+H Disease #

  Human Diseases in ICD-11 Classification

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A01 Certain infectious or parasitic diseases B Gastroenteritis or colitis of infectious origin C Bacterial intestinal infections D 1A00 Cholera E H00110 Cholera D 1A01 Intestinal infection due to other Vibrio E H00307 Vibrio parahaemolyticus infection E H00308 Vibrio vulnificus infection D 1A02 Intestinal infections due to Shigella E H00299 Shigellosis D 1A03 Intestinal infections due to Escherichia coli E H00278 Enteropathogenic Escherichia coli (EPEC) infection E H00280 Enterotoxigenic Escherichia coli (ETEC) infection E H01311 Enteroinvasive Escherichia coli (EIEC) infection E H00277 Enterohemorrhagic Escherichia coli (EHEC) infection E H01312 Enteroaggregative Escherichia coli (EAEC) infection D 1A04 Intestinal infections due to Clostridioides difficile E H00338 Pseudomembranous colitis D 1A05 Intestinal infections due to Yersinia enterocolitica E H00298 Yersiniosis D 1A06 Gastroenteritis due to Campylobacter E H00321 Campylobacter infection D 1A07 Typhoid fever E H00111 Typhoid fever D 1A08 Paratyphoid fever E H00112 Paratyphoid fever D 1A09 Infections due to other Salmonella E H00113 Salmonellosis D 1A0Y Other specified bacterial intestinal infections E H01454 Colonic spirochetosis D 1A0Z Bacterial intestinal infections, unspecified C Bacterial foodborne intoxications D 1A10 Foodborne staphylococcal intoxication E H01175 Staphylococcal infection D 1A11 Botulism E H00339 Botulism D 1A12 Foodborne Clostridium perfringens intoxication E H00335 Foodborne Clostridium perfringens intoxication D 1A13 Foodborne Bacillus cereus intoxication E H00329 Foodborne Bacillus cereus intoxication D 1A1Y Other specified bacterial foodborne intoxications E H00300 Enterobacter infection D 1A1Z Bacterial foodborne intoxications, unspecified C Viral intestinal infections D 1A20 Enteritis due to Adenovirus D 1A21 Gastroenteritis due to Astrovirus D 1A22 Gastroenteritis due to Rotavirus E H00975 Rotaviral enteritis D 1A23 Enteritis due to Norovirus E H01323 Enteritis due to Norovirus D 1A24 Intestinal infections due to Cytomegalovirus D 1A2Y Other specified viral intestinal infections D 1A2Z Viral intestinal infections, unspecified E H01430 Viral gastroenteritis C Protozoal intestinal infections D 1A30 Infections due to Balantidium coli E H01087 Balantidiasis D 1A31 Giardiasis E H00362 Giardiasis D 1A32 Cryptosporidiosis E H00356 Cryptosporidiosis D 1A33 Cystoisosporiasis E H02372 Cystoisosporiasis D 1A34 Sarcocystosis E H02373 Sarcocystosis D 1A35 Blastocystosis E H02374 Blastocystosis D 1A36 Amoebiasis E H00360 Amoebiasis D 1A3Y Other specified protozoal intestinal infections E H01089 Dientamoebiasis D 1A3Z Protozoal intestinal infections, unspecified C 1A40 Gastroenteritis or colitis without specification of infectious agent B Predominantly sexually transmitted infections C Syphilis D 1A60 Congenital syphilis E H00354 Syphilis D 1A61 Early syphilis E H00354 Syphilis D 1A62 Late syphilis E H00354 Syphilis D 1A63 Latent syphilis, unspecified as early or late D 1A6Z Syphilis, unspecified C Gonococcal infection D 1A70 Gonococcal genitourinary infection E H00315 Gonococcal infection D 1A71 Gonococcal pelviperitonitis E H00315 Gonococcal infection D 1A72 Gonococcal infection of other sites E H00315 Gonococcal infection D 1A73 Disseminated gonococcal infection D 1A7Z Gonococcal infection, unspecified C Sexually transmissible infections due to chlamydia D 1A80 Chlamydial lymphogranuloma E H00348 Lymphogranuloma venereum D 1A81 Non-ulcerative sexually transmitted chlamydial infection E H00347 Chlamydia infection D 1A8Y Other specified sexually transmissible infections due to chlamydia D 1A8Z Sexually transmissible infections due to chlamydia, unspecified C 1A90 Chancroid D H00305 Chancroid C 1A91 Granuloma inguinale D H01415 Donovanosis C 1A92 Trichomoniasis D H00812 Trichomoniasis C 1A93 Sexually transmissible infestations C 1A94 Anogenital herpes simplex infection D H00365 Herpes simplex virus infection C 1A95 Anogenital warts D H01418 Condyloma acuminatum C 1A9Y Other specified predominantly sexually transmitted infections D H00388 Non-chlamydial non-gonococcal urethritis C 1A9Z Predominantly sexually transmitted infections, unspecified B Mycobacterial diseases C Tuberculosis D 1B10 Tuberculosis of the respiratory system E H00342 Tuberculosis D 1B11 Tuberculosis of the nervous system E H00342 Tuberculosis D 1B12 Tuberculosis of other systems and organs E H00342 Tuberculosis D 1B13 Miliary tuberculosis D 1B14 Latent tuberculosis D 1B1Y Other specified tuberculosis D 1B1Z Tuberculosis, unspecified C 1B20 Leprosy D H00344 Leprosy D H01473 Erythema nodosum leprosum C 1B21 Infections due to non-tuberculous mycobacteria D H01458 Nontuberculous mycobacterial infection D H01462 Rapidly growing mycobacteria infection D H02029 Mycobacterium avium complex (MAC) pulmonary disease D H01042 Buruli ulcer C 1B2Y Other specified mycobacterial diseases C 1B2Z Mycobacterial diseases, unspecified D H01021 Rhodococcus equi infection D H01049 Gordonia bronchialis infection D H01050 Tsukamurella infection B Certain staphylococcal or streptococcal diseases C Acute rheumatic fever D 1B40 Acute rheumatic fever without mention of heart involvement D 1B41 Acute rheumatic fever with heart involvement D 1B42 Rheumatic chorea E H01924 Sydenham chorea C 1B50 Scarlet fever D H01515 Scarlet fever C 1B51 Streptococcal pharyngitis D H00333 Streptococcal infection D H01424 Group A streptococcal pharyngitis C 1B53 Meningitis due to Streptococcus D H00333 Streptococcal infection D H01406 Streptococcus suis infection C 1B54 Meningitis due to Staphylococcus C 1B5Y Other specified staphylococcal or streptococcal diseases C 1B5Z Staphylococcal or streptococcal diseases, unspecified B Pyogenic bacterial infections of the skin or subcutaneous tissues C 1B70 Bacterial cellulitis, erysipelas or lymphangitis D H01517 Erysipelas C 1B71 Necrotising fasciitis D H01455 Necrotizing fasciitis C 1B72 Impetigo C 1B73 Ecthyma C 1B74 Superficial bacterial folliculitis C 1B75 Deep bacterial folliculitis or pyogenic abscess of the skin C 1B7Y Other specified pyogenic bacterial infection of skin and subcutaneous tissue D H01407 Capnocytophaga ochracea infection B Certain zoonotic bacterial diseases C 1B90 Rat-bite fevers D H01314 Rat-bite fever C 1B91 Leptospirosis D H00355 Leptospirosis C 1B92 Glanders D H00316 Glanders C 1B93 Plague D H00297 Plague C 1B94 Tularaemia D H00312 Tularemia C 1B95 Brucellosis D H00325 Brucellosis C 1B96 Erysipeloid D H01315 Erysipeloid C 1B97 Anthrax D H00328 Anthrax C 1B98 Cat-scratch disease D H00326 Bartonellosis C 1B99 Pasteurellosis D H00306 Pasteurellosis C 1B9A Extraintestinal yersiniosis D H00298 Yersiniosis C 1B9Z Unspecified zoonotic bacterial disease B Other bacterial diseases C 1C10 Actinomycosis D H01325 Actinomycosis C 1C11 Bartonellosis D H00326 Bartonellosis D H00327 Trench fever C 1C12 Whooping cough D H00319 Pertussis C 1C13 Tetanus D H00337 Tetanus C 1C14 Obstetrical tetanus C 1C15 Tetanus neonatorum C 1C16 Gas gangrene D H00336 Gas gangrene C 1C17 Diphtheria D H00343 Diphtheria D H01051 Corynebacterium ulcerans infection C 1C18 Brazilian purpuric fever D H01330 Brazilian purpuric fever C 1C19 Legionellosis D H00311 Legionellosis C 1C1A Listeriosis D H00332 Listeriosis C 1C1B Nocardiosis D H00345 Nocardiosis C 1C1C Meningococcal disease D H00314 Meningococcal infection C 1C1D Yaws D H01318 Yaws C 1C1E Pinta D H01530 Pinta C 1C1F Endemic non-venereal syphilis D H01531 Bejel C 1C1G Lyme borreliosis D H00353 Lyme borreliosis C 1C1H Necrotising ulcerative gingivitis D H01440 Acute necrotizing ulcerative gingivitis C 1C1J Relapsing fever D H00427 Relapsing fever C Other diseases due to chlamydiae D 1C20 Chlamydial conjunctivitis D 1C21 Chlamydial peritonitis D 1C22 Infections due to Chlamydia psittaci E H00350 Psittacosis D 1C23 Trachoma E H00349 Trachoma D 1C2Y Other specified diseases due to chlamydiae D 1C2Z Diseases due to chlamydiae, unspecified C Rickettsioses D 1C30 Typhus fever E H00322 Epidemic typhus E H00324 Scrub typhus D 1C31 Spotted fever E H00323 Spotted fever D 1C32 Rickettsialpox E H02379 Rickettsialpox D 1C33 Q fever E H00310 Q fever D 1C3Y Other specified rickettsioses E H01140 Sennetsu neorickettsiosis D 1C3Z Rickettsioses, unspecified C 1C40 Campylobacteriosis D H00321 Campylobacter infection C 1C41 Bacterial infection of unspecified site D H00302 Citrobacter infection D H00303 Serratia infection D H01441 Pseudomonas aeruginosa infection C 1C42 Melioidosis D H00317 Melioidosis C 1C43 Actinomycetoma D H01451 Actinomycetoma C 1C44 Non-pyogenic bacterial infections of the skin C 1C45 Toxic shock syndrome D H01426 Invasive streptococcal disease C 1C4Y Other specified bacterial diseases D H01335 Photorhabdus asymbiotica infection D H01343 Pantoea ananatis infection D H01446 Propionibacterium acnes infection C 1C4Z Unspecified bacterial disease B Human immunodeficiency virus disease C 1C60 Human immunodeficiency virus disease associated with tuberculosis C 1C61 Human immunodeficiency virus disease associated with malaria C 1C62 Human immunodeficiency virus disease without mention of tuberculosis or malaria D H01563 HIV infection B Viral infections of the central nervous system C 1C80 Viral encephalitis not elsewhere classified D H02511 Jamestown Canyon encephalitis D H02512 Cache Valley virus infection D H02536 Infection-induced acute encephalopathy C 1C81 Acute poliomyelitis D H00376 Acute poliomyelitis C 1C82 Rabies D H00377 Rabies D H00378 Lyssavirus infection C 1C83 Western equine encephalitis D H01534 Western equine encephalitis C 1C84 Eastern equine encephalitis D H01535 Eastern equine encephalitis C 1C85 Japanese encephalitis D H01533 Japanese encephalitis C 1C86 St Louis encephalitis D H02166 Saint Louis encephalitis C 1C87 Rocio viral encephalitis D H02171 Rocio viral encephalitis C 1C88 Murray Valley encephalitis D H01536 Murray Valley encephalitis C 1C89 Far Eastern tick-borne encephalitis D H00380 Tick-borne viral encephalitis C 1C8A Central European tick-borne encephalitis D H00380 Tick-borne viral encephalitis C 1C8B California encephalitis C 1C8C Venezuelan equine encephalitis D H01547 Venezuelan equine encephalitis C 1C8D La Crosse encephalitis D H01537 La Crosse encephalitis C 1C8E Viral meningitis not elsewhere classified D H00393 Enterovirus infection C 1C8F Lymphocytic choriomeningitis D H01324 Lymphocytic choriomeningitis C 1C8Y Other specified viral infections of the central nervous system C 1C8Z Viral infections of the central nervous system, unspecified D H00379 Mosquito-borne viral encephalitis B Non-viral and unspecified infections of the central nervous system C 1D00 Infectious encephalitis not elsewhere classified D H01417 Acute encephalitis C 1D01 Infectious meningitis not elsewhere classified D H00304 Haemophilus influenzae infection D H01313 Escherichia coli meningitis D H01429 Aseptic meningitis C 1D02 Infectious myelitis not elsewhere classified C 1D03 Infectious abscess of the central nervous system C 1D04 Infectious granulomas of the central nervous system C 1D05 Infectious cysts of the central nervous system C 1D0Y Other specified non-viral and unspecified infections of the central nervous system C 1D0Z Non-viral and unspecified infections of the central nervous system, unspecified B Dengue C 1D20 Dengue without warning signs D H00381 Dengue C 1D21 Dengue with warning signs D H00381 Dengue C 1D22 Severe dengue D H00381 Dengue C 1D2Z Dengue fever, unspecified D H00381 Dengue B Certain arthropod-borne viral fevers C 1D40 Chikungunya virus disease D H01540 Chikungunya fever C 1D41 Colorado tick fever D H02165 Colorado tick fever C 1D42 O'nyong-nyong fever D H01545 O'nyong-nyong fever C 1D43 Oropouche virus disease D H02163 Oropouche fever C 1D44 Rift Valley fever D H01549 Rift Valley fever C 1D45 Sandfly fever D H02164 Sandfly fever C 1D46 West Nile virus infection D H01548 West Nile fever C 1D47 Yellow fever D H00384 Yellow fever C 1D48 Zika virus disease D H01553 Zika fever C 1D49 Crimean-Congo haemorrhagic fever D H00284 Crimean-Congo hemorrhagic fever C 1D4A Omsk haemorrhagic fever D H00416 Omsk hemorrhagic fever C 1D4B Kyasanur Forest disease D H01322 Kyasanur Forest disease C 1D4C Alkhurma haemorrhagic fever D H01560 Alkhumra hemorrhagic fever C 1D4D Ross River disease D H00397 Ross River fever C 1D4E Severe fever with thrombocytopenia syndrome D H01416 Severe fever with thrombocytopenia syndrome C 1D4Y Other specified arthropod-borne viral fevers D H00385 South American hemorrhagic fever D H01546 Mayaro fever D H01550 Bunyamwera fever D H02509 Vesicular stomatitis fever C 1D4Z Arthropod-borne viral fever, virus unspecified D H00382 Mosquito-borne viral fever D H00383 Arthropod-borne viral fever B Certain zoonotic viral diseases C 1D60 Filovirus disease D H00283 Ebola disease D H00405 Marburg disease C 1D61 Arenavirus disease D H02173 Arenaviral hemorrhagic fever D H01541 Argentine hemorrhagic fever D H01542 Bolivian hemorrhagic fever D H00386 Lassa fever D H01543 Venezuelan hemorrhagic fever D H01544 Brazilian hemorrhagic fever C 1D62 Hantavirus disease D H00389 Hemorrhagic fever with renal syndrome D H00390 Hantavirus pulmonary syndrome C 1D63 Henipavirus encephalitis D H00391 Henipavirus infection D H01538 Hendra virus infection D H01539 Nipah virus infection C 1D64 Middle East respiratory syndrome D H01419 Middle East respiratory syndrome C 1D65 Severe acute respiratory syndrome D H00402 Severe acute respiratory syndrome C 1D6Y Other specified zoonotic viral diseases C 1D6Z Zoonotic viral disease, virus unspecified B Certain other viral diseases C 1D80 Mumps D H00396 Mumps C 1D81 Infectious mononucleosis D H00367 Infectious mononucleosis C 1D82 Cytomegaloviral disease D H00368 Cytomegalovirus infection C 1D83 Epidemic myalgia D H00393 Enterovirus infection D H02413 Epidemic myalgia C 1D84 Viral conjunctivitis D H01320 Epidemic keratoconjunctivitis D H00393 Enterovirus infection D H01421 Acute hemorrhagic conjunctivitis D H01420 Pharyngoconjunctival fever C 1D85 Viral carditis C 1D86 Viral haemorrhagic fever, not elsewhere classified C Viral infection of unspecified site D 1D90 Adenovirus infection of unspecified site E H00371 Adenovirus infection D 1D91 Enterovirus infection of unspecified site E H00393 Enterovirus infection D 1D92 Coronavirus infection, unspecified site D 1D93 Parvovirus infection of unspecified site D 1D9Y Other viral infections of unspecified site D 1D9Z Unspecified viral infection of unspecified site C 1E1Y Other specified viral diseases C 1E1Z Unspecified viral disease B Influenza C 1E30 Influenza due to identified seasonal influenza virus D H00398 Influenza C 1E31 Influenza due to identified zoonotic or pandemic influenza virus D H00399 Avian influenza C 1E32 Influenza, virus not identified B Viral hepatitis C 1E50 Acute viral hepatitis D H02162 Viral hepatitis D H00411 Hepatitis A D H00412 Hepatitis B D H00413 Hepatitis C D H00414 Hepatitis D D H00415 Hepatitis E C 1E51 Chronic viral hepatitis D H02162 Viral hepatitis D H00412 Hepatitis B D H00413 Hepatitis C D H00414 Hepatitis D D H00415 Hepatitis E C 1E5Z Viral hepatitis, unspecified B Viral infections characterised by skin or mucous membrane lesions C Infections due to poxvirus D 1E70 Smallpox E H00372 Smallpox D 1E71 Monkeypox E H00373 Mpox (Monkeypox) D 1E72 Cowpox E H02351 Cowpox D 1E73 Vaccinia E H02352 Vaccinia D 1E74 Buffalopox D 1E75 Orf E H02354 Orf D 1E76 Molluscum contagiosum E H01052 Molluscum contagiosum D 1E7Y Other specified infections due to poxvirus D 1E7Z Infections due to poxvirus, unspecified C Human papillomavirus infection of skin or mucous membrane D 1E80 Common warts D 1E81 Plane warts D 1E82 Warts of lips or oral cavity D 1E83 Wart virus proliferation in immune-deficient states E H00842 Epidermodysplasia verruciformis D 1E8Z Viral warts, not elsewhere classified E H00374 Viral wart C Varicella zoster virus infections D 1E90 Varicella E H00366 Varicella D 1E91 Zoster E H00366 Varicella E H01624 Postherpetic neuralgia C 1F00 Herpes simplex infections D H00365 Herpes simplex virus infection D H00387 B virus infection C 1F01 Roseola infantum D H00369 Exanthema subitum C 1F02 Rubella D H00395 Rubella C 1F03 Measles D H00394 Measles C 1F04 Erythema infectiosum D H00404 Erythema infectiosum C 1F05 Picornavirus infections presenting in the skin or mucous membranes D H00393 Enterovirus infection D H01327 Herpangina D H01326 Hand, foot and mouth disease C 1F0Y Other specified viral infections characterised by skin or mucous membrane lesions C 1F0Z Viral infections characterised by skin or mucous membrane lesions, unspecified B Mycoses C 1F20 Aspergillosis D H01328 Aspergillosis C 1F21 Basidiobolomycosis D H01503 Zygomycosis D H02032 Entomophthoramycosis C 1F22 Blastomycosis D H01501 Blastomycosis C 1F23 Candidosis D H00363 Candidiasis D H01109 Chronic mucocutaneous candidiasis C 1F24 Chromoblastomycosis D H01520 Chromomycosis C 1F25 Coccidioidomycosis D H01319 Coccidioidomycosis C 1F26 Conidiobolomycosis D H01503 Zygomycosis D H02032 Entomophthoramycosis C 1F27 Cryptococcosis D H00364 Cryptococcosis C 1F28 Dermatophytosis D H01316 Dermatophytosis C 1F29 Eumycetoma D H02385 Eumycetoma C 1F2A Histoplasmosis D H01062 Histoplasmosis C 1F2B Lobomycosis D H01518 Lobomycosis C 1F2C Mucormycosis D H01503 Zygomycosis D H02033 Mucormycosis C 1F2D Non-dermatophyte superficial dermatomycoses D H01334 Tinea versicolor D H02428 Trichosporonosis C 1F2E Paracoccidioidomycosis D H01329 Paracoccidioidomycosis C 1F2F Phaeohyphomycosis D H02386 Phaeohyphomycosis C 1F2G Pneumocystosis D H01521 Pneumocystis pneumonia C 1F2H Scedosporiosis D H02392 Scedosporiosis C 1F2J Sporotrichosis D H01499 Sporotrichosis C 1F2K Talaromycosis D H02393 Talaromycosis C 1F2L Emmonsiosis C 1F2Y Other specified mycoses C 1F2Z Mycoses, unspecified B Parasitic diseases C Malaria D 1F40 Malaria due to Plasmodium falciparum E H00361 Malaria D 1F41 Malaria due to Plasmodium vivax E H00361 Malaria D 1F42 Malaria due to Plasmodium malariae E H00361 Malaria D 1F43 Malaria due to Plasmodium ovale E H00361 Malaria D 1F44 Other parasitologically confirmed malaria D 1F45 Malaria without parasitological confirmation D 1F4Z Malaria, unspecified C Nonintestinal protozoal diseases D 1F50 Acanthamoebiasis E H02401 Acanthamoebiasis D 1F51 African trypanosomiasis E H00357 African trypanosomiasis D 1F52 Babesiosis E H01060 Babesiosis D 1F53 Chagas disease E H00358 Chagas disease D 1F54 Leishmaniasis E H00359 Leishmaniasis D 1F55 Naegleriasis E H02399 Primary amoebic meningoencephalitis (PAM) D 1F56 Rhinosporidiosis E H02400 Rhinosporidiosis D 1F57 Toxoplasmosis E H00435 Toxoplasmosis D 1F58 Microsporidiosis E H01336 Encephalitozoon infection D 1F5Z Unspecified protozoal disease C Helminthiases D Diseases due to nematodes E 1F60 Angiostrongyliasis F H02403 Angiostrongyliasis E 1F61 Anisakiasis F H01058 Anisakiasis E 1F62 Ascariasis F H01090 Ascariasis E 1F63 Capillariasis F H02404 Capillariasis E 1F64 Dracunculiasis F H01044 Dracunculiasis E 1F65 Enterobiasis F H01091 Enterobiasis E 1F66 Filariasis F H02028 Filariasis F H01104 Loiasis F H01061 Mansonelliasis F H01086 Lymphatic filariasis E 1F67 Gnathostomiasis F H01057 Gnathostomiasis E 1F68 Hookworm diseases F H01092 Hookworm disease E 1F69 Oesophagostomiasis F H02405 Oesophagostomiasis E 1F6A Onchocerciasis F H01043 Onchocerciasis E 1F6B Strongyloidiasis F H01100 Strongyloidiasis E 1F6C Syngamosis F H02406 Syngamosis E 1F6D Toxocariasis F H01056 Toxocariasis E 1F6E Trichinosis F H01099 Trichinosis E 1F6F Trichostrongyliasis F H02407 Trichostrongyliasis E 1F6G Trichuriasis F H01046 Trichuriasis E 1F6H Uncinariosis E 1F6Y Other specified diseases due to nematodes F H01137 Baylisascariasis E 1F6Z Diseases due to nematodes, unspecified D Diseases due to cestodes E 1F70 Cysticercosis F H01047 Cysticercosis E 1F71 Diphyllobothriasis F H01085 Diphyllobothriasis E 1F72 Dipylidiasis F H02408 Dipylidiasis E 1F73 Echinococcosis F H01153 Human echinococcosis E 1F74 Hymenolepiasis F H01138 Hymenolepiasis E 1F75 Sparganosis F H01014 Sparganosis E 1F76 Taeniasis F H01152 Taenia saginata infection E 1F7Y Other specified diseases due to cestodes E 1F7Z Diseases due to cestodes, unspecified D Diseases due to trematodes E 1F80 Clonorchiasis F H01610 Clonorchiasis E 1F81 Dicrocoeliasis F H02409 Dicrocoeliasis E 1F82 Fascioliasis F H01048 Liver fluke disease E 1F83 Fasciolopsiasis E 1F84 Opisthorchiasis F H01628 Opisthorchiasis E 1F85 Paragonimiasis F H01093 Paragonimiasis E 1F86 Schistosomiasis F H01045 Schistosomiasis E 1F8Y Other specified diseases due to trematodes F H01617 Foodborne trematodiasis E 1F8Z Diseases due to trematodes, unspecified D 1F90 Other and unspecified infestation by parasitic worms D 1F91 Diphyllobothriasis and sparganosis D 1F9Z Helminthiases, unspecified E H01055 Giant kidney worm infection C Infestations by ectoparasites D 1G00 Pediculosis E H01054 Pediculosis D 1G01 Myiasis E H01178 Myiasis D 1G02 External hirudiniasis D 1G03 Pthiriasis E H02423 Phthiriasis D 1G04 Scabies E H01519 Scabies D 1G05 Tungiasis E H01179 Tungiasis D 1G06 Cimicosis E H02416 Cimicosis D 1G07 Infestation by mites D 1G0Y Infestation by other specified ectoparasite D 1G0Z Infestation by unknown or unspecified ectoparasite E H01098 Pentastomiasis C 1G2Y Other specified parasitic diseases C 1G2Z Unspecified parasitic diseases B Sepsis C 1G40 Sepsis without septic shock C 1G41 Sepsis with septic shock B 1G60 Certain other disorders of infectious origin B Sequelae of infectious diseases C 1G80 Sequelae of tuberculosis C 1G81 Sequelae of trachoma C 1G82 Sequelae of leprosy C 1G83 Sequelae of poliomyelitis C 1G84 Sequelae of viral encephalitis C 1G85 Sequelae of diphtheria C 1G8Y Sequelae of other specified infectious diseases B 1H0Z Infection, unspecified # A02 Neoplasms B Neoplasms of brain or central nervous system C 2A00 Primary neoplasms of brain D H00042 Glioma D H01692 Subependymal giant cell astrocytoma D H01667 Medulloblastoma D H01007 Choroid plexus papilloma C 2A01 Primary neoplasms of meninges D H01556 Meningioma C 2A02 Primary neoplasm of spinal cord, cranial nerves or remaining parts of central nervous system D H00043 Neuroblastoma C 2A0Z Other and unspecified neoplasms of brain or central nervous system B Neoplasms of haematopoietic or lymphoid tissues C Myeloproliferative neoplasms D 2A20 Non mast cell myeloproliferative neoplasms E H00004 Chronic myeloid leukemia E H01605 Myelofibrosis E H01590 Chronic eosinophilic leukemia E H01599 Hypereosinophilic syndrome E H00012 Polycythemia vera D 2A21 Mastocytosis E H01511 Mast-cell leukemia D 2A22 Other and unspecified myeloproliferative neoplasms C Myelodysplastic syndromes D 2A30 Refractory anaemia D 2A31 Refractory neutropaenia D 2A32 Refractory thrombocytopenia D 2A33 Refractory anaemia with ring sideroblasts D 2A34 Refractory cytopenia with multi-lineage dysplasia D 2A35 Refractory anaemia with excess of blasts D 2A36 Myelodysplastic syndrome with isolated del(5q) E H01481 Myelodysplastic syndrome E H01484 5q- syndrome D 2A37 Myelodysplastic syndrome, unclassifiable E H01481 Myelodysplastic syndrome D 2A38 Refractory cytopenia of childhood D 2A3Y Other specified myelodysplastic syndromes D 2A3Z Myelodysplastic syndromes, unspecified E H01481 Myelodysplastic syndrome C Myelodysplastic and myeloproliferative neoplasms D 2A40 Chronic myelomonocytic leukaemia E H02411 Chronic myelomonocytic leukemia D 2A41 Atypical chronic myeloid leukaemia, BCR-ABL1negative E H02412 Atypical chronic myeloid leukemia D 2A42 Juvenile myelomonocytic leukaemia E H02541 Juvenile myelomonocytic leukemia D 2A43 Refractory anaemia with ring sideroblasts associated with marked thrombocytosis D 2A44 Myeloproliferative and myelodysplastic disease, unclassifiable D 2A4Y Other specified myelodysplastic and myeloproliferative neoplasms D 2A4Z Myelodysplastic and myeloproliferative neoplasms, unspecified E H02410 Myelodysplastic/myeloproliferative neoplasms C Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1 D 2A50 Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement D 2A51 Myeloid neoplasm associated with PDGFRB rearrangement D 2A52 Myeloid or lymphoid neoplasms with FGFR1 abnormalities D 2A5Z Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1, unspecified C 2A60 Acute myeloid leukaemias and related precursor neoplasms D H00003 Acute myeloid leukemia D H02542 Acute promyelocytic leukemia C 2A61 Acute leukaemias of ambiguous lineage C Precursor lymphoid neoplasms D 2A70 Precursor B-lymphoblastic neoplasms E H00001 B-cell acute lymphoblastic leukemia D 2A71 Precursor T-lymphoblastic neoplasms E H00002 T-cell acute lymphoblastic leukemia D 2A7Z Precursor lymphoid neoplasms, unspecified C Mature B-cell neoplasms D 2A80 Follicular lymphoma E H01613 Follicular lymphoma D 2A81 Diffuse large B-cell lymphomas E H02424 Primary central nervous system lymphoma E H02434 Diffuse large B-cell lymphoma, not otherwise specified D 2A82 Mature B-cell neoplasm with leukaemic behaviour E H00005 Chronic lymphocytic leukemia E H00006 Hairy cell leukemia D 2A83 Plasma cell neoplasms E H00010 Multiple myeloma E H01461 Crow-Fukase syndrome D 2A84 Heavy chain diseases or malignant immunoproliferative diseases D 2A85 Other specified mature B-cell neoplasms or lymphoma E H00011 Lymphoplasmacytic lymphoma E H01464 Mantle cell lymphoma E H00008 Burkitt lymphoma D 2A86 B-cell lymphoma, mixed features E H02664 Joint contracture, osteochondromas, and B-cell lymphoma D 2A8Z Mature B-cell neoplasms, unspecified C Mature T-cell or NK-cell neoplasms D 2A90 Mature T-cell lymphoma, specified types, nodal or systemic E H01892 Peripheral T cell lymphoma E H00009 Adult T-cell leukemia E H01601 Anaplastic large-cell lymphoma D Mature T-cell or NK-cell lymphomas and lymphoproliferative disorders, primary cutaneous specified types E 2B00 Subcutaneous panniculitis-like T-cell lymphoma F H02661 Subcutaneous panniculitis-like T-cell lymphoma E 2B01 Mycosis fungoides F H01463 Mycosis fungoides E 2B02 Sézary syndrome E 2B03 Primary cutaneous CD-30 positive T-cell lymphoproliferative disorders E 2B0Y Other specified primary cutaneous mature T-cell or NK-cell lymphomas and lymphoproliferative disorders E 2B0Z Primary cutaneous T-cell lymphoma of undetermined or unspecified type D 2B2Y Other specified mature T-cell or NK-cell neoplasms D 2B2Z Mature T-cell or NK-cell neoplasms, unspecified C 2B30 Hodgkin lymphoma D H00007 Hodgkin lymphoma C 2B31 Histiocytic or dendritic cell neoplasms D H01512 Langerhans cell histiocytosis D H02425 Erdheim-Chester disease C 2B32 Immunodeficiency-associated lymphoproliferative disorders C 2B33 Malignant haematopoietic neoplasms without further specification D H02418 Non-Hodgkin lymphoma C 2B3Z Neoplasms of haematopoietic or lymphoid tissues, unspecified B Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues C Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues D Malignant mesenchymal neoplasms E 2B50 Chondrosarcoma, primary site F H00053 Extraskeletal myxoid chondrosarcoma E 2B51 Osteosarcoma, primary site F H00036 Osteosarcoma F H01470 Giant cell tumor of bone F H00881 Li-Fraumeni syndrome E 2B52 Ewing sarcoma, primary site F H00035 Ewing sarcoma E 2B53 Fibroblastic or myofibroblastic tumour, primary site E 2B54 Unclassified pleomorphic sarcoma, primary site E 2B55 Rhabdomyosarcoma, primary site F H00037 Rhabdomyosarcoma F H02427 Soft tissue sarcomas E 2B56 Angiosarcoma, primary site F H01666 Angiosarcoma F H01557 Hepatic angiosarcoma E 2B57 Kaposi sarcoma, primary site F H00041 Kaposi sarcoma E 2B58 Leiomyosarcoma, primary site E 2B59 Liposarcoma, primary site F H00049 Myxoid liposarcoma E 2B5A Synovial sarcoma, primary site F H00050 Synovial sarcoma F H02427 Soft tissue sarcomas E 2B5B Gastrointestinal stromal tumour, primary site F H01591 Gastrotintestinal stromal tumor E 2B5C Endometrial stromal sarcoma, primary site E 2B5D Malignant mixed epithelial mesenchymal tumour, primary site E 2B5E Malignant nerve sheath tumour of peripheral nerves or autonomic nervous system, primary site E 2B5F Sarcoma, not elsewhere classified, primary site E 2B5G Myosarcoma of uterus, part not specified E 2B5H Well differentiated lipomatous tumour, primary site E 2B5J Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites E 2B5K Unspecified malignant soft tissue tumours or sarcomas of bone or articular cartilage of other or unspecified sites F H00051 Alveolar soft part sarcoma F H00052 Clear cell sarcoma of soft tissue F H01985 Desmoplastic small round cell tumor E 2B5Y Other specified malignant mesenchymal neoplasms E 2B5Z Malignant mesenchymal neoplasm of unspecified type D Malignant neoplasms of lip, oral cavity or pharynx E 2B60 Malignant neoplasms of lip F H00016 Oral cancer E 2B61 Malignant neoplasms of base of tongue F H00016 Oral cancer E 2B62 Malignant neoplasms of other or unspecified parts of tongue F H00016 Oral cancer E 2B63 Malignant neoplasms of gum F H00016 Oral cancer E 2B64 Malignant neoplasms of floor of mouth F H00016 Oral cancer E 2B65 Malignant neoplasms of palate F H00016 Oral cancer E 2B66 Malignant neoplasms of other or unspecified parts of mouth F H00016 Oral cancer E 2B67 Malignant neoplasms of parotid gland E 2B68 Malignant neoplasms of submandibular or sublingual glands F H01508 Salivary gland cancer F H02420 Head and neck cancer E 2B69 Malignant neoplasms of tonsil F H01509 Tonsillar cancer F H02420 Head and neck cancer E 2B6A Malignant neoplasms of oropharynx F H01559 Oropharyngeal cancer F H02420 Head and neck cancer E 2B6B Malignant neoplasms of nasopharynx F H00054 Nasopharyngeal cancer E 2B6C Malignant neoplasms of piriform sinus E 2B6D Malignant neoplasms of hypopharynx E 2B6E Malignant neoplasms of other or ill-defined sites in the lip, oral cavity or pharynx F H02420 Head and neck cancer E 2B6Y Other specified malignant neoplasms of lip, oral cavity or pharynx E 2B6Z Malignant neoplasms of lip, oral cavity or pharynx, unspecified D Malignant neoplasms of digestive organs E 2B70 Malignant neoplasms of oesophagus F H00017 Esophageal cancer E 2B71 Malignant neoplasms of oesophagogastric junction E 2B72 Malignant neoplasms of stomach F H00018 Gastric cancer E Malignant neoplasms of intestine F 2B80 Malignant neoplasms of small intestine G H00034 Carcinoid F 2B81 Malignant neoplasms of appendix F Malignant neoplasms of large intestine G 2B90 Malignant neoplasms of colon H H00020 Colorectal cancer H H02565 Hereditary nonpolyposis colorectal cancer H H02568 Polymerase proofreading-associated polyposis G 2B91 Malignant neoplasms of rectosigmoid junction H H00020 Colorectal cancer G 2B92 Malignant neoplasms of rectum H H00020 Colorectal cancer G 2B93 Malignant neoplasms of large intestine, site unspecified G 2B9Y Other specified malignant neoplasms of large intestine H H00876 Mismatch repair deficiency F 2C00 Malignant neoplasms of anus or anal canal G H00044 Cancer of the anal canal F 2C0Y Other specified malignant neoplasms of intestine F 2C0Z Malignant neoplasms of intestine, unspecified E 2C10 Malignant neoplasm of pancreas F H00019 Pancreatic cancer F H00045 Pancreatic neuroendocrine tumor E 2C11 Malignant neoplasms of other or ill-defined digestive organs E 2C12 Malignant neoplasms of liver or intrahepatic bile ducts F H00048 Hepatocellular carcinoma F H02302 Hepatoblastoma F H00046 Cholangiocarcinoma E 2C13 Malignant neoplasms of gallbladder F H00047 Gallbladder cancer E 2C14 Malignant neoplasms of proximal biliary tract, cystic duct E 2C15 Malignant neoplasms of biliary tract, distal bile duct E 2C16 Malignant neoplasms of ampulla of Vater E 2C17 Malignant neoplasms of other or unspecified parts of biliary tract E 2C18 Malignant neoplasms of perihilar bile duct E 2C1Z Malignant neoplasms of digestive organs, unspecified D Malignant neoplasms of middle ear, respiratory or intrathoracic organs E 2C20 Malignant neoplasms of nasal cavity F H00043 Neuroblastoma E 2C21 Malignant neoplasms of middle ear E 2C22 Malignant neoplasms of accessory sinuses E 2C23 Malignant neoplasms of larynx F H00055 Laryngeal cancer F H02420 Head and neck cancer E 2C24 Malignant neoplasms of trachea E 2C25 Malignant neoplasms of bronchus or lung F H00014 Non-small cell lung cancer F H00013 Small cell lung cancer E 2C26 Malignant neoplasms of the pleura F H00015 Malignant pleural mesothelioma E 2C27 Malignant neoplasms of thymus E 2C28 Malignant neoplasms of heart, mediastinum or non-mesothelioma of pleura E 2C29 Malignant neoplasms of other or ill-defined sites in the respiratory system or intrathoracic organs E 2C2Y Other specified malignant neoplasms of middle ear, respiratory or intrathoracic organs E 2C2Z Malignant neoplasms of middle ear, respiratory or intrathoracic organs, unspecified D Malignant neoplasms of skin E 2C30 Melanoma of skin F H00038 Melanoma E 2C31 Squamous cell carcinoma of skin F H00040 Squamous cell carcinoma F H02566 Muir-Torre syndrome E 2C32 Basal cell carcinoma of skin F H00039 Basal cell carcinoma E 2C33 Adnexal carcinoma of skin E 2C34 Cutaneous neuroendocrine carcinoma F H01555 Merkel cell carcinoma E 2C35 Cutaneous sarcoma E 2C3Y Other specified malignant neoplasms of skin E 2C3Z Malignant neoplasm of skin of unknown or unspecified type D Malignant neoplasms of peripheral nerves or autonomic nervous system E 2C40 Malignant neuroepitheliomatous neoplasms of peripheral nerves or autonomic nervous system E 2C41 Malignant perineurioma E 2C4Y Other specified malignant neoplasms of peripheral nerves and autonomic nervous system E 2C4Z Malignant neoplasms of peripheral nerves or autonomic nervous system, unspecified