 Burn of third degree, body region unspecified",9292,T30.3,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T30.3,ORPHAcode: 90076 Partial deep dermal and full thickness burns +"T30.3 Burn of third degree, body region unspecified",9292,T30.3,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T30.3,ORPHAcode: 90076 Partial deep dermal and full thickness burns,ICD-10 "T30.4 Corrosion of unspecified body region, unspecified degree",9293,T30.4,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T30.4,,ICD-10 "T30.5 Corrosion of first degree, body region unspecified",9294,T30.5,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T30.5,,ICD-10 "T30.6 Corrosion of second degree, body region unspecified",9295,T30.6,T29-T32 Burns and corrosions of multiple and unspecified body regions,http://identifiers.org/icd/T30.6,,ICD-10 @@ -9392,12 +9392,12 @@ T38.9 Other and unspecified hormone antagonists,9379,T38.9,"T36-T50 Poisoning by "T39.8 Other nonopioid analgesics and antipyretics, not elsewhere classified",9386,T39.8,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T39.8,,ICD-10 "T39.9 Nonopioid analgesic, antipyretic and antirheumatic, unspecified",9387,T39.9,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T39.9,,ICD-10 T40 Poisoning by narcotics and psychodysleptics [hallucinogens],9388,T40,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40,,ICD-10 -T40.0 Poisoning by narcotics and psychodysleptics [hallucinogens] - Opium,9389,T40.0,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.0,ORPHAcode: 35889 Acute opioid poisoning +T40.0 Poisoning by narcotics and psychodysleptics [hallucinogens] - Opium,9389,T40.0,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.0,ORPHAcode: 35889 Acute opioid poisoning,ICD-10 T40.1 Poisoning by narcotics and psychodysleptics [hallucinogens] - Heroin,9390,T40.1,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.1,,ICD-10 T40.2 Poisoning by narcotics and psychodysleptics [hallucinogens] - Other opioids,9391,T40.2,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.2,,ICD-10 T40.3 Poisoning by narcotics and psychodysleptics [hallucinogens] - Methadone,9392,T40.3,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.3,,ICD-10 T40.4 Other synthetic narcotics,9393,T40.4,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.4,,ICD-10 -T40.5 Poisoning by narcotics and psychodysleptics [hallucinogens] - Cocaine,9394,T40.5,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.5,ORPHAcode: 90068 Cocaine intoxication +T40.5 Poisoning by narcotics and psychodysleptics [hallucinogens] - Cocaine,9394,T40.5,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.5,ORPHAcode: 90068 Cocaine intoxication,ICD-10 T40.6 Other and unspecified narcotics,9395,T40.6,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.6,,ICD-10 T40.7 Poisoning by narcotics and psychodysleptics [hallucinogens] - Cannabis (derivatives),9396,T40.7,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.7,,ICD-10 T40.8 Poisoning by narcotics and psychodysleptics [hallucinogens] - Lysergide [LSD],9397,T40.8,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T40.8,,ICD-10 @@ -9419,7 +9419,7 @@ T42.2 Succinimides and oxazolidinediones,9409,T42.2,"T36-T50 Poisoning by drugs, W17 Other fall from one level to another,9413,W17,W00-W19 Falls,http://identifiers.org/icd/W17,,ICD-10 T42.8 Antiparkinsonism drugs and other central muscle-tone depressants,9414,T42.8,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T42.8,,ICD-10 "T43 Poisoning by psychotropic drugs, not elsewhere classified",9415,T43,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T43,,ICD-10 -"T43.0 Poisoning by psychotropic drugs, not elsewhere classified - Tricyclic and tetracyclic antidepressants",9416,T43.0,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T43.0,ORPHAcode: 43117 Acute tricyclic antidepressant poisoning +"T43.0 Poisoning by psychotropic drugs, not elsewhere classified - Tricyclic and tetracyclic antidepressants",9416,T43.0,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T43.0,ORPHAcode: 43117 Acute tricyclic antidepressant poisoning,ICD-10 "T43.1 Poisoning by psychotropic drugs, not elsewhere classified - Monoamine-oxidase-inhibitor antidepressants",9417,T43.1,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T43.1,,ICD-10 "T43.2 Poisoning by psychotropic drugs, not elsewhere classified - Other and unspecified antidepressants",9418,T43.2,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T43.2,,ICD-10 T43.3 Phenothiazine antipsychotics and