D Malignant neoplasms of retroperitoneum, peritoneum or omentum E 2C50 Malignant neoplasms of retroperitoneum E 2C51 Malignant neoplasms of peritoneum F H01665 Primary peritoneal carcinoma E 2C52 Malignant neoplasms of omentum E 2C53 Malignant neoplasm involving overlapping sites of retroperitoneum, peritoneum or omentum E 2C5Y Other specified malignant neoplasms of retroperitoneum, peritoneum or omentum E 2C5Z Malignant neoplasms of retroperitoneum, peritoneum or omentum, unspecified D Malignant neoplasms of breast E 2C60 Carcinoma of breast, specialised type E 2C61 Invasive carcinoma of breast F H00031 Breast cancer E 2C62 Inflammatory carcinoma of breast E 2C63 Malignant phyllodes tumour of breast E 2C64 Solid papillary carcinoma of breast with evidence of invasion E 2C65 Hereditary breast and ovarian cancer syndrome F H02531 Familial breast-ovarian cancer E 2C6Y Other specified malignant neoplasms of breast E 2C6Z Malignant neoplasms of breast, unspecified D Malignant neoplasms of female genital organs E 2C70 Malignant neoplasms of vulva F H00029 Vulvar cancer E 2C71 Malignant neoplasms of vagina E 2C72 Malignant neoplasms of uterine ligament, parametrium, or uterine adnexa E 2C73 Malignant neoplasms of ovary F H00027 Ovarian cancer E 2C74 Malignant neoplasms of fallopian tube F H01554 Fallopian tube cancer E 2C75 Malignant neoplasms of placenta F H00028 Choriocarcinoma E 2C76 Malignant neoplasms of corpus uteri F H00026 Endometrial cancer E 2C77 Malignant neoplasms of cervix uteri F H00030 Cervical cancer E 2C78 Malignant neoplasms of uterus, part not specified E 2C79 Malignant neoplasm involving overlapping sites of female genital organs E 2C7Y Other specified malignant neoplasms of female genital organs E 2C7Z Malignant neoplasms of female genital organs, unspecified D Malignant neoplasms of male genital organs E 2C80 Malignant neoplasms of testis F H00023 Testicular cancer E 2C81 Malignant neoplasms of penis F H00025 Penile cancer E 2C82 Malignant neoplasms of prostate F H00024 Prostate cancer F H02530 Hereditary prostate cancer E 2C83 Malignant neoplasms of scrotum E 2C84 Malignant neoplasms of other specified male genital organs E 2C8Z Malignant neoplasms of male genital organs, unspecified D Malignant neoplasms of urinary tract E 2C90 Malignant neoplasms of kidney, except renal pelvis F H00021 Renal cell carcinoma F H02301 Nephroblastoma E 2C91 Malignant neoplasms of renal pelvis E 2C92 Malignant neoplasms of ureter E 2C93 Malignant neoplasms of urethra or paraurethral gland E 2C94 Malignant neoplasms of bladder F H00022 Bladder cancer E 2C95 Malignant neoplasm involving overlapping sites of urinary organs E 2C9Y Other specified malignant neoplasms of urinary tract E 2C9Z Malignant neoplasms of urinary tract, unspecified D Malignant neoplasms of eye or ocular adnexa E 2D00 Malignant neoplasm of conjunctiva E 2D01 Malignant neoplasm of cornea E 2D02 Malignant neoplasm of retina F H01513 Retinoblastoma E 2D03 Malignant neoplasm of lacrimal apparatus E 2D04 Malignant neoplasm of orbit E 2D05 Malignant neoplasm of choroid E 2D06 Malignant neoplasm of ciliary body E 2D07 Malignant neoplasm of iris E 2D0Y Other specified malignant neoplasms of eye and ocular adnexa E 2D0Z Malignant neoplasms of eye or ocular adnexa, unspecified D Malignant neoplasms of endocrine glands E 2D10 Malignant neoplasms of thyroid gland F H00032 Thyroid cancer F H01592 Medullary thyroid cancer E 2D11 Malignant neoplasms of adrenal gland F H00033 Adrenal carcinoma E 2D12 Malignant neoplasms of other endocrine glands or related structures F H01510 Malignant paraganglioma E 2D1Z Malignant neoplasms of endocrine glands, unspecified D 2D3Y Other specified malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues D 2D3Z Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues, unspecified C Malignant neoplasms of ill-defined or unspecified primary sites D 2D40 Adenocarcinoma of unspecified site D 2D41 Unspecified carcinoma of unspecified site D 2D42 Malignant neoplasms of ill-defined sites D 2D43 Malignant neoplasms of independent, multiple primary sites D 2D4Y Other specified malignant neoplasms of unspecified primary sites D 2D4Z Unspecified malignant neoplasms of unspecified sites C Malignant neoplasm metastases D 2D50 Malignant neoplasm metastasis in brain D 2D51 Malignant neoplasm metastasis in meninges D 2D52 Malignant neoplasm metastasis in spinal cord, cranial nerves or remaining parts of central nervous system D Malignant neoplasm metastasis in lymph nodes E 2D60 Malignant neoplasm metastasis in lymph node of a single region F H02610 Head and neck squamous cell carcinoma E 2D61 Malignant neoplasm metastases in lymph nodes of multiple regions E 2D6Z Metastatic malignant neoplasm to unspecified lymph node D Malignant neoplasm metastasis in thoracic or respiratory organs E 2D70 Malignant neoplasm metastasis in lung E 2D71 Malignant neoplasm metastasis in mediastinum E 2D72 Malignant neoplasm metastasis in pleura E 2D73 Malignant neoplasm metastasis in upper respiratory tract organs E 2D7Y Malignant neoplasm metastasis in other specified thoracic organs E 2D7Z Malignant neoplasm metastasis in thoracic or respiratory organs, unspecified D Malignant neoplasm metastasis in digestive system E 2D80 Malignant neoplasm metastasis in liver or intrahepatic bile duct E 2D81 Malignant neoplasm metastasis in pancreas E 2D82 Malignant neoplasm metastasis in extrahepatic bile ducts E 2D83 Malignant neoplasm metastasis in ampulla of Vater E 2D84 Malignant neoplasm metastasis in the small intestine E 2D85 Malignant neoplasm metastasis in large intestine E 2D86 Malignant neoplasm metastasis in anus E 2D8Y Malignant neoplasm metastasis in other specified digestive system organ E 2D8Z Malignant neoplasm metastasis in unspecified digestive system organ D Malignant neoplasm metastasis in retroperitoneum or peritoneum E 2D90 Malignant neoplasm metastasis in retroperitoneum E 2D91 Malignant neoplasm metastasis in peritoneum D Malignant neoplasm metastasis in other sites E 2E00 Malignant neoplasm metastasis in kidney or renal pelvis E 2E01 Malignant neoplasm metastasis in bladder E 2E02 Malignant neoplasm metastasis in other or unspecified urinary system organs E 2E03 Malignant neoplasm metastasis in bone or bone marrow E 2E04 Malignant neoplasm metastasis in soft tissue E 2E05 Malignant neoplasm metastasis in female reproductive system E 2E06 Malignant neoplasm metastasis in male genital organs E 2E07 Malignant neoplasm metastasis in adrenal gland E 2E08 Metastatic malignant neoplasm involving skin E 2E09 Malignant neoplasm metastasis in peripheral nervous system E 2E0Y Malignant neoplasm metastasis in other specified sites D 2E2Z Malignant neoplasm metastasis, unspecified B In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues C 2E60 Carcinoma in situ of oral cavity, oesophagus or stomach C 2E61 Carcinoma in situ of other or unspecified digestive organs C 2E62 Carcinoma in situ of middle ear or respiratory system C 2E63 Melanoma in situ neoplasms C 2E64 Carcinoma in situ of skin C 2E65 Carcinoma in situ of breast C 2E66 Carcinoma in situ of cervix uteri C 2E67 Carcinoma in situ of other or unspecified genital organs C 2E68 Carcinoma in situ of bladder C 2E69 Carcinoma in situ of other or unspecified urinary organs C 2E6A Carcinoma in situ of the eye or ocular adnexa C 2E6B Carcinoma in situ of thyroid and other endocrine glands D H01558 Parathyroid carcinoma C 2E6Y Carcinoma in situ of other specified site C 2E6Z Carcinoma in situ of unspecified site B Benign neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues C Benign mesenchymal neoplasms D 2E80 Benign lipomatous neoplasm D 2E81 Benign vascular neoplasms E H01471 Lymphangioma E H01735 Lymphangiomatosis E H01482 Infantile hemangioma E H01875 Infantile hepatic hemangioma D 2E82 Benign chondrogenic tumours D 2E83 Benign osteogenic tumours D 2E84 Benign fibrogenic or myofibrogenic tumour D 2E85 Benign fibrohistiocytic tumour D 2E86 Benign smooth muscle or skeletal muscle tumour E H01640 Uterine leiomyoma D 2E87 Benign gastrointestinal stromal tumour D 2E88 Benign endometrial stromal nodule D 2E89 Benign mesenchymal tumours of uncertain differentiation D 2E8A Other mixed or unspecified benign mesenchymal tumours D 2E8Y Other specified benign mesenchymal neoplasm D 2E8Z Benign mesenchymal neoplasms, unspecified E H00804 Multiple cutaneous and uterine leiomyomata C Benign non-mesenchymal neoplasms D 2E90 Benign neoplasm of lip, oral cavity or pharynx D 2E91 Benign neoplasm of major salivary glands D 2E92 Benign neoplasm of digestive organs E H02538 Paraganglioma E H01025 Familial adenomatous polyposis E H00539 PTEN hamartoma tumor syndrome E H01023 Juvenile polyposis syndrome E H01024 Hereditary mixed polyposis syndrome D Benign neoplasm of respiratory or intrathoracic organs E 2F00 Benign neoplasm of middle ear or respiratory system E 2F01 Benign neoplasm of intrathoracic organs E 2F0Y Benign neoplasms of other specified respiratory and intrathoracic organs E 2F0Z Benign neoplasms of unspecified respiratory and intrathoracic organs D 2F10 Benign neoplasm of mesothelial tissue D Benign cutaneous neoplasms E 2F20 Benign cutaneous melanocytic neoplasms E 2F21 Benign keratinocytic acanthomas E 2F22 Benign neoplasms of epidermal appendages F H00827 Brooke-Spiegler syndrome F H00828 Familial cylindromatosis F H00829 Multiple familial trichoepithelioma F H00947 Pilomatricoma E 2F23 Benign dermal fibrous or fibrohistiocytic neoplasms F H01910 Infantile myofibromatosis E 2F24 Benign cutaneous neoplasms of neural or nerve sheath origin E 2F25 Cherry angioma E 2F26 Lobular capillary haemangioma E 2F2Y Other specified benign cutaneous neoplasms E 2F2Z Benign cutaneous neoplasm of unspecified type D 2F30 Benign neoplasm of breast D 2F31 Benign non-mesenchymal neoplasms of uterus D 2F32 Benign neoplasm of ovary D 2F33 Benign neoplasm of other or unspecified female genital organs D 2F34 Benign neoplasm of male genital organs D 2F35 Benign neoplasm of urinary organs E H01691 Renal angiomyolipoma D 2F36 Benign neoplasm of eye or ocular adnexa E H01149 Ring dermoid of cornea D 2F37 Benign neoplasm of endocrine glands E H01102 Pituitary adenomas D 2F3Y Benign non-mesenchymal neoplasms of other specified site D 2F3Z Benign non-mesenchymal neoplasms of unspecified site C 2F5Y Other specified benign neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues C 2F5Z Benign neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues, unspecified B Neoplasms of uncertain behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues C 2F70 Neoplasms of uncertain behaviour of oral cavity or digestive organs C 2F71 Neoplasms of uncertain behaviour of middle ear, respiratory or intrathoracic organs C 2F72 Neoplasms of uncertain behaviour of skin C 2F73 Neoplasms of uncertain behaviour of retroperitoneum C 2F74 Neoplasms of uncertain behaviour of peritoneum C 2F75 Neoplasms of uncertain behaviour of breast C 2F76 Neoplasms of uncertain behaviour of female genital organs C 2F77 Neoplasms of uncertain behaviour of male genital organs C 2F78 Neoplasms of uncertain behaviour of urinary organs C 2F79 Neoplasms of uncertain behaviour of eye or ocular adnexa C 2F7A Neoplasms of uncertain behaviour of endocrine glands D H00247 Multiple endocrine neoplasia syndrome C 2F7B Neoplasms of uncertain behaviour of bone or articular cartilage C 2F7C Neoplasms of uncertain behaviour of connective or other soft tissue C 2F7Y Neoplasms of uncertain behaviour of other specified site D H01134 Rhabdoid predisposition syndrome D H02624 Tumor predisposition syndrome C 2F7Z Neoplasms of uncertain behaviour of unspecified site B Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues C 2F90 Neoplasms of unknown behaviour of oral cavity or digestive organs C 2F91 Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs C 2F92 Neoplasms of unknown behaviour of skin C 2F93 Neoplasms of unknown behaviour of retroperitoneum C 2F94 Neoplasms of unknown behaviour of peritoneum C 2F95 Neoplasms of unknown behaviour of breast C 2F96 Neoplasms of unknown behaviour of female genital organs C 2F97 Neoplasms of unknown behaviour of male genital organs C 2F98 Neoplasms of unknown behaviour of urinary organs C 2F99 Neoplasms of unknown behaviour of eye or ocular adnexa C 2F9A Neoplasms of unknown behaviour of endocrine glands C 2F9B Neoplasms of unknown behaviour of bone or articular cartilage C 2F9C Neoplasms of unknown behaviour of connective or other soft tissue C 2F9Y Neoplasms of unknown behaviour of other specified site C 2F9Z Neoplasms of unknown behaviour of unspecified site # A03 Diseases of the blood or blood-forming organs B Anaemias or other erythrocyte disorders C Nutritional or metabolic anaemias D 3A00 Iron deficiency anaemia E H01145 Atransferrinemia E H01196 Hypochromic microcytic anemia E H01278 Iron-refractory iron deficiency anemia E H02206 Aceruloplasminemia D 3A01 Megaloblastic anaemia due to vitamin B12 deficiency E H01277 Vitamin B12 deficiency anaemia E H01190 Transcobalamin II deficiency D 3A02 Folate deficiency anaemia E H01197 Dihydrofolate reductase deficiency E H01262 Formiminotransferase deficiency D 3A03 Other nutritional or metabolic anaemias E H00198 Orotic aciduria C Haemolytic anaemias D Congenital haemolytic anaemia E 3A10 Hereditary haemolytic anaemia F H00668 Anemia due to disorders of glutathione metabolism F H00231 Hereditary elliptocytosis F H01125 Hereditary pyropoikilocytosis F H02001 Familial pseudohyperkalemia F H00230 Hereditary spherocytosis F H00232 Hereditary stomatocytosis F H00664 Anemia due to disorders of glycolytic enzymes F H00674 Anemia due to disorders of nucleotide metabolism F H00832 Core neuroacanthocytosis syndromes F H01214 Rh-null hemolytic anemia (RHN) F H01432 Choreoacanthocytosis F H01434 Atypical hemolytic uremic syndrome F H01720 Southeast Asian ovalocytosis F H01978 Dehydrated hereditary stomatocytosis F H01979 Overhydrated hereditary stomatocytosis F H02002 Cryohydrocytosis F H02658 X-linked congenital hemolytic anemia E 3A1Y Other specified congenital haemolytic anaemia D Acquired haemolytic anaemia E 3A20 Acquired haemolytic anaemia, immune F H01585 Autoimmune hemolytic anemia E 3A21 Acquired haemolytic anaemia, non-immune F H01053 Paroxysmal nocturnal hemoglobinuria E 3A2Z Acquired haemolytic anaemia, unspecified D 3A4Z Haemolytic anaemias, unspecified C 3A50 Thalassaemias D H00228 Thalassemia C 3A51 Sickle cell disorders or other haemoglobinopathies D H00229 Sickle cell disease C Pure red cell aplasia D 3A60 Congenital pure red cell aplasia E H00237 Diamond-Blackfan anemia D 3A61 Acquired pure red cell aplasia E H01586 Acquired pure red cell aplasia D 3A6Z Pure red cell aplasia, unspecified C 3A70 Aplastic anaemia D H01132 Aplastic anemia D H00238 Fanconi anemia D H00439 Shwachman-Diamond syndrome D H00507 Dyskeratosis congenita D H00788 Hoyeraal-Hreidarsson syndrome D H00921 Revesz syndrome D H02524 Ataxia-pancytopenia syndrome D H02529 Bone marrow failure syndrome D H02569 Pulmonary fibrosis and/or bone marrow failure, telomere-related D H02608 Autoinflammatory-pancytopenia syndrome C 3A71 Anaemia due to chronic disease D H01642 Renal anemia C 3A72 Sideroblastic anaemia D H00982 Sideroblastic anemia D H02670 Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay D H00898 Myopathy with lactic acidosis and sideroblastic anaemia C 3A73 Congenital dyserythropoietic anaemia D H00917 Congenital dyserythropoietic anemia C Polycythaemia D 3A80 Congenital polycythaemia E H00236 Congenital polycythemia D 3A81 Acquired polycythaemia D 3A8Z Polycythaemia, unspecified C 3A90 Anaemia due to acute disease C 3A91 Congenital methaemoglobinaemia D H00235 Methemoglobinemia C 3A92 Hereditary methaemoglobinaemia D H00235 Methemoglobinemia C 3A93 Acquired methaemoglobinaemia C 3A94 Acute posthaemorrhagic anaemia C 3A9Y Other specified anaemias or erythrocyte disorders C 3A9Z Anaemias or other erythrocyte disorders, unspecified B Coagulation defects, purpura or other haemorrhagic or related conditions C Coagulation defects D Congenital or constitutional haemorrhagic condition E 3B10 Hereditary factor VIII deficiency F H00219 Hemophilia E 3B11 Hereditary factor IX deficiency F H00219 Hemophilia E 3B12 Von Willebrand disease F H00219 Hemophilia F H02092 von Willebrand disease E 3B13 Haemophilia C F H00938 Factor XI deficiency E 3B14 Other inherited coagulation factor deficiency with bleeding tendency F H01254 Congenital prothrombin deficiency F H00222 Afibrinogenemia F H02257 Factor X deficiency F H00995 Combined deficiency of vitamin K-dependent clotting factors F H02256 Factor VII deficiency F H00220 Factor V deficiency F H00221 Combined deficiency of factors V and VIII F H00945 Factor XIII deficiency E 3B15 Inherited coagulation factor deficiency without bleeding tendency F H00941 Factor XII deficiency F H01078 Fletcher factor deficiency E 3B1Z Congenital or constitutional haemorrhagic condition, unspecified D Haemorrhagic diseases due to acquired coagulation factor defects E 3B20 Disseminated intravascular coagulation F H01587 Disseminated intravascular coagulation E 3B21 Haemorrhagic disorder due to circulating anticoagulants and coagulation factors F H01759 Autoimmune acquired factor XIII (F13) deficiency E 3B22 Acquired haemophilia E 3B2Y Other specified haemorrhagic diseases due to acquired coagulation factor defects D 3B4Z Coagulation defects, unspecified C Fibrinolytic defects D 3B50 Inherited fibrinolytic defects E H00983 Alpha-2-plasmin inhibitor (a2-PI) deficiency E H01106 Plasminogen activator inhibitor type 1 deficiency E H01206 Plasminogen deficiency D 3B51 Acquired fibrinolytic defects C 3B60 Non-thrombocytopenic purpura C 3B61 Thrombophilia D H00223 Inherited thrombophilia D H01381 Antithrombin III deficiency C 3B62 Qualitative platelet defects D H01235 Bleeding disorder platelet-type D H02097 Gray platelet syndrome D H00224 Bernard-Soulier syndrome D H00226 Glanzmann thrombasthenia D H01523 Wiskott-Aldrich syndrome D H01162 Scott syndrome D H02093 Platelet-type von Willebrand disease D H02259 Stormorken syndrome C 3B63 Thrombocytosis D H01612 Essential thrombocythemia C 3B64 Thrombocytopenia D H00978 Thrombocytopenia (THC) D H00227 Congenital amegakaryocytic thrombocytopenia D H00233 MYH9-related disease D H00578 Epstein syndrome D H00867 Radioulnar synostosis with amegakaryocytic thrombocytopenia D H01740 Macrothrombocytopenia D H01847 Thrombocytopenia-absent radius syndrome D H02052 Sebastian syndrome D H02053 Fechtner syndrome D H01240 Immune thrombocytopenia D H00225 Thrombotic thrombocytopenic purpura C 3B65 Thrombotic microangiopathy, not elsewhere classified C 3B6Y Other specified coagulation defects, purpura or other haemorrhagic or related conditions C 3B6Z Coagulation defects, purpura or other haemorrhagic or related conditions, unspecified B Diseases of spleen C 3B80 Congenital disorders of spleen C 3B81 Acquired disorders of spleen C 3B8Z Diseases of spleen, unspecified B 3C0Y Other specified diseases of the blood or blood-forming organs B 3C0Z Diseases of the blood or blood-forming organs, unspecified # A04 Diseases of the immune system B Primary immunodeficiencies C 4A00 Primary immunodeficiencies due to disorders of innate immunity D H01725 Primary immunodeficiency disease D H02525 Disorders of innate immunity D H02620 Autoinflammation with episodic fever and lymphadenopathy D H00098 Chronic granulomatous disease D H01094 Eosinophil peroxidase deficiency D H02024 Neutrophil specific granule deficiency D H02025 Myeloperoxidase deficiency D H00104 Alternative complement pathway component defects D H00102 Classic complement pathway component defects D H00103 Late complement pathway defects D H01006 Hereditary angioedema D H00105 Mannose-binding lectin pathway component defects D H00106 Complement regulatory protein defects D H01136 Carboxypeptidase N deficiency D H00089 IFN-gamma/IL-12 axis D H00096 Defects of toll-like receptor signaling D H00721 Pyogenic bacterial infections, recurrent, due to MYD88 deficiency D H00090 NK cell defects D H00097 WHIM syndrome C 4A01 Primary immunodeficiencies due to disorders of adaptive immunity D H01725 Primary immunodeficiency disease D H02526 Disorders of adaptive immunity D H00085 Agammaglobulinemias D H02308 Immunodeficiency-centromeric instability-facial anomalies syndrome D H00086 Hyper IgM syndromes, autosomal recessive type D H00088 Common variable immunodeficiency D H00093 Combined immunodeficiency D H00091 T-B+Severe combined immunodeficiency D H00092 T-B-Severe combined immunodeficiency D H01128 Reticular dysgenesis D H01244 T+B+Severe combined immunodeficiencies (SCIDs) D H02309 Adenosine deaminase deficiency D H02554 Omenn syndrome D H00984 Bare lymphocyte syndrome type1 D H00985 Bare lymphocyte syndrome type2 D H00087 Other humoral immunodeficiencies D H00924 Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation D H01181 T-cell immunodeficiency congenital alopecia and nail dystrophy D H01387 Activated PI3K-delta syndrome D H02015 LIG4 syndrome D H02133 Vici syndrome D H02585 Roifman-Chitayat syndrome D H01971 IPEX syndrome D H00108 Autoimmune lymphoproliferative syndromes D H01969 X-linked lymphoproliferative syndrome D H01970 Lymphoproliferative syndrome D H00109 Familial hemophagocytic lymphohistiocytosis D H02491 Immunoskeletal dysplasia with neurodevelopmental abnormalities D H02574 BILU syndrome D H00064 Ataxia telangiectasia D H00094 Immunodeficiency associated with DNA repair defects D H00962 RIDDLE syndrome D H01344 Nijmegen breakage syndrome D H01346 Bloom syndrome D H02014 Ataxia-telangiectasia-like syndrome D H00580 Schimke immunoosseous dysplasia D H01264 Hepatic venoocclusive disease with immunodeficiency D H01968 Hyper-IgE syndrome C 4A0Y Other specified primary immunodeficiencies D H01245 Immunodeficiency without anhidrotic ectodermal dysplasia C 4A0Z Primary immunodeficiencies, unspecified B 4A20 Acquired immunodeficiencies C H00406 Acquired immunodeficiency syndrome (AIDS) B Nonorgan specific systemic autoimmune disorders C 4A40 Lupus erythematosus D H00080 Systemic lupus erythematosus D H01500 Lupus nephritis C 4A41 Idiopathic inflammatory myopathy D H01604 Polymyositis and dermatomyositis D H01229 Inclusion body myopathy 3 D H01505 Inclusion body myositis D H02031 Inclusion body myopathy with Paget disease of bone and frontotemporal dementia C 4A42 Systemic sclerosis D H01492 Systemic sclerosis C 4A43 Overlap or undifferentiated nonorgan specific systemic autoimmune disease D H01761 Immunoglobulin G4-related disease D H01502 Sjogren syndrome D H01710 Mixed connective tissue disease D H01693 Eosinophilic fasciitis D H01133 Reynolds syndrome D H01232 Syndromic multisystem autoimmune disease D H02540 Infantile-onset multisystem autoimmune disease C 4A44 Vasculitis D H01698 Giant cell arteritis D H01382 Polyarteritis nodosa D H01718 Kawasaki disease D H01625 Buerger disease D H01584 IgA vasculitis D H01767 Henoch-Schonlein purpura nephritis D H01658 Microscopic polyangiitis D H01655 Granulomatosis with polyangiitis D H01468 Eosinophilic granulomatosis with polyangiitis D H01465 Large-vessel vasculitis C 4A45 Antiphospholipid syndrome D H01697 Antiphospholipid syndrome C 4A4Y Other specified nonorgan specific systemic autoimmune disorders D H02537 Autoinflammation, immune dysregulation, and eosinophilia D H02621 X-linked systemic autoinflammatory disease C 4A4Z Nonorgan specific systemic autoimmune disorders, unspecified B Autoinflammatory disorders C 4A60 Monogenic autoinflammatory syndromes D H02588 NLRP1-associated autoinflammation with arthritis and dyskeratosis D H02589 Periodic fever, immunodeficiency, and thrombocytopenia syndrome D H02591 Interleukin-18 binding protein deficiency D H02592 Familial Behcet-like autoinflammatory syndrome D H02593 Chronic mucocutaneous ulceration D H02599 Inherited autoinflammatory disease D H00288 Familial Mediterranean fever D H00282 Cryopyrin associated periodic syndrome D H02159 Familial cold autoinflammatory syndrome D H02555 Muckle-Wells syndrome D H02556 CINCA syndrome D H00912 Tumor necrosis factor receptor-associated periodic syndrome D H00285 Blau syndrome D H00287 Pyogenic sterile arthritis, pyoderma gangrenosum, and acne syndrome D H01743 Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation D H01744 Polyglucosan body myopathy D H02414 Autoinflammation, panniculitis, and dermatosis syndrome D H02467 Neonatal inflammatory skin and bowel disease D H02532 Proteasome-associated autoinflammatory syndrome D H02561 Familial autoinflammatory syndrome with or without immunodeficiency D H02656 X-linked multisystem autoinflammatory disease with immune dysregulation D H02660 Autoinflammation with pulmonary and cutaneous vasculitis D H02672 Systemic autoinflammatory disease with vasculitis C 4A61 SAPHO syndrome C 4A62 Behçet disease D H01476 Behcet disease C 4A6Y Other specified autoinflammatory disorders D H01117 Chronic recurrent multifocal osteomyelitis D H01275 Interleukin 1 receptor antagonist deficiency D H01748 NLRC4 inflammasomopathy C 4A6Z Autoinflammatory disorders, unspecified B Allergic or hypersensitivity conditions C 4A80 Allergic or hypersensitivity disorders involving the respiratory tract C 4A81 Allergic or hypersensitivity disorders involving the eye C 4A82 Allergic or hypersensitivity disorders involving skin or mucous membranes C 4A83 Allergic or hypersensitivity disorders involving the gastrointestinal tract D H01782 Eosinophilic gastrointestinal disorder C 4A84 Anaphylaxis D H01359 Anaphylaxis C 4A85 Complex allergic or hypersensitivity conditions C 4A8Y Allergic or hypersensitivity conditions of other specified type C 4A8Z Allergic or hypersensitivity conditions of unspecified type B Immune system disorders involving white cell lineages C 4B00 Disorders of neutrophil number D H00100 Neutropenic disorders D H00939 Darsun syndrome D H01218 P14 deficiency C 4B01 Disorders of neutrophil function C 4B02 Eosinopenia C 4B03 Eosinophilia C 4B04 Disorders with decreased monocyte counts C 4B05 Disorders with increased monocyte counts C 4B06 Acquired lymphopenia C 4B07 Acquired lymphocytosis C 4B0Y Other specified immune system disorders involving white cell lineages D H00234 Pelger-Huet anomaly D H02051 May-Hegglin anomaly C 4B0Z Immune system disorders involving white cell lineages, unspecified B Certain disorders involving the immune system C 4B20 Sarcoidosis D H01309 Sarcoidosis, early-onset C 4B21 Polyclonal hypergammaglobulinaemia C 4B22 Cryoglobulinaemia C 4B23 Immune reconstitution inflammatory syndrome C 4B24 Graft-versus-host disease D H00084 Graft-versus-host disease C 4B2Y Other specified disorders involving the immune system D H01479 Castleman disease D H02669 Inflammatory bowel disease, immunodeficiency, and encephalopathy B 4B40 Diseases of thymus B 4B4Y Other specified diseases of the immune system B 4B4Z Diseases of the immune system, unspecified # A05 Endocrine, nutritional or metabolic diseases B Endocrine diseases C Disorders of the thyroid gland or thyroid hormones system D 5A00 Hypothyroidism E H01186 Abnormal thyroid hormone metabolism E H00251 Thyroid dyshormonogenesis E H00249 Thyroid hormone resistance syndrome E H00250 Congenital nongoitrous hypothyroidism (CHNG) E H00650 Allan-Herndon-Dudley syndrome E H01040 Bamforth-Lazarus syndrome D 5A01 Nontoxic goitre D 5A02 Thyrotoxicosis E H01269 Congenital hyperthyroidism E H01645 Hyperthyroidism E H00082 Graves disease E H02402 Thyroid eye disease D 5A03 Thyroiditis E H01647 Subacute thyroiditis E H00081 Hashimoto thyroiditis D 5A04 Hypersecretion of calcitonin D 5A05 Generalised resistance to thyroid hormone D 5A06 Sick-euthyroid syndrome D 5A0Y Other specified disorders of the thyroid gland or thyroid hormones system D 5A0Z Disorders of the thyroid gland or thyroid hormones system, unspecified C Diabetes mellitus D 5A10 Type 1 diabetes mellitus E H00408 Type 1 diabetes mellitus E H01224 Ketosis-prone diabetes mellitus D 5A11 Type 2 diabetes mellitus E H00409 Type 2 diabetes mellitus D 5A12 Malnutrition-related diabetes mellitus D 5A13 Diabetes mellitus, other specified type E H00410 Maturity onset diabetes of the young (MODY) E H01228 Insulin-resistant diabetes mellitus with acanthosis nigricans E H00766 Wolcott-Rallison syndrome D 5A14 Diabetes mellitus, type unspecified D Acute complications of diabetes mellitus E 5A20 Diabetic hyperosmolar hyperglycaemic state E 5A21 Hypoglycaemia in the context of diabetes mellitus E 5A22 Diabetic acidosis E 5A23 Diabetic coma E 5A24 Uncontrolled or unstable diabetes mellitus E 5A2Y Other specified acute complications of diabetes mellitus C Other disorders of glucose regulation or pancreatic internal secretion D 5A40 Intermediate hyperglycaemia D 5A41 Hypoglycaemia without associated diabetes E H01909 Hypoinsulinemic hypoglycemia with hemihypertrophy D 5A42 Increased secretion of glucagon D 5A43 Abnormal secretion of gastrin E H01522 Zollinger-Ellison syndrome D 5A44 Insulin-resistance syndromes E H00419 Congenital generalized lipodystrophy E H00420 Familial partial lipodystrophy E H00719 Leprechaunism E H00942 Rabson-Mendenhall syndrome E H01474 Acquired generalized lipodystrophy E H02384 Abdominal obesity-metabolic syndrome D 5A45 Persistent hyperinsulinaemic hypoglycaemia of infancy E H01267 Familial hyperinsulinemic hypoglycemia D 5A4Y Other specified disorders of glucose regulation or pancreatic internal secretion D 5A4Z Disorders of glucose regulation or pancreatic internal secretion, unspecified C Disorders of the parathyroids or parathyroid hormone system D 5A50 Hypoparathyroidism E H01862 Hypoparathyroidism E H00244 Pseudohypoparathyroidism D 5A51 Hyperparathyroidism E H00246 Primary hyperparathyroidism E H01669 Secondary hyperparathyroidism E H02026 Familial hypocalciuric hypercalcemia E H02030 Neonatal hyperparathyroidism D 5A5Y Other specified disorders of the parathyroids or parathyroid hormone system D 5A5Z Disorders of the parathyroids or parathyroid hormone system, unspecified C Disorders of the pituitary hormone system D 5A60 Hyperfunction of pituitary gland E H01683 Disorders of antidiuretic hormone (ADH) secretion E H01483 Acromegaly E H01618 Pituitary gigantism E H01864 Excessive secretion of growth hormone E H01388 Hyperprolactinemia E H01682 Syndrome of inappropriate antidiuretic hormone secretion E H01294 Nephrogenic syndrome of inappropriate antidiuresis E H00937 Precocious puberty E H02018 Central precocious puberty E H01701 Pituitary TSH hypersecretion D 5A61 Hypofunction or certain other specified disorders of pituitary gland E H01683 Disorders of antidiuretic hormone (ADH) secretion E H00254 Growth hormone deficiency E H00931 Growth hormone insensitivity with immunodeficiency E H01253 Isolated follicle-stimulating hormone deficiency E H01274 Growth delay due to insulin-like growth factor I resistance E H01700 Hypopituitarism E H01907 Acid-labile subunit deficiency E H01973 Fertile eunuch syndrome E H02035 Isolated growth hormone deficiency E H02036 Combined pituitary hormone deficiency E H02037 Laron syndrome E H02038 X-linked panhypopituitarism E H02039 Kowarski syndrome E H02040 Insulin-like growth factor I deficiency E H01011 Adrenocorticotropic hormone deficiency E H00255 Hypogonadotropic hypogonadism E H01860 Abnormal pituitary gonadotropin secretion E H01699 Isolated TSH deficiency E H02034 Central hypothyroidism and testicular enlargement E H00253 Neurohypophyseal diabetes insipidus E H00854 Wolfram syndrome E H00682 Woodhouse-Sakati syndrome D 5A6Z Disorders of the pituitary hormone system, unspecified C Disorders of the adrenal glands or adrenal hormone system D 5A70 Cushing syndrome E H01431 Cushing syndrome E H00260 Pigmented micronodular adrenocortical disease E H01820 Carney complex E H02049 Bilateral macronodular adrenal hyperplasia D 5A71 Adrenogenital disorders E H01702 Glucocorticoid resistance syndrome E H00216 Congenital adrenal hyperplasia E H02315 Disordered steroidogenesis due to cytochrome P450 oxidoreductase E H01111 Cortisone reductase deficiency D 5A72 Hyperaldosteronism E H00602 Glucocorticoid-remediable aldosteronism (GRA) E H01603 Primary aldosteronism E H00259 Apparent mineralocorticoid excess syndrome D 5A73 Hypoaldosteronism E H00258 Aldosterone synthase deficiency D 5A74 Adrenocortical insufficiency E H01598 Addison disease E H00177 Neonatal adrenoleukodystrophy E H00256 Familial glucocorticoid deficiency E H00257 Achalasia Addisonianism Alacrima syndrome E H02314 Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete E H02316 Adrenal insufficiency, NR5A1 related E H02319 IMAGE syndrome D 5A75 Adrenomedullary hyperfunction D 5A76 Certain specified disorders of adrenal gland E H01163 Corticosteroid-binding globulin (CBG) deficiency D 5A7Z Disorders of the adrenal glands or adrenal hormone system, unspecified C Disorders of the gonadal hormone system D 5A80 Ovarian dysfunction E H01739 Polycystic ovary syndrome D 5A81 Testicular dysfunction or testosterone-related disorders E H02019 Familial male-limited precocious puberty E H02027 Male hypogonadism D 5A8Z Disorders of the gonadal hormone system, unspecified C Certain disorders of puberty D 5A90 Disorder of puberty due to oestrogen resistance E H02061 Estrogen resistance syndrome D 5A91 Delayed puberty D 5A92 Peripheral precocious puberty E H00794 Aromatase excess syndrome E H00937 Precocious puberty D 5A9Y Other disorders of puberty E H02020 Aromatase deficiency D 5A9Z Disorders of puberty, unspecified C Polyglandular dysfunction D 5B00 Autoimmune polyendocrinopathy E H01972 Autoimmune polyendocrinopathy syndrome type 1 D 5B01 Polyglandular hyperfunction D 5B0Y Other specified polyglandular dysfunction D 5B0Z Polyglandular dysfunction, unspecified C Endocrine disorders, not elsewhere classified D 5B10 Carcinoid syndrome D 5B11 Short stature, not elsewhere classified D 5B12 Constitutional tall stature D 5B1Y Other specified endocrine disorders, not elsewhere classified C 5B3Y Other specified endocrine diseases C 5B3Z Endocrine diseases, unspecified B Nutritional disorders C Undernutrition D 5B50 Underweight in infants, children or adolescents D 5B51 Wasting in infants, children or adolescents D 5B52 Acute malnutrition in infants, children or adolescents D 5B53 Stunting in infants, children or adolescents D 5B54 Underweight in adults D 5B55 Vitamin A deficiency E H01266 Hypercarotenemia and vitamin A deficiency D 5B56 Vitamin C deficiency E H01580 Vitamin C deficiency D 5B57 Vitamin D deficiency E H01143 Vitamin D-dependent rickets D 5B58 Vitamin E deficiency E H00981 Ataxia with isolated vitamin E deficiency (AVED) D 5B59 Vitamin K deficiency D 5B5A Vitamin B1 deficiency E H01566 Beriberi E H01565 Wernicke encephalopathy D 5B5B Vitamin B2 deficiency E H02544 Riboflavin deficiency D 5B5C Vitamin B3 deficiency E H01582 Pellagra D 5B5D Vitamin B6 deficiency D 5B5E Folate deficiency D 5B5F Vitamin B12 deficiency D 5B5G Biotin deficiency D 5B5H Pantothenic acid deficiency D 5B5J Choline deficiency D 5B5K Mineral deficiencies E H01925 Transient neonatal zinc deficiency D Sequelae of malnutrition or certain specified nutritional deficiencies E 5B60 Sequelae of protein-energy malnutrition E 5B61 Sequelae of vitamin A deficiency E 5B62 Sequelae of vitamin C deficiency E 5B63 Sequelae of rickets E 5B6Y Other specified sequelae of malnutrition or certain specified nutritional deficiencies E 5B6Z Sequelae of malnutrition or certain specified nutritional deficiencies, unspecified D 5B70 Essential fatty acid deficiency D 5B71 Protein deficiency D 5B7Y Other specified undernutrition D 5B7Z Unspecified undernutrition C Overweight, obesity or specific nutrient excesses D Overweight or obesity E 5B80 Overweight or localised adiposity E 5B81 Obesity F H02059 Leptin deficiency F H02060 Leptin receptor deficiency F H02105 Prohormone convertase 1/3 deficiency F H02106 Genetic obesity F H02235 Morbid obesity and spermatogenic failure D Certain specified nutrient excesses E 5B90 Vitamin excesses F H01266 Hypercarotenemia and vitamin A deficiency E 5B91 Mineral excesses E 5B9Y Other specified nutrient excesses E 5B9Z Certain specified nutrient excesses, unspecified D 5C1Y Other specified overweight, obesity or specific nutrient excesses D 5C1Z Overweight, obesity or specific nutrient excesses, unspecified C 5C3Y Other specified nutritional disorders C 5C3Z Nutritional disorders, unspecified B Metabolic disorders C Inborn errors of metabolism D 5C50 Inborn errors of amino acid or other organic acid metabolism E H00167 Phenylketonuria E H02419 Glycine encephalopathy with normal serum glycine E H00163 Alkaptonuria E H00165 Tyrosinemia E H00171 Histidinemia E H01233 Urocanase deficiency E H01583 Hydroxykynureninuria E H02545 Hypertryptophanemia E H00188 Hyperlysinemia E H01242 Saccharopinuria E H02644 Alpha-aminoadipic and alpha-ketoadipic aciduria E H02313 5-Oxoprolinase deficiency E H01079 3-Phosphoglycerate dehydrogenase (3-PGDH) deficiency E H01082 Phosphoserine aminotransferase deficiency E H02116 Phosphoserine phosphatase deficiency E H01003 Dimethylglycine dehydrogenase deficiency E H00191 Nonketotic hyperglycinemia E H02657 Sarcosinemia E H02380 D-glyceric aciduria E H00190 Hyperprolinemia E H00187 Ornithine transcarbamylase deficiency E H00189 Ornithinaemia E H01398 Primary hyperammonemia (Urea cycle disorders) E H01400 Secondary hyperammonemia E H01028 Argininosuccinic aciduria E H00164 Carbamoyl phosphate synthetase I deficiency E H00186 Hyperargininemia E H00185 Citrullinemia E H01032 N-acetylglutamate synthase deficiency E H01268 Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome E H00182 Cystathioninuria E H00183 Homocystinuria E H00184 Hypermethioninemia E H01237 Sulfite oxidase deficiency E H01285 Methylcobalamin deficiency type G E H02311 Molybdenum cofactor deficiency E H02485 Extraoral halitosis due to MTO deficiency E H00172 Maple syrup urine disease E H01076 Beta-ketothiolase deficiency E H01279 Isobutyryl-CoA dehydrogenase deficiency E H02136 Branched-chain ketoacid dehydrogenase kinase deficiency E H02285 Methylmalonate semialdehyde dehydrogenase deficiency E H02546 Hypervalinemia and hyperleucine-isoleucinemia E H01349 Methacrylic aciduria E H00173 Isovaleric acidemia E H00174 Methylmalonic aciduria E H00175 Propionic acidemia E H00180 Holocarboxylase synthetase deficiency E H00181 3-Methylcrotonylglycinuria E H00375 SBCAD deficiency E H00754 3-Methylglutaconic aciduria E H01182 Biotinidase deficiency E H02221 Methylmalonic aciduria and homocystinuria E H02222 Methylmalonic acidemia and hyperhomocysteinemia, cblX type E H00074 Canavan disease E H00178 Glutaric acidemia E H00835 Succinic semialdehyde dehydrogenase deficiency E H01146 Aminoacylase 1 deficiency E H01225 D-2-hydroxyglutaric aciduria E H01280 L-2-hydroxyglutaric aciduria E H01283 Malonyl-CoA decarboxylase deficiency E H02304 Combined D-2- and L-2-hydroxyglutaric aciduria E H02109 Combined malonic and methylmalonic aciduria E H01119 Prolidase deficiency E H01234 Trimethylaminuria E H00923 Congenital systemic glutamine deficiency E H01386 Asparagine synthetase deficiency E H02312 Glutathione synthetase deficiency D 5C51 Inborn errors of carbohydrate metabolism E H01065 Pentosuria E H01135 Ribose 5-phosphate isomerase deficiency E H01189 Transaldolase deficiency E H02439 Short stature, developmental delay, congenital heart defect E H02013 Glycerol kinase deficiency E H00117 Primary hyperoxaluria E H00069 Glycogen storage disease E H00150 Danon disease E H01375 Glucose 6-phosphate dehydrogenase deficiency E H01760 Hepatic glycogen storage disease E H01762 Muscle glycogen storage disease E H01939 Glycogen storage disease type I E H01940 Glycogen storage disease type II E H01941 Glycogen storage disease type III E H01942 Glycogen storage disease type IV E H01943 Glycogen storage disease type V E H01944 Glycogen storage disease type VI E H01945 Glycogen storage disease type VII E H01946 Glycogen storage disease type XI E H01947 Fanconi-Bickel syndrome E H01948 Glycogen storage disease type IX E H01949 Glycogen storage disease type 0b E H01950 Glycogen storage disease type 0a E H01951 Glycogen storage disease type X E H01952 Glycogen storage disease type XII E H01953 Glycogen storage disease type XIII E H01954 Glycogen storage disease type XIV E H01955 Glycogen storage disease type XV E H01956 Glycogen storage disease of heart E H00070 Galactosemia E H02008 Galactose-1P uridylyltransferase deficiency E H02009 Galactokinase deficiency E H02010 Galactose epimerase deficiency E H00071 Hereditary fructose intolerance E H00114 Fructose-1,6-bisphosphatase deficiency E H02567 Sorbitol dehydrogenase deficiency with peripheral neuropathy D 5C52 Inborn errors of lipid metabolism E H01589 Systemic primary carnitine deficiency E H01981 Carnitine palmitoyltransferase I deficiency E H01982 Carnitine palmitoyltransferase II deficiency E H01983 Carnitine-acylcarnitine translocase deficiency E H02596 Disorders of carnitine transport and the carnitine cycle E H00392 VLCAD deficiency E H00488 MCAD deficiency E H00489 LCHAD deficiency E H00525 Disorders of mitochondrial fatty-acid oxidation E H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency E H01352 Mitochondrial trifunctional protein deficiency E H01364 3-Hydroxyacyl-CoA dehydrogenase deficiency E H01929 2,4-Dienoyl-CoA reductase deficiency E H01980 SCAD deficiency E H02085 Acyl-CoA dehydrogenase 9 deficiency E H00179 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency E H01121 Succinyl CoA:3-oxoacid CoA transferase (SCOT) deficiency E H01123 HMG-CoA synthase deficiency E H00162 Sjogren-Larsson syndrome E H02284 Leukotriene C4 synthase deficiency E H02689 Retinal dystrophy with leukodystrophy E H00161 Smith-Lemli-Opitz syndrome E H00206 Mevalonate kinase deficiency E H00617 Desmosterolosis E H01281 Lathosterolosis E H00151 Cerebrotendinous xanthomatosis E H00624 Progressive familial intrahepatic cholestasis E H00628 Congenital bile acid synthesis defect E H02099 Alpha-methylacyl-CoA racemase deficiency E H00152 Sitosterolemia E H00736 Dorfman-Chanarin syndrome E H01297 Neutral lipid storage disease with myopathy E H00654 Barth syndrome E H02527 Lipid storage myopathy due to FLAD1 deficiency E H02711 Acetyl-CoA carboxylase-alpha deficiency D 5C53 Inborn errors of energy metabolism E H01427 Mitochondrial disease E H01096 Pyruvate kinase deficiency E H00072 Pyruvate dehydrogenase complex deficiency E H01996 Pyruvate dehydrogenase phosphatase deficiency E H01997 Pyruvate dehydrogenase E1-alpha deficiency E H01998 Pyruvate dehydrogenase E1-beta deficiency E H01999 Pyruvate dehydrogenase E2 deficiency E H02000 Dihydrolipoamide dehydrogenase deficiency E H02003 Pyruvate dehydrogenase E3-binding protein deficiency E H00073 Pyruvate carboxylase deficiency E H02197 Mitochondrial pyruvate carrier deficiency E H02438 Hyperglycinemia, lactic acidosis, and seizures E H02520 Phosphoenolpyruvate carboxykinase deficiency E H01022 Diseases of the tricarboxylic acid cycle E H02004 Fumarase deficiency E H02006 Alpha-ketoglutarate dehydrogenase complex deficiency E H02113 Infantile cerebellar-retinal degeneration E H02562 Yoon-Bellen neurodevelopmental syndrome E H00469 Mitochondrial DNA depletion syndrome E H01389 Alpers syndrome E H01390 Mitochondrial neurogastrointestinal encephalomyopathy E H01384 Mitochondrial recessive ataxia syndrome E H00999 Coenzyme Q10 deficiency E H00871 Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation E H01367 Infantile liver failure E H01354 Leigh syndrome E H01369 ATP synthase deficiency E H00473 Mitochondrial complex I deficiency E H00891 Combined oxidative phosphorylation deficiency E H00920 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis E H01201 Jensen syndrome E H01368 Cytochrome c oxidase (COX) deficiency E H01894 Multiple mitochondrial dysfunctions syndrome E H02005 Mitochondrial complex II deficiency E H02007 GRACILE syndrome E H02086 Mitochondrial complex III deficiency E H01305 Global cerebral hypomyelination E H01348 Mitochondrial phosphate carrier deficiency E H00834 Guanidinoacetate methyltransferase deficiency E H00849 Cerebral creatine deficiency syndrome E H02181 Idiopathic hyperCKemia E H02196 X-linked creatine deficiency syndrome E H01248 Monocarboxylate transporter 1 deficiency E H01900 Encephalopathy due to defective mitochondrial and peroxisomal fission E H02518 Neonatal severe encephalopathy with lactic acidosis and brain abnormalities E H02643 Lipoyltransferase 1 deficiency D 5C54 Inborn errors of glycosylation or other specified protein modification E H01486 Multiple congenital anomalies-hypotonia-seizures syndrome E H01487 CHIME syndrome E H00118 Congenital disorders of glycosylation type I E H00119 Congenital disorders of glycosylation type II E H01188 Tn syndrome E H01193 Familial tumoral calcinosis E H00996 Amish infantile epilepsy syndrome E H01127 PIGM-congenital disorder of glycosylation E H01489 Inherited glycosylphosphatidylinositol deficiencies E H02451 Congenital disorder of glycosylation with defective fucosylation E H02690 Structural heart defects and renal anomalies syndrome D 5C55 Inborn errors of purine, pyrimidine or nucleotide metabolism E H00192 Xanthinuria E H00194 Lesch-Nyhan syndrome E H00195 Adenine phosphoribosyltransferase deficiency E H00196 Phosphoribosylpyrophosphate synthetase superactivity E H00197 Adenylosuccinate lyase deficiency E H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) E H00966 AICA-ribosiduria E H02011 Familial juvenile hyperuricemic nephropathy E H02237 AMP deaminase deficiency E H00193 Dihydropyrimidine dehydrogenase deficiency E H00199 Dihydropyrimidinase deficiency E H00200 Beta-ureidopropionase deficiency E H00290 Aicardi-Goutieres syndrome E H00878 Cystic leukoencephalopathy without megalencephaly E H02433 Hypomyelination with brainstem and spinal cord involvement and leg spasticity D 5C56 Lysosomal diseases E H01425 Lysosomal storage disease E H00423 Sphingolipidosis E H00124 GM2 gangliosidoses E H00281 GM1 gangliosidosis E H00426 Gangliosidosis E H02016 Tay-Sachs disease E H02017 Sandhoff disease E H00125 Fabry disease E H00127 Metachromatic leukodystrophy E H00272 Multiple sulfatase deficiency E H00126 Gaucher disease E H00136 Niemann-Pick disease type C E H00137 Niemann-Pick disease type A/B E H00138 Farber lipogranulomatosis E H00148 Lysosomal acid lipase deficiency E H00424 Defects in the degradation of sphingomyelin E H01239 Combined SAP deficiency E H02468 Early childhood-onset progressive leukodystrophy E H00149 Neuronal ceroid lipofuscinosis E H02275 Batten disease E H02276 Kufs disease E H02277 Santavuori-Haltia disease E H02278 Jansky-Bielschowsky disease E H02279 Cathepsin D deficiency E H00422 Glycoproteinoses E H00143 Mucolipidosis II E H00144 Mucolipidosis IV E H02130 Mucolipidosis III E H00139 alpha-Mannosidosis E H00140 beta-Mannosidosis E H00141 Fucosidosis E H00142 Sialidosis E H00145 Aspartylglucosaminuria E H00146 Alpha-N-acetylgalactosaminidase deficiency E H00276 Galactosialidosis E H00421 Mucopolysaccharidosis E H00128 Mucopolysaccharidosis type I E H00129 Mucopolysaccharidosis type II E H00123 Mucopolysaccharidosis type IV E H00131 Mucopolysaccharidosis type VI E H00130 Mucopolysaccharidosis type III E H00132 Mucopolysaccharidosis type VII E H00133 Mucopolysaccharidosis type IX E H02205 Mucopolysaccharidosis-plus syndrome E H02729 Ain-Naz type of dysostosis multiplex E H00147 Sialuria E H00273 Pycnodysostosis E H00274 Papillon-Lefevre syndrome E H00425 Lysosomal cysteine protease deficiencies E H02128 Defects in lysosomal trafficking D 5C57 Peroxisomal diseases E H00177 Neonatal adrenoleukodystrophy E H00205 Peroxisome biogenesis disorder E H00207 Rhizomelic chondrodysplasia punctata E H01342 Zellweger syndrome E H02100 Peroxisomal fatty acyl-CoA reductase 1 disorder E H00075 Refsum disease E H00176 Adrenoleukodystrophy E H00407 Peroxisomal beta-oxidation enzyme deficiency E H00874 Leukoencephalopathy with dystonia and motor neuropathy E H02096 Peroxisomal acyl-CoA oxidase deficiency E H02098 D-bifunctional protein deficiency E H02099 Alpha-methylacyl-CoA racemase deficiency E H00203 Acatalasemia D 5C58 Inborn errors of porphyrin or heme metabolism E H02025 Myeloperoxidase deficiency E H00208 Hyperbilirubinemia E H02054 Crigler-Najjar syndrome E H02055 Gilbert syndrome E H02056 Dubin-Johnson syndrome E H00624 Progressive familial intrahepatic cholestasis E H02192 Benign recurrent intrahepatic cholestasis E H00950 Arthrogryposis, renal dysfunction, and cholestasis E H01936 Hyperbiliverdinemia E H02057 Rotor syndrome E H01763 Porphyria E H00202 Hepatic porphyria E H00201 Erythropoietic porphyria D 5C59 Inborn errors of neurotransmitter metabolism E H01005 Dopamine beta-hydroxylase deficiency E H01161 Aromatic L-amino acid decarboxylase deficiency E H02597 Sepiapterin reductase deficiency E H00548 Brunner syndrome E H01257 GABA-transaminase deficiency E H02432 Butyrylcholinesterase deficiency D 5C5A Alpha-1-antitrypsin deficiency E H01103 Alpha-1-antitrypsin deficiency D 5C5Y Other specified inborn errors of metabolism E H00967 Adiponectin deficiency E H01567 Thiamine pyrophosphokinase deficiency E H02441 HUPRA syndrome E H02727 Triokinase and FMN cyclase deficiency syndrome D 5C5Z Inborn errors of metabolism, unspecified C Disorders of metabolite absorption or transport D 5C60 Disorders of amino acid absorption or transport E H00692 Lowe syndrome E H00275 Cystinosis E H00901 Cystinuria E H00843 Hartnup disorder E H00899 Lysinuric protein intolerance E H00905 Iminoglycinuria E H00911 Dicarboxylic aminoaciduria E H01304 Hyperglycinuria D 5C61 Disorders of carbohydrate absorption or transport E H00115 Congenital sucrase-isomaltase deficiency E H02090 Trehalase deficiency E H00836 GLUT1 deficiency syndrome E H01126 Familial renal glucosuria E H02575 Lactose intolerance, adult type E H00116 Congenital lactase deficiency E H01261 Congenital glucose-galactose malabsorption D 5C62 Disorders of lipid absorption or transport E H02330 Pancreatic lipase deficiency D 5C63 Disorders of vitamin or non-protein cofactor absorption or transport E H01252 Hereditary folate malabsorption E H01262 Formiminotransferase deficiency E H01295 Neurodegeneration due to cerebral folate transport deficiency E H00214 Hypophosphatemic rickets E H02139 Autosomal recessive hypophosphatemic rickets E H02141 Autosomal dominant hypophosphatemic rickets E H02142 X-linked recessive hypophosphatemic rickets E H02143 X-linked dominant hypophosphatemic rickets E H01124 Pyridoxamine-5'-phosphate oxidase (PNPO) deficiency E H01183 Thiamine-responsive megaloblastic anemia E H01231 Biotin-thiamine-responsive basal ganglia disease E H02662 Sulfide quinone oxidoreductase deficiency E H02671 Sodium-dependent multivitamin transporter deficiency E H02699 Folate-responsive megaloblastic anemia D 5C64 Disorders of mineral absorption or transport E H00210 Wilson disease E H00209 Menkes syndrome E H00833 Neurodegeneration with brain iron accumulation E H02207 Kufor-Rakeb syndrome E H02208 Pantothenate kinase-associated neurodegeneration E H02209 HARP syndrome E H00211 Hemochromatosis E H00212 Acrodermatitis enteropathica E H02550 Birk-Landau-Perez syndrome E H00213 Hypophosphatasia E H01113 Acid phosphatase deficiency E H02138 Hereditary hypophophatemic rickets with hypercalciuria E H00240 Gitelman syndrome E H01210 Hypomagnesemia E H00245 Calcium sensing receptor (CASR) related disease E H01371 Hypercalcemia infantile E H01938 Hypermanganesemia with dystonia D 5C6Y Other specified disorders of metabolite absorption or transport D 5C6Z Disorders of metabolite absorption or transport, unspecified C Disorders of fluid, electrolyte or acid-base balance D 5C70 Volume depletion D 5C71 Hyperosmolality or hypernatraemia D 5C72 Hypo-osmolality or hyponatraemia D 5C73 Acidosis D 5C74 Alkalosis D 5C75 Mixed disorder of acid-base balance D 5C76 Hyperkalaemia D 5C77 Hypokalaemia D 5C78 Fluid overload D 5C7Y Other specified disorders of fluid, electrolyte or acid-base balance D 5C7Z Disorders of fluid, electrolyte or acid-base balance, unspecified C Disorders of lipoprotein metabolism or certain specified lipidaemias D 5C80 Hyperlipoproteinaemia E H01101 Combined lipase deficiency E H01635 Hyperlipidemia E H00155 Familial hypercholesterolemia E H01383 Hyperlipoproteinemia type IIa E H01918 Familial autosomal recessive hypercholesterolemia E H00154 Hyperlipoproteinemia, type I E H00157 Hyperlipoproteinemia, type V E H01637 Hypertriglyceridemia E H01784 Primary hyperchylomicronemia E H02731 Transient infantile hypertriglyceridemia E H00153 Familial combined hyperlipidemia E H00156 Hyperlipoproteinemia, type III E H01199 Hyperalphalipoproteinemia E H01108 CD36 deficiency E H02329 Hepatic lipase deficiency D 5C81 Hypolipoproteinaemia E H00159 Tangier disease E H00930 Hypoalphalipoproteinemia E H00160 Abetalipoproteinemia E H00927 Chylomicron retention disease E H01270 Familial hypobetalipoproteinemia E H00158 Lecithin:cholesterol acyltransferase deficiency D 5C8Y Other specified disorders of lipoprotein metabolism or lipidaemias D 5C8Z Unspecified disorders of lipoprotein metabolism or lipidaemias C 5C90 Metabolic or transporter liver disease C Other metabolic disorders D 5D00 Amyloidosis E H01185 Cerebral amyloid angiopathy E H01217 Primary localized cutaneous amyloidosis E H02499 AL amyloidosis E H00845 Familial amyloidosis E H02484 X-linked reticulate pigmentary disorder with systemic manifestations E H02322 Amyloidosis, Finnish type D 5D01 Tumour lysis syndrome D 5D0Y Other specified metabolic disorders C 5D2Z Metabolic disorders, unspecified B Postprocedural endocrine or metabolic disorders C 5D40 Postprocedural hypothyroidism C 5D41 Postprocedural hypoinsulinaemia C 5D42 Postprocedural hypoparathyroidism C 5D43 Postprocedural hypopituitarism C 5D44 Postprocedural ovarian failure C 5D45 Postprocedural testicular hypofunction C 5D46 Postprocedural adrenocortical hypofunction # A06 Mental, behavioural or neurodevelopmental disorders B Neurodevelopmental disorders C 6A00 Disorders of intellectual development D H00480 X-linked intellectual developmental disorder D H00658 X-linked syndromic intellectual developmental disorder D H00768 Autosomal recessive intellectual developmental disorder D H00773 Autosomal dominant intellectual developmental disorder D H01306 FRA12A mental retardation D H01911 Syndromic autosomal recessive mental retardation C 6A01 Developmental speech or language disorders D H00902 Speech-language disorder 1 C 6A02 Autism spectrum disorder D H02111 Autism D H01882 Asperger syndrome D H02371 Intellectual developmental disorder with autism and speech delay D H02507 Pilarowski-Bjornsson syndrome C 6A03 Developmental learning disorder C 6A04 Developmental motor coordination disorder C 6A05 Attention deficit hyperactivity disorder D H01895 Attention deficit hyperactivity disorder (ADHD) C 6A06 Stereotyped movement disorder C 6A0Y Other specified neurodevelopmental disorders D H02387 Snijders Blok-Fisher syndrome D H02490 Gabriele-de Vries syndrome D H02510 Jaberi-Elahi syndrome D H02521 Diets-Jongmans syndrome D H02571 Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities D H02692 Usmani-Riazuddin syndrome D H02705 Neurodevelopmental disorder with glutamatergic synapse dysfunction C 6A0Z Neurodevelopmental disorders, unspecified B Schizophrenia or other primary psychotic disorders C 6A20 Schizophrenia D H01649 Schizophrenia C 6A21 Schizoaffective disorder C 6A22 Schizotypal disorder C 6A23 Acute and transient psychotic disorder C 6A24 Delusional disorder C 6A25 Symptomatic manifestations of primary psychotic disorders C 6A2Y Other specified primary psychotic disorder C 6A2Z Schizophrenia or other primary psychotic disorders, unspecified B Catatonia C 6A40 Catatonia associated with another mental disorder C 6A41 Catatonia induced by substances or medications C 6A4Z Catatonia, unspecified B Mood disorders C Bipolar or related disorders D 6A60 Bipolar type I disorder E H01653 Bipolar disorder D 6A61 Bipolar type II disorder E H01653 Bipolar disorder D 6A62 Cyclothymic disorder D 6A6Y Other specified bipolar or related disorders D 6A6Z Bipolar or related disorders, unspecified C Depressive disorders D 6A70 Single episode depressive disorder E H01646 Major depressive disorder D 6A71 Recurrent depressive disorder E H01646 Major depressive disorder D 6A72 Dysthymic disorder D 6A73 Mixed depressive and anxiety disorder D 6A7Y Other specified depressive disorders D 6A7Z Depressive disorders, unspecified C 6A80 Symptomatic and course presentations for mood episodes in mood disorders C 6A8Y Other specified mood disorders C 6A8Z Mood disorders, unspecified B Anxiety or fear-related disorders C 6B00 Generalised anxiety disorder D H01662 Generalized anxiety disorder C 6B01 Panic disorder D H01664 Panic disorder C 6B02 Agoraphobia C 6B03 Specific phobia C 6B04 Social anxiety disorder D H01670 Social anxiety disorder C 6B05 Separation anxiety disorder C 6B06 Selective mutism C 6B0Y Other specified anxiety or fear-related disorders C 6B0Z Anxiety or fear-related disorders, unspecified B Obsessive-compulsive or related disorders C 6B20 Obsessive-compulsive disorder D H01450 Obsessive-compulsive disorder C 6B21 Body dysmorphic disorder D H01447 Body dysmorphic disorder C 6B22 Olfactory reference disorder C 6B23 Hypochondriasis C 6B24 Hoarding disorder D H01448 Hoarding disorder C 6B25 Body-focused repetitive behaviour disorders D H00864 Trichotillomania D H01449 Excoriation disorder C 6B2Y Other specified obsessive-compulsive or related disorders C 6B2Z Obsessive-compulsive or related disorders, unspecified D H01453 Obsessive-Compulsive and Related Disorder B Disorders specifically associated with stress C 6B40 Post traumatic stress disorder C 6B41 Complex post traumatic stress disorder C 6B42 Prolonged grief disorder C 6B43 Adjustment disorder C 6B44 Reactive attachment disorder C 6B45 Disinhibited social engagement disorder C 6B4Y Other specified disorders specifically associated with stress C 6B4Z Disorders specifically associated with stress, unspecified B Dissociative disorders C 6B60 Dissociative neurological symptom disorder C 6B61 Dissociative amnesia C 6B62 Trance disorder C 6B63 Possession trance disorder C 6B64 Dissociative identity disorder C 6B65 Partial dissociative identity disorder C 6B66 Depersonalization-derealization disorder C 6B6Y Other specified dissociative disorders C 6B6Z Dissociative disorders, unspecified B Feeding or eating disorders C 6B80 Anorexia Nervosa C 6B81 Bulimia Nervosa C 6B82 Binge eating disorder C 6B83 Avoidant-restrictive food intake disorder C 6B84 Pica C 6B85 Rumination-regurgitation disorder C 6B8Y Other specified feeding or eating disorders D H01703 Eating Disorders C 6B8Z Feeding or eating disorders, unspecified B Elimination disorders C 6C00 Enuresis C 6C01 Encopresis C 6C0Z Elimination disorders, unspecified B Disorders of bodily distress or bodily experience C 6C20 Bodily distress disorder C 6C21 Body integrity dysphoria C 6C2Y Other specified disorders of bodily distress or bodily experience C 6C2Z Disorders of bodily distress or bodily experience, unspecified B Disorders due to substance use or addictive behaviours C Disorders due to substance use D 6C40 Disorders due to use of alcohol E H01611 Alcohol dependence E H01071 Acute alcohol sensitivity D 6C41 Disorders due to use of cannabis D 6C42 Disorders due to use of synthetic cannabinoids D 6C43 Disorders due to use of opioids D 6C44 Disorders due to use of sedatives, hypnotics or anxiolytics D 6C45 Disorders due to use of cocaine D 6C46 Disorders due to use of stimulants including amphetamines, methamphetamine or methcathinone D 6C47 Disorders due to use of synthetic cathinones D 6C48 Disorders due to use of caffeine D 6C49 Disorders due to use of hallucinogens D 6C4A Disorders due to use of nicotine D 6C4B Disorders due to use of volatile inhalants D 6C4C Disorders due to use of MDMA or related drugs, including MDA D 6C4D Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP] D 6C4E Disorders due to use of other specified psychoactive substances, including medications D 6C4F Disorders due to use of multiple specified psychoactive substances, including medications D 6C4G Disorders due to use of unknown or unspecified psychoactive substances D 6C4H Disorders due to use of non-psychoactive substances D 6C4Y Other specified disorders due to substance use D 6C4Z Disorders due to substance use, unspecified C Disorders due to addictive behaviours D 6C50 Gambling disorder D 6C51 Gaming disorder D 6C5Y Other specified disorders due to addictive behaviours D 6C5Z Disorders due to addictive behaviours, unspecified B Impulse control disorders C 6C70 Pyromania C 6C71 Kleptomania C 6C72 Compulsive sexual behaviour disorder C 6C73 Intermittent explosive disorder C 6C7Y Other specified impulse control disorders C 6C7Z Impulse control disorders, unspecified B Disruptive behaviour or dissocial disorders C 6C90 Oppositional defiant disorder C 6C91 Conduct-dissocial disorder C 6C9Y Other specified disruptive behaviour or dissocial disorders C 6C9Z Disruptive behaviour or dissocial disorders, unspecified B Personality disorders and related traits C 6D10 Personality disorder C 6D11 Prominent personality traits or patterns B Paraphilic disorders C 6D30 Exhibitionistic disorder C 6D31 Voyeuristic disorder C 6D32 Pedophilic disorder C 6D33 Coercive sexual sadism disorder C 6D34 Frotteuristic disorder C 6D35 Other paraphilic disorder involving non-consenting individuals C 6D36 Paraphilic disorder involving solitary behaviour or consenting individuals C 6D3Z Paraphilic disorders, unspecified B Factitious disorders C 6D50 Factitious disorder imposed on self C 6D51 Factitious disorder imposed on another C 6D5Z Factitious disorders, unspecified B Neurocognitive disorders C 6D70 Delirium C 6D71 Mild neurocognitive disorder C 6D72 Amnestic disorder C Dementia D 6D80 Dementia due to Alzheimer disease D 6D81 Dementia due to cerebrovascular disease D 6D82 Dementia due to Lewy body disease D 6D83 Frontotemporal dementia D 6D84 Dementia due to psychoactive substances including medications D 6D85 Dementia due to diseases classified elsewhere D 6D86 Behavioural or psychological disturbances in dementia D 6D8Y Dementia, other specified cause D 6D8Z Dementia, unknown or unspecified cause C 6E0Y Other specified neurocognitive disorders C 6E0Z Neurocognitive disorders, unspecified B Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium C 6E20 Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms C 6E21 Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, with psychotic symptoms C 6E2Z Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, unspecified B 6E40 Psychological or behavioural factors affecting disorders or diseases classified elsewhere B Secondary mental or behavioural syndromes associated with disorders or diseases classified elsewhere C 6E60 Secondary neurodevelopmental syndrome C 6E61 Secondary psychotic syndrome C 6E62 Secondary mood syndrome C 6E63 Secondary anxiety syndrome C 6E64 Secondary obsessive-compulsive or related syndrome C 6E65 Secondary dissociative syndrome C 6E66 Secondary impulse control syndrome C 6E67 Secondary neurocognitive syndrome C 6E68 Secondary personality change C 6E69 Secondary catatonia syndrome C 6E6Y Other specified secondary mental or behavioural syndrome C 6E6Z Secondary mental or behavioural syndrome, unspecified B 6E8Y Other specified mental, behavioural or neurodevelopmental disorders B 6E8Z Mental, behavioural or neurodevelopmental disorders, unspecified # A07 Sleep-wake disorders B Insomnia disorders C 7A00 Chronic insomnia D H01609 Insomnia C 7A01 Short-term insomnia D H01609 Insomnia C 7A0Z Insomnia disorders, unspecified B Hypersomnolence disorders C 7A20 Narcolepsy D H01293 Narcolepsy C 7A21 Idiopathic hypersomnia C 7A22 Kleine-Levin syndrome C 7A23 Hypersomnia due to a medical condition C 7A24 Hypersomnia due to a medication or substance C 7A25 Hypersomnia associated with a mental disorder C 7A26 Insufficient sleep syndrome C 7A2Y Other specified hypersomnolence disorders C 7A2Z Hypersomnolence disorders, unspecified B Sleep-related breathing disorders C 7A40 Central sleep apnoeas C 7A41 Obstructive sleep apnoea C 7A42 Sleep-related hypoventilation or hypoxemia disorders D H01727 Primary alveolar hypoventilation syndrome D H01729 Premature ventricular complexes D H01715 Obesity hypoventilation syndrome D H00916 Congenital central hypoventilation syndrome C 7A4Y Other specified sleep-related breathing disorders C 7A4Z Sleep-related breathing disorders, unspecified B Circadian rhythm sleep-wake disorders C 7A60 Delayed sleep-wake phase disorder D H00689 Delayed sleep phase disorder C 7A61 Advanced sleep-wake phase disorder D H00688 Familial advanced sleep phase syndrome C 7A62 Irregular sleep-wake rhythm disorder C 7A63 Non-24 hour sleep-wake rhythm disorder C 7A64 Circadian rhythm sleep-wake disorder, shift work type C 7A65 Circadian rhythm sleep-wake disorder, jet lag type C 7A6Z Circadian rhythm sleep-wake disorders, unspecified B Sleep-related movement disorders C 7A80 Restless legs syndrome D H01597 Restless legs syndrome C 7A81 Periodic limb movement disorder C 7A82 Sleep-related leg cramps C 7A83 Sleep-related bruxism C 7A84 Sleep-related rhythmic movement disorder C 7A85 Benign sleep myoclonus of infancy C 7A86 Propriospinal myoclonus at sleep onset C 7A87 Sleep-related movement disorder due to a medical condition C 7A88 Sleep-related movement disorder due to a medication or substance C 7A8Y Other specified sleep-related movement disorders C 7A8Z Sleep-related movement disorders, unspecified B Parasomnia disorders C 7B00 Disorders of arousal from non-REM sleep C 7B01 Parasomnias related to REM sleep C 7B02 Other parasomnias C 7B0Y Other specified parasomnia disorders C 7B0Z Parasomnia disorders, unspecified B 7B2Y Other specified sleep-wake disorders B 7B2Z Sleep-wake disorders, unspecified # A08 Diseases of the nervous system B Movement disorders C 8A00 Parkinsonism D H01600 Parkinsonian syndrome D H00057 Parkinson disease D H00077 Progressive supranuclear palsy D H00879 Perry syndrome D H01574 Familial idiopathic basal ganglia calcification C 8A01 Choreiform disorders D H00860 Benign hereditary chorea D H00059 Huntington disease D H01243 Huntington disease-like syndrome D H00060 Dentatorubropallidoluysian atrophy (DRPLA) D H00655 McLeod syndrome D H00832 Core neuroacanthocytosis syndromes D H01779 Neuroferritinopathy D H02367 Chorea, childhood-onset, with psychomotor retardation C 8A02 Dystonic disorders D H00831 Primary dystonia D H01255 Juvenile-onset dystonia D H01608 Cervical dystonia D H02706 Early-onset dystonia and/or spastic paraplegia D H02557 Dopa-responsive dystonia D H00989 Mohr-Tranebjaerg syndrome D H02676 Infantile-onset parkinsonism-dystonia C 8A03 Ataxic disorders D H01616 Spinocerebellar degeneration D H00067 Friedreich ataxia D H00749 Episodic ataxias D H00063 Spinocerebellar ataxia (SCA) D H01478 Machado-Joseph disease D H01891 Autosomal recessive spinocerebellar ataxias D H02573 Autosomal recessive spinocerebellar ataxias with axonal neuropathy D H00848 Ataxia with ocular apraxia D H01036 Posterior column ataxia with retinitis pigmentosa D H01038 Cerebellar ataxia cayman type D H01170 Autosomal recessive spastic