neuroleptics,9419,T43.3,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T43.3,,ICD-10 @@ -9441,7 +9441,7 @@ T44.1 Other parasympathomimetics [cholinergics],9427,T44.1,"T36-T50 Poisoning by T44.9 Other and unspecified drugs primarily affecting the autonomic nervous system,9435,T44.9,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T44.9,,ICD-10 "T45 Poisoning by primarily systemic and haematological agents, not elsewhere classified",9436,T45,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45,,ICD-10 T45.0 Antiallergic and antiemetic drugs,9437,T45.0,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.0,,ICD-10 -T45.1 Antineoplastic and immunosuppressive drugs,9438,T45.1,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.1,ORPHAcode: 217064 5-fluorouracil poisoning +T45.1 Antineoplastic and immunosuppressive drugs,9438,T45.1,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.1,ORPHAcode: 217064 5-fluorouracil poisoning,ICD-10 "T45.2 Vitamins, not elsewhere classified",9439,T45.2,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.2,,ICD-10 "T45.3 Enzymes, not elsewhere classified",9440,T45.3,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.3,,ICD-10 T45.4 Iron and its compounds,9441,T45.4,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.4,,ICD-10 @@ -9453,7 +9453,7 @@ T45.4 Iron and its compounds,9441,T45.4,"T36-T50 Poisoning by drugs, medicaments T45.8 Other primarily systemic and haematological agents,9447,T45.8,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.8,,ICD-10 "T45.9 Primarily systemic and haematological agent, unspecified",9448,T45.9,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T45.9,,ICD-10 T46 Poisoning by agents primarily affecting the cardiovascular system,9449,T46,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T46,,ICD-10 -T46.0 Poisoning by agents primarily affecting the cardiovascular system - Cardiac-stimulant glycosides and drugs of similar action,9450,T46.0,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T46.0,ORPHAcode: 31828 Digitalis poisoning +T46.0 Poisoning by agents primarily affecting the cardiovascular system - Cardiac-stimulant glycosides and drugs of similar action,9450,T46.0,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T46.0,ORPHAcode: 31828 Digitalis poisoning,ICD-10 T46.1 Poisoning by agents primarily affecting the cardiovascular system - Calcium-channel blockers,9451,T46.1,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T46.1,,ICD-10 "T46.2 Other antidysrhythmic drugs, not elsewhere classified",9452,T46.2,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T46.2,,ICD-10 "T46.3 Poisoning by agents primarily affecting the cardiovascular system - Coronary vasodilators, not elsewhere classified",9453,T46.3,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T46.3,,ICD-10 @@ -9497,7 +9497,7 @@ T50.0 Mineralocorticoids and their antagonists,9490,T50.0,"T36-T50 Poisoning by T50.1 Loop [high-ceiling] diuretics,9491,T50.1,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.1,,ICD-10 "T50.2 Carbonic-anhydrase inhibitors, benzothiadiazides and other diuretics",9492,T50.2,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.2,,ICD-10 "T50.3 Electrolytic, caloric and water-balance agents",9493,T50.3,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.3,,ICD-10 -T50.4 Drugs affecting uric acid metabolism,9494,T50.4,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.4,ORPHAcode: 31824 Colchicine poisoning +T50.4 Drugs affecting uric acid metabolism,9494,T50.4,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.4,ORPHAcode: 31824 Colchicine poisoning,ICD-10 "T50.5 Poisoning by diuretics and other and unspecified drugs, medicaments and biological substances - Appetite depressants",9495,T50.5,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.5,,ICD-10 "T50.6 Antidotes and chelating agents, not elsewhere classified",9496,T50.6,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.6,,ICD-10 T50.7 Analeptics and opioid receptor antagonists,9497,T50.7,"T36-T50 Poisoning by drugs, medicaments and biological substances",http://identifiers.org/icd/T50.7,,ICD-10 @@ -9508,7 +9508,7 @@ T51 Toxic effect of alcohol,9501,T51,T51-T65 Toxic effects of substances chiefly T51.0 Toxic effect of alcohol - Ethanol,9502,T51.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T51.0,,ICD-10 "T59 Toxic effect of other gases, fumes and vapours",9503,T59,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T59,,ICD-10 "T73.9 Effect of deprivation, unspecified",9504,T73.9,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T73.9,,ICD-10 -T51.1 Toxic effect of alcohol - Methanol,9505,T51.