ataxia of Charlevoix-Saguenay D H01204 Cerebellar ataxia, mental retardation (MR), and dysequilibrium syndrome (CAMRQ) D H01432 Choreoacanthocytosis D H02101 Autosomal dominant sensory ataxia D H02140 Boucher-Neuhauser syndrome D H02144 Gordon Holmes syndrome D H02273 Nonprogressive cerebellar ataxia with mental retardation D H02552 Ataxia, intention tremor, and hypotonia syndrome C 8A04 Disorders associated with tremor D H01577 Essential tremor C 8A05 Tic disorders D H00862 Tourette syndrome C 8A06 Myoclonic disorders C 8A07 Certain specified movement disorder D H01287 Congenital mirror movements D H01528 Neuroleptic malignant syndrome C 8A0Y Other specified movement disorders D H01570 Autosomal dominant striatal degeneration C 8A0Z Movement disorders, unspecified B Disorders with neurocognitive impairment as a major feature C 8A20 Alzheimer disease D H00056 Alzheimer disease C 8A21 Progressive focal atrophies C 8A22 Lewy body disease D H00066 Lewy body dementia (LBD) C 8A23 Frontotemporal lobar degeneration D H00078 Frontotemporal lobar degeneration C 8A2Y Other specified disorders with neurocognitive impairment as a major feature D H00290 Aicardi-Goutieres syndrome C 8A2Z Disorders with neurocognitive impairment as a major feature, unspecified B Multiple sclerosis or other white matter disorders C 8A40 Multiple sclerosis D H01490 Multiple sclerosis C 8A41 Isolated demyelinating syndromes of the central nervous system C 8A42 Acute disseminated encephalomyelitis C 8A43 Neuromyelitis optica D H01491 Neuromyelitis optica C 8A44 Leukodystrophies D H02598 Progressive leukoencephalopathy D H00176 Adrenoleukodystrophy D H00065 Alexander disease D H00438 Nasu-Hakola disease D H00679 Hypomyelinating leukodystrophy D H00869 Leukoencephalopathy with vanishing white matter D H00875 Megaloencephalic leukoencephalopathy with subcortical cysts D H01230 Adult-onset autosomal dominant leukodystrophy D H01807 Hereditary diffuse leukoencephalopathy with spheroids D H02200 Leukoencephalopathy, progressive, with ovarian failure D H02377 Leukodystrophy and acquired microcephaly with or without dystonia D H00135 Krabbe disease C 8A45 Secondary white matter disorders D H01724 HTLV1-associated myelopathy D H01696 Subacute sclerosing panencephalitis D H00370 Progressive multifocal leukoencephalopathy C 8A46 Central demyelination of corpus callosum C 8A4Y Other specified multiple sclerosis or other white matter disorders D H02457 Developmental delay, leukoencephalopathy, and neurologic decompensation C 8A4Z Multiple sclerosis or other white matter disorders, unspecified B Epilepsy or seizures C 8A60 Epilepsy due to structural or metabolic conditions or diseases D H01826 Mesial temporal lobe epilepsy with hippocampal sclerosis C 8A61 Genetic or presumed genetic syndromes primarily expressed as epilepsy D H00577 Symptomatic generalized epilepsies D H00808 Idiopathic generalized epilepsies D H01247 Pyridoxine-dependent epilepsy D H01819 Early myoclonic encephalopathy D H02250 Early-onset vitamin B6-dependent epilepsy D H02696 Early-onset epilepsy D H00806 Benign familial neonatal seizure D H01818 Dravet syndrome D H01815 Malignant migrating partial seizures in infancy D H01775 PCDH19-related epilepsy syndrome D H02212 Familial infantile myoclonic epilepsy D H02215 Childhood absence epilepsy D H01823 Myoclonic-astatic epilepsy D H01822 Epilepsy with myoclonic absence D H01258 Generalized epilepsy and paroxysmal dyskinesia D H02361 Myoclonic-atonic epilepsy D H02564 Generalized epilepsy with febrile seizures plus D H02217 Juvenile myoclonic epilepsy D H02216 Juvenile absence epilepsy D H02213 Familial adult myoclonic epilepsy D H00809 Familial epilepsy temporal lobe (ETL) D H00810 Progressive myoclonic epilepsy D H01212 Familial encephalopathy with neuroserpin inclusion bodies D H01994 Myoclonic epilepsy of Lafora D H01995 Unverricht-Lundborg disease D H00807 Nocturnal frontal lobe epilepsy D H00836 GLUT1 deficiency syndrome D H02214 Familial focal epilepsy with variable foci C 8A62 Epileptic encephalopathies D H01460 West syndrome D H01813 Lennox-Gastaut syndrome D H01514 Landau-Kleffner syndrome D H00606 Early infantile epileptic encephalopathy D H01808 Hemiconvulsion-hemiplegia-epilepsy syndrome D H01812 Rasmussen encephalitis D H01827 Rolandic epilepsy, mental retardation, and speech dyspraxia D H01829 Acute encephalitis with refractory repetitive partial seizures D H02150 Infantile or early childhood epileptic encephalopathy D H02360 Epileptic encephalopathy, childhood-onset D H02472 Early-onset progressive encephalopathy C 8A63 Seizure due to acute causes D H00783 Febrile seizures C 8A64 Single seizure due to remote causes C 8A65 Single unprovoked seizure C 8A66 Status epilepticus C 8A67 Acute repetitive seizures C 8A68 Types of seizures C 8A6Y Other specified epilepsy or seizures C 8A6Z Epilepsy or seizures, unspecified B Headache disorders C 8A80 Migraine D H00775 Hemiplegic migraine D H02362 Benign familial infantile seizure C 8A81 Tension-type headache C 8A82 Trigeminal autonomic cephalalgias D H01588 Cluster headache C 8A83 Other primary headache disorder C 8A84 Secondary headache C 8A85 Painful cranial neuropathies or other facial pains C 8A8Y Other specified headache disorders C 8A8Z Headache disorders, unspecified B Cerebrovascular diseases C Intracranial haemorrhage D 8B00 Intracerebral haemorrhage D 8B01 Subarachnoid haemorrhage D 8B02 Nontraumatic subdural haemorrhage D 8B03 Nontraumatic epidural haemorrhage D 8B0Z Intracranial haemorrhage, unspecified C Cerebral ischaemia D 8B10 Transient ischaemic attack D 8B11 Cerebral ischaemic stroke D 8B1Y Other specified cerebral ischaemia D 8B1Z Cerebral ischaemia, unspecified C 8B20 Stroke not known if ischaemic or haemorrhagic C 8B21 Cerebrovascular disease with no acute cerebral symptom C 8B22 Certain specified cerebrovascular diseases D H01184 Familial dementia D H00534 Cerebral cavernous malformation D H01396 Moyamoya disease D H00536 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) D H01757 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy D H00877 Brain small vessel disease D H02718 Autosomal dominant pontine microangiopathy and leukoencephalopathy C 8B23 Cerebrovascular abnormalities C 8B24 Hypoxic-ischaemic encephalopathy C 8B25 Late effects of cerebrovascular disease C 8B26 Vascular syndromes of brain in cerebrovascular diseases D H01120 Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome C 8B2Z Cerebrovascular diseases, unspecified B Spinal cord disorders excluding trauma C 8B40 Cauda equina syndrome C 8B41 Myelitis D H01863 Atopic myelitis C 8B42 Myelopathy C 8B43 Non-compressive vascular myelopathies C 8B44 Degenerative myelopathic disorders D H00266 Hereditary spastic paraplegia D H01351 Spastic ataxia D H02114 Spastic paraplegia, optic atrophy, and neuropathy D H02293 Spastic paraplegia-psychomotor retardation-seizures syndrome D H02178 MASA syndrome D H01172 Infantile-onset ascending hereditary spastic paralysis C 8B4Y Other specified spinal cord disorders excluding trauma C 8B4Z Spinal cord disorders excluding trauma, unspecified B Motor neuron diseases or related disorders C 8B60 Motor neuron disease D H00058 Amyotrophic lateral sclerosis (ALS) D H00970 Juvenile primary lateral sclerosis D H02342 Frontotemporal dementia and amyotrophic lateral sclerosis D H00841 Infantile progressive bulbar palsy C 8B61 Spinal muscular atrophy D H00455 Spinal muscular atrophy D H00062 Spinal and bulbar muscular atrophy (SBMA) D H00524 Scapuloperoneal spinal muscular atrophy D H00856 Distal hereditary motor neuropathies D H02238 Spinal muscular atrophy with congenital bone fractures C 8B62 Post polio progressive muscular atrophy C 8B6Y Other specified motor neuron diseases or related disorders C 8B6Z Motor neuron diseases or related disorders, unspecified B Disorders of nerve root, plexus or peripheral nerves C Disorders of cranial nerves D 8B80 Disorders of olfactory nerve D 8B81 Disorders of vestibulocochlear nerve D 8B82 Disorders of trigeminal nerve D 8B83 Disorders of spinal accessory nerve D 8B84 Disorders of hypoglossal nerve D 8B85 Disorders of multiple cranial nerves D 8B86 Disorders of vagus nerve D 8B87 Disorders of glossopharyngeal nerve D 8B88 Disorders of facial nerve D 8B8Y Other specified disorders of cranial nerves E H02594 Congenital facial palsy with ptosis and velopharyngeal dysfunction D 8B8Z Disorders of cranial nerves, unspecified C Nerve root or plexus disorders D 8B90 Nerve root and plexus compressions D 8B91 Brachial plexus disorders D 8B92 Lumbosacral plexus disorders D 8B93 Radiculopathy D 8B94 Diabetic radiculoplexoneuropathy D 8B95 Secondary brachial plexus lesion due to certain specified disorders D 8B9Y Other specified nerve root or plexus disorders D 8B9Z Nerve root or plexus disorders, unspecified C Polyneuropathy D 8C00 Idiopathic progressive neuropathy D 8C01 Inflammatory polyneuropathy E H01436 Guillain-Barre syndrome E H01689 Fisher syndrome E H01842 Bickerstaff brainstem encephalitis E H01527 Chronic inflammatory demyelinating polyradiculoneuropathy D 8C03 Other secondary polyneuropathy E H01459 Diabetic neuropathy E H02559 Microvascular complications of diabetes D 8C0Y Other specified polyneuropathy D 8C0Z Polyneuropathy, unspecified C Mononeuropathy D 8C10 Mononeuropathies of upper limb E H00798 Familial carpal tunnel syndrome D 8C11 Mononeuropathies of lower limb D 8C12 Certain specified mononeuropathies D 8C1Y Mononeuropathy of other specified site D 8C1Z Mononeuropathy of unspecified site C Hereditary neuropathy D 8C20 Hereditary motor and sensory neuropathy E H00264 Charcot-Marie-Tooth disease E H02357 Congenital hypomyelinating neuropathy E H01131 Hereditary neuralgic amyotrophy E H01155 Roussy-Levy syndrome E H01296 Hereditary neuropathy with liability to pressure palsies E H02344 Cowchock syndrome E H02345 Autosomal recessive peripheral neuropathy (PNRIID) E H02359 Dejerine-Sottas disease E H02649 Autosomal dominant slowed nerve conduction velocity D 8C21 Hereditary sensory or autonomic neuropathy E H00265 Hereditary sensory and autonomic neuropathy E H02580 Hereditary sensory neuropathy with spastic paraplegia E H01987 Familial dysautonomia E H01836 Congenital pain insensitivity with anhidrosis E H00774 Congenital insensitivity to pain E H00935 Cold-induced sweating syndrome D 8C2Y Other specified hereditary neuropathy E H01259 Giant axonal neuropathy D 8C2Z Hereditary neuropathy, unspecified C 8C4Y Other specified disorders of nerve root, plexus or peripheral nerves C 8C4Z Disorders of nerve root, plexus or peripheral nerves, unspecified B Diseases of neuromuscular junction or muscle C Myasthenia gravis or certain specified neuromuscular junction disorders D 8C60 Myasthenia gravis E H01594 Myasthenia gravis D 8C61 Congenital myasthenic syndromes E H00770 Congenital myasthenic syndrome D 8C62 Lambert-Eaton syndrome E H01596 Lambert-Eaton myasthenic syndrome D 8C6Y Other specified myasthenia gravis and neuromuscular junction disorders D 8C6Z Unspecified myasthenia gravis or neuromuscular junction disorders C Primary disorders of muscles D 8C70 Muscular dystrophy E H00562 Dystrophinopathies E H01964 Becker muscular dystrophy E H01963 Duchenne muscular dystrophy E H00563 Emery-Dreifuss muscular dystrophy E H00591 Facioscapulohumeral muscular dystrophy E H00565 Sarcoglycanopathies E H00593 Limb-girdle muscular dystrophy E H00567 Limb-girdle muscular dystrophy 1C E H00592 Calpainopathy E H01959 Muscular dystrophy-dystroglycanopathy type C E H01962 Congenital muscular dystrophy type 1D E H01974 Limb-girdle muscular dystrophy 2B E H00656 Scapuloperoneal myopathy E H00120 Muscular dystrophy-dystroglycanopathy type A E H00590 Congenital muscular dystrophies (CMD/MDC) E H01284 Marinesco-Sjogren syndrome E H01340 Bethlem myopathy E H01341 Collagen VI myopathy E H01778 Ullrich disease E H01957 Fukuyama congenital muscular dystrophy E H01958 Merosin-deficient congenital muscular dystrophy E H01960 Muscular dystrophy-dystroglycanopathy type B E H01961 Congenital muscular dystrophy type 1C E H02307 Muscular dystrophy-dystroglycanopathy E H00697 X-linked myopathy with postural muscle atrophy E H02721 Scapulohumeroperoneal myopathy D 8C71 Myotonic disorders E H00568 Myotonic dystrophy E H01777 Schwartz-Jampel syndrome E H00705 Myotonia congenita E H00744 Potassium-aggravated myotonia E H01804 Isaacs syndrome E H02390 Autosomal recessive neuromyotonia and axonal neuropathy E H01780 Non-dystrophic myotonia E H02179 Rippling muscle disease D 8C72 Congenital myopathies E H01810 Congenital myopathy E H00698 Nemaline myopathy E H00702 Cap myopathy E H00700 Centronuclear myopathy E H00699 Central core disease E H00703 Myosin storage myopathy E H01291 Spheroid body myopathy E H01310 Multi-minicore disease E H01338 Myosclerosis E H02678 External ophthalmoplegia with rib and vertebral anomalies E H00701 Congenital fiber type disproportion E H00657 Reducing body myopathy E H01781 Autophagic vacuolar myopathy E H02084 Native American myopathy E H02258 Tubular aggregate myopathy E H02320 Vacuolar myopathy with CASQ1 aggregates E H02321 Early-onset myopathy, areflexia, respiratory distress, and dysphagia D 8C73 Mitochondrial myopathies E H01363 NARP syndrome E H00068 Leber hereditary optic atrophy E H01200 Fatal infantile cardioencephalomyopathy E H01347 MELAS syndrome E H01356 Myoclonic Epilepsy and Ragged-Red Fiber Disease E H01365 Leber hereditary optic neuropathy and dystonia E H02201 Mitochondrial myopathy with lactic acidosis E H02447 Myopathy with extrapyramidal signs E H02448 Harel-Yoon syndrome E H02684 Mitochondrial progressive myopathy with congenital cataract and developmental delay E H02701 Recurrent metabolic crises with variable encephalomyopathic features and neurologic regression E H02704 Mitochondrial myopathy and ataxia D 8C74 Periodic paralyses or disorders of muscle membrane excitability E H00743 Paramyotonia congenita E H00215 Periodic paralysis E H00746 Hypokalemic periodic paralysis E H00745 Hyperkalemic periodic paralysis E H00747 Thyrotoxic hypokalemic periodic paralysis E H00748 Andersen-Tawil syndrome D 8C75 Distal myopathies E H00566 Distal myopathy with anterior tibial onset E H00594 Distal myopathy E H00596 Nonaka myopathy (NM) E H01965 Miyoshi muscular dystrophy E H01975 Welander distal myopathy E H01976 Tibial muscular dystrophy E H01977 Laing distal myopathy E H02182 Distal myopathy, Tateyama type E H02586 Distal myopathy with rimmed vacuoles D 8C76 Myofibrillar myopathy E H00595 Myofibrillar myopathies D 8C77 Ocular myopathy D 8C78 Malignant hyperthermia or hyperpyrexia E H02646 Malignant hyperthermia D 8C7Y Other specified primary disorders of muscles E H01129 Brody myopathy D 8C7Z Primary disorders of muscles, unspecified C Secondary myopathies D 8C80 Drug-induced myopathy D 8C81 Autoimmune myopathy D 8C82 Myopathy in certain specified infectious or parasitic disease D 8C83 Myopathy in certain specified endocrine disease D 8C84 Secondary rhabdomyolysis D 8C8Y Other specified secondary myopathies D 8C8Z Secondary myopathies, unspecified C 8D0Y Other specified diseases of neuromuscular junction or muscle C 8D0Z Diseases of neuromuscular junction or muscle, unspecified B Cerebral palsy C 8D20 Spastic cerebral palsy D H01097 Spastic quadriplegic cerebral palsy C 8D21 Dyskinetic cerebral palsy C 8D22 Ataxic cerebral palsy C 8D23 Worster-Drought syndrome D H01837 Congenital suprabulbar paresis C 8D2Y Other specified cerebral palsy C 8D2Z Cerebral palsy, unspecified B Nutritional or toxic disorders of the nervous system C 8D40 Neurological disorders due to nutrient deficiency C 8D41 Neurological disorders due to an excess of micro or macro nutrients C 8D42 Neurological disorders due to overweight or obesity in adults or children C 8D43 Neurological disorders due to toxicity D H01578 Subacute myelo-optico-neuropathy (SMON) C 8D44 Alcohol-related neurological disorders C 8D4Y Other specified nutritional or toxic disorders of the nervous system C 8D4Z Nutritional or toxic disorders of the nervous system, unspecified B Disorders of cerebrospinal fluid pressure or flow C 8D60 Increased intracranial pressure C 8D61 Intracranial hypotension C 8D62 Cerebrospinal fluid rhinorrhoea C 8D63 Cerebrospinal fluid otorrhoea C 8D64 Hydrocephalus D H01676 Normal pressure hydrocephalus C 8D65 Cerebrospinal fluid fistula C 8D66 Syringomyelia or syringobulbia D H01675 Syringomyelia C 8D67 Intracranial arachnoid cyst C 8D68 Porencephalic cyst C 8D6Y Other specified disorders of cerebrospinal fluid pressure or flow C 8D6Z Disorders of cerebrospinal fluid pressure or flow, unspecified B Disorders of autonomic nervous system C 8D80 Congenital malformations of the autonomic nervous system C 8D81 Inherited autonomic nervous system disorders C 8D82 Autoimmune disorders involving the autonomic nervous system C 8D83 Autonomic nervous system disorder due to infection C 8D84 Pure autonomic nervous system failure C 8D85 Autonomic nervous system disorder due to substances C 8D86 Autonomic nervous system hyperactivity C 8D87 Autonomic nervous system disorder due to certain specified neurodegenerative disorder D H01614 Multiple system atrophy D H01177 Infantile bilateral striatal necrosis C 8D88 Autonomic neuropathies C 8D89 Disorders of orthostatic tolerance D H01031 Orthostatic intolerance C 8D8A Focal or segmental autonomic disorders C 8D8B Disorders affecting autonomic synaptic neurotransmission C 8D8C Autonomic dysreflexia C 8D8D Hypoglycaemia unawareness C 8D8Y Other specified disorders of autonomic nervous system C 8D8Z Disorders of autonomic nervous system, unspecified B Human prion diseases C 8E00 Sporadic Creutzfeldt-Jakob Disease D H00061 Prion disease C 8E01 Acquired prion disease D H00061 Prion disease C 8E02 Genetic prion diseases D H00061 Prion disease C 8E03 Variably protease sensitive prionopathy D H00061 Prion disease C 8E0Y Other specified human prion diseases D H00061 Prion disease C 8E0Z Human prion diseases, unspecified B Disorders of consciousness C 8E20 Persistent vegetative state C 8E21 Permanent vegetative state C 8E22 Minimally conscious state C 8E2Y Other specified disorders of consciousness C 8E2Z Disorders of consciousness, unspecified B Other disorders of the nervous system C 8E40 Disorders of the meninges excluding infection D H01668 Neoplastic meningitis C 8E41 Pachymeningitis C 8E42 Superficial siderosis of the nervous system D H01846 Superficial siderosis C 8E43 Pain disorders D H01638 Neuropathic pain D H00772 Paroxysmal extreme pain disorder D H01391 Familial episodic pain syndrome C 8E44 Post anoxic brain damage C 8E45 Locked-in syndrome C 8E46 Reye syndrome C 8E47 Encephalopathy, not elsewhere classified D H01841 Acute encephalopathy with biphasic seizures and late reduced diffusion D H02261 PEBAT D H02262 PEBEL C 8E48 Encephalitis, not elsewhere classified C 8E49 Postviral fatigue syndrome C 8E4A Paraneoplastic or autoimmune disorders of the nervous system D H01452 Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection C 8E4Y Other specified disorders of the nervous system D H02473 Leukoencephalopathy, brain calcifications, and cysts D H02476 Childhood-onset neurodegeneration with brain atrophy D H02489 Mild encephalopathy with reversible myelin vacuolization D H02572 Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures B Postprocedural disorders of the nervous system C 8E60 Post ventricular shunting leak C 8E61 Post radiation injury of the nervous system C 8E62 Postprocedural meningitis C 8E63 Post pump encephalopathy C 8E64 Multifocal cerebral infarctions C 8E66 Intracranial hypotension due to lumbar puncture B 8E7Y Other specified diseases of the nervous system B 8E7Z Diseases of the nervous system, unspecified # A09 Diseases of the visual system B Disorders of the ocular adnexa or orbit C Disorders of eyelid or peri-ocular area D 9A00 Congenital malposition of eyelids D 9A01 Infectious disorders of eyelid E H01644 Blepharitis D 9A02 Inflammatory disorders of eyelid E H01644 Blepharitis D 9A03 Acquired malposition of eyelid D 9A04 Acquired disorders of eyelashes D 9A05 Movement disorders of eyelid D 9A06 Certain specified disorders of eyelid D 9A0Y Other specified disorders of eyelid or peri-ocular area D 9A0Z Disorders of eyelid or peri-ocular area, unspecified C Disorders of lacrimal apparatus D 9A10 Disorders of lacrimal gland D 9A11 Disorders of lacrimal drainage system D 9A1Y Other specified disorders of lacrimal apparatus D 9A1Z Disorders of lacrimal apparatus, unspecified C Disorders of orbit D 9A20 Displacement of eyeball D 9A21 Orbital infection D 9A22 Orbital inflammation D 9A23 Orbital cyst D 9A24 Bony deformity of orbit D 9A25 Soft tissue deformity of orbit D 9A26 Combined bony and soft tissue deformity of orbit D 9A2Y Other specified disorders of orbit D 9A2Z Disorders of orbit, unspecified C 9A4Y Other specified disorders of the ocular adnexa or orbit C 9A4Z Disorders of the ocular adnexa or orbit, unspecified B Disorders of the eyeball anterior segment C Disorders of conjunctiva D 9A60 Conjunctivitis E H01366 Bacterial conjunctivitis D 9A61 Certain specified disorders of conjunctiva D 9A62 Mucous membrane pemphigoid with ocular involvement D 9A6Y Other specified disorders of conjunctiva D 9A6Z Disorders of conjunctiva, unspecified C Disorders of the cornea D 9A70 Hereditary corneal dystrophies E H00960 Fuchs corneal dystrophy E H00963 Congenital hereditary endothelial dystrophy E H00726 Meesmann corneal dystrophy E H00951 Reis-Bucklers corneal dystrophy E H00952 Thiel-Behnke dystrophies E H00953 Gelatinous drop-like corneal dystrophy E H00954 Macular corneal dystrophy E H00955 Granular corneal dystrophies E H00956 Lattice corneal dystrophies E H00957 Fleck corneal dystrophy E H00958 Congenital stromal corneal dystrophy E H00959 Schnyder corneal dystrophy E H01221 Epithelial basement membrane corneal dystrophy D 9A71 Infectious keratitis D 9A72 Traumatic keratitis D 9A73 Exposure keratitis D 9A74 Neurotrophic keratitis D 9A75 Autoimmune keratitis D 9A76 Corneal ulcer D 9A77 Corneal scars or opacities D 9A78 Certain specified disorders of cornea E H00789 Keratoconus E H02426 EDICT syndrome D 9A79 Keratoconjunctivitis sicca E H01641 Dry eye disease D 9A7Y Other specified disorders of the cornea E H01273 Autosomal dominant keratitis D 9A7Z Disorders of the cornea, unspecified C Disorders of the anterior chamber D 9A80 Hyphaema D 9A81 Parasites in the anterior chamber of the eye D 9A82 Cyst in the anterior chamber of the eye D 9A83 Flat anterior chamber hypotony of eye D 9A8Y Other specified disorders of the anterior chamber D 9A8Z Disorders of the anterior chamber, unspecified C Disorders of the anterior uvea D 9A90 Degeneration of iris or ciliary body D 9A91 Cyst of iris or ciliary body D 9A92 Persistent pupillary membranes D 9A93 Adhesions or disruptions of iris or ciliary body D 9A94 Certain specified disorders of iris or ciliary body D 9A96 Anterior uveitis D 9A9Y Other specified disorders of the anterior uvea D 9A9Z Disorders of the anterior uvea, unspecified C Functional disorders of the pupil D 9B00 Disorders of the afferent pupillary system D 9B01 Disorders of the efferent pupillary system D 9B02 Light-near dissociations D 9B0Y Other specified functional disorders of the pupil D 9B0Z Functional disorders of the pupil, unspecified C Disorders of lens D 9B10 Cataract E H01202 Cataract E H02204 Hereditary hyperferritinaemia-cataract syndrome D 9B11 Certain specified disorders of lens D 9B1Z Disorders of lens, unspecified C 9B3Y Other specified disorders of the eyeball anterior segment C 9B3Z Disorders of the eyeball anterior segment, unspecified B Disorders of the eyeball posterior segment C Disorders of sclera D 9B50 Episcleritis D 9B51 Scleritis D 9B52 Scleral staphyloma D 9B5Y Other specified disorders of sclera D 9B5Z Disorders of sclera, unspecified C Disorders of the choroid D 9B60 Choroidal degeneration D 9B61 Choroidal dystrophy E H00732 Sorsby fundus dystrophy E H01116 Choroideremia E H01768 Central areolar choroidal dystrophy E H01880 Autosomal recessive microcephaly and chorioretinopathy E H02107 Bietti crystalline corneoretinal dystrophy D 9B62 Chorioretinal scars D 9B63 Choroidal haemorrhage or rupture D 9B64 Choroidal detachment D 9B65 Choroiditis D 9B66 Intermediate choroiditis D 9B6Y Other specified disorders of the choroid D 9B6Z Disorders of the choroid, unspecified C Disorders of the retina D 9B70 Inherited retinal dystrophies E H00481 Cone-rod dystrophy and cone dystrophy E H00527 Retinitis pigmentosa E H00814 Vitelliform macular dystrophy E H00819 Stargardt disease E H00825 Familial flecked retina syndrome E H00837 Leber congenital amaurosis E H00971 Achromatopsia E H00974 Blue cone monochromacy E H01009 Newfoundland rod-cone dystrophy E H01130 Late-onset retinal degeneration E H01770 Macular dystrophy E H01890 Pattern dystrophies of the retinal pigment epithelium E H02075 Enhanced S-cone syndrome E H02077 Snowflake vitreoretinal degeneration E H02078 Autosomal dominant vitreoretinochoroidopathy E H02108 Basal laminar drusen E H02110 Doyne honeycomb retinal dystrophy E H02288 Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities E H02289 Retinal dystrophy with or without extraocular anomalies E H02290 Retinal dystrophy and iris coloboma with or without congenital cataract E H02291 Retinal dystrophy, iris coloboma, and comedogenic acne syndrome E H02341 Goldmann-Favre syndrome E H02440 Fleck retina, familial benign D 9B71 Retinopathy E H01457 Diabetic retinopathy E H02559 Microvascular complications of diabetes D 9B72 Inflammatory diseases of the retina D 9B73 Retinal detachments or breaks E H01766 Juvenile retinoschisis D 9B74 Retinal vascular occlusions D 9B75 Macular disorders E H00821 Age-related macular degeneration E H01480 Idiopathic macular hole E H01010 Occult macular dystrophy E H01651 Macular edema D 9B76 Degenerative high myopia D 9B77 Eales disease D 9B78 Certain specified retinal disorders E H01000 Retinal vasculopathy with cerebral leukodystrophy E H02251 Cerebroretinal microangiopathy with calcifications and cysts E H01798 Autosomal dominant neovascular inflammatory vitreoretinopathy E H01180 Sveinsson chorioretinal atrophy (SCRA) D 9B7Y Other specified disorders of the retina E H00690 Aland Island eye disease E H01088 Pigmented paravenous chorioretinal atrophy E H02469 Cone-rod synaptic disorder E H02642 Retinal arterial macroaneurysm with supravalvular pulmonic stenosis D 9B7Z Disorders of the retina, unspecified C Disorders of the vitreous body D 9B80 Inherited vitreoretinal disorders E H00805 Vitreoretinal degeneration E H02073 Wagner syndrome D 9B81 Posterior vitreous detachment D 9B82 Vitreous prolapse D 9B83 Vitreous haemorrhage D 9B84 Vitreous opacities, membranes or strands D 9B8Y Other specified disorders of the vitreous body D 9B8Z Disorders of the vitreous body, unspecified C 9C0Y Other specified disorders of the eyeball posterior segment C 9C0Z Disorders of the eyeball posterior segment, unspecified B Disorders of the eyeball affecting both anterior and posterior segments C 9C20 Panuveitis C 9C21 Endophthalmitis C 9C22 Eyeball deformity C 9C2Y Other specified disorders of the eyeball affecting both anterior and posterior segments C 9C2Z Disorders of the eyeball affecting both anterior and posterior segments, unspecified B Disorders of the visual pathways or centres C 9C40 Disorder of the optic nerve D H01719 Optic neuropathy D H01717 Optic neuritis D H00068 Leber hereditary optic atrophy D H01020 Optic atrophy D H01365 Leber hereditary optic neuropathy and dystonia D H01378 Bosch-Boonstra optic atrophy syndrome C 9C41 Disorder of optic chiasm C 9C42 Disorder of post chiasmal visual pathways C 9C43 Disorder of visual cortex C 9C44 Disorder of higher visual centres C 9C4Y Other specified disorders of the visual pathways or centres C 9C4Z Disorders of the visual pathways or centres, unspecified B Glaucoma or glaucoma suspect C 9C60 Glaucoma suspect C 9C61 Glaucoma D H00612 Primary open angle glaucoma D H01203 Primary congenital glaucoma C 9C6Y Other specified glaucoma or glaucoma suspect C 9C6Z Glaucoma or glaucoma suspect, unspecified B Strabismus or ocular motility disorders C 9C80 Non paralytic strabismus C 9C81 Ocular motor nerve palsies C 9C82 Disorders of extraocular muscles D H01118 Progressive external ophthalmoplegia D H01355 Kearns-Sayre syndrome D H01395 Autosomal recessive progressive external ophthalmoplegia D H00704 Oculopharyngeal muscular dystrophy D H02513 Oculopharyngodistal myopathy D H00633 Duane retraction syndrome D H00838 Congenital fibrosis of the extraocular muscles D H02151 Hereditary congenital facial paresis D H02693 Congenital cranial dysinnervation disorder with absent corneal reflex and developmental delay C 9C83 Disorders of binocular movement D H02450 Horizontal gaze palsy with progressive scoliosis C 9C84 Nystagmus D H00776 Congenital motor nystagmus (CMN) C 9C85 Certain specified irregular eye movements C 9C8Y Other specified strabismus or ocular motility disorders C 9C8Z Strabismus or ocular motility disorders, unspecified B Disorders of refraction or accommodation C 9D00 Disorders of refraction D H02041 Myopia C 9D01 Disorders of accommodation C 9D0Y Other specified disorders of refraction or accommodation C 9D0Z Disorders of refraction or accommodation, unspecified B Postprocedural disorders of eye or ocular adnexa C 9D20 Bullous aphakic keratopathy following cataract surgery C 9D21 Cataract lens fragments in eye following cataract surgery C 9D22 Chorioretinal scars after surgery for detachment C 9D23 Conjunctival blebitis after glaucoma surgery C 9D24 Complications with glaucoma drainage devices C 9D25 Glaucoma due to ocular surgery or laser B Impairment of visual functions C 9D41 Impairment of visual field C 9D42 Patterns of visual field impairment C 9D43 Impairment of contrast vision C 9D44 Impairment of colour vision D H00971 Achromatopsia D H00976 Colorblindness C 9D45 Impairment of light sensitivity D H00787 Congenital stationary night blindness C 9D46 Impairment of binocular functions C Subjective visual experiences D 9D50 Visual discomfort D 9D51 Transient visual loss D 9D52 Hemifield losses D 9D53 Entoptic phenomena D 9D54 Visual illusions D 9D55 Nonorganic visual loss D 9D56 Visual release hallucinations D 9D5Y Other specified subjective visual experiences D 9D5Z Subjective visual experiences, unspecified C 9D7Y Other specified impairment of visual functions D H00973 Bradyopsia C 9D7Z Impairment of visual functions, unspecified B Vision impairment C 9D90 Vision impairment including blindness C 9D92 Specific vision dysfunctions C 9D93 Complex vision-related dysfunctions C 9D94 Impairment of presenting visual acuity C 9D95 Impairment of best corrected visual acuity C 9D96 Impairment of uncorrected visual acuity C 9D9Y Other specified vision impairment C 9D9Z Vision impairment, unspecified B 9E1Y Other specified diseases of the visual system C H00169 Ocular albinism B 9E1Z Diseases of the visual system, unspecified # A10 Diseases of the ear or mastoid process B Diseases of external ear C Infectious diseases of external ear D AA00 Abscess of external ear D AA01 Cellulitis of external ear D AA02 Malignant otitis externa D AA03 Otomycosis D AA04 Perichondritis of external ear D AA0Y Other specified infectious diseases of external ear D AA0Z Infectious diseases of external ear, unspecified C Otitis externa D Noninfectious inflammation of external ear E AA10 Seborrhoeic otitis externa E AA11 Acute noninfectious otitis externa E AA12 Chondrodermatitis nodularis E AA13 Chronic otitis externa E AA1Y Other specified noninfectious inflammation of external ear E AA1Z Noninfectious inflammation of external ear, unspecified D AA3Y Other specified otitis externa D AA3Z Otitis externa, unspecified C Noninflammatory disorders of the external ear D AA40 Acquired deformity of external auditory canal D AA41 Acquired deformity of pinna D AA42 Impacted cerumen D AA4Y Other specified noninflammatory disorders of the external ear D AA4Z Noninflammatory disorders of the external ear, unspecified C AA6Z Diseases of external ear, unspecified B Diseases of middle ear or mastoid C Otitis media D Nonsuppurative otitis media E AA80 Acute serous or mucoid otitis media E AA81 Acute nonserous nonsuppurative otitis media E AA82 Chronic serous or mucoid otitis media E AA83 Noninfected otitis media with effusion E AA8Z Nonsuppurative otitis media, unspecified D Suppurative otitis media E AA90 Acute suppurative otitis media E AA91 Chronic suppurative otitis media E AA9Y Other specified suppurative otitis media E AA9Z Suppurative otitis media, unspecified D AB00 Acute otitis media D AB01 Chronic otitis media D AB0Y Other specified otitis media D AB0Z Otitis media, unspecified C AB10 Disorders of Eustachian tube C AB11 Mastoiditis or related conditions C AB12 Cholesteatoma of middle ear C AB13 Perforation of tympanic membrane C AB14 Acute myringitis C AB15 Chronic myringitis C AB16 Tympanosclerosis C AB17 Adhesive middle ear disease C AB18 Discontinuity or dislocation of ear ossicles C AB19 Acquired abnormalities of ear ossicles not related to discontinuity or dislocation C AB1A Polyp of middle ear C AB1B Middle ear cicatrix C AB1Y Other specified diseases of middle ear or mastoid C AB1Z Diseases of middle ear or mastoid, unspecified B Diseases of inner ear C AB30 Acute vestibular syndrome C AB31 Episodic vestibular syndrome D H01495 Meniere disease D H01706 Delayed endolymphatic hydrops C AB32 Chronic vestibular syndrome C AB33 Otosclerosis C AB34 Disorders of vestibular function C AB35 Labyrinthine fistula C AB36 Labyrinthine dysfunction C AB37 Noise effects on inner ear C AB3Y Other specified diseases of inner ear C AB3Z Diseases of inner ear, unspecified B Disorders with hearing impairment C AB50 Congenital hearing impairment D H00604 Deafness, autosomal dominant D H00605 Deafness, autosomal recessive D H01209 Deafness, X-linked D H02336 Deafness, Y-linked D H02636 Sinoatrial node dysfunction and deafness C AB51 Acquired hearing impairment D H01704 Sudden sensorineural hearing loss D H01705 Bilateral sudden sensorineural hearing loss C AB52 Deafness not otherwise specified C AB53 Ototoxic hearing loss C AB54 Presbycusis C AB55 Sudden idiopathic hearing loss C AB56 Hereditary hearing loss C AB57 Auditory synaptopathy or neuropathy D H02339 Auditory neuropathy C AB5Y Other specified disorders with hearing impairment C AB5Z Disorders with hearing impairment, unspecified B Disorders of ear, not elsewhere classified C AB70 Otalgia or effusion of ear C AB71 Degenerative or vascular disorders of ear C AB72 Disorders of acoustic nerve C AB73 Atrophy ear C AB7Y Other specified disorders of ear, not elsewhere classified B Postprocedural disorders of ear or mastoid process C AB90 Recurrent cholesteatoma of postmastoidectomy cavity C AB91 Mucosal cyst of postmastoidectomy cavity C AB92 Granulation of postmastoidectomy cavity C AB93 Chronic inflammation of postmastoidectomy cavity B AC0Y Other specified diseases of the ear or mastoid process B AC0Z Diseases of the ear or mastoid process, unspecified # A11 Diseases of the circulatory system B Hypertensive diseases C BA00 Essential hypertension D H01633 High blood pressure C BA01 Hypertensive heart disease C BA02 Hypertensive renal disease C BA03 Hypertensive crisis C BA04 Secondary hypertension D H00242 Liddle syndrome D H00603 Hypertension exacerbated in pregnancy B Hypotension C BA20 Idiopathic hypotension C BA21 Orthostatic hypotension C BA2Y Other specified hypotension C BA2Z Hypotension, unspecified B Ischaemic heart diseases C Acute ischaemic heart disease D BA40 Angina pectoris E H01632 Angina pectoris D BA41 Acute myocardial infarction E H01730 Myocardial infarction D BA42 Subsequent myocardial infarction D BA43 Coronary thrombosis not resulting in myocardial infarction D BA4Z Acute ischaemic heart disease, unspecified C Chronic ischaemic heart disease D BA50 Old myocardial infarction D BA51 Ischaemic cardiomyopathy D BA52 Coronary atherosclerosis D BA5Y Other specified chronic ischaemic heart disease D BA5Z Chronic ischaemic heart disease, unspecified C BA60 Certain current complications following acute myocardial infarction C BA6Z Ischaemic heart diseases, unspecified B Diseases of coronary artery C BA81 Coronary artery aneurysm C BA82 Coronary artery dissection C BA83 Coronary artery fistula, acquired C BA84 Chronic total occlusion of coronary artery C BA85 Coronary vasospastic disease C BA86 Coronary microvascular disease C BA8Y Other specified diseases of coronary artery C BA8Z Diseases of coronary artery, unspecified D H01742 Coronary artery disease B Pulmonary heart disease or diseases of pulmonary circulation C BB00 Pulmonary thromboembolism C BB01 Pulmonary hypertension D H01619 Primary pulmonary hypertension D H01621 Pulmonary arterial hypertension D H01866 Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis D H01622 Chronic thromboembolic pulmonary hypertension C BB02 Certain specified diseases of pulmonary vessels C BB03 Acquired pulmonary venous abnormality C BB0Y Other specified pulmonary heart disease or diseases of pulmonary circulation C BB0Z Pulmonary heart disease or diseases of pulmonary circulation, unspecified B Pericarditis C BB20 Acute pericarditis C BB21 Chronic rheumatic pericarditis C BB22 Constrictive pericarditis C BB23 Cardiac tamponade C BB24 Haemopericardium C BB25 Pericardial effusion C BB2Y Other specified pericarditis C BB2Z Pericarditis, unspecified B Acute or subacute endocarditis C BB40 Acute or subacute infectious endocarditis C BB41 Myoendocarditis C BB42 Periendocarditis C BB4Y Other specified acute or subacute endocarditis C BB4Z Acute or subacute endocarditis, unspecified B Heart valve diseases C Mitral valve disease D BB60 Mitral valve stenosis D BB61 Mitral valve insufficiency D BB62 Mitral valve prolapse E H01868 Mitral valve prolapse D BB63 Mitral valve stenosis with insufficiency D BB64 Mitral valvar abscess D BB65 Mitral valve rupture D BB6Y Other specified mitral valve disease D BB6Z Mitral valve disease, unspecified C Aortic valve disease D BB70 Aortic valve stenosis D BB71 Aortic valve insufficiency D BB72 Aortic valve stenosis with insufficiency D BB73 Aortic valvar abscess D BB74 Aortic valvar prolapse D BB7Y Other specified aortic valve disease D BB7Z Aortic valve disease, unspecified C Tricuspid valve disease D BB80 Tricuspid valve stenosis D BB81 Tricuspid valve insufficiency D BB82 Tricuspid valve stenosis with insufficiency D BB83 Tricuspid valvular abscess D BB84 Tricuspid valve rupture D BB8Y Other specified tricuspid valve disease D BB8Z Tricuspid valve disease, unspecified C Pulmonary valve disease D BB90 Pulmonary valve stenosis D BB91 Pulmonary valve insufficiency D BB92 Pulmonary valve stenosis with insufficiency D BB93 Pulmonary valvar abscess D BB9Y Other specified pulmonary valve disease D BB9Z Pulmonary valve disease, unspecified C BC00 Multiple valve disease C BC01 Prosthetic valve disease C BC02 Acquired abnormality of congenitally malformed valve C BC0Z Heart valve diseases, unspecified D H00334 Bacterial endocarditis B BC20 Chronic rheumatic heart diseases, not elsewhere classified B Diseases of the myocardium or cardiac chambers C BC40 Acquired atrial abnormality C BC41 Acquired ventricular abnormality C BC42 Myocarditis D H00295 Viral myocarditis C BC43 Cardiomyopathy D H00294 Dilated cardiomyopathy D H02697 Long-Olsen-Distelmaier syndrome D H00292 Hypertrophic cardiomyopathy D H01219 Restrictive cardiomyopathy D H00293 Arrhythmogenic right ventricular cardiomyopathy D H00669 Naxos disease D H02094 Carvajal syndrome D H02498 Diabetic cardiomyopathy D H02683 Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities C BC44 Noncompaction cardiomyopathy D H01216 Left ventricular noncompaction C BC45 Cardiomegaly C BC46 Intracardiac thrombosis C BC4Y Other specified diseases of the myocardium or cardiac chambers C BC4Z Diseases of the myocardium or cardiac chambers, unspecified B Cardiac arrhythmia C BC60 Atrial premature depolarization C BC61 Junctional premature depolarization C BC62 Accessory pathway C BC63 Conduction disorders D H01263 Progressive cardiac conduction defect (PCCD) D H02125 Cardiac conduction disease with or without dilated cardiomyopathy C BC64 Sudden arrhythmic death syndrome C BC65 Cardiac arrhythmia associated with genetic disorder D H00720 Long QT syndrome D H00748 Andersen-Tawil syndrome D H02091 Jervell and Lange-Nielsen syndrome D H00728 Brugada syndrome D H00725 Short QT syndrome D H00730 Familial idiopathic ventricular fibrillation D H01019 Catecholaminergic polymorphic ventricular tachycardia D H02122 Chronic atrial and intestinal dysrhythmia C Ventricular rhythm disturbance D BC70 Ventricular premature depolarization D BC71 Ventricular tachyarrhythmia E H02269 Familial ventricular tachycardia D BC7Y Other specified ventricular rhythm disturbance D BC7Z Ventricular rhythm disturbance, unspecified C Supraventricular rhythm disturbance D BC80 Supraventricular bradyarrhythmia E H02636 Sinoatrial node dysfunction and deafness E H00729 Sick sinus syndrome E H02674 Atrial standstill D BC81 Supraventricular tachyarrhythmia E H00731 Atrial fibrillation E H01154 Wolff-Parkinson-White (WPW) syndrome D BC8Y Other specified supraventricular rhythm disturbance D BC8Z Supraventricular rhythm disturbance, unspecified C BC90 Rhythm disturbance at level of atrioventricular junction C BC91 Pacemaker or implantable cardioverter defibrillator battery at end of battery life C BC9Y Other specified cardiac arrhythmia C BC9Z Cardiac arrhythmia, unspecified B Heart failure C BD10 Congestive heart failure C BD11 Left ventricular failure C BD12 High output syndromes C BD13 Right ventricular failure C BD14 Biventricular failure C BD1Y Other specified heart failure D H01631 Acute heart failure C BD1Z Heart failure, unspecified B Diseases of arteries or arterioles C BD30 Acute arterial occlusion C Chronic arterial occlusive disease D BD40 Atherosclerotic chronic arterial occlusive disease E H01626 Arteriosclerosis obliterans E H01629 Chronic arterial occlusive disease E H02505 Atherosclerosis D BD41 Non-atherosclerotic chronic arterial occlusive disease E H01629 Chronic arterial occlusive disease E H02719 Multifocal fibromuscular dysplasia D BD42 Raynaud phenomenon E H01620 Raynaud syndrome E H01629 Chronic arterial occlusive disease D BD4Y Other specified chronic arterial occlusive disease D BD4Z Chronic arterial occlusive disease, unspecified C BD50 Aortic aneurysm or dissection D H00801 Familial thoracic aortic aneurysm and dissection C BD51 Arterial aneurysm or dissection, excluding aorta C BD52 Certain specified disorders of arteries or arterioles D H00824 Calcification of joints and arteries D H01002 Generalized arterial calcification of infancy C BD53 Secondary disorders of arteries and arterioles C BD54 Diabetic foot ulcer C BD55 Asymptomatic stenosis of intracranial or extracranial artery C BD56 Asymptomatic occlusion of intracranial or extracranial artery C BD5Y Other specified diseases of arteries or arterioles C BD5Z Diseases of arteries or arterioles, unspecified B Diseases of veins C BD70 Superficial thrombophlebitis C BD71 Deep vein thrombosis D H01723 Deep vein thrombosis C BD72 Venous thromboembolism C BD73 Acquired systemic vein abnormality C BD74 Chronic peripheral venous insufficiency of lower extremities C BD75 Venous varicosities of sites other than lower extremity C BD7Y Other specified diseases of veins C BD7Z Diseases of veins, unspecified B Disorders of lymphatic vessels or lymph nodes C BD90 Lymphadenitis D H01397 Tick-borne lymphadenopathy C BD91 Lymphangitis C BD92 Lymphangiectasia C BD93 Lymphoedema D H00535 Lymphatic malformation D H01017 Choanal atresia and lymphedema D H02167 Lymphedema-distichiasis syndrome D H02168 Hypotrichosis-lymphedema-telangiectasia syndrome D H02169 Hennekam lymphangiectasia-lymphedema syndrome C BD9Y Other specified disorders of lymphatic vessels or lymph nodes C BD9Z Disorders of lymphatic vessels or lymph nodes, unspecified B Postprocedural disorders of circulatory system C BE10 Postcardiotomy syndrome C BE11 Other functional disturbances following cardiac surgery C BE12 Postprocedural valve disorders C BE13 Postprocedural true or false aortic aneurysm C BE14 Postprocedural disorder of circulatory system following repair of congenital heart or great vessel anomaly C BE15 Postprocedural pulmonary arterial tree disorder C BE16 Postprocedural pulmonary venous disorder C BE17 Postprocedural residual or recurrent interatrial communication C BE19 Postprocedural ventricular abnormality C BE1A Cardiac transplant associated coronary allograft vasculopathy C BE1B Lymphoedema due to surgery or radiotherapy C BE1C Inferior caval vein obstruction due to foreign body C BE1D Superior caval vein obstruction due to foreign body C BE1E Postprocedural right atrial complication C BE1F Postprocedural left atrial complication B BE2Y Other specified diseases of the circulatory system B BE2Z Diseases of the circulatory system, unspecified # A12 Diseases of the respiratory system B Upper respiratory tract disorders C CA00 Acute nasopharyngitis D H02442 Common cold C CA01 Acute sinusitis C CA02 Acute pharyngitis C CA03 Acute tonsillitis C CA04 Acute laryngopharyngitis C CA05 Acute laryngitis or tracheitis C CA06 Acute obstructive laryngitis or epiglottitis C CA07 Acute upper respiratory infections of multiple and unspecified sites C CA08 Vasomotor or allergic rhinitis D H01360 Allergic rhinitis C CA09 Chronic rhinitis, nasopharyngitis or pharyngitis C CA0A Chronic rhinosinusitis D H01765 Eosinophilic sinusitis C CA0B Silent sinus syndrome C CA0C Cyst or mucocele of nose or nasal sinus C CA0D Deviated nasal septum C CA0E Hypertrophy of nasal turbinates C CA0F Chronic diseases of tonsils or adenoids C CA0G Chronic laryngitis or laryngotracheitis C CA0H Diseases of vocal cords or larynx, not elsewhere classified C CA0J Nasal polyp C CA0K Abscess of upper respiratory tract C CA0Y Other specified upper respiratory tract disorders C CA0Z Upper respiratory tract disorders, unspecified B Certain lower respiratory tract diseases C CA20 Bronchitis C CA21 Emphysema C CA22 Chronic obstructive pulmonary disease D H01714 Chronic obstructive pulmonary disease (COPD) D H01873 Obliterative bronchiolitis C CA23 Asthma D H00079 Asthma D H01191 Asthma with nasal polyps and aspirin intolerance C CA24 Bronchiectasis D H00892 Bronchiectasis with or without elevated sweat chloride C CA25 Cystic fibrosis D H00218 Cystic fibrosis C CA26 Chronic bronchiolitis D H01873 Obliterative bronchiolitis D H01713 Diffuse panbronchiolitis C CA27 Tracheobronchitis C CA2Y Other specified lower respiratory tract disease C CA2Z Lower respiratory tract disease, unspecified B Lung infections C CA40 Pneumonia D H00351 Chlamydial pneumonia D H00304 Haemophilus influenzae infection D H00301 Klebsiella infection D H00341 Mycoplasma pneumonia D H01441 Pseudomonas aeruginosa infection D H00333 Streptococcal infection D H01321 Pneumococcal disease D H00401 Respiratory syncytial virus infection D H00400 Parainfluenza infection D H01063 Human metapneumovirus infection D H01521 Pneumocystis pneumonia C CA41 Acute bronchiolitis D H00401 Respiratory syncytial virus infection C CA42 Acute bronchitis D H00341 Mycoplasma pneumonia D H00401 Respiratory syncytial virus infection D H00400 Parainfluenza infection D H00304 Haemophilus influenzae infection C CA43 Abscess of lung or mediastinum C CA44 Pyothorax C CA45 Respiratory infections, not elsewhere classified C CA4Y Other specified lung infections C CA4Z Lung infections, unspecified B Lung diseases due to external agents C CA60 Pneumoconiosis C Pneumonitis D CA70 Hypersensitivity pneumonitis due to organic dust E H00346 Extrinsic allergic alveolitis E H01411 Saccharomonospora viridis infection D CA71 Pneumonitis due to solids and liquids D CA72 Mendelson syndrome D CA7Y Other specified pneumonitis D CA7Z Pneumonitis, unspecified C CA80 Airway disease due to specific organic dust C CA81 Respiratory conditions due to inhalation of chemicals, gases, fumes or vapours C CA82 Respiratory conditions due to other external agents C CA8Y Other specified lung diseases due to external agents C CA8Z Lung diseases due to external agents, unspecified B Respiratory diseases principally affecting the lung interstitium C CB00 Acute respiratory distress syndrome C CB01 Pulmonary oedema C CB02 Pulmonary eosinophilia C CB03 Idiopathic interstitial pneumonitis D H01716 Idiopathic interstitial pneumonias D H01299 Idiopathic pulmonary fibrosis C CB04 Primary interstitial lung diseases specific to infancy or childhood D H00830 Alveolar capillary dysplasia with misalignment of pulmonary veins D H00217 Pulmonary alveolar proteinosis D H01122 Congenital pulmonary alveolar proteinosis D H02124 Interstitial lung and liver disease D H00913 Brain-lung-thyroid syndrome C CB05 Interstitial lung diseases associated with systemic diseases D H02466 Rajab interstitial lung disease with brain calcification C CB06 Pulmonary alveolar microlithiasis D H01298 Pulmonary alveolar microlithiasis C CB07 Lymphangioleiomyomatosis D H00896 Lymphangioleiomyomatosis C CB0Y Other specified respiratory diseases principally affecting the lung interstitium C CB0Z Respiratory diseases principally affecting the lung interstitium, unspecified B Pleural, diaphragm or mediastinal disorders C CB20 Pleural plaque C CB21 Pneumothorax D H01110 Pneumothorax C CB22 Diseases of mediastinum, not elsewhere classified C CB23 Disorders of diaphragm C CB24 Chylous effusion C CB25 Fibrothorax C CB26 Haemothorax C CB27 Pleural effusion C CB2Y Other specified pleural, diaphragm or mediastinal disorders C CB2Z Pleural, diaphragm or mediastinal disorders, unspecified B CB40 Certain diseases of the respiratory system B CB41 Respiratory failure B Postprocedural disorders of the respiratory system C CB60 Tracheostomy malfunction C CB61 Chronic pulmonary insufficiency following surgery C CB62 Postprocedural subglottic stenosis C CB63 Postprocedural stenosis of the trachea C CB64 Transfusion related acute lung injury B CB7Z Diseases of the respiratory system, unspecified # A13 Diseases of the digestive system B Diseases or disorders of orofacial complex C DA00 Disorders of lips C DA01 Disorders of oral mucosa D H02648 Acantholytic blistering of the oral and laryngeal mucosa C DA02 Miscellaneous specified disorders of lips or oral mucosa D H00724 White sponge nevus C DA03 Diseases of tongue C DA04 Diseases of salivary glands C DA05 Cysts of oral or facial-neck region C DA06 Certain specified diseases of jaws C DA07 Disorders of tooth development or eruption D H00680 Primary failure of tooth eruption C DA08 Diseases of hard tissues of teeth D H01331 Dental caries C DA09 Diseases of pulp or periapical tissues C DA0A Certain specified disorders of teeth or supporting structures C DA0B Gingival diseases C DA0C Periodontal disease D H01408 Periodontal disease D H02050 Prepubertal periodontitis D H01317 Aggressive periodontitis C DA0D Certain specified disorders of gingiva or edentulous alveolar ridge D H01250 Hereditary gingival fibromatosis C DA0E Dentofacial anomalies C DA0F Sensory disturbances affecting orofacial complex C DA0Y Other specified diseases or disorders of orofacial complex C DA0Z Diseases or disorders of orofacial complex, unspecified D H01407 Capnocytophaga ochracea infection B Diseases of oesophagus C DA20 Acquired anatomical alterations of the oesophagus C DA21 Motility disorders of oesophagus C DA22 Gastro-oesophageal reflux disease D H01602 Gastroesophageal reflux disease C DA23 Columnar metaplastic epithelium of the oesophagus D H01901 Barrett esophagus C DA24 Oesophagitis D H01361 Eosinophilic esophagitis C DA25 Oesophageal ulcer C DA26 Vascular disorders of the oesophagus C DA2Y Other specified diseases of oesophagus C DA2Z Diseases of oesophagus, unspecified B Diseases of the stomach or the duodenum C Diseases of stomach D DA40 Acquired anatomical alterations of the stomach D DA41 Gastroduodenal motor or secretory disorders D DA42 Gastritis D DA43 Vascular disorders of the stomach D DA44 Gastric polyp D DA4Y Other specified diseases of stomach C Diseases of duodenum D DA50 Acquired anatomical alterations of the duodenum D DA51 Duodenitis E H00320 Helicobacter pylori infection D DA52 Vascular disorders of the duodenum D DA53 Duodenal polyp D DA5Y Other specified diseases of duodenum C Ulcer of stomach or duodenum D DA60 Gastric ulcer E H01634 Peptic ulcer E H00320 Helicobacter pylori infection E H02504 Gastrointestinal ulceration, recurrent, with dysfunctional platelets D DA61 Peptic ulcer, site unspecified E H01634 Peptic ulcer D DA62 Anastomotic ulcer E H01634 Peptic ulcer E H00320 Helicobacter pylori infection D DA63 Duodenal ulcer E H01634 Peptic ulcer E H00320 Helicobacter pylori infection C DA7Z Diseases of the stomach or the duodenum, unspecified B Diseases of small intestine C DA90 Nonstructural developmental anomalies of small intestine D H01805 Tricho-hepato-enteric syndrome D H01276 Chronic idiopathic intestinal pseudo-obstruction D H02553 Visceral myopathy C DA91 Obstruction of small intestine C DA92 Other acquired anatomical alterations of small intestine C DA93 Motility disorders of small intestine C DA94 Noninfectious enteritis or ulcer of small intestine D H01853 Chronic nonspecific multiple ulcers of the small intestine C DA95 Coeliac disease D H02123 Celiac disease C DA96 Intestinal malabsorption or protein-losing enteropathy D H00352 Whipple disease D H00988 Enterokinase deficiency D H01016 Primary bile acid malabsorption D H01935 Familial hypercholanemia C DA97 Certain vascular disorders of small intestine C DA98 Polyps of small intestine C DA9Y Other specified diseases of small intestine C DA9Z Diseases of small intestine, unspecified B Diseases of appendix C DB10 Appendicitis C DB11 Certain specified diseases of appendix C DB1Y Other specified diseases of appendix C DB1Z Diseases of appendix, unspecified B Diseases of large intestine C DB30 Obstruction of large intestine C DB31 Other acquired anatomical alterations of large intestine C DB32 Motility disorders of large intestine D H01871 Isolated hypoganglionosis C DB33 Certain noninfectious colitis or proctitis C DB34 Certain vascular disorders of large intestine C DB35 Polyp of large intestine C DB36 Certain infections of the large intestine C DB3Y Other specified diseases of large intestine C DB3Z Diseases of large intestine, unspecified B Diseases of anal canal C Acquired anatomical alterations of the anal canal D DB50 Fissure or fistula of anal regions D DB51 Stenosis of anal canal D DB52 Ulcer of anus D DB53 Anal prolapse D DB5Y Other specified acquired anatomical alterations of the anal canal D DB5Z Acquired anatomical alterations of the anal canal, unspecified C Haemorrhoids or perianal venous conditions D DB60 Haemorrhoids D DB61 Perianal venous thrombosis D DB62 Residual haemorrhoidal skin tags D DB6Y Other specified haemorrhoids or perianal venous conditions D DB6Z Haemorrhoids or perianal venous conditions, unspecified C DB70 Infections of the anal region C DB71 Anal polyp C DB72 Certain specified diseases of anal canal C DB7Y Other specified diseases of anal canal C DB7Z Diseases of anal canal, unspecified B Diseases of liver C DB90 Infectious liver disease C DB91 Acute or subacute hepatic failure D H01712 Fulminant hepatic failure C DB92 Non-alcoholic fatty liver disease D H01333 Non-alcoholic fatty liver disease C DB93 Hepatic fibrosis or cirrhosis D H02194 North American Indian childhood cirrhosis D H02225 Familial cirrhosis C DB94 Alcoholic liver disease D H02516 Alcoholic liver disease C DB95 Drug-induced or toxic liver disease C DB96 Autoimmune liver disease D H01685 Autoimmune hepatitis D H01467 Primary biliary cholangitis D H01684 Primary sclerosing cholangitis D H00742 Neonatal ichthyosis-sclerosing cholangitis (NISCH) syndrome C DB97 Certain specified inflammatory liver diseases C DB98 Vascular disorders of the liver D H01687 Extrahepatic portal vein obstruction D H01433 Budd-Chiari syndrome D H01686 Idiopathic portal hypertension C DB99 Certain specified diseases of liver D H00545 Polycystic liver disease D H01506 Hepatic encephalopathy C DB9Z Diseases of liver, unspecified B Diseases of gallbladder or biliary tract C DC10 Acquired anatomical alterations of gallbladder or bile ducts C DC11 Cholelithiasis D H01213 Gallbladder disease D H01679 Intrahepatic lithiasis C DC12 Cholecystitis D H01213 Gallbladder disease C DC13 Cholangitis C DC14 Certain specified biliary diseases C DC1Y Other specified diseases of gallbladder or biliary tract C DC1Z Diseases of gallbladder or biliary tract, unspecified B Diseases of pancreas C DC30 Cystic diseases of the pancreas C DC31 Acute pancreatitis D H01681 Acute pancreatitis C DC32 Chronic pancreatitis D H01680 Chronic pancreatitis D H00933 Hereditary pancreatitis D H00932 Tropical calcific pancreatitis C DC33 Autoimmune pancreatitis C DC34 Obstructive pancreatitis C DC35 Certain specified diseases of pancreas C DC3Y Other specified diseases of pancreas C DC3Z Diseases of pancreas, unspecified B Diseases of peritoneum C DC50 Peritonitis C DC51 Certain specified disorders of peritoneum or retroperitoneum C DC5Z Diseases of peritoneum, unspecified B Diverticular disease of intestine C Diverticular disease of small intestine D DC70 Diverticulitis of small intestine D DC71 Diverticulosis of small intestine D DC72 Diverticulum of small intestine C Diverticular disease of large intestine D DC80 Diverticulitis of large intestine D DC81 Diverticulosis of large intestine D DC82 Diverticulum of large intestine C Diverticular disease of intestine of overlapping sites D DC90 Diverticular disease of small and large intestine C Diverticular disease of unspecified part of intestine D DD00 Diverticulitis of unspecified part of intestine D DD01 Diverticulosis of unspecified part of intestine D DD02 Diverticulum of unspecified part of intestine C DD1Z Diverticular disease of intestine, unspecified B Ischaemic vascular disorders of intestine C DD30 Acute vascular disorders of intestine C DD31 Chronic vascular disorders of intestine C DD3Y Other specified ischaemic vascular disorders of intestine C DD3Z Ischaemic vascular disorders of intestine, unspecified B Hernias C DD50 Non-abdominal wall hernia C DD51 Inguinal hernia C DD52 Femoral hernia C DD53 Umbilical hernia C DD54 Paraumbilical hernia C DD55 Epigastric hernia C DD56 Incisional hernia C DD57 Parastomal hernia C DD5Y Other specified hernias C DD5Z Hernias, unspecified B Inflammatory bowel diseases C DD70 Crohn disease D H00286 Crohn disease D H01227 Inflammatory bowel disease (IBD) C DD71 Ulcerative colitis D H01227 Inflammatory bowel disease (IBD) D H01466 Ulcerative colitis C DD72 Indeterminate colitis D H01227 Inflammatory bowel disease (IBD) C DD7Y Other specified inflammatory bowel diseases C DD7Z Inflammatory bowel diseases, unspecified B Functional gastrointestinal disorders C DD90 Functional oesophageal or gastroduodenal disorders C DD91 Irritable bowel syndrome or certain specified functional bowel disorders D H01615 Irritable bowel syndrome C DD92 Functional anorectal disorders C DD93 Functional digestive disorders of infants, toddlers or children C DD94 Functional gallbladder disorder C DD95 Functional sphincter of Oddi disorder C DD9Y Other specified functional gastrointestinal disorders C DD9Z Functional gastrointestinal disorders, unspecified B Postprocedural disorders of digestive system C DE10 Vomiting following gastrointestinal surgery C DE11 Dumping syndrome C DE12 Malfunction or complication of external stoma of digestive organs C DE13 Postsurgical malabsorption, not elsewhere classified B DE2Y Other specified diseases of the digestive system B DE2Z Diseases of the digestive system, unspecified # A14 Diseases of the skin B Certain skin disorders attributable to infection or infestation C Certain skin disorders attributable to viral infection D Viral exanthems E EA00 Viral exanthem due to unknown or unspecified agent E EA0Y Viral exanthem due to other specified virus D Certain dermatoses with suspected viral aetiology E EA10 Pityriasis rosea F H01660 Pityriasis rosea E EA11 Papular purpuric gloves and socks syndrome E EA12 Infantile papular acrodermatitis D Dermatoses from distant or systemic viral infection E EA20 Necrolytic acral erythema D EA3Z Unspecified skin disorder attributable to viral infection C Certain skin disorders attributable to bacterial infection D Predominantly tropical or subtropical bacterial infections affecting skin E EA40 Tropical phagedaenic ulcer D EA50 Toxin-mediated cutaneous reactions to distant or systemic bacterial infection D EA51 Skin complications of BCG immunisation D EA5Y Cutaneous involvement by other specified bacterial infection D EA5Z Cutaneous involvement by unspecified bacterial infection C EA60 Certain skin disorders attributable to fungal infection C EA6Y Cutaneous involvement by other specified infection or infestation B Inflammatory dermatoses C Dermatitis and eczema D EA80 Atopic eczema E H01358 Atopic dermatitis D EA81 Seborrhoeic dermatitis and related conditions E H00795 Seborrhea-like dermatitis with psoriasiform element E H01652 Seborrheic dermatitis D EA82 Nummular dermatitis D EA83 Lichen simplex or lichenification D EA84 Asteatotic eczema D EA85 Dermatitis or eczema of hands and feet D EA86 Dermatitis and eczema of lower legs D EA87 Dermatitis or eczema of anogenital region D EA88 Miscellaneous specified eczematous dermatoses D EA89 Generalised eczematous dermatitis of unspecified type D EA8Y Other specified eczematous dermatosis D EA8Z Dermatitis or eczema, unspecified C Papulosquamous dermatoses D EA90 Psoriasis E H01656 Psoriasis E H01663 Pustular psoriasis D EA91 Lichen planus E H01654 Lichen planus D EA92 Lichenoid dermatoses D EA93 Pityriasis lichenoides D EA94 Pityriasis rubra pilaris E H01659 Pityriasis rubra pilaris D EA95 Small plaque parapsoriasis C Urticaria, angioedema and other urticarial disorders D EB00 Spontaneous urticaria D EB01 Inducible urticaria and angioedema E H01799 Vibratory urticaria D EB02 Cholinergic urticaria and related conditions D EB03 Syndromes with urticarial reactions or angioedema D EB04 Idiopathic angioedema D EB05 Urticaria of unspecified type D EB0Y Other specified urticarial disorders C Inflammatory erythemas and other reactive inflammatory dermatoses D EB10 Diffuse inflammatory erythemas D EB11 Annular erythema D EB12 Erythema multiforme E H01695 Erythema multiforme D EB13 Stevens-Johnson syndrome or toxic epidermal necrolysis E H01694 Stevens-Johnson syndrome D Neutrophilic dermatoses E EB20 Acute febrile neutrophilic dermatosis F H02590 Acute febrile neutrophilic dermatosis E EB21 Pyoderma gangrenosum E EB2Y Other specified neutrophilic dermatoses D EB30 Eosinophilic cellulitis D EB31 Erythema nodosum E H01473 Erythema nodosum leprosum C Immunobullous diseases of the skin D EB40 Pemphigus E H01648 Pemphigus D EB41 Pemphigoid E H01650 Pemphigoid D EB42 Linear IgA bullous dermatosis D EB43 Epidermolysis bullosa acquisita D EB44 Dermatitis herpetiformis E H01362 Dermatitis herpetiformis D EB4Y Other specified immunobullous disorder C Cutaneous lupus erythematosus D EB50 Subacute cutaneous lupus erythematosus E H01595 Cutaneous lupus erythematosus D EB51 Chronic cutaneous lupus erythematosus E H01595 Cutaneous lupus erythematosus D EB5Z Cutaneous lupus erythematosus of unspecified type C Scarring or sclerosing inflammatory dermatoses D EB60 Lichen sclerosus E H01690 Lichen sclerosus et atrophicus D EB61 Morphoea E H01493 Localized Scleroderma C EB7Y Other specified inflammatory dermatoses B Metabolic and nutritional disorders affecting the skin C EB90 Dermatoses resulting from disturbed metabolic processes D H01661 Xanthoma C EB9Y Other specified metabolic and nutritional disorders affecting the skin B Genetic and developmental disorders affecting the skin C Genetic syndromes affecting the skin D EC10 Genetic syndromes with poikiloderma E H00793 Poikiloderma with neutropenia E H01906 Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis D EC1Y Other specified genetic syndromes affecting the skin C EC20 Genetic disorders of keratinisation D H01771 Congenital ichthyosis D H00735 Ichthyosis vulgaris D H00134 X-linked ichthyosis D H00733 Harlequin ichthyosis D H00734 Autosomal recessive congenital ichthyosis D H00691 Bullous congenital ichthyosiform erythroderma (BCIE) D H00693 Ichthyosis bullosa of Siemens D H00707 Ichthyosis hystrix, Curth-Macklin type D H02265 Annular epidermolytic ichthyosis D H00710 Erythrokeratodermia variabilis D H00738 Ichthyosis with confetti D H00790 Keratosis linearis with ichthyosis congenita and sclerosing keratoderma D H02449 Autosomal dominant lamellar ichthyosis D H00737 Peeling skin syndrome D H00715 Darier disease D H00844 Familial benign chronic pemphigus D H00716 Palmoplantar keratoderma with deafness D H00274 Papillon-Lefevre syndrome D H00695 Mal de Meleda D H00714 Vohwinkel syndrome D H00722 Epidermolytic palmoplantar keratoderma D H00723 Non-epidermolytic palmoplantar keratoderma D H02264 Palmoplantar keratoderma, Nagashima type D H02266 Palmoplantar keratoderma, Bothnian type D H02517 Olmsted syndrome D H00717 Striate palmoplantar keratoderma D H02263 Focal nonepidermolytic palmoplantar keratoderma D H02702 Tylosis with esophageal cancer D H00755 Acrokeratosis verruciformis D H01394 Cole disease C EC21 Genetic defects of hair or hair growth D H00667 Woolly hair D H00670 Monilethrix D H01796 Uncombable hair syndrome D H00820 Bjornstad syndrome D H00866 Trichothiodystrophy D H00893 Cardiomyopathy, dilated, with woolly hair and keratoderma D H00780 Atrichia with papular lesions D H00784 Localized autosomal recessive hypotrichosis D H00786 Hypotrichosis D H00858 Marie-Unna hereditary hypotrichosis D H00782 Hypotrichosis and recurrent skin vesicles C EC22 Genetic defects of nails or nail growth D H00683 Anonychia congenita D H01307 Nonsyndromic congenital nail disorder C EC23 Genetic disorders of skin pigmentation D H00884 Familial progressive hyperpigmentation D H00944 Dowling-Degos disease D H02188 Watson syndrome D H00166 Hermansky-Pudlak syndrome D H00168 Oculocutaneous albinism D H02021 Chediak-Higashi syndrome D H00170 Piebaldism D H00759 Waardenburg syndrome D H00885 Hypomelanosis of Ito D H01187 Tietz syndrome D H02022 Griscelli syndrome D H00880 Dyschromatosis symmetrica hereditaria D H02350 Dyschromatosis universalis hereditaria D H02665 Reticulate acropigmentation of Kitamura C Genetically-determined epidermolysis bullosa D EC30 Epidermolysis bullosa simplex E H00584 Epidermolysis bullosa simplex E H00585 Epidermolysis bullosa, hemidesmosomal E H00644 Ectodermal dysplasia/skin fragility syndrome D EC31 Junctional epidermolysis bullosa E H00586 Epidermolysis bullosa, junctional D EC32 Dystrophic epidermolysis bullosa E H00587 Epidermolysis bullosa, dystrophica E H00763 Transient bullous dermolysis of the newborn D EC33 Syndromic epidermolysis bullosa E H00588 Kindler syndrome D EC3Z Epidermolysis bullosa E H00813 Laryngo onycho cutaneous syndrome E H01737 Epidermolysis bullosa C Genetic disorders affecting dermal collagen, elastin or other matrix proteins D EC40 Pseudoxanthoma elasticum E H00560 