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T51.1,ORPHAcode: 31825 Methanol poisoning +T51.1 Toxic effect of alcohol - Methanol,9505,T51.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T51.1,ORPHAcode: 31825 Methanol poisoning,ICD-10 T51.2 Toxic effect of alcohol - 2-Propanol,9506,T51.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T51.2,,ICD-10 T51.3 Toxic effect of alcohol - Fusel oil,9507,T51.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T51.3,,ICD-10 T51.8 Other alcohols,9508,T51.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T51.8,,ICD-10 @@ -9519,7 +9519,7 @@ T52.1 Toxic effect of organic solvents - Benzene,9512,T52.1,T51-T65 Toxic effect T52.2 Homologues of benzene,9513,T52.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T52.2,,ICD-10 T52.3 Toxic effect of organic solvents - Glycols,9514,T52.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T52.3,,ICD-10 T52.4 Toxic effect of organic solvents - Ketones,9515,T52.4,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T52.4,,ICD-10 -T52.8 Other organic solvents,9516,T52.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T52.8,ORPHAcode: 31826 Ethylene glycol poisoning +T52.8 Other organic solvents,9516,T52.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T52.8,ORPHAcode: 31826 Ethylene glycol poisoning,ICD-10 "T52.9 Organic solvent, unspecified",9517,T52.9,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T52.9,,ICD-10 T53 Toxic effect of halogen derivatives of aliphatic and aromatic hydrocarbons,9518,T53,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T53,,ICD-10 T53.0 Toxic effect of halogen derivatives of aliphatic and aromatic hydrocarbons - Carbon tetrachloride,9519,T53.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T53.0,,ICD-10 @@ -9540,21 +9540,21 @@ T54.3 Corrosive alkalis and alkali-like substances,9532,T54.3,T51-T65 Toxic effe T55 Toxic effect of soaps and detergents,9534,T55,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T55,,ICD-10 T56 Toxic effect of metals,9535,T56,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56,,ICD-10 "T57.9 Inorganic substance, unspecified",9536,T57.9,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57.9,,ICD-10 -T56.0 Toxic effect of metals - Lead and its compounds,9537,T56.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.0,ORPHAcode: 330015 Lead poisoning +T56.0 Toxic effect of metals - Lead and its compounds,9537,T56.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.0,ORPHAcode: 330015 Lead poisoning,ICD-10 W18 Other fall on same level,9538,W18,W00-W19 Falls,http://identifiers.org/icd/W18,,ICD-10 -T56.1 Toxic effect of metals - Mercury and its compounds,9539,T56.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.1,ORPHAcode: 1917 Fetal methylmercury syndrome +T56.1 Toxic effect of metals - Mercury and its compounds,9539,T56.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.1,ORPHAcode: 1917 Fetal methylmercury syndrome,ICD-10 T56.2 Toxic effect of metals - Chromium and its compounds,9540,T56.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.2,,ICD-10 T56.3 Toxic effect of metals - Cadmium and its compounds,9541,T56.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.3,,ICD-10 T56.4 Toxic effect of metals - Copper and its compounds,9542,T56.4,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.4,,ICD-10 T56.5 Toxic effect of metals - Zinc and its compounds,9543,T56.5,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.5,,ICD-10 T56.6 Toxic effect of metals - Tin and its compounds,9544,T56.6,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.6,,ICD-10 T56.7 Toxic effect of metals - Beryllium and its compounds,9545,T56.7,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.7,,ICD-10 -T56.8 Other metals,9546,T56.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.8,ORPHAcode: 60014 Argyria +T56.8 Other metals,9546,T56.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.8,ORPHAcode: 60014 Argyria,ICD-10 "T56.9 Toxic effect of metals - Metal, unspecified",9547,T56.9,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T56.9,,ICD-10 T57 Toxic effect of other inorganic substances,9548,T57,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57,,ICD-10 T57.0 Toxic effect of other inorganic substances - Arsenic and its compounds,9549,T57.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57.0,,ICD-10 T57.1 Toxic effect of other inorganic substances - Phosphorus and its compounds,9550,T57.