Pseudoxanthoma elasticum D EC4Y Other specified genetic disorders affecting dermal matrix proteins C Specified developmental anomalies affecting the skin D EC50 Developmental anomalies of the umbilicus D EC5Y Other specified developmental anomalies affecting the skin C EC7Y Other specified genetic and developmental disorders affecting the skin B Sensory and psychological disorders affecting the skin C Disturbances of cutaneous sensation D EC90 Pruritus D EC91 Prurigo D EC92 Mucocutaneous or cutaneous pain syndromes D EC9Y Other specified disturbances of cutaneous sensation C Psychological or psychiatric conditions affecting the skin D Self-inflicted skin disorders E ED00 Artefactual skin disorder E ED01 Simulated skin disease E ED02 Painful bruising syndrome E ED0Y Other specified self-inflicted skin disorders D ED2Y Other specified psychological or psychiatric conditions affecting the skin C Neurological conditions affecting the skin D ED30 Neuropathic skin damage D ED31 Burning feet syndrome D ED3Y Cutaneous involvement in other specified neurological condition B Skin disorders involving specific cutaneous structures C Disorders of the epidermis and epidermal appendages D Disorders of epidermal keratinisation E ED50 Ichthyoses E ED51 Diffuse epidermal hyperkeratosis and acanthosis E ED52 Porokeratoses F H00791 Disseminated superficial actinic porokeratosis (DSAP) F H01933 Porokeratosis E ED53 Skin peeling E ED54 Xerosis cutis or asteatosis E ED55 Palmoplantar keratodermas F H01673 Palmoplantar keratoderma F H02318 Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal E ED56 Keratosis pilaris F H00750 Keratosis pilaris atrophicans E ED5Y Other specified disorders of epidermal keratinisation D Disorders of skin colour E ED60 Acquired hypermelanosis E ED61 Acquired melanotic macules or lentigines E ED62 Endogenous non-melanin pigmentation E ED63 Acquired hypomelanotic disorders F H01372 Vitiligo F H01504 Vogt-Koyanagi-Harada syndrome E ED64 Abnormal skin pigmentation E ED6Y Other specified disorders of skin pigmentation D Disorders of hair E ED70 Alopecia or hair loss F H01158 Alopecia universalis E ED71 Hypertrichosis E ED72 Hirsutism and syndromes with hirsutism E ED73 Acquired disorders of the hair shaft E ED7Y Other specified disorders of hair D Disorders of the hair follicle E Acne and related disorders F ED80 Acne G H01445 Acne vulgaris F ED81 Acneform inflammatory disorders E ED90 Rosacea and related disorders E ED91 Disorders of the sebaceous gland E ED92 Disorders involving the apocrine follicular unit F H00681 Acne inversa E ED9Y Other specified disorders involving the hair follicle F H00672 Pseudofolliculitis barbae D Disorders of eccrine sweat glands or sweating E EE00 Hyperhidrosis E EE01 Hypohidrosis F H01848 Acquired idiopathic generalized anhidrosis F H02281 Isolated anhidrosis with normal sweat glands E EE02 Miliaria E EE0Y Other specified disorders of eccrine sweat glands or sweating D Disorders of the nail or perionychium E EE10 Acquired deformities of the nail plate E EE11 Acquired abnormalities of nail colour E EE12 Infections of the nail or perionychium E EE13 Certain disorders affecting the nails or perionychium E EE1Y Other specified disorders of the nail or perionychium E EE1Z Disorders of the nail or perionychium, unspecified D Disorders of epidermal integrity E EE20 Acute cutaneous distension syndrome E EE21 Epidermal fragility C Disorders of the dermis and subcutis D Disorders of cutaneous connective tissue E EE40 Atrophy or degeneration of dermal or subcutaneous connective tissue E EE41 Abnormalities of dermal elastin F H00557 Cutis laxa E Poikiloderma F EE50 Acquired poikiloderma E Fibromatoses and keloids F EE60 Keloid or hypertrophic scars F EE61 Superficial fibromatoses F EE6Y Other specified fibromatous disorders of skin and soft tissue G H00663 Restrictive dermopathy G H01173 Stiff skin syndrome E EE70 Perforating dermatoses E EE7Y Other specified disorders of cutaneous connective tissue D Histiocytic-granulomatous disorders of the skin E EE80 Necrobiotic granulomatous skin disorders E EE81 Dermal dendrocyte, Class IIa histiocytoses E EE8Y Other specified histiocytic and granulomatous disorders of the skin D Benign dermal lymphocytic or lymphoplasmacytic infiltrations or proliferations E EE90 Benign lymphocytic infiltration of the skin E EE91 Lymphocytoma cutis D Disorders of subcutaneous fat E EF00 Panniculitis E EF01 Lipoatrophy or lipodystrophy F H01475 Lipodystrophy E EF02 Certain noninflammatory disorders of subcutaneous fat E EF0Y Other specified disorders of subcutaneous fat C Disorders of cutaneous blood and lymphatic vessels D Malformations involving cutaneous blood vessels E EF20 Acquired malformations of cutaneous blood vessels E EF2Z Cutaneous vascular malformation, unspecified D Purpura or bruising E EF30 Purpura or bruising due to disorders of coagulation E EF31 Traumatic purpura E EF3Y Other specified purpura E EF3Z Purpura of unspecified aetiology D EF40 Vasculitis or capillaritis involving the skin D Dermatoses attributable to hyperviscosity or microvascular occlusion E EF50 Livedoid vasculopathy E EF5Y Other specified dermatoses attributable to hyperviscosity or microvascular occlusion D Dermatoses resulting from vascular insufficiency E EF60 Ischaemic ulceration of skin E Dermatoses due to venous disease F EF70 Lower limb venous eczema F EF7Y Other specified dermatoses due to venous disease F EF7Z Dermatoses due to venous disease, unspecified E EF9Y Other specified dermatoses resulting from vascular insufficiency D Functional vascular disorders of the skin E EG00 Vasodilatation of extremities F H00771 Inherited erythromelalgia E EG01 Vasoconstriction of extremities E EG02 Flushing disorders B Skin disorders involving certain specific body regions C Skin disorders involving the head and neck D EG30 Skin disorders localised to the scalp E H01446 Propionibacterium acnes infection D Disorders of the external ear involving the skin E Inflammatory disorders of the external ear F EG40 Contact dermatitis of external ear F EG4Y Other specified inflammatory disorder of external ear F EG4Z Inflammatory disorder of external ear, unspecified C Skin disorders involving the genital and perianal regions D Dermatoses of the anus, perianal area or perineum E EG60 Anal pruritus E EG61 Infections of the anus or perianal skin E EG62 Inflammatory dermatoses of the perianal area E EG63 Sacrococcygeal pilonidal disease D EG7Y Other specified skin disorders involving the genital and perianal regions C EG9Y Skin disorders involving other specific body regions C EG9Z Skin disorders involving certain specific body regions, unspecified B Skin disorders associated with pregnancy, the neonatal period and infancy C Skin disorders specific to the perinatal or neonatal period D Neonatal skin infection E EH10 Neonatal viral infections involving the skin E EH11 Neonatal pyogenic skin infections E EH12 Neonatal fungal infections involving the skin E EH1Z Neonatal skin infection, unspecified D EH3Y Other specified skin disorders specific to the perinatal or neonatal period C EH40 Dermatoses of infancy B Adverse cutaneous reactions to medication C Drug eruptions D EH60 Exanthematic drug eruption D EH61 Drug-induced urticaria, angioedema and anaphylaxis D EH62 Lichenoid drug eruption D EH63 Stevens-Johnson syndrome and toxic epidermal necrolysis due to drug D EH64 Drug-induced erythroderma D EH65 DRESS syndrome D EH66 Fixed drug eruption D EH67 Acne or acneform reactions attributable to drugs D EH6Y Drug eruption of other specified type D EH6Z Drug eruption of unspecified type C EH70 Pigmentary abnormalities of skin due to drug C EH71 Dermatoses precipitated by drug therapy C EH72 Drug-induced hair abnormalities C EH73 Drug-induced nail abnormalities C EH74 Drug-induced oral conditions C EH75 Photosensitivity due to drug C EH76 Dermatoses associated with specific classes of medication C EH77 Localised adverse cutaneous reactions to administration of drug C EH78 Adverse cutaneous reactions to herbal, homoeopathic or other alternative therapies C EH7Y Other specified adverse cutaneous reactions to medication C EH7Z Unspecified adverse cutaneous reactions to medication B Skin disorders provoked by external factors C EH90 Pressure ulceration C EH92 Dermatoses provoked by friction or mechanical stress C EH93 Dermatoses due to foreign bodies C EH94 Scar of skin, not elsewhere classified C Dermatoses provoked or exacerbated by exposure to cold D EJ0Y Other specified dermatoses provoked or exacerbated by exposure to cold C Dermatoses provoked by heat or electricity D EJ10 Erythema ab igne D EJ1Y Other specified dermatoses provoked by heat or electricity C Dermatoses provoked by light or UV radiation D Chronic effects of ultraviolet radiation on the skin E EJ20 Photoaging of the skin E EJ2Y Other specified chronic effects of ultraviolet radiation on the skin D EJ30 Autoimmune or other photodermatoses D Acute effects of ultraviolet radiation on normal skin E EJ40 Sunburn E EJ41 Burn from exposure to artificial source of ultraviolet radiation E EJ4Z Acute effects of ultraviolet radiation on normal skin, unspecified D EJ6Y Other specified dermatoses provoked by light or UV radiation E H02131 UV-sensitive syndrome C Dermatoses due to ionizing radiation D EJ71 Chronic effects of ionizing radiation on the skin D EJ7Z Dermatoses due to ionizing radiation, unspecified C EK00 Allergic contact dermatitis D H01357 Allergic contact dermatitis C EK01 Photo-allergic contact dermatitis C EK02 Irritant contact dermatitis C EK10 Allergic contact urticaria C EK11 Protein contact dermatitis C EK12 Allergic contact sensitisation C Phototoxic reactions to skin contact with photoactive agents D EK20 Phototoxic reaction to fragrance or cosmetics D EK2Y Phototoxic reaction to skin contact with other specified photoactive agent D EK2Z Phototoxic dermatitis, unspecified C EK50 Cutaneous reactions to venomous or noxious animals C EK5Y Other specified skin disorders provoked by external factors B Benign proliferations, neoplasms and cysts of the skin C EK70 Cutaneous cysts C EK71 Skin tags or polyps B Disorders of the skin of uncertain or unpredictable malignant potential C EK90 Actinic keratosis and other discrete epidermal dysplasias D H02429 Actinic keratosis C EK91 Dermatoses which may presage cutaneous lymphoma C EK92 Histiocytoses of uncertain malignant potential D H01168 Sea-blue histiocyte disease B Cutaneous markers of internal disorders C Cutaneous markers of internal malignancy D EL10 Paraneoplastic syndromes involving skin D EL1Y Other specified cutaneous markers of internal malignancy C EL3Y Other specified cutaneous markers of internal disorders B Postprocedural disorders of the skin C EL50 Unsatisfactory surgical scar of skin C EL51 Cutaneous flap necrosis C EL52 Myocutaneous flap necrosis C EL53 Skin graft failure C EL54 Composite graft failure C Adverse cutaneous effects of therapeutic ionizing irradiation D EL60 Acute radiodermatitis following radiotherapy D EL61 Chronic radiodermatitis following radiotherapy D EL63 Radionecrosis of skin due to therapeutic ionizing irradiation C Complications of cutaneous cosmetic procedures D EL73 Unsatisfactory outcome from cutaneous cosmetic surgical procedure C EL80 Adverse cutaneous effects of diagnostic procedures B EM0Y Other specified diseases of the skin B EM0Z Skin disease of unspecified nature # A15 Diseases of the musculoskeletal system or connective tissue B Arthropathies C Osteoarthritis D FA00 Osteoarthritis of hip D FA01 Osteoarthritis of knee D FA02 Osteoarthritis of wrist or hand D FA03 Osteoarthritis of other specified joint D FA04 Oligoosteoarthritis D FA05 Polyosteoarthritis D FA0Z Osteoarthritis, unspecified C Infection related arthropathies D FA10 Direct infections of joint E H01442 Septic arthritis D FA11 Reactive arthropathies D FA12 Postinfectious arthropathies D FA13 Infectious spondyloarthritis D FA1Y Other specified infection related arthropathies D FA1Z Infection related arthropathies, unspecified C Inflammatory arthropathies D FA20 Rheumatoid arthritis E H00630 Rheumatoid arthritis D FA21 Psoriatic arthritis D FA22 Polymyalgia rheumatica E H01606 Polymyalgia rheumatica D FA23 Adult-onset Still disease E H01516 Adult onset Still disease D FA24 Juvenile idiopathic arthritis E H01672 Juvenile idiopathic arthritis D FA25 Gout E H01532 Gout D FA26 Certain specified crystal arthropathies E H01236 Familial articular chondrocalcinosis D FA27 Certain specified inflammatory arthropathies E H01507 Seronegative arthritis D FA2Z Inflammatory arthropathies, unspecified C Certain specified joint disorders or deformities of limbs D FA30 Acquired deformities of fingers or toes D FA31 Other acquired deformities of limbs D FA32 Disorders of patella D FA33 Internal derangement of knee D FA34 Certain specified joint derangements D FA35 Wear of articular bearing surface of joint prosthesis D FA36 Effusion of joint D FA37 Certain joint disorders, not elsewhere classified D FA38 Arthropathy in diseases classified elsewhere D FA3Z Unspecified joint disorders and deformities of limbs C FA5Y Other specified arthropathies C FA5Z Arthropathies, unspecified B Conditions associated with the spine C Structural disorders of spine D FA70 Spinal deformities D FA71 Torticollis D FA72 Disorders of vertebra E H01708 Diffuse idiopathic skeletal hyperostosis D FA7Y Other specified structural disorders of spine D FA7Z Structural disorders of spine, unspecified C Degenerative condition of spine D FA80 Intervertebral disc degeneration E H02539 Intervertebral disc disease D FA81 Spondylolysis D FA82 Spinal stenosis E H01711 Spinal stenosis D FA83 Ossification of spinal ligaments E H00431 Ossification of the posterior longitudinal ligament of spine E H01707 Ossified ligamentum flavum D FA84 Spondylolisthesis D FA85 Spinal endplate defects D FA8Y Other specified degenerative condition of spine D FA8Z Degenerative condition of spine, unspecified C Inflammation of spine D FA90 Infection of vertebra D FA91 Infection of intervertebral disc D FA92 Inflammatory spondyloarthritis E H01674 Ankylosing spondylitis D FA9Y Other specified inflammation of spine D FA9Z Inflammation of spine, unspecified C Spondylopathies D FB00 Ankylosis of spinal joint D FB0Y Other specified spondylopathies D FB0Z Spondylopathies, unspecified C FB10 Spinal instabilities C FB1Y Other specified conditions associated with the spine C FB1Z Conditions associated with the spine, unspecified B Soft tissue disorders C Disorders of muscles D FB30 Infectious myositis D FB31 Calcification or ossification of muscle E H00441 Progressive osseous heteroplasia E H00430 Fibrodysplasia ossificans progressiva D FB32 Certain specified disorders of muscle E H02452 Muscle hypertrophy D FB33 Secondary disorders of muscle D FB3Z Disorders of muscles, unspecified C Disorders of synovium or tendon D FB40 Tenosynovitis D FB41 Spontaneous rupture of synovium or tendon D FB42 Certain specified disorders of synovium or tendon D FB43 Secondary disorders of synovium or tendon D FB4Y Other specified disorders of synovium or tendon D FB4Z Disorders of synovium or tendon, unspecified C Miscellaneous specified soft tissue disorders D FB50 Bursitis D FB51 Fibroblastic disorders D FB52 Soft tissue disorders in diseases classified elsewhere D FB53 Shoulder lesions D FB54 Enthesopathies of lower limb D FB55 Certain specified enthesopathies D FB56 Specified soft tissue disorders, not elsewhere classified C FB6Z Soft tissue disorders, unspecified B Osteopathies or chondropathies C FB80 Certain specified disorders of bone density or structure D H00501 Fibrous dysplasia, polyostotic D H01774 Hyperostosis corticalis generalisata D H02609 Craniodiaphyseal dysplasia C FB81 Osteonecrosis D H01709 Glucocorticoid-induced osteonecrosis C FB82 Chondropathies D H00448 Familial osteochondritis dissecans D H01526 Legg-Calve-Perthes Disease D H01529 Avascular necrosis of femoral head D H01758 Relapsing polychondritis C FB83 Low bone mass disorders D H01593 Osteoporosis C FB84 Osteomyelitis or osteitis C FB85 Paget disease of bone D H00437 Paget disease of bone C FB86 Disorders associated with bone growth D H00457 Primary hypertrophic osteoarthropathy D H00472 Torg syndrome D H00614 Hyaline fibromatosis syndrome D H00623 Hajdu-Cheney syndrome D H01865 Multicentric carpotarsal osteolysis syndrome D H02042 Familial expansile osteolysis D H02089 Winchester syndrome C FB8Y Other specified osteopathies or chondropathies C FB8Z Osteopathies or chondropathies, unspecified B FC00 Certain specified acquired deformities of musculoskeletal system or connective tissue, not elsewhere classified B FC01 Postprocedural disorders of the musculoskeletal system B FC0Y Other specified diseases of the musculoskeletal system or connective tissue B FC0Z Diseases of the musculoskeletal system or connective tissue, unspecified # A16 Diseases of the genitourinary system B Diseases of the female genital system C Inflammatory disorders of the female genital tract D GA00 Vulvitis D GA01 Inflammatory disorders of the uterus, except cervix D GA02 Vaginitis D GA03 Diseases of Bartholin gland D GA04 Cervicitis D GA05 Female pelvic inflammatory diseases D GA06 Pelvic peritoneal adhesions of unknown or combined origin D GA07 Salpingitis and oophoritis D GA0Z Inflammatory disorders of the female genital tract, unspecified C GA10 Endometriosis D H01639 Endometriosis C GA11 Adenomyosis C Noninflammatory disorders of female genital tract D GA12 Dyspareunia D GA13 Acquired abnormalities of vulva or perineum D GA14 Acquired abnormalities of vagina D GA15 Acquired abnormalities of cervix uteri D GA16 Acquired abnormalities of uterus, except cervix D GA17 Acquired abnormalities of fallopian tube D GA18 Acquired abnormalities of ovary D GA19 Acquired abnormalities of broad ligament D GA1Y Other specified noninflammatory disorders of female genital tract D GA1Z Noninflammatory disorders of female genital tract, unspecified C Abnormal uterine or vaginal bleeding D GA20 Menstrual cycle bleeding disorders D GA21 Nonmenstrual bleeding disorders D GA22 Excessive menstruation with irregular cycle D GA23 Anovulatory bleeding D GA2Y Other specified abnormal uterine or vaginal bleeding D GA2Z Abnormal uterine or vaginal bleeding, unspecified C GA30 Menopausal or certain specified perimenopausal disorders D H00627 Premature ovarian failure C GA31 Female infertility D H01897 Oocyte/zygote/embryo maturation arrest D H02335 Preimplantation embryonic lethality C GA32 Complications associated with medically assisted reproduction D H01039 Ovarian hyperstimulation syndrome C GA33 Recurrent pregnancy loss C GA34 Female pelvic pain associated with genital organs or menstrual cycle C Dermatoses of female genitalia D GA40 Inflammatory dermatoses of the vulva D GA41 Ulcerative or erosive disorders of the vulva D GA42 Sensory disturbance of the vulva D GA43 Miscellaneous dermatoses of female genitalia D GA4Y Other specified dermatoses of female genitalia C GA6Y Other specified diseases of the female genital system C GA6Z Diseases of the female genital system, unspecified B Diseases of the male genital system C Dermatoses of male genitalia D GA80 Ulcerative disorders of the penis or scrotum D GA81 Miscellaneous dermatoses of male genitalia C Diseases of prostate D GA90 Hyperplasia of prostate D GA91 Inflammatory and other diseases of prostate C GB00 Hydrocele or spermatocele C GB01 Torsion of testis, epididymis or appendices C GB02 Orchitis or epididymitis C GB03 Atrophy of testis C GB04 Male infertility D H00890 Azoospermia D H01208 Globozoospermia D H01282 Spermatogenic failure D H02534 Y-linked spermatogenic failure C GB05 Redundant prepuce, phimosis or paraphimosis C GB06 Certain specified disorders of penis C GB07 Inflammatory disorders of male genital organs, not elsewhere classified C GB08 Vascular disorders of male genital organs C GB0Y Other specified diseases of the male genital system C GB0Z Diseases of the male genital system, unspecified B Disorders of breast C GB20 Benign breast disease C GB21 Inflammatory disorders of breast C GB22 Hypertrophy of breast C GB23 Certain specified disorders of breast C GB2Z Disorders of breast, unspecified B Diseases of the urinary system C Glomerular diseases D GB40 Nephritic syndrome E H01688 Rapidly progressive glomerulonephritis D GB41 Nephrotic syndrome E H00576 Pierson syndrome E H01657 Nephrotic syndrome E H01722 Galloway-Mowat syndrome D GB42 Persistent proteinuria or albuminuria D GB4Y Other specified glomerular diseases E H00582 Benign familial hematuria D GB4Z Glomerular diseases, unspecified C Renal tubulo-interstitial diseases D GB50 Acute tubulo-interstitial nephritis D GB51 Acute pyelonephritis D GB52 Acute tubular necrosis D GB53 Acute renal papillary necrosis D GB54 Tubulo-interstitial nephritis, not specified as acute or chronic D GB55 Chronic tubulo-interstitial nephritis E H02577 Karyomegalic interstitial nephritis D GB56 Obstructive or reflux nephropathy E H01037 Vesicoureteral reflux D GB57 Nephrocalcinosis D GB58 Pyonephrosis D GB59 Renal or perinephric abscess D GB5Y Other specified renal tubulo-interstitial diseases D GB5Z Renal tubulo-interstitial diseases, unspecified C Kidney failure D GB60 Acute kidney failure D GB61 Chronic kidney disease E H01456 Diabetic nephropathy E H02559 Microvascular complications of diabetes D GB6Z Kidney failure, unspecified C Urolithiasis D GB70 Calculus of upper urinary tract E H02145 Calcium oxalate nephrolithiasis E H02626 Kalamiella piersonii infection D GB71 Calculus of lower urinary tract D GB7Z Urolithiasis, unspecified C Cystic or dysplastic kidney disease D GB80 Nonfamilial nongenetic cystic kidney disease D GB81 Autosomal dominant polycystic kidney disease E H00542 Polycystic kidney disease D GB82 Autosomal dominant tubulointerstitial disease E H00541 Autosomal dominant tubulointerstitial kidney disease E H02012 Medullary cystic kidney disease D GB83 Nephronophthisis E H00537 Nephronophthisis E H00538 Senior-Loken syndrome D GB8Y Other specified cystic or dysplastic kidney disease E H00542 Polycystic kidney disease D GB8Z Cystic or dysplastic kidney disease, unspecified C GB90 Certain specified disorders of kidney or ureter D H01198 Fanconi renotubular syndrome D H00239 Bartter syndrome D H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) D H00243 Hyperkalemic distal renal tubular acidosis (RTA type 4) D H00428 Distal renal tubular acidosis (RTA type 1) D H00429 Proximal renal tubular acidosis (RTA type 2) D H02310 Renal tubular acidosis D H00888 Nephrolithiasis/osteoporosis, hypophosphatemic D H00252 Congenital nephrogenic diabetes insipidus D H00694 Dent disease D H00948 Renal hypouricemia D H02147 X-linked recessive nephrolithiasis with renal failure D H02148 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis D H02149 X-linked hypercalciuric nephrolithiasis C Certain specified diseases of urinary system D GC00 Cystitis E H01551 Interstitial cystitis D GC01 Other disorders of bladder D GC02 Urethritis and urethral syndrome D GC03 Urethral stricture D GC04 Fistula of the genitourinary tract D GC05 Prolapsed urethral mucosa D GC06 Urethral diverticulum D GC07 Urethral caruncle D GC08 Urinary tract infection, site not specified E H01176 Uncomplicated urinary tract infection E H00279 Uropathogenic Escherichia coli (UPEC) infection E H01339 Asymptomatic bacteriuria D GC0Y Other diseases of urinary system C GC2Z Diseases of the urinary system, unspecified B Other conditions of the genitourinary system C Female pelvic floor dysfunction D GC40 Pelvic organ prolapse D GC41 Anorectal dysfunction associated with pelvic organ prolapse D GC42 Sexual dysfunction associated with pelvic organ prolapse D GC4Z Female pelvic floor dysfunction, unspecified C GC50 Functional bladder disorders, not otherwise specified C GC51 Female Genital Mutilation B Postprocedural disorders of genitourinary system C GC70 Postoperative adhesions of vagina C GC71 Prolapse of vaginal vault after hysterectomy C GC72 Postprocedural urethral stricture C GC73 Postprocedural pelvic peritoneal adhesions C GC74 Malfunction or complication of external stoma of urinary tract C GC75 Malfunction of the afferent segment of a continent urinary pouch C GC76 Malfunction of the efferent segment of a continent urinary pouch C GC77 Postprocedural nonmenstrual uterine bleeding C GC78 Postprocedural acute female pelvic inflammatory disease C GC79 Disorders of breast reduction C GC7A Disorders of breast augmentation C GC7B Postinterventional ischemia or infarction of kidney B GC8Y Other specified diseases of the genitourinary system B GC8Z Diseases of the genitourinary system, unspecified # A17 Conditions related to sexual health B Sexual dysfunctions C HA00 Hypoactive sexual desire dysfunction C HA01 Sexual arousal dysfunctions C HA02 Orgasmic dysfunctions C HA03 Ejaculatory dysfunctions C HA0Y Other specified sexual dysfunctions C HA0Z Sexual dysfunctions, unspecified B Sexual pain disorders C HA20 Sexual pain-penetration disorder C HA2Y Other specified sexual pain disorders C HA2Z Sexual pain disorders, unspecified B HA40 Aetiological considerations in sexual dysfunctions and sexual pain disorders B Gender incongruence C HA60 Gender incongruence of adolescence or adulthood C HA61 Gender incongruence of childhood C HA6Z Gender incongruence, unspecified B HA8Y Other specified conditions related to sexual health B HA8Z Conditions related to sexual health, unspecified # A18 Pregnancy, childbirth or the puerperium B Abortive outcome of pregnancy C JA00 Abortion C JA01 Ectopic pregnancy C JA02 Molar pregnancy D H00289 Recurrent hydatidiform moles C JA03 Missed abortion C JA04 Blighted ovum or nonhydatidiform mole C JA05 Complications following abortion, ectopic or molar pregnancy C JA0Z Abortive outcome of pregnancy, unspecified B Oedema, proteinuria, or hypertensive disorders in pregnancy, childbirth, or the puerperium C JA20 Pre-existing hypertension complicating pregnancy, childbirth or the puerperium C JA21 Pre-eclampsia superimposed on chronic hypertension C JA22 Gestational oedema or proteinuria without hypertension C JA23 Gestational hypertension C JA24 Pre-eclampsia C JA25 Eclampsia C JA2Z Oedema, proteinuria, or hypertensive disorders in pregnancy, childbirth, or the puerperium, unspecified B Obstetric haemorrhage C JA40 Haemorrhage in early pregnancy C JA41 Antepartum haemorrhage C JA42 Intrapartum haemorrhage C JA43 Postpartum haemorrhage C JA4Z Obstetric haemorrhage, unspecified B Certain specified maternal disorders predominantly related to pregnancy C JA60 Excessive vomiting in pregnancy C JA61 Venous complications in pregnancy C JA62 Infections of genitourinary tract in pregnancy C JA63 Diabetes mellitus in pregnancy C JA64 Malnutrition in pregnancy C JA65 Maternal care for other conditions predominantly related to pregnancy D H02193 Intrahepatic cholestasis of pregnancy C JA66 Clinical findings on antenatal screening of mother C JA67 Complications of anaesthesia during pregnancy C JA6Z Maternal disorders predominantly related to pregnancy, unspecified B Maternal care related to the fetus, amniotic cavity or possible delivery problems C JA80 Maternal care related to multiple gestation C JA81 Maternal care related to complications specific to multiple gestation C JA82 Maternal care for known or suspected malpresentation of fetus C JA83 Maternal care for known or suspected disproportion C JA84 Maternal care for known or suspected abnormality of pelvic organs C JA85 Maternal care for known or suspected fetal abnormality or damage C JA86 Maternal care for other known or suspected fetal problems C JA87 Maternal care related to polyhydramnios C JA88 Maternal care related to certain specified disorders of amniotic fluid or membranes C JA89 Maternal care related to premature rupture of membranes C JA8A Maternal care related to placental disorders C JA8B Maternal care related to placenta praevia or low lying placenta C JA8C Maternal care related to premature separation of placenta C JA8D Maternal care related to false labour C JA8E Maternal care related to prolonged pregnancy C JA8Y Maternal care related to other specified fetus, amniotic cavity or possible delivery problems C JA8Z Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems B Complications of labour or delivery C JB00 Preterm labour or delivery C JB01 Failed induction of labour C JB02 Abnormalities of forces of labour C JB03 Long labour C JB04 Obstructed labour due to malposition or malpresentation of fetus C JB05 Obstructed labour due to maternal pelvic abnormality C JB06 Obstructed labour due to other causes C JB07 Labour or delivery complicated by fetal distress C JB08 Labour or delivery complicated by umbilical cord complications C JB09 Perineal laceration during delivery C JB0A Certain specified obstetric trauma C JB0B Retained placenta or membranes, without haemorrhage C JB0C Complications of anaesthesia during labour or delivery C JB0D Certain specified complications of labour or delivery, not elsewhere classified C JB0Y Other specified complications of labour or delivery C JB0Z Complications of labour or delivery, unspecified B Delivery C JB20 Single spontaneous delivery C JB21 Single delivery by forceps or vacuum extractor C JB22 Single delivery by caesarean section C JB23 Other assisted single delivery C JB24 Multiple delivery C JB2Z Delivery, unspecified B Complications predominantly related to the puerperium C JB40 Infections in the puerperium C JB41 Venous complications in the puerperium C JB42 Obstetric embolism C JB43 Complications of anaesthesia during the puerperium C JB44 Certain specified complications of the puerperium C JB45 Infections of breast associated with childbirth C JB46 Certain specified disorders of breast or lactation associated with childbirth D H01607 Galactorrhea C JB4Z Complications predominantly related to the puerperium, unspecified B Certain obstetric conditions, not elsewhere classified C JB60 Obstetric death of unspecified cause C JB61 Death from any obstetric cause occurring more than 42 days but less than one year after delivery C JB62 Death from sequelae of obstetric causes C JB63 Maternal infectious diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium C JB64 Certain maternal diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium C JB65 Sequelae of complication of pregnancy, childbirth or the puerperium C JB6Y Other specified obstetric conditions, not elsewhere classified C JB6Z Unspecified obstetric condition # A19 Certain conditions originating in the perinatal period B Fetus or newborn affected by maternal factors or by complications of pregnancy, labour or delivery C KA00 Fetus or newborn affected by maternal conditions that may be unrelated to present pregnancy C KA01 Fetus or newborn affected by maternal complications of pregnancy C KA02 Fetus or newborn affected by complications of placenta C KA03 Fetus or newborn affected by complications of umbilical cord C KA04 Fetus or newborn affected by other abnormalities of membranes C KA05 Fetus or newborn affected by certain complications of labour or delivery C KA06 Fetus or newborn affected by noxious influences transmitted via placenta or breast milk C KA07 Neonatal dermatoses due to maternal antibodies C KA0Z Fetus or newborn affected by unspecified maternal factors or by complications of pregnancy, labour or delivery B Disorders of newborn related to length of gestation or fetal growth C KA20 Disorders of newborn related to slow fetal growth or fetal malnutrition C KA21 Disorders of newborn related to short gestation or low birth weight, not elsewhere classified C KA22 Disorders of newborn related to long gestation or high birth weight C KA2Y Other specified disorders of newborn related to length of gestation or fetal growth C KA2Z Disorders of newborn related to length of gestation or fetal growth, unspecified B Birth injury C KA40 Birth injury to central nervous system C KA41 Birth injury to eye C KA42 Birth injury to scalp C KA43 Birth injury to skin or soft tissues C KA44 Birth injury to peripheral nervous system C KA45 Birth injury to skeleton C KA46 Birth injury to other organs C KA4Z Birth injury, unspecified B Infections of the fetus or newborn C KA60 Sepsis of fetus or newborn C KA61 Other bacterial infections of the fetus or newborn C KA62 Viral infection in the fetus or newborn C KA63 Fungal infection of fetus or newborn C KA64 Parasitic diseases in the fetus or newborn C KA65 Neonatal infections of certain specified sites C KA6Y Other specified infections of the fetus or newborn C KA6Z Infections of the fetus or newborn, unspecified B Haemorrhagic or haematological disorders of fetus or newborn C KA80 Fetal blood loss C KA81 Umbilical haemorrhage of newborn C KA82 Intracranial nontraumatic haemorrhage of fetus or newborn C KA83 Certain specified neonatal haemorrhages C KA84 Haemolytic disease of fetus or newborn C KA85 Hydrops fetalis due to haemolytic disease C KA86 Neonatal kernicterus C KA87 Neonatal hyperbilirubinaemia D H02152 Transient familial neonatal hyperbilirubinemia C KA88 Disseminated intravascular coagulation of fetus or newborn C KA89 Transient neonatal thrombocytopaenia C KA8A Polycythaemia neonatorum C KA8B Anaemia of prematurity C KA8C Congenital hypoplastic anaemia C KA8D Transient neonatal neutropaenia C KA8E Alloimmune neonatal neutropaenia C KA8F Neonatal vitamin K deficiency C KA8Y Other specified haemorrhagic or haematological disorders of fetus or newborn C KA8Z Haemorrhagic or haematological disorders of fetus or newborn, unspecified B Neurological disorders specific to the perinatal or neonatal period C KB00 Neonatal cerebral ischaemia C KB01 Periventricular cysts of newborn C KB02 Neonatal cerebral leukomalacia C KB03 Neonatal encephalopathy D H01211 MECP2-related severe neonatal encephalopathy C KB04 Hypoxic ischaemic encephalopathy of newborn C KB05 Neonatal hydrocephalus C KB06 Neonatal seizures C KB07 Compression of brain in neonate C KB08 Disorders of muscle tone of newborn C KB0Y Other specified neurological disorders specific to the perinatal or neonatal period C KB0Z Neurological disorders specific to the perinatal or neonatal period, unspecified B Respiratory disorders specific to the perinatal or neonatal period C KB20 Intrauterine hypoxia C KB21 Birth asphyxia C KB22 Metabolic acidaemia in newborn C KB23 Respiratory distress of newborn C KB24 Congenital pneumonia C KB25 Neonatal tracheitis C KB26 Neonatal aspiration syndromes C KB27 Pulmonary air leak or related conditions originating in the perinatal period C KB28 Pulmonary haemorrhage originating in the perinatal period C KB29 Chronic respiratory disease originating in the perinatal period C KB2A Apnoea of newborn C KB2B Primary atelectasis of newborn C KB2C Cyanotic attacks of newborn C KB2D Respiratory failure of newborn C KB2E Respiratory arrest of newborn C KB2F Congenital lung or lobar atelectasis C KB2G Tracheal haemorrhage of newborn due to airway trauma C KB2H Acquired vocal cord paralysis in newborn C KB2J Airway obstruction in the neonate due to airway abnormality C KB2K Pulmonary cysts in newborn C KB2Y Other specified respiratory disorders specific to the perinatal or neonatal period C KB2Z Respiratory disorders specific to the perinatal or neonatal period, unspecified B Cardiovascular disorders present in the perinatal or neonatal period C KB40 Neonatal cardiac failure C KB41 Cardiac arrhythmias in the neonate C KB42 Persistent pulmonary hypertension of the newborn C KB44 Transient myocardial ischaemia of newborn C KB45 Neonatal hypertension C KB46 Neonatal hypotension C KB47 Benign or innocent cardiac murmurs in newborn C KB48 Patent arterial duct of prematurity C KB4Y Other specified cardiovascular disorders present in the perinatal or neonatal period C KB4Z Cardiovascular disorders present in the perinatal or neonatal period, unspecified B Transitory endocrine or metabolic disorders specific to fetus or newborn C KB60 Transitory disorders of carbohydrate metabolism specific to fetus or newborn D H00513 Transient neonatal diabetes mellitus D H00512 Permanent neonatal diabetes mellitus D H01377 Mitchell-Riley syndrome C KB61 Transitory neonatal disorders of calcium or magnesium metabolism C KB62 Transitory neonatal disorders of thyroid function C KB63 Certain specified transitory neonatal electrolyte or metabolic disturbances C KB64 Transitory neonatal hypoparathyroidism C KB6Z Transitory endocrine or metabolic disorders specific to fetus or newborn, unspecified B Digestive system disorders of fetus or newborn C KB80 Gastro-oesophageal reflux disease in newborn C KB81 Oesophagitis in newborn C KB82 Prenatal gastric perforation C KB83 Postnatal gastric perforation C KB84 Postnatal isolated ileal perforation C KB85 Prenatal intrauterine intestinal perforation C KB86 Postnatal intestinal perforation C KB87 Intestinal obstruction of newborn C KB88 Necrotising enterocolitis of newborn C KB89 Neonatal malabsorption syndromes D H01469 Short bowel syndrome D H01477 Congenital short bowel syndrome C KB8A Neonatal haematemesis or melaena due to swallowed maternal blood C KB8B Neonatal peritonitis C KB8C Noninfectious neonatal diarrhoea D H01174 Congenital diarrhea C KB8Y Other specified digestive system disorders of fetus or newborn D H02730 Severe congenital liver disease C KB8Z Digestive system disorders of fetus or newborn, unspecified B Genitourinary system disorders specific to the perinatal or neonatal period C KC00 Congenital hydrocele C KC01 Congenital renal failure C KC0Y Other specified genitourinary system disorders specific to the perinatal or neonatal period C KC0Z Genitourinary system disorders specific to the perinatal or neonatal period, unspecified B Disorders involving the integument of fetus or newborn C KC20 Conditions involving the umbilical cord C KC21 Inflammatory dermatoses of the newborn C KC22 Neonatal disorders of subcutaneous fat C KC23 Neonatal disorders of the oral mucosa C KC24 Neonatal nutritional disorders affecting the skin C Skin disorders associated with prematurity D KC30 Skin fragility of prematurity D KC31 Congenital erosive or vesicular dermatosis healing with reticulated supple scarring D KC3Y Other specified skin disorders associated with prematurity C KC40 Miscellaneous skin disorders in the neonate C KC41 Miscellaneous specified conditions of integument specific to fetus or newborn C Iatrogenic injuries involving the skin of the neonate D Postnatal iatrogenic skin injury E KC50 Neonatal phototherapy burn E KC5Y Other specified postnatal iatrogenic skin injury E KC5Z Postnatal iatrogenic skin injury, unspecified D KC7Y Other specified iatrogenic injuries involving the skin of the neonate C KC9Z Disorders involving the integument of fetus or newborn, unspecified B Disturbances of temperature regulation of newborn C KD10 Environmental hyperthermia of newborn C KD11 Fever of newborn C KD12 Hypothermia of newborn C KD1Y Other specified disturbances of temperature regulation of newborn C KD1Z Disturbances of temperature regulation of newborn, unspecified B Certain disorders originating in the perinatal period C KD30 Birth depression C KD31 Wide cranial sutures of newborn C KD32 Feeding problems of newborn C KD33 Jittery baby, not elsewhere classified C KD34 Reactions or intoxications due to drugs administered to fetus or newborn C KD35 Neonatal withdrawal syndrome from maternal use of drugs of addiction C KD36 Withdrawal symptoms from therapeutic use of drugs in newborn C KD37 Exposure to tobacco smoke in the perinatal period C KD38 Meconium staining C KD39 Complications of intrauterine procedures, not elsewhere classified C KD3A Termination of pregnancy, affecting surviving fetus or newborn C KD3B Fetal death, cause not specified C KD3C Vomiting in newborn C KD3Y Other specified disorders originating in the perinatal period B KD5Z Conditions originating in the perinatal or neonatal period, unspecified # A20 Developmental anomalies B Structural developmental anomalies primarily affecting one body system C Structural developmental anomalies of the nervous system D LA00 Anencephaly or similar anomalies E H02120 Anencephaly D LA01 Cephalocele D LA02 Spina bifida E H00262 Neural tube defects, folate-sensitive E H02563 Neural tube defects D LA03 Arnold-Chiari malformation type II E H01561 Chiari malformation D LA04 Congenital hydrocephalus E H01677 Congenital hydrocephalus E H02458 Hydrocephalus due to congenital stenosis of aqueduct of Sylvius D LA05 Cerebral structural developmental anomalies E H00269 Primary microcephaly E H01833 Hemimegalencephaly E H02446 Autosomal recessive macrocephaly/megalencephaly syndrome E H00267 Holoprosencephaly E H00263 Acrocallosal syndrome E H01835 Neuronal migration disorder E H00271 Polymicrogyria E H01251 Focal cortical dysplasia of Taylor E H01881 Complex cortical dysplasia with other brain malformations E H00270 Periventricular nodular heterotopia E H00839 Porencephaly E H01160 Schizencephaly E H01870 Microhydranencephaly E H02501 Occipital cortical malformation D LA06 Cerebellar structural developmental anomalies E H01678 Dandy-Walker syndrome D LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column E H01675 Syringomyelia E H01561 Chiari malformation E H01893 Lateral meningocele syndrome D LA0Y Other specified structural developmental anomalies of the nervous system E H02494 Alkuraya-Kucinskas syndrome D LA0Z Structural developmental anomalies of the nervous system, unspecified C Structural developmental anomalies of the eye, eyelid or lacrimal apparatus D LA10 Structural developmental anomalies of ocular globes E H01027 Microphthalmia E H02172 Nanophthalmos D LA11 Structural developmental anomalies of the anterior segment of eye E H01114 Ocular coloboma E H01029 Cornea plana congenita E H02104 Megalocornea E H00620 Axenfeld-Rieger syndrome E H01159 Anterior segment dysgenesis E H00635 Aniridia E H00961 Posterior polymorphous corneal dystrophy E H01075 Peters anomaly D LA12 Structural developmental anomalies of lens or zonula E H00676 Congenital primary aphakia E H00662 Ectopia lentis D LA13 Structural developmental anomalies of the posterior segment of eye E H02112 Persistent hyperplastic primary vitreous E H00589 Familial exudative vitreoretinopathy E H02475 Retinoschisis E H02203 Optic nerve hypoplasia E H02270 Cavitary optic disc anomalies E H01256 Foveal hypoplasia E H02231 Optic disc anomalies with retinal and/or macular dystrophy D LA14 Structural developmental anomalies of eyelid, lacrimal apparatus or orbit E H00677 Aplasia of lacrimal and salivary glands E H02514 Lacrimal duct defect D LA1Y Other specified structural developmental anomalies of the eye, eyelid or lacrimal apparatus D LA1Z Structural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecified C Structural developmental anomalies of the ear D LA20 Structural anomaly of eustachian apparatus D LA21 Minor anomalies of pinnae D LA22 Structural developmental anomalies of ear causing hearing impairment E H02115 Congenital aural atresia D LA23 Otocephaly E H02118 Agnathia-otocephaly complex D LA24 Accessory auricle D LA2Y Other specified structural developmental anomalies of the ear D LA2Z Structural developmental anomalies of the ear, unspecified C Structural developmental anomalies of the face, mouth or teeth D LA30 Structural developmental anomalies of teeth and periodontal tissues E H00625 Tooth agenesis E H00652 Solitary median maxillary central incisor syndrome E H00615 Amelogenesis imperfecta E H00618 Amelogenesis imperfecta hypoplastic-hypomaturation with taurodontism E H01015 Jalili syndrome E H02348 Dentin dysplasia E H00432 Hereditary dentine disorders D LA31 Structural developmental anomalies of mouth or tongue D Clefts of lip, alveolus or palate E LA40 Cleft lip F H00516 Cleft lip and/or cleft palate E LA41 Cleft lip and alveolus F H00516 Cleft lip and/or cleft palate E LA42 Cleft palate F H00516 Cleft lip and/or cleft palate F H00909 Cleft palate with ankyloglossia E LA4Y Other specified clefts of lip, alveolus or palate E LA4Z Clefts of lip, alveolus or palate, unspecified D LA50 Congenital velopharyngeal incompetence D LA51 Facial clefts E H02202 Oblique facial cleft D LA52 Facial asymmetry D LA53 Macrocheilia D LA54 Microcheilia D LA55 Compression facies D LA56 Pierre Robin syndrome D LA5Y Other specified structural developmental anomalies of the face D LA5Z Structural developmental anomalies of the face, unspecified C Structural developmental anomalies of the neck D LA60 Webbed neck D LA61 Congenital sternomastoid tumour D LA62 Congenital torticollis D LA6Y Other specified structural developmental anomalies of the neck D LA6Z Structural developmental anomalies of the neck, unspecified C Structural developmental anomalies of the respiratory system D LA70 Structural developmental anomalies of the nose or cavum E H01017 Choanal atresia and lymphedema D LA71 Structural developmental anomalies of larynx D LA72 Laryngotracheooesophageal cleft D LA73 Structural developmental anomalies of trachea E H02600 Congenital tracheal stenosis D LA74 Structural developmental anomalies of bronchi D LA75 Structural developmental anomalies of lungs E H00564 Primary ciliary dyskinesia D LA76 Structural developmental anomalies of pleura D LA77 Congenital cyst of mediastinum D LA7Y Other specified structural developmental anomalies of the respiratory system D LA7Z Structural developmental anomalies of the respiratory system, unspecified C Structural developmental anomalies of the circulatory system D Structural developmental anomaly of heart or great vessels E LA80 Anomalous position-orientation of heart E LA81 Abnormal ventricular relationships E LA82 Total mirror imagery E LA83 Right isomerism E LA84 Left isomerism F H01764 Polysplenia syndrome E LA85 Congenital anomaly of an atrioventricular or ventriculo-arterial connection F H01786 Congenitally corrected transposition of the great arteries F H00550 Complete transposition of the great arteries F H00918 Double-outlet right ventricle F H01736 Persistent truncus arteriosus E LA86 Congenital anomaly of mediastinal vein F H02605 Congenital pulmonary venous stenosis E LA87 Congenital anomaly of an atrioventricular valve or atrioventricular septum F H02230 X-linked cardiac valvular dysplasia F H02602 Congenital tricuspid valve stenosis F H01783 Ebstein anomaly F H02603 Congenital mitral valve stenosis F H00547 Atrioventricular septal defect E LA88 Congenital anomaly of a ventricle or the ventricular septum F H00549 Tetralogy of Fallot F H01803 Pulmonary atresia with ventricular septal defect F H01926 Ventricular septal defect E LA89 Functionally univentricular heart F H01787 Univentricular heart F H01785 Tricuspid atresia F H01272 Hypoplastic left heart syndrome F H02375 Cardiac valvular dysplasia E LA8A Congenital anomaly of a ventriculo-arterial valve or adjacent regions F H01802 Pulmonary atresia with intact ventricular septum F H00554 Aortic valve disease F H00553 Congenital supravalvular aortic stenosis E LA8B Congenital anomaly of great arteries including arterial duct F H01630 Patent ductus arteriosus F H02601 Pulmonary arterial sling E LA8C Congenital anomaly of coronary artery E LA8D Congenital pericardial anomaly E LA8E Congenital anomaly of atrial septum F H00546 Atrial septal defect E LA8F Congenital anomaly of right atrium E LA8G Congenital anomaly of left atrium E LA8Y Other specified structural developmental anomaly of heart or great vessels F H00632 Heterotaxy F H02199 Congenital heart defects, multiple type E LA8Z Structural developmental anomaly of heart or great vessels, unspecified D LA90 Structural developmental anomalies of the peripheral vascular system E H00533 Hereditary hemorrhagic telangiectasia E H00531 Venous malformations E H01849 Peripheral arteriovenous malformation E H02043 Capillary malformation-arteriovenous malformation D LA9Y Other specified structural developmental anomalies of the circulatory system D LA9Z Structural developmental anomalies of the circulatory system, unspecified C Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord D LB00 Structural developmental anomalies of diaphragm E H01241 Congenital diaphragmatic hernia D LB01 Omphalocele D LB02 Gastroschisis D LB03 Structural developmental anomalies of umbilical cord D LB0Y Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord D LB0Z Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord, unspecified C Structural developmental anomalies of the digestive tract D LB10 Structural developmental anomalies of salivary glands or ducts D LB11 Congenital diverticulum of pharynx D LB12 Structural developmental anomalies of oesophagus D LB13 Structural developmental anomalies of stomach D LB14 Structural developmental anomalies of duodenum D LB15 Structural developmental anomalies of small intestine D LB16 Structural developmental anomalies of large intestine E H00910 Hirschsprung disease E H01871 Isolated hypoganglionosis D LB17 Structural developmental anomalies of anal canal E H01858 Persistent cloaca E H01856 Cloacal exstrophy D LB18 Congenital anomalies of intestinal fixation D LB1Y Other specified structural developmental anomalies of the digestive tract E H02331 Gastrointestinal defects and immunodeficiency syndrome D LB1Z Structural developmental anomalies of the digestive tract, unspecified C Structural developmental anomalies of the liver, biliary tract, pancreas or spleen D LB20 Structural developmental anomalies of gallbladder, bile ducts or liver E H01855 Biliary atresia E H00551 Alagille syndrome D LB21 Structural developmental anomalies of pancreas E H00861 Pancreatic agenesis D LB22 Structural developmental anomalies of spleen E H01435 Congenital asplenia D LB2Y Other specified structural developmental anomalies of the liver, biliary tract, pancreas or spleen D LB2Z Structural developmental anomalies of the liver, biliary tract, pancreas or spleen, unspecified C Structural developmental anomalies of the urinary system D LB30 Structural developmental anomalies of kidneys E H01867 Congenital anomalies of kidney and urinary tract E H00822 Renal hypodysplasia and aplasia E H00575 Renal tubular dysgenesis D LB31 Structural developmental anomalies of urinary tract E H01867 Congenital anomalies of kidney and urinary tract E H02495 Congenital megabladder D LB3Y Other specified structural developmental anomalies of the urinary system D LB3Z Structural developmental anomalies of the urinary system, unspecified C Structural developmental anomalies of the female genital system D LB40 Structural developmental anomalies of vulva D LB41 Structural developmental anomalies of clitoris D LB42 Structural developmental anomalies of vagina D LB43 Structural developmental anomalies of cervix uteri D LB44 Structural developmental anomalies of uterus, except cervix E H00600 Mullerian agenesis D LB45 Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments E H00599 Ovarian dysgenesis D LB4Y Other specified structural developmental anomalies of the female genital system D LB4Z Structural developmental anomalies of the female genital system, unspecified C Structural developmental anomalies of the male genital system D LB50 Micropenis or penis agenesis D LB51 Anorchia or microorchidia D LB52 Cryptorchidism E H02176 Cryptorchidism D LB53 Hypospadias E H02175 Hypospadias D LB54 Congenital chordee D LB55 Epispadias D LB56 Bifid scrotum D LB57 Agenesis of vas deferens E H01033 Congenital bilateral absence of vas deferens D LB58 Polyorchidism D LB59 Hypoplasia of testis or scrotum D LB5Y Other specified structural developmental anomalies of the male genital system D LB5Z Structural developmental anomalies of the male genital system, unspecified C Structural developmental anomalies of the breast D LB60 Breast aplasia D LB61 Absent nipple D LB62 Supernumerary breasts D LB63 Accessory nipple D LB6Y Other specified structural developmental anomalies of the breast D LB6Z Structural developmental anomalies of the breast, unspecified C Structural developmental anomalies of the skeleton D LB70 Structural developmental anomalies of cranium E H02160 Craniosynostoses E H01207 Trigonocephaly E H00475 Enlarged parietal foramina/cranium bifidum E H01105 Cranio-lenticulo-sutural dysplasia D LB71 Structural developmental anomalies of facial bones D LB72 Structural developmental anomalies of shoulder girdle D LB73 Structural developmental anomalies of spine or bony thorax E H01851 Congenital scoliosis associated with rib anomalies E H00852 Klippel-Feil syndrome D LB74 Structural developmental anomalies of pelvic girdle E H01817 Beukes hip dysplasia D LB75 Brachydactyly E H00482 Brachydactyly D LB76 Triphalangeal thumb D LB77 Hyperphalangy D LB78 Polydactyly E H01226 Polysyndactyly E H01852 Postaxial polydactyly E H02332 Preaxial polydactyly D LB79 Syndactyly E H01095 Syndactyly E H00459 Synpolydactyly E H01854 Metacarpal 4-5 fusion D Congenital deformities of fingers or toes E LB80 Congenital deformities of fingers F H01246 Isolated congenital nail clubbing E LB81 Congenital deformities of toes E LB8Z Congenital deformities of fingers or toes, unspecified D LB90 Joint formation defects E H00484 Multiple synostosis syndrome E H00851 Proximal symphalangism D LB91 Congenital shoulder dislocation D LB92 Congenital elbow dislocation D LB93 Congenital knee dislocation D LB94 Congenital patella dislocation D LB95 Patella aplasia or hypoplasia D LB96 Congenital bowing of long bones D LB97 Limb overgrowth E H02647 Macrodactyly D LB98 Congenital deformities of feet E H00903 Congenital clubfoot E H00929 Congenital vertical talus D LB99 Reduction defects of upper limb E H00471 Split-hand/foot malformation D LB9A Reduction defects of lower limb E H00471 Split-hand/foot malformation D LB9B Reduction defects of upper and lower limbs E H00629 Acheiropodia E H00636 Tetra-amelia syndrome D LB9Y Other specified structural developmental anomalies of the skeleton E H00873 Cousin syndrome D LB9Z Structural developmental anomalies of the skeleton, unspecified E H00762 Spondyloepiphyseal dysplasia with congenital joint dislocations C Structural developmental anomalies of the skin D Developmental hamartomata of the epidermis and epidermal appendages E LC00 Keratinocytic epidermal hamartoma F H02627 Epidermal nevus E LC01 Pilosebaceous hamartoma E LC02 Complex epidermal hamartoma F H02716 Becker nevus syndrome E LC0Y Other specified developmental hamartomata of the epidermis and epidermal appendages D Developmental anomalies of skin pigmentation E LC10 Dermal melanocytosis E LC1Y Other specified developmental anomalies of skin pigmentation D Hamartomata derived from dermal connective tissue E LC20 Connective tissue hamartoma E LC2Y Other specified hamartomata derived from dermal connective tissue D Developmental defects of hair or nails E LC30 Developmental defects of hair or hair growth E LC31 Developmental defects of the nail apparatus D LC40 Dermoid cyst D Developmental anomalies of cutaneous vasculature E LC50 Developmental capillary vascular malformations of the skin E LC51 Developmental venous malformations involving the skin F H02044 Cutaneous and mucosal venous malformation E LC52 Complex or combined developmental vascular malformations involving the skin E LC5Y Other specified developmental anomalies of cutaneous vasculature E LC5Z Developmental anomalies of cutaneous vasculature, unspecified D Congenital anomalies of skin development E LC60 Aplasia cutis congenita F H01896 Aplasia cutis congenita D LC7Y Other specified structural developmental anomalies of the skin E H02295 Adermatoglyphia D LC7Z Structural developmental anomalies of the skin, unspecified C Structural developmental anomalies of the adrenal glands D LC80 Congenital adrenal hypoplasia E H01772 Adrenal hypoplasia, congenital D LC8Y Other specified structural developmental anomalies of the adrenal glands D LC8Z Structural developmental anomalies of the adrenal glands, unspecified C LD0Y Other specified structural developmental anomalies primarily affecting one body system C LD0Z Structural developmental anomalies primarily affecting one body system, unspecified B Multiple developmental anomalies or syndromes C LD20 Syndromes with central nervous system anomalies as a major feature D H00530 Joubert syndrome and related disorders D H00897 Pontocerebellar hypoplasia D H01001 COACH syndrome D H01811 Arima syndrome D H02272 CAPOS syndrome D H02431 Cerebellar hypoplasia, epilepsy, and global developmental delay D H02464 Poretti-Boltshauser syndrome D H00268 Lissencephaly D H00792 Warburg micro syndrome D H02117 Neu-Laxova syndrome D H00616 Bowen-Conradi syndrome D H00840 Pseudo-TORCH syndrome D H00990 Microcephaly, Amish type D H00991 Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II) D H00993 Microcephalic osteodysplastic primordial dwarfism, type I (MOPD I) D H01872 Microcephaly-capillary malformation syndrome D H01876 Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation D H01921 MICPCH syndrome D H02132 Microcephaly syndrome D H02282 Spastic tetraplegia, thin corpus callosum, and progressive microcephaly D H02461 Neurodevelopmental disorder with microcephaly D H02492 Microcephaly, growth restriction, and increased sister chromatid exchange D H02668 Heyn-Sproul-Jackson syndrome D H02707 Khan-Khan-Katsanis syndrome D H02708 Baralle-Macken syndrome D H02709 Neurodevelopmental disorder with aminoacyl-tRNA synthetase defect D H02726 Kaya-Barakat-Masson syndrome D H00544 Septo-optic dysplasia D H00816 Agenesis of the corpus callosum with peripheral neuropathy D H01034 L1 syndrome D H01035 Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia D H01776 Aicardi syndrome D H01789 You-Hoover-Fong syndrome D H01919 Proud syndrome D H01937 Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly D H02366 Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome D H02396 Corpus callosum agenesis with facial anomalies and cerebellar ataxia D H02487 Diencephalic-mesencephalic junction dysplasia syndrome D H02519 Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations D H02606 Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures D H02645 Cerebellar atrophy with seizures and variable developmental delay D H02652 Macrocephaly, acquired, with impaired intellectual development D H02653 Faundes-Banka syndrome D H02675 Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features D H02680 Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities D H02695 Fibrosis, neurodegeneration, and cerebral angiomatosis D H02723 Macrocephaly/autism syndrome C LD21 Syndromes with eye anomalies as a major feature D H01904 Microphthalmia with linear skin defects syndrome D H02134 Microphthalmia with limb anomalies D H02170 Microphthalmia, syndromic D H00673 Weill-Marchesani syndrome D H00826 Blepharophimosis-ptosis-epicanthus inversus syndrome D H01012 Oculo-auricular syndrome D H02045 Norrie disease D H02292 Retinal dystrophy, juvenile cataracts, and short stature syndrome D H02422 Retinitis pigmentosa with skeletal anomalies D H02445 Microcornea, myopic chorioretinal atrophy, and telecanthus D H02655 Retinal dystrophy and microvillus inclusion disease C LD22 Syndromes with dental anomalies as a major feature C LD23 Syndromes with vascular anomalies as a major feature D H00579 Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps (HANAC) D H01809 Sturge-Weber syndrome D H02088 Primary intraosseous vascular malformation C LD24 Syndromes with skeletal anomalies as a major feature D H00520 Type II collagenopathies D H00505 FGFR3-related short limb skeletal dysplasia D H01749 Achondroplasia D H02069 SADDAN D H02068 Hypochondroplasia D H01750 Thanatophoric dysplasia D H00515 Atelosteogenesis type II D H02063 Diastrophic dysplasia D H00207 Rhizomelic chondrodysplasia punctata D H00447 HEM skeletal dysplasia D H00496 Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD) D H01194 X-linked chondrodysplasia punctata D H00436 Osteopetrosis D H00452 Buschke-Ollendorff syndrome D H00434 Camurati-Engelmann disease D H00444 Osteopathia striata with cranial sclerosis D H00450 Worth type autosomal dominant osteosclerosis D H00486 Sclerosteosis D H00490 Diaphyseal dysplasia with anemia D H00491 Craniometaphyseal dysplasia D H00508 Blomstrand syndrome D H00613 Infantile cortical hyperostosis D H00968 Raine syndrome D H01832 Lenz-Majewski syndrome D H02631 Melorheostosis D H00122 Multiple exostoses D H00493 Heparan sulfate proteoglycan gene defects D H00497 Cherubism D H02127 Yunis-Varon syndrome D H00443 Osteoglophonic dysplasia D H00498 Gnathodiaphyseal dysplasia D H00521 Cleidocranial dysplasia D H01018 Metachondromatosis D H02558 Craniotubular dysplasia, Ikegawa type D H00445 Osteoarthritis with mild chondrodysplasia D H00474 Schneckenbecken dysplasia D H00483 Angel shaped phalangoepiphyseal dysplasia D H00499 Spondylocarpotarsal synostosis syndrome D H00519 Spondyloepiphyseal dysplasia congenita D H00757 Dyggve-Melchior-Clausen disease D H00758 Progressive pseudorheumatoid dysplasia D H00760 Spondyloepiphyseal dysplasia tarda D H00761 SEMD, Pakistani type D H00765 Spondyloepiphyseal dysplasia, Kimberley type D H00767 SEMD, Matrilin type D H00777 SEMD, short limb-hand type D H00863 Spondylo-megaepiphyseal-metaphyseal dysplasia D H01494 SEMD with joint laxity type D H01575 Roifman syndrome D H01576 Spondyloenchondrodysplasia with immune dysregulation (SPENCDI) D H01967 Anauxetic dysplasia D H02070 Kniest dysplasia D H02071 Czech dysplasia D H02079 Oto-spondylo-megaepiphyseal dysplasia D H02080 Fibrochondrogenesis D H02155 Dyssegmental dysplasia D H02183 Parastremmatic dwarfism D H02184 Metatropic dysplasia D H02186 Spondyloepiphyseal dysplasia, Maroteaux type D H02187 Spondyloepimetaphyseal dysplasia D H02462 Spondyloepiphyseal dysplasia D H02497 Smith-McCort dysplasia D H01821 Spondylometaphyseal dysplasia with cone-rod dystrophy D H01825 Spondylometaphyseal dysplasia, Sedaghatian type D H01830 Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type D H02185 Spondylometaphyseal dysplasia D H02732 Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly D H00678 Achondrogenesis type IA D H02065 Achondrogenesis type IB D H02066 Achondrogenesis type II D H00522 Brachyolmia D H01828 Opsismodysplasia D H01844 Diaphanospondylodysostosis D H00495 Eiken dysplasia D H00477 Pseudoachondroplasia D H00476 Multiple epiphyseal dysplasia D H02436 Al-Gazali syndrome D H00479 Metaphyseal dysplasias D H00518 Metaphyseal dysplasia without hypotrichosis D H00675 Acrocapitofemoral dysplasia D H00900 Geleophysic dysplasia D H02062 Familial digital arthropathy-brachydactyly D H02228 Acromicric dysplasia D H02229 Terminal osseous dysplasia D H00466 Grebe dysplasia D H00468 Acromesomelic dysplasia, Demirhan type D H00470 Acromesomelic dysplasia, Maroteaux type D H02543 Acromesomelic dysplasia D H00485 Robinow syndrome D H00492 SHOX-related short stature D H02154 Omodysplasia D H00511 Short rib-polydactyly syndrome D H00751 Asphyxiating thoracic dystrophy D H02157 Short-rib thoracic dysplasia D H00462 Stuve-Wiedemann syndrome D H02629 Bent bone dysplasia syndrome D H00509 3M syndrome D H00619 Kenny-Caffey syndrome D H00622 Hypoparathyroidism-retardation-dysmorphism syndrome D H00992 Seckel syndrome D H02223 Osteocraniostenosis D H00494 Desbuquois syndrome D H01498 Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects D H02048 Larsen syndrome D H02064 Atelosteogenesis type I and III D H02067 Boomerang dysplasia D H00458 Syndromic craniosynostoses D H01756 Pfeiffer syndrome D H01754 Crouzon syndrome D H01755 Apert syndrome D H01008 C syndrome D H01753 Antley-Bixler syndrome D H01888 Carpenter syndrome D H01988 Jackson-Weiss syndrome D H01989 Beare-Stevenson syndrome D H01990 Muenke syndrome D H01991 Saethre-Chotzen syndrome D H01992 Craniofrontonasal syndrome D H01993 Baller-Gerold syndrome D H02047 Bohring-Opitz syndrome D H02254 Craniosynostosis and dental anomalies D H02637 Brachycephaly, trichomegaly, and developmental delay D H00517 Spondylocostal dysostosis D H01843 Cerebrocostomandibular syndrome D H00464 Nail-patella syndrome D H00461 Ischiocoxopodopatellar syndrome D H01889 Meier-Gorlin syndrome D H00506 Osteogenesis imperfecta D H00451 Osteoporosis-pseudoglioma syndrome D H00514 Bruck syndrome D H01496 Spondyloocular syndrome D H01571 Singleton-Merten syndrome D H01572 Cole-Carpenter syndrome D H02395 Calvarial doughnut lesions with bone fragility D H00969 Skeletal defects, genital hypoplasia, and mental retardation D H02233 Alazami syndrome D H02280 Complex lethal osteochondrodysplasia D H02300 Steel syndrome D H02306 Chondrodysplasia with joint dislocations, GPAPP type D H02349 Odontochondrodysplasia D H02415 Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome D H02551 Skeletal dysplasia with joint laxity and advanced bone age C LD25 Syndromes with face or limb anomalies as a major feature D H00454 Oral-facial-digital syndrome D H00456 Fronto-otopalatodigital syndromes D H01816 Frank-ter Haar syndrome D H02227 Frontometaphyseal dysplasia D H01376 Acrofacial dysostosis D H02158 Weyers acrofacial dysostosis D H00528 Frontonasal dysplasia D H00850 Frontorhiny D H01884 Auriculocondylar syndrome D H02210 Acromelic frontonasal dysostosis D H02234 Hamamy syndrome D H02640 Vertebral hypersegmentation and orofacial anomalies C LD26 Syndromes with limb anomalies as a major feature D H00467 Fibular hypoplasia and complex brachydactyly D H00853 Cenani-Lenz syndactyly syndrome D H00855 Triphalangeal thumb-polysyndactyly syndrome D H00859 Guttmacher syndrome D H00870 Brachydactyly-syndactyly syndrome D H02161 Greig cephalopolysyndactyly syndrome D H02333 Laurin-Sandrow syndrome D H00778 Tarsal-carpal coalition syndrome D H00986 Multiple pterygium syndrome D H00935 Cold-induced sweating syndrome D H01392 Arthrogryposis, mental retardation, and seizures D H01886 Van den Ende-Gupta syndrome D H02299 Arthrogryposis multiplex congenita D H02358 Arthrogryposis multiplex congenita, neurogenic, with myelin defect D H00811 Distal arthrogryposis D H00865 Lethal congenital contractural syndrome D H00872 Trismus-pseudocamptodactyly syndrome D H01931 Lethal-type popliteal pterygium syndrome D H02268 Wieacker-Wolff syndrome D H00532 Parkes Weber syndrome D H01788 Klippel-Trenaunay-Weber syndrome D H01497 Temtamy preaxial brachydactyly syndrome D H00846 Fuhrmann syndrome D H00847 Al-Awadi/Raas-Rothschild syndrome D H02717 Contractures, pterygia, and spondylocarpostarsal fusion syndrome C LD27 Syndromes with skin or mucosal anomalies as a major feature D H00651 Hypohidrotic ectodermal dysplasia D H00645 Incontinentia pigmenti D H01874 Cronkhite-Canada syndrome D H02456 Ectodermal dysplasia D H00648 Ectodermal dysplasia, Clouston type D H00095 Ectodermal dysplasia and immunodeficiency D H00204 Heimler syndrome D H00449 Oculodentodigital dysplasia D H00487 Tricho-dento-osseous syndrome D H00503 Ellis-van Creveld syndrome D H00529 Cranioectodermal dysplasia D H00540 Osteoporosis, lymphedema, anhydrotic ectodermal dysplasia with immunodeficiency (OLEDAID) D H00571 Johanson-Blizzard syndrome D H00638 Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome D H00639 Ectodermal dysplasia, ectrodactyly, and macular dystrophy D H00640 Limb-mammary syndrome D H00641 ADULT syndrome D H00642 Lacrimo-auriculo-dento-digital syndrome D H00643 Tooth and nail syndrome D H00646 