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57.1,,ICD-10 -T57.2 Toxic effect of other inorganic substances - Manganese and its compounds,9551,T57.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57.2,ORPHAcode: 306682 Manganese poisoning +T57.2 Toxic effect of other inorganic substances - Manganese and its compounds,9551,T57.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57.2,ORPHAcode: 306682 Manganese poisoning,ICD-10 T57.3 Toxic effect of other inorganic substances - Hydrogen cyanide,9552,T57.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57.3,,ICD-10 T57.8 Other specified inorganic substances,9553,T57.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T57.8,,ICD-10 T58 Toxic effect of carbon monoxide,9554,T58,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T58,,ICD-10 @@ -9572,7 +9572,7 @@ T60 Toxic effect of pesticides,9565,T60,T51-T65 Toxic effects of substances chie T60.0 Toxic effect of pesticides - Organophosphate and carbamate insecticides,9566,T60.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T60.0,,ICD-10 T60.1 Toxic effect of pesticides - Halogenated insecticides,9567,T60.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T60.1,,ICD-10 T60.2 Toxic effect of pesticides - Other insecticides,9568,T60.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T60.2,,ICD-10 -T60.3 Toxic effect of pesticides - Herbicides and fungicides,9569,T60.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T60.3,ORPHAcode: 31827 Paraquat poisoning +T60.3 Toxic effect of pesticides - Herbicides and fungicides,9569,T60.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T60.3,ORPHAcode: 31827 Paraquat poisoning,ICD-10 W19 Unspecified fall,9570,W19,W00-W19 Falls,http://identifiers.org/icd/W19,,ICD-10 T60.4 Toxic effect of pesticides - Rodenticides,9571,T60.4,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T60.4,,ICD-10 T60.8 Other pesticides,9572,T60.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T60.8,,ICD-10 @@ -9586,13 +9586,13 @@ T61.9 Toxic effect of unspecified seafood,9579,T61.9,T51-T65 Toxic effects of su T62 Toxic effect of other noxious substances eaten as food,9580,T62,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T62,,ICD-10 T62.0 Toxic effect of other noxious substances eaten as food - Ingested mushrooms,9581,T62.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T62.0,,ICD-10 T62.1 Toxic effect of other noxious substances eaten as food - Ingested berries,9582,T62.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T62.1,,ICD-10 -T62.2 Other ingested (parts of) plant(s),9583,T62.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T62.2,ORPHAcode: 73423 Acute ackee fruit intoxication +T62.2 Other ingested (parts of) plant(s),9583,T62.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T62.2,ORPHAcode: 73423 Acute ackee fruit intoxication,ICD-10 T62.8 Other specified noxious substances eaten as food,9584,T62.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T62.8,,ICD-10 "T62.9 Noxious substance eaten as food, unspecified",9585,T62.9,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T62.9,,ICD-10 T63 Toxic effect of contact with venomous animals,9586,T63,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63,,ICD-10 -T63.0 Toxic effect of contact with venomous animals - Snake venom,9587,T63.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.0,ORPHAcode: 449285 Snakebite envenomation +T63.0 Toxic effect of contact with venomous animals - Snake venom,9587,T63.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.0,ORPHAcode: 449285 Snakebite envenomation,ICD-10 T63.1 Venom of other reptiles,9588,T63.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.1,,ICD-10 -T63.2 Venom of scorpion,9589,T63.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.2,ORPHAcode: 466677 Scorpion envenomation +T63.2 Venom of scorpion,9589,T63.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.2,ORPHAcode: 466677 Scorpion envenomation,ICD-10 T63.3 Venom of spider,9590,T63.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.3,,ICD-10 T63.4 Venom of other arthropods,9591,T63.4,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.4,,ICD-10 T63.5 Toxic effect of contact with fish,9592,T63.5,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.5,,ICD-10 @@ -9601,7 +9601,7 @@ T63.8 Toxic effect of contact with other venomous animals,9594,T63.8,T51-T65 Tox T63.9 Toxic effect of contact with unspecified venomous animal,9595,T63.9,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T63.9,,ICD-10 T64 Toxic effect of aflatoxin and other mycotoxin food contaminants,9596,T64,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T64,,ICD-10 T65 Toxic effect of other and unspecified substances,9597,T65,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65,,ICD-10 -T65.0 Toxic effect of other and unspecified substances - Cyanides,9598,T65.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65.0,ORPHAcode: 466670 Cyanide poisoning +T65.0 Toxic effect of other and unspecified substances - Cyanides,9598,T65.0,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65.0,ORPHAcode: 466670 Cyanide poisoning,ICD-10 T65.1 Strychnine and its salts,9599,T65.1,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65.1,,ICD-10 T65.2 Tobacco and nicotine,9600,T65.2,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65.2,,ICD-10 T65.3 Nitroderivatives and aminoderivatives of benzene and its homologues,9601,T65.3,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65.3,,ICD-10 @@ -9612,7 +9612,7 @@ T65.5 Nitroglycerin and other nitric acids and esters,9604,T65.5,T51-T65 Toxic e T65.8 Toxic effect of other specified substances,9606,T65.8,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65.8,,ICD-10 T65.9 Toxic effect of unspecified substance,9607,T65.9,T51-T65 Toxic effects of substances chiefly nonmedicinal as to source,http://identifiers.org/icd/T65.9,,ICD-10 T66-T78 Other and unspecified effects of external causes,9608,,"XIX Injury, poisoning and certain other consequences of external causes",,,ICD-10 -T66 Unspecified effects of radiation,9609,T66,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T66,ORPHAcode: 454831 Acute radiation syndrome +T66 Unspecified effects of radiation,9609,T66,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T66,ORPHAcode: 454831 Acute radiation syndrome,ICD-10 T67 Effects of heat and light,9610,T67,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T67,,ICD-10 T67.0 Heatstroke and sunstroke,9611,T67.0,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T67.0,,ICD-10 T67.1 Heat syncope,9612,T67.1,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T67.1,,ICD-10 @@ -9663,8 +9663,8 @@ T78.0 Anaphylactic shock due to adverse food reaction,9656,T78.0,T66-T78 Other a V01-V99 Transport accidents,9657,V01-V99,V01-X59 Accidents,,,ICD-10 "T78.1 Other adverse food reactions, not elsewhere classified",9658,T78.1,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.1,,ICD-10 "T78.2 Adverse effects, not elsewhere classified - Anaphylactic shock, unspecified",9659,T78.2,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.2,,ICD-10 -"T78.3 Adverse effects, not elsewhere classified - Angioneurotic oedema",9660,T78.3,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.3,ORPHAcode: 100057 Renin-angiotensin-aldosterone system-blocker-induced angioedema -"T78.4 Adverse effects, not elsewhere classified - Allergy, unspecified",9661,T78.4,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.4,ORPHAcode: 139402 Drug rash with eosinophilia and systemic symptoms +"T78.3 Adverse effects, not elsewhere classified - Angioneurotic oedema",9660,T78.3,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.3,ORPHAcode: 100057 Renin-angiotensin-aldosterone system-blocker-induced angioedema,ICD-10 +"T78.4 Adverse effects, not elsewhere classified - Allergy, unspecified",9661,T78.4,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.4,ORPHAcode: 139402 Drug rash with eosinophilia and systemic symptoms,ICD-10 "T78.8 Other adverse effects, not elsewhere classified",9662,T78.8,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.8,,ICD-10 "T78.9 Adverse effect, unspecified",9663,T78.9,T66-T78 Other and unspecified effects of external causes,http://identifiers.org/icd/T78.9,,ICD-10 T79-T79 Certain early complications of trauma,9664,,"XIX Injury, poisoning and certain other consequences of external causes",,,ICD-10 @@ -9748,12 +9748,12 @@ T85.4 Mechanical complication of breast prosthesis and implant,9738,T85.4,"T80-T "T85.8 Other complications of internal prosthetic devices, implants and grafts, not elsewhere classified",9742,T85.8,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T85.8,,ICD-10 "T85.9 Unspecified complication of internal prosthetic device, implant and graft",9743,T85.9,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T85.9,,ICD-10 T86 Failure and rejection of transplanted organs and tissues,9744,T86,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86,,ICD-10 -T86.0 Bone-marrow transplant rejection,9745,T86.0,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.0,ORPHAcode: 39812 Graft versus