Odontoonychodermal dysplasia D H00647 Ectodermal dysplasia-syndactyly syndrome D H00649 Ectodermal dysplasia, hair-nail type D H00708 Naegeli-Franceschetti-Jadassohn syndrome D H00752 Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome and Rapp-Hodgkin syndrome D H00781 Schopf-Schulz-Passarge syndrome D H00796 Dermatopathia pigmentosa reticularis D H00857 Oligodontia-colorectal cancer syndrome D H00922 Schinzel-Giedion midface retraction syndrome D H00949 Focal dermal hypoplasia D H00977 Trichorhinophalangeal syndrome D H01271 Hypoparathyroidism with sensorineural deafness and renal dysplasia D H01403 Coffin-Siris syndrome D H01905 Trichomegaly D H01966 Cartilage-hair hypoplasia D H02058 Kohlschutter-Tonz syndrome D H02081 Marshall syndrome D H02083 Focal facial dermal dysplasia D H02218 DOORS syndrome D H02219 DDOD syndrome D H02296 Basan syndrome D H02303 Alopecia-mental retardation syndrome D H02417 Gingival fibromatosis with hypertrichosis D H02474 Blepharocheilodontic syndrome D H02691 Scalp-ear-nipple syndrome D H01428 Xeroderma pigmentosum D H00671 Netherton syndrome D H00712 KID/HID syndrome D H00739 Ichthyosis with hypotrichosis D H00740 Ichthyosis follicularis, alopecia, and photophobia syndrome D H00741 Ichthyosis prematurity syndrome D H00799 CEDNIK syndrome D H01934 Barber-Say syndrome D H00818 Birt-Hogg-Dube syndrome D H01986 Legius syndrome D H02189 Neurofibromatosis-Noonan syndrome D H01741 Autoinflammation lipodystrophy and dermatosis syndrome D H00665 Mandibuloacral dysplasia D H02236 Keppen-Lubinsky syndrome D H00684 Pachyonychia congenita D H00696 Haim-Munk syndrome D H00785 Congenital hypotrichosis with juvenile macular dystrophy D H00815 H syndrome D H00883 Lipoid proteinosis D H02486 HELIX syndrome D H02713 Inflammatory poikiloderma with hair abnormalities and acral keratoses C LD28 Syndromes with connective tissue involvement as a major feature D H00660 Congenital contractural arachnodactyly D H00653 Marfan syndrome D H00800 Loeys-Dietz syndrome D H00659 Shprintzen-Goldberg syndrome D H00661 MASS phenotype D H01385 Rienhoff syndrome D H02720 Meester-Loeys syndrome D H00802 Ehlers-Danlos syndrome D H01902 Brittle cornea syndrome D H02239 Ehlers-Danlos syndrome, spondylodysplastic type D H02240 Ehlers-Danlos syndrome periodontal type D H02241 Ehlers-Danlos syndrome cardiac valvular type D H02242 Ehlers-Danlos syndrome vascular type D H02243 Ehlers-Danlos syndrome arthrochalasia type D H02244 Ehlers-Danlos syndrome dermatosparaxis type D H02245 Ehlers-Danlos syndrome kyphoscoliosis type D H02246 Ehlers-Danlos syndrome musculocontractural type D H02247 Ehlers-Danlos syndrome myopathic type D H02724 Combined osteogenesis imperfecta and Ehlers-Danlos syndrome D H00904 Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities D H00906 Macrocephaly, alopecia, cutis laxa, and scoliosis D H01859 Occipital horn syndrome D H00919 Arterial tortuosity syndrome D H02224 Grange syndrome D H02502 Joint laxity, short stature, and myopia D H02654 Boudin-Mortier syndrome D H02703 VISS syndrome C LD29 Syndromes with obesity as a major feature D H01915 Borjeson-Forssman-Lehmann syndrome D H02195 MEHMO syndrome D H02267 Wilson-Turner syndrome C LD2A Malformative disorders of sex development D H00607 46,XY gonadal dysgenesis D H00608 46,XY disorder of sex development due to testosterone secretion defect D H02177 Androgen insensitivity syndrome D H00442 Campomelic dysplasia D H00598 46,XX testicular disorder of sex development D H00609 Persistent Mullerian duct syndrome D H02317 SERKAL syndrome D H02318 Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal C LD2B Syndromes with premature ageing appearance as a major feature D H00076 Cockayne syndrome D H00558 Geroderma osteodysplasticum D H00601 Hutchinson-Gilford progeria syndrome D H01733 Werner syndrome D H01734 Rothmund-Thomson syndrome D H01883 Nestor-Guillermo progeria syndrome D H02323 Ruijs-Aalfs syndrome D H02480 Fontaine progeroid syndrome D H02570 Cerebro-oculo-facio-skeletal syndrome D H02677 Progeroid laminopathy C LD2C Overgrowth syndromes D H00713 Beckwith-Wiedemann syndrome D H00718 Sotos syndrome D H00980 Nevo syndrome D H01215 Simpson-Golabi-Behmel syndrome D H01308 Macrocephaly macrosomia facial dysmorphism syndrome D H01412 Perlman syndrome D H01751 Weaver syndrome D H01806 Tenorio syndrome D H01834 Marshall-Smith syndrome D H01885 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome D H01909 Hypoinsulinemic hypoglycemia with hemihypertrophy D H01912 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi D H02119 Proteus syndrome D H02153 Megalencephaly-capillary malformation syndrome D H02294 Tatton-Brown-Rahman syndrome D H02297 CLAPO syndrome D H02298 Macrocephaly, dysmorphic facies, and psychomotor retardation D H02347 Thauvin-Robinet-Faivre syndrome D H02444 Luscan-Lumish syndrome D H02477 Cohen-Gibson syndrome D H02522 Imagawa-Matsumoto syndrome D H02679 Miura-type epiphyseal chondrodysplasia C LD2D Phakomatoses or hamartoneoplastic syndromes D H00666 Peutz-Jeghers syndrome D H01437 Neurofibromatosis type 1 D H01438 Neurofibromatosis type 2 D H00915 Tuberous sclerosis complex D H00895 Basal cell nevus syndrome D H00559 von Hippel-Lindau syndrome D H01222 Cowden syndrome D H02576 Familial cutaneous telangiectasia and cancer syndrome D H02628 Schimmelpenning-Feuerstein-Mims syndrome D H02722 Nevus comedonicus C LD2E Syndromes with structural anomalies due to inborn errors of metabolism C LD2F Syndromes with multiple structural anomalies, without predominant body system involvement D H00979 Sacral defect with anterior meningocele D H02129 Prune belly syndrome D H01195 VACTERL/VATER association D H00261 Meckel syndrome D H01738 Noonan syndrome D H00610 Treacher Collins syndrome D H01838 Mandibulofacial dysostosis with microcephaly D H02126 Mandibulofacial dysostosis with alopecia D H02211 Acrodysostosis D H02673 Craniofacial microsomia D H00433 Holt-Oram syndrome D H00453 Branchio-oto-renal syndrome D H00460 Hand-foot-genital syndrome D H00463 Currarino syndrome D H00500 Keutel syndrome D H00502 Pallister-Hall syndrome D H00504 Rubinstein-Taybi syndrome D H00510 Feingold syndrome D H00523 Noonan syndrome and related disorders D H00555 Char syndrome D H00556 CHARGE syndrome D H00569 Aarskog-Scott syndrome D H00570 Kabuki syndrome D H00572 Roberts-SC phocomelia syndrome D H00573 Townes-Brocks syndrome D H00574 Coffin-Lowry syndrome D H00583 Opitz-GBBB syndrome D H00611 Popliteal pterygium syndrome (PPS) D H00631 Cornelia de Lange syndrome D H00634 Duane-radial ray syndrome D H00637 Ulnar-mammary syndrome D H00685 Bifid nose with or without anorectal and renal anomalies D H00686 Manitoba oculotrichoanal syndrome D H00709 Birk Barel mental retardation syndrome (BBMRS) D H00711 Russell-Silver syndrome D H00753 Urofacial syndrome D H00756 Pitt-Hopkins syndrome D H00797 Martsolf syndrome D H00817 Branchiooculofacial syndrome D H00868 Stapes ankylosis with broad thumb and toes D H00886 Donnai-Barrow syndrome D H00889 Lujan-Fryns syndrome D H00894 FG syndrome D H00907 Kleefstra syndrome D H00908 Mowat-Wilson syndrome D H00914 Warsaw breakage syndrome D H00926 Growth retardation, developmental delay, coarse facies, and early death D H00934 Caudal duplication anomaly D H00936 Goldberg-Shprintzen megacolon syndrome D H00943 TARP syndrome D H00965 RAPADILINO syndrome D H00972 Endocrine-cerebro-osteodysplasia syndrome D H00987 Fetal akinesia deformation sequence D H00997 CATSHL syndrome D H01026 Renal coloboma syndrome D H01030 Congenital arthrogryposis with anterior horn cell disease D H01156 STAR syndrome D H01220 Congenital cataracts, facial dysmorphism, and neuropathy D H01265 Hydrolethalus syndrome D H01289 Mulibrey nanism D H01292 Nance-Horan syndrome D H01370 SHORT syndrome D H01393 Van Maldergem syndrome D H01402 Nicolaides-Baraitser syndrome D H01413 Adams-Oliver syndrome D H01568 3C syndrome D H01569 CHOPS syndrome D H01573 Zimmermann-Laband syndrome D H01745 Cardiofaciocutaneous syndrome D H01747 Costello syndrome D H01793 Young-Simpson syndrome D H01794 Genitopatellar syndrome D H01795 Blepharophimosis-mental retardation syndrome D H01797 Webb-Dattani syndrome D H01814 Stromme syndrome D H01839 Burn-McKeown syndrome D H01840 Moebius syndrome D H01845 Catel-Manzke syndrome D H01869 Megacystis microcolon intestinal hypoperistalsis syndrome D H01878 Al-Raqad syndrome D H01879 Wiedemann-Steiner syndrome D H01887 3MC syndrome D H01908 Carey-Fineman-Ziter syndrome D H01917 CK syndrome D H01923 Microcephaly, short stature, and impaired glucose metabolism D H01927 Van der Woude syndrome D H01930 Au-Kline syndrome D H01932 Ablepharon-macrostomia syndrome D H01984 Leopard syndrome D H02023 Baraitser-Winter syndrome D H02046 OFC syndrome D H02072 Stickler syndrome D H02074 Knobloch syndrome D H02082 Floating-Harbor syndrome D H02087 Vertebral, cardiac, renal, and limb defects syndrome D H02102 Myhre syndrome D H02180 McKusick-Kaufman syndrome D H02190 CBL syndrome D H02191 Noonan-like syndrome with loose anagen hair D H02198 Pancreatic agenesis and congenital heart disease D H02232 CAGSSS syndrome D H02248 MEND syndrome D H02249 Primrose syndrome D H02253 Beaulieu-Boycott-Innes syndrome D H02255 FDLAB syndrome D H02260 Chondrodysplasia Chassaing-Lacombe type D H02271 Cerebellofaciodental syndrome D H02274 Cerebellar atrophy, visual impairment, and psychomotor retardation D H02283 IVIC syndrome D H02324 Sacral agenesis with vertebral anomalies D H02327 KBG syndrome D H02328 Sifrim-Hitz-Weiss syndrome D H02334 Pierpont syndrome D H02364 Heart and brain malformation syndrome D H02368 Developmental delay with short stature, dysmorphic facial features, and sparse hair D H02369 IMAGE-I syndrome D H02370 FILS syndrome D H02376 Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies D H02381 Cleft palate, psychomotor retardation, and distinctive facial features D H02382 Bainbridge-Ropers syndrome D H02383 Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis D H02391 Infantile-onset multisystem neurologic, endocrine, and pancreatic disease D H02394 Cleft palate, cardiac defects, and mental retardation D H02453 Congenital heart defects and ectodermal dysplasia D H02454 Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder D H02455 Congenital heart defects, hamartomas of tongue, and polysyndactyly D H02478 CATIFA syndrome D H02479 Nivelon-Nivelon-Mabille syndrome D H02481 Syndromic disorder with short stature D H02482 ROSAH syndrome D H02483 Basel-Vanagaite-Smirin-Yosef syndrome D H02493 Al Kaissi syndrome D H02496 Cerebellar, ocular, craniofacial, and genital syndrome D H02500 Congenital interstitial lung disease with nephrotic syndrome and epidermolysis bullosa D H02503 Richieri-Costa-Pereira syndrome D H02506 Cardioacrofacial dysplasia D H02508 Agenesis of corpus callosum, cardiac, ocular, and genital syndrome D H02533 Kaufman oculocerebrofacial syndrome D H02581 Juberg-Hayward syndrome D H02595 Oculoskeletodental syndrome D H02607 Short stature and microcephaly with genital anomalies D H02619 Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome D H02625 Primordial dwarfism-immunodeficiency-lipodystrophy syndrome D H02641 Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development D H02650 Menke-Hennekam syndrome D H02694 Alazami-Yuan syndrome D H02725 Heart-hand syndrome D H01824 CODAS syndrome D H01850 Hartsfield syndrome D H01857 Filippi syndrome D H02343 EVEN-plus syndrome D H02465 Weiss-Kruszka syndrome D H02547 BRENS syndrome D H02548 CIMDAG syndrome D H02549 Cerebellar ataxia, brain abnormalities, and cardiac conduction defects D H02578 Short stature, microcephaly, and endocrine dysfunction D H02638 Zaki syndrome D H02639 Atelis syndrome D H02663 Braddock-Carey syndrome D H02667 Takenouchi-Kosaki syndrome D H02710 Yuksel-Vogel-Bauer syndrome D H02733 Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies C LD2G Conjoined twins C LD2H Syndromic genetic deafness D H00687 Fraser syndrome D H02356 PCWH syndrome D H00779 Usher syndrome D H00446 Craniofacial-deafness-hand syndrome D H00581 Alport syndrome D H00706 Bart-Pumphrey syndrome D H00727 Athabascan brainstem dysgenesis syndrome D H00803 Seizures-sensorineural deafness-ataxia-mental retardation-electrolyte imbalance (SESAME) D H00823 ABCD syndrome D H00946 Arts syndrome D H01286 Microtia hearing impairment and cleft palate D H01903 Brown-Vialetto-Van Laere syndrome D H02095 Perrault syndrome D H02135 Cone-rod dystrophy and hearing loss D H02220 MEDNIK syndrome D H02226 Cardiospondylocarpofacial syndrome D H02286 Congenital deafness with inner ear agenesis, microtia, and microdontia D H02287 Deafness, dystonia, and cerebral hypomyelination D H02326 Keipert syndrome D H02355 Deafness and myopia D H02430 Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus D H02435 Deafness-infertility syndrome D H02634 Deafness, cataract, impaired intellectual development, and polyneuropathy D H02687 Congenital deafness and adult-onset progressive leukoencephalopathy C LD2Y Other specified multiple developmental anomalies or syndromes D H00417 Alstrom syndrome D H00418 Bardet-Biedl syndrome D H01623 MDPL syndrome D H02488 Cardiac-urogenital syndrome D H02523 Genitourinary and/or brain malformation syndrome D H02630 Chitayat syndrome C LD2Z Multiple developmental anomalies or syndromes, unspecified D H00493 Heparan sulfate proteoglycan gene defects B Chromosomal anomalies, excluding gene mutations C LD40 Complete trisomies of the autosomes D H01552 Down syndrome D H01562 Patau syndrome D H01564 Edwards syndrome C LD41 Duplications of the autosomes D H02604 Chromosome 1q21.1 duplication syndrome D H01790 Emanuel syndrome C LD42 Polyploidies C LD43 Complete monosomies of the autosomes C LD44 Deletions of the autosomes D H01831 Ring chromosome 20 syndrome D H01792 1p36 deletion syndrome D H02471 Brain malformations with urinary tract defects D H00561 Brachydactyly-mental retardation syndrome D H02146 Glass syndrome D H01773 4p deletion syndrome D H01223 Mental retardation-stereotypic movements-epilepsy and/or cerebral malformations D H00764 Chromosome 5p deletion syndrome D H01439 Williams-Beuren syndrome D H01800 Verheij syndrome D H02103 DeSanto-Shinawi syndrome D H02156 Lamb-Shaffer syndrome D H01861 Chromosome 15q24 microdeletion syndrome D H01877 Chromosome 15q13.3 microdeletion syndrome D H02121 Koolen-De Vries syndrome D H01791 Smith-Magenis syndrome D H01004 Velocardiofacial syndrome D H01524 DiGeorge syndrome D H01525 22q11.2 deletion syndrome D H01238 Phelan-McDermid syndrome C LD45 Uniparental disomies D H01801 Kagami-Ogata syndrome C LD46 Imprinting errors C LD47 Balanced rearrangements or structural rearrangements C Sex chromosome anomalies D LD50 Number anomalies of chromosome X D LD51 Structural anomalies of chromosome X, excluding Turner syndrome E H00552 Chromosome Xp21 deletion syndrome E H00994 Familial skewed X-chromosome inactivation D LD52 Number anomalies of chromosome Y D LD53 Structural anomalies of chromosome Y D LD54 Male with sex chromosome mosaicism D LD55 Fragile X chromosome E H00465 Fragile X syndrome E H01731 Fragile X tremor/ataxia syndrome D LD56 Chimaera 46, XX, 46, XY D LD5Y Other specified sex chromosome anomalies D LD5Z Sex chromosome anomalies, unspecified C LD7Y Other specified chromosomal anomalies, excluding gene mutations D H01288 Mosaic variegated aneuploidy syndrome C LD7Z Chromosomal anomalies, excluding gene mutations, unspecified B LD90 Conditions with disorders of intellectual development as a relevant clinical feature C H01732 Angelman syndrome C H00478 Prader-Willi syndrome C H00440 Rett syndrome C H00597 Snyder-Robinson syndrome C H00769 Hyperekplexia C H00940 Cohen syndrome C H01752 ATR-X syndrome C H01769 ZTTK syndrome C H01913 Renpenning syndrome C H01914 Christianson syndrome C H01916 Stocco dos Santos X-linked mental retardation syndrome C H01920 Partington syndrome C H01922 Infantile hypotonia with psychomotor retardation and characteristic facies C H02137 Laurence-Moon syndrome C H02252 PEHO syndrome C H02305 RERE-related neurodevelopmental syndrome C H02325 Schaaf-Yang syndrome C H02337 Skraban-Deardorff syndrome C H02338 PEHO-like syndrome C H02346 Intellectual developmental disorder with short stature C H02353 Hyperekplexia and epilepsy C H02363 Ververi-Brady syndrome C H02365 Helsmoortel-van der Aa syndrome C H02378 Hypotonia, ataxia, and delayed development syndrome C H02397 Neurodevelopmental disorder with movement abnormalities or hypotonia C H02437 Growth retardation, impaired intellectual development, hypotonia, and hepatopathy C H02459 Syndromic neurodevelopmental disorder C H02460 Neurodevelopmental disorder with dysmorphic facies and skeletal anomalies C H02461 Neurodevelopmental disorder with microcephaly C H02463 Syndromic intellectual developmental disorder C H02470 Neurodevelopmental disorder with structural brain abnormalities C H02515 Li-Ghorbani-Weisz-Hubshman syndrome C H02528 Hao-Fountain syndrome C H02535 Neurodevelopmental disorder with dysmorphic facies C H02560 White-Kernohan syndrome C H02582 Mullegama-Klein-Martinez syndrome C H02583 X-linked intellectual disability-hypotonic facies syndrome C H02584 Ferguson-Bonni neurodevelopmental syndrome C H02587 Luo-Schoch-Yamamoto syndrome C H02611 Turnpenny-Fry syndrome C H02612 Radio-Tartaglia syndrome C H02613 Brunet-Wagner neurodevelopmental syndrome C H02614 Snijders Blok-Campeau syndrome C H02615 Parenti-Mignot neurodevelopmental syndrome C H02616 Neurodevelopmental disorder with macrocephaly C H02617 Bryant-Li-Bhoj neurodevelopmental syndrome C H02618 Developmental delay with variable intellectual disability and dysmorphic facies C H02622 Shukla-Vernon syndrome C H02623 Kury-Isidor syndrome C H02632 PP2A-related neurodevelopmental disorder C H02633 Beck-Fahrner syndrome C H02635 Poirier-Bienvenu neurodevelopmental syndrome C H02651 Lessel-Kreienkamp syndrome C H02659 Dentici-Novelli neurodevelopmental syndrome C H02666 Chilton-Okur-Chung neurodevelopmental syndrome C H02682 Nizon-Isidor syndrome C H02685 Developmental delay with neuropsychiatric disorders C H02686 Developmental delay with dysmorphic facies and dental anomalies C H02688 Dworschak-Punetha neurodevelopmental syndrome C H02698 Trichohepatoneurodevelopmental syndrome C H02700 Intellectual developmental disorder with impaired language and dysmorphic facies C H02712 Li-Campeau syndrome C H02714 Tessadori-Bicknell-van Haaften neurodevelopmental syndrome C H02715 Neurodevelopmental disorder with defects of ubiquitin-proteasome system C H02728 Marbach-Schaaf neurodevelopmental syndrome C H02734 Hengel-Maroofian-Schols syndrome B LD9Y Other specified developmental anomalies B LD9Z Developmental anomalies, unspecified # A21 Symptoms, signs or clinical findings, not elsewhere classified B Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system C Symptoms of blood, blood-forming organs, or the immune system D MA00 Symptom or complaint of the blood D MA01 Enlarged lymph nodes D MA0Y Other specified symptoms of blood, blood-forming organs, or the immune system C Clinical findings in blood, blood-forming organs, or the immune system D MA10 Abnormal serum enzyme levels D MA11 Clinical findings of hormones in blood, blood-forming organs, or the immune system D MA12 Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system D MA13 Clinical findings of substances chiefly nonmedicinal as to source in blood, blood-forming organs, or the immune system D MA14 Immunological findings in blood, blood-forming organs, or the immune system D MA15 Microbiological findings in blood, blood-forming organs, or the immune system D MA16 Cytological findings in blood, blood-forming organs, or the immune system D MA17 Histological findings in blood, blood-forming organs, or the immune system D MA18 Certain clinical findings of blood chemistry D MA19 Certain abnormalities of plasma proteins D MA1A Elevated erythrocyte sedimentation rate or abnormality of plasma viscosity D MA1Y Other specified clinical findings in blood, blood-forming organs, or the immune system C MA3Y Other specified symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system B Symptoms, signs or clinical findings of endocrine, nutritional or metabolic diseases C Results of function studies of the endocrine, nutritional or metabolic diseases D MA50 Abnormal results of thyroid function studies D MA51 Abnormal results of other endocrine function studies C MA6Y Other specified symptoms, signs or clinical findings of endocrine, nutritional or metabolic diseases B Symptoms, signs or clinical findings of speech or voice C Symptoms or signs involving speech or voice D MA80 Speech disturbances D MA81 Speech dysfluency D MA82 Voice disturbances D MA8Y Other specified symptoms or signs involving speech or voice C MB0Y Other specified symptoms, signs or clinical findings of speech or voice B Mental or behavioural symptoms, signs or clinical findings C MB20 Symptoms, signs or clinical findings involving consciousness C MB21 Symptoms, signs or clinical findings involving cognition C MB22 Symptoms or signs involving motivation or energy C MB23 Symptoms or signs involving appearance or behaviour C MB24 Symptoms or signs involving mood or affect C MB25 Symptoms or signs involving form of thought C MB26 Symptoms or signs involving content of thought C MB27 Symptoms or signs involving perceptual disturbance C MB28 Symptoms or signs related to personality features C MB29 Symptoms or signs involving eating and related behaviour C MB2A Symptoms or signs involving elimination C MB2Y Other specified mental or behavioural symptoms, signs or clinical findings B Symptoms, signs or clinical findings of the nervous system C Symptoms or signs involving the nervous system D MB40 Sensation disturbance D MB41 Disturbances of smell and taste D MB42 Phonophobia D MB43 Dyssomnia D MB44 Abnormalities of gait and mobility D MB45 Lack of coordination D MB46 Abnormal involuntary movements D MB47 Abnormality of tonus and reflex E H02388 Infantile-onset limb and orofacial dyskinesia E H02389 Familial dyskinesia with facial myokymia D MB48 Dizziness and giddiness D MB49 Aura D MB4A Apraxia D MB4B Symbolic dysfunctions E H01899 Dyslexia D MB4C Gerstmann syndrome D MB4D Headache, not elsewhere classified D Paralytic symptoms E MB50 Tetraplegia E MB51 Diplegia of upper extremities E MB52 Diplegia of lower extremities E MB53 Hemiplegia F H00998 Alternating hemiplegia of childhood E MB54 Monoplegia of upper extremity E MB55 Monoplegia of lower extremity E MB56 Paraplegia E MB57 Functional level of injury of spinal cord E MB5Y Other specified paralytic symptoms E MB5Z Paralytic symptoms, unspecified D MB60 Sleeptalking D MB6Y Other specified symptoms or signs involving the nervous system C Clinical findings in the nervous system D MB70 Clinical findings in cerebrospinal fluid D MB71 Clinical findings on diagnostic imaging of central nervous system D MB72 Results of function studies of the nervous system D MB7Y Other specified clinical findings in the nervous system C MB9Y Other specified symptoms, signs or clinical findings of the nervous system B Symptoms, signs or clinical findings of the visual system C Symptoms or signs involving the visual system D MC10 Eye appearance abnormal D MC11 Eye sensation abnormal D MC12 Chronic enlargement of lacrimal gland D MC13 Epiphora D MC14 Eye discharge D MC15 Red eye D MC16 Pallor conjunctiva D MC17 Icteric sclera D MC18 Ocular pain D MC19 Quadrantanopia D MC1A Visual floaters D MC1B Symptom or complaint of the eyelid D MC1C Symptom or complaint of glasses D MC1D Symptom or complaint of contact lens D MC1Y Other specified symptoms or signs involving the visual system C MC20 Clinical findings of the visual system C MC21 Impairment of electrophysiological functions C MC2Y Other specified symptoms, signs or clinical findings of the visual system B Symptoms, signs or clinical findings of ear or mastoid process C Symptoms or signs involving the ear or mastoid process D MC40 Plugged feeling ear D MC41 Tinnitus D MC4Y Other specified symptoms or signs involving the ear or mastoid process C MC6Y Other specified symptoms, signs or clinical findings of ear or mastoid process B Symptoms, signs or clinical findings of the circulatory system C Symptoms or signs involving the circulatory system D MC80 Abnormal blood-pressure reading, without diagnosis D MC81 Abnormalities of heart beat D MC82 Cardiac arrest D MC83 Cardiac murmurs and other cardiac sounds D MC84 Cardiovascular pain D MC85 Gangrene D MC86 Precordial pain D MC87 Pressure or tightness of heart D MC88 Prominent veins D MC8Y Other specified symptoms or signs involving the circulatory system C MC90 Clinical findings on diagnostic imaging of heart or coronary circulation C MC91 Results of function studies of the circulatory system C MC9Y Other specified symptoms, signs or clinical findings of the circulatory system B Symptoms, signs or clinical findings of the respiratory system C Symptoms or signs involving the respiratory system D MD10 Abnormal sputum D MD11 Abnormalities of breathing D MD12 Cough D Haemorrhage from respiratory passages E MD20 Epistaxis E MD21 Haemorrhage from throat E MD22 Haemoptysis E MD23 Haemorrhage from other sites in respiratory passages E MD24 Acute idiopathic pulmonary haemorrhage in infants over 28 days of age E MD2Z Haemorrhage from respiratory passages, unspecified D MD30 Pain in throat or chest D MD31 Pleurisy D MD32 Rales D MD33 Respiratory arrest D MD34 Symptom or complaint of the nose D MD35 Symptom or complaint of the sinus D MD36 Symptom or complaint of the throat D MD3Y Other specified symptoms or signs involving the respiratory system C Clinical findings in the respiratory system D MD40 Clinical findings in specimens from respiratory organs and thorax D MD41 Clinical findings on diagnostic imaging of lung D MD42 Results of function studies of the respiratory system D MD4Y Other specified clinical findings in the respiratory system C MD6Y Other specified symptoms, signs or clinical findings of the respiratory system B Symptoms, signs or clinical findings of the digestive system or abdomen C Symptoms or signs involving the digestive system or abdomen D MD80 Symptoms or signs of the orofacial complex D MD81 Abdominal or pelvic pain D MD82 Intra-abdominal or pelvic swelling, mass or lump D Symptoms related to the upper gastrointestinal tract E MD90 Nausea or vomiting E MD91 Belching E MD92 Dyspepsia E MD93 Dysphagia E MD94 Halitosis E MD95 Heartburn E MD9Y Other specified symptoms related to the upper gastrointestinal tract D Symptoms related to the lower gastrointestinal tract or abdomen E ME00 Abdominal compartment syndrome E ME01 Abdominal distension E ME02 Abdominal rigidity E ME03 Abnormal bowel sounds E ME04 Ascites E ME05 Change in bowel habit E ME06 Chronic enteritis of uncertain aetiology E ME07 Faecal incontinence E ME08 Flatulence and related conditions E ME09 Rectal tenesmus E ME0A Visible peristalsis E ME0B Problems with defaecation, not otherwise specified E ME0Y Other specified symptoms related to the lower gastrointestinal tract or abdomen D ME10 Abnormalities related to hepatobiliary system D ME1Y Other specified symptoms or signs involving the digestive system or abdomen C Clinical findings in the digestive system D ME20 Clinical findings in specimens from digestive organs or abdominal cavity D ME21 Clinical findings on diagnostic imaging of liver or biliary tract D ME22 Clinical findings on diagnostic imaging of digestive tract D ME23 Results of function studies of the digestive system D ME24 Clinical manifestations of the digestive system D ME2Y Other specified clinical findings in the digestive system C ME4Y Other specified symptoms, signs or clinical findings of the digestive system or abdomen B Symptoms, signs or clinical findings involving the skin C Symptoms or signs involving the skin D ME60 Skin lesion of uncertain or unspecified nature D ME61 Subcutaneous swelling, mass or lump of uncertain or unspecified nature D ME62 Acute skin eruption of uncertain or unspecified nature D ME63 Chronic skin disorder of uncertain or unspecified nature D ME64 Non-specific cutaneous vascular signs D ME65 Disturbances of skin sensation of unspecified aetiology D ME66 Miscellaneous non-specific skin-related symptoms and signs D ME67 Skin disorder of uncertain or unspecified nature D ME6Y Other specified symptoms or signs involving the skin B Symptoms, signs or clinical findings of the musculoskeletal system C Symptoms or signs of the musculoskeletal system D ME80 Clicking hip D ME81 Musculoskeletal chest pain D ME82 Pain in joint D ME83 Rheumatism, unspecified D ME84 Spinal pain D ME85 Stiffness of joint D ME86 Symptom or complaint of a body part D ME8Y Other specified symptoms or signs of the musculoskeletal system C Clinical findings in the musculoskeletal system D ME90 Clinical findings on diagnostic imaging of skull and head D ME91 Clinical findings on diagnostic imaging of limbs D ME92 Clinical findings on diagnostic imaging of other parts of musculoskeletal system D ME93 Biomechanical lesions, not elsewhere classified D ME9Y Other specified clinical findings in the musculoskeletal system C MF1Y Other specified symptoms, signs or clinical findings of the musculoskeletal system B Symptoms, signs or clinical findings of the genitourinary system C Symptoms, signs or clinical findings involving the female genital system D MF30 Breast lump or mass female D MF31 Breast or lactation symptom or complaint D MF32 Menopausal symptom or complaint D MF33 Premenstrual symptom or complaint D MF34 Pregnancy symptom or complaint D MF35 Postpartum symptom or complaint D MF36 Other symptom or complaint of vagina D MF37 Symptom or complaint of female nipple D MF38 Symptom or complaint of female pelvis D MF39 Symptom or complaint of the vulva D MF3A Vaginal discharge E H01380 Bacterial vaginosis D MF3Y Other specified symptoms, signs or clinical findings involving the female genital system C Symptoms, signs or clinical findings involving the male genital system D MF40 Problems of male genital organs D MF41 Symptom or complaint of male sexual function D MF42 Retractile testis migrans D MF4Y Other specified symptoms, signs or clinical findings involving the male genital system C Symptoms, signs or clinical findings involving the urinary system D MF50 Abnormal micturition D MF51 Anuria or oliguria D MF52 Bladder pain D MF53 Extrarenal uraemia D MF54 Macroscopic changes of size of the kidney D MF55 Polyuria D MF56 Renal colic D MF57 Symptom or complaint of bladder D MF58 Urethral discharge D MF59 Urinary symptom or complaint D MF5Y Other specified symptoms, signs or clinical findings involving the urinary system C Clinical findings in specimens from female genital organs D MF60 Abnormal level of enzymes in specimens from female genital organs D MF61 Abnormal level of hormones in specimens from female genital organs D MF62 Abnormal level of drugs, medicaments and biological substances in specimens from female genital organs D MF63 Abnormal level of substances chiefly nonmedicinal as to source in specimens from female genital organs D MF64 Abnormal immunological findings in specimens from female genital organs D MF65 Abnormal microbiological findings in specimens from female genital organs D MF66 Abnormal cytological findings in specimens from female genital organs D MF67 Abnormal histological findings in specimens from female genital organs D MF68 Abnormal chromosomal findings in specimens from female genital organs D MF6Y Other specified clinical findings in specimens from female genital organs D MF6Z Clinical findings in specimens from female genital organs, unspecified C Clinical findings in specimens from male genital organs D MF70 Abnormal level of enzymes in specimens from male genital organs D MF71 Abnormal level of hormones in specimens from male genital organs D MF72 Abnormal level of drugs, medicaments and biological substances in specimens from male genital organs D MF73 Abnormal level of substances chiefly nonmedicinal as to source in specimens from male genital organs D MF74 Abnormal immunological findings in specimens from male genital organs D MF75 Abnormal microbiological findings in specimens from male genital organs D MF76 Abnormal cytological findings in specimens from male genital organs D MF77 Abnormal histological findings in specimens from male genital organs D MF78 Abnormal chromosomal findings in specimens from male genital organs D MF7Y Other specified clinical findings in specimens from male genital organs D MF7Z Clinical findings in specimens from male genital organs, unspecified C Clinical findings in specimens from the urinary system D MF80 Diffuse mesangial sclerosis D MF81 Fibronectin glomerulopathy E H01260 Glomerulopathy with fibronectin deposits D MF82 Lipoprotein glomerulopathy E H00887 Lipoprotein glomerulopathy D MF83 Diabetic glomerular changes D MF84 Pauci-immune proliferative glomerulonephritis D MF85 Anti-glomerular basement membrane antibody mediated disease E H01721 Anti-glomerular basement membrane (GBM) disease D MF8Y Other specified clinical findings in specimens from the urinary system E H00626 Focal segmental glomerulosclerosis E H01581 IgA nephropathy E H01726 Membranoproliferative glomerulonephritis E H01767 Henoch-Schonlein purpura nephritis E H02579 C3 glomerulopathy D MF8Z Clinical findings in specimens from the urinary system, unspecified C Clinical findings on examination of urine, without diagnosis D MF90 Acetonuria D MF91 Bilirubinuria D MF92 Chyluria D MF93 Glycosuria D MF94 Haemoglobinuria D MF95 Myoglobinuria E H01290 Acute recurrent myoglobinuria D MF96 Proteinuria D MF97