host disease +T86.0 Bone-marrow transplant rejection,9745,T86.0,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.0,ORPHAcode: 39812 Graft versus host disease,ICD-10 T86.1 Kidney transplant failure and rejection,9746,T86.1,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.1,,ICD-10 T86.2 Heart transplant failure and rejection,9747,T86.2,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.2,,ICD-10 T86.3 Heart-lung transplant failure and rejection,9748,T86.3,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.3,,ICD-10 T86.4 Liver transplant failure and rejection,9749,T86.4,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.4,,ICD-10 -T86.8 Failure and rejection of other transplanted organs and tissues,9750,T86.8,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.8,ORPHAcode: 306644 Complication after organ transplantation +T86.8 Failure and rejection of other transplanted organs and tissues,9750,T86.8,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.8,ORPHAcode: 306644 Complication after organ transplantation,ICD-10 T86.9 Failure and rejection of unspecified transplanted organ and tissue,9751,T86.9,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T86.9,,ICD-10 T87.0 Complications of reattached (part of) upper extremity,9752,T87.0,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T87.0,,ICD-10 T87.1 Complications of reattached (part of) lower extremity,9753,T87.1,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T87.1,,ICD-10 @@ -9766,7 +9766,7 @@ T87.6 Other and unspecified complications of amputation stump,9758,T87.6,"T80-T8 "T88.0 Other complications of surgical and medical care, not elsewhere classified - Infection following immunization",9760,T88.0,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.0,,ICD-10 "T88.1 Other complications following immunization, not elsewhere classified",9761,T88.1,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.1,,ICD-10 "T88.2 Other complications of surgical and medical care, not elsewhere classified - Shock due to anaesthesia",9762,T88.2,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.2,,ICD-10 -"T88.3 Other complications of surgical and medical care, not elsewhere classified - Malignant hyperthermia due to anaesthesia",9763,T88.3,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.3,ORPHAcode: 423 Malignant hyperthermia of anesthesia +"T88.3 Other complications of surgical and medical care, not elsewhere classified - Malignant hyperthermia due to anaesthesia",9763,T88.3,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.3,ORPHAcode: 423 Malignant hyperthermia of anesthesia,ICD-10 "T88.4 Other complications of surgical and medical care, not elsewhere classified - Failed or difficult intubation",9764,T88.4,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.4,,ICD-10 T88.5 Other complications of anaesthesia,9765,T88.5,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.5,,ICD-10 T88.6 Anaphylactic shock due to adverse effect of correct drug or medicament properly administered,9766,T88.6,"T80-T88 Complications of surgical and medical care, not elsewhere classified",http://identifiers.org/icd/T88.6,,ICD-10 @@ -10918,7 +10918,7 @@ Z32.1 Pregnancy confirmed,10910,Z32.1,Z30-Z39 Persons encountering health servic "Z33 Pregnant state, incidental",10911,Z33,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z33,,ICD-10 Z34 Supervision of normal pregnancy,10912,Z34,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z34,,ICD-10 Z34.0 Supervision of normal first pregnancy,10913,Z34.0,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z34.0,,ICD-10 -Z34.8 Supervision of other normal pregnancy,10914,Z34.8,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z34.8,ORPHAcode: 289385 Malignancy diagnosed during pregnancy +Z34.8 Supervision of other normal pregnancy,10914,Z34.8,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z34.8,ORPHAcode: 289385 Malignancy diagnosed during pregnancy,ICD-10 "Z34.9 Supervision of normal pregnancy, unspecified",10915,Z34.9,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z34.9,,ICD-10 Z35 Supervision of high-risk pregnancy,10916,Z35,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z35,,ICD-10 Z35.0 Supervision of pregnancy with history of infertility,10917,Z35.0,Z30-Z39 Persons encountering health services in circumstances related to reproduction,http://identifiers.org/icd/Z35.0,,ICD-10 @@ -11396,7 +11396,7 @@ Z94.4 Liver transplant status,11389,Z94.4,Z80-Z99 Persons with potential health Z94.5 Skin transplant status,11390,Z94.5,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z94.5,,ICD-10 Z94.6 Bone transplant status,11391,Z94.6,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z94.6,,ICD-10 Z94.7 Corneal transplant status,11392,Z94.7,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z94.7,,ICD-10 -Z94.8 Other transplanted organ and tissue status,11393,Z94.8,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z94.8,ORPHAcode: 90053 Complications after hematopoietic stem cell transplantation +Z94.8 Other transplanted organ and tissue status,11393,Z94.8,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z94.8,ORPHAcode: 90053 Complications after hematopoietic stem cell transplantation,ICD-10 "Z94.9 Transplanted organ and tissue status, unspecified",11394,Z94.9,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z94.9,,ICD-10 Z95 Presence of cardiac and vascular implants and grafts,11395,Z95,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z95,,ICD-10 U83.7 Resistance to multiple antibiotics,11396,U83.7,U82-U85 Resistance to antimicrobial and antineoplastic drugs,http://identifiers.org/icd/U83.7,,ICD-10 @@ -11441,8 +11441,8 @@ Z99.8 Dependence on other enabling machines and devices,11434,Z99.8,Z80-Z99 Pers Z99.9 Dependence on unspecified enabling machine and device,11435,Z99.9,Z80-Z99 Persons with potential health hazards related to family and personal history and certain conditions influencing health status,http://identifiers.org/icd/Z99.9,,ICD-10 XXII Codes for special purposes,11436,,,,,ICD-10 U04 Severe acute respiratory syndrome [SARS],11437,U04,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U04,,ICD-10 -"U04.9 Severe acute respiratory syndrome [SARS], unspecified",11438,U04.9,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U04.9,ORPHAcode: 140896 Severe acute respiratory syndrome -U06 Emergency use of U06,11439,U06,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U06,ORPHAcode: 448237 Zika virus disease +"U04.9 Severe acute respiratory syndrome [SARS], unspecified",11438,U04.9,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U04.9,ORPHAcode: 140896 Severe acute respiratory syndrome,ICD-10 +U06 Emergency use of U06,11439,U06,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U06,ORPHAcode: 448237 Zika virus disease,ICD-10 U06.0 Emergency use of U06.0,11440,U06.0,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U06.0,,ICD-10 U06.1 Emergency use of U06.1,11441,U06.1,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U06.1,,ICD-10 U06.2 Emergency use of U06.2,11442,U06.2,U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use,http://identifiers.org/icd/U06.2,,ICD-10 @@ -11489,7 +11489,7 @@ U84.9 Resistance to unspecified antimicrobial drugs,11479,U84.9,U82-U85 Resistan U85 Resistance to antineoplastic drugs,11480,U85,U82-U85 Resistance to antimicrobial and antineoplastic drugs,http://identifiers.org/icd/U85,,ICD-10 ORPHAcodes,11481,,,,,Orphanet "48,XXYY syndrome",11482,10,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_10,,Orphanet -Ataxia-telangiectasia,11483,100,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_100,Column6 +Ataxia-telangiectasia,11483,100,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_100,,Orphanet OBSOLETE: Genetic optic atrophy,,103,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_103,,Orphanet Ocular albinism with late-onset sensorineural deafness,11484,1000,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_1000,,Orphanet Reticular perineurioma,11485,100000,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_100000,,Orphanet @@ -12867,7 +12867,7 @@ Reticulate acropigmentation of Kitamura,12856,178307,ORPHAcodes,http://www.orpha Isolated sternocostoclavicular hyperostosis,12857,178311,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178311,,Orphanet Undifferentiated embryonal sarcoma of the liver,12858,178315,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178315,,Orphanet Acute lung injury,12859,178320,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178320,,Orphanet - land Islands eye disease,12860,178333,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178333,,Orphanet +land Islands eye disease,12860,178333,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178333,,Orphanet UV-sensitive syndrome,12861,178338,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178338,,Orphanet Inflammatory myofibroblastic tumor,12862,178342,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178342,,Orphanet Aromatase excess syndrome,12863,178345,ORPHAcodes,http://www.orpha.net/ORDO/Orphanet_178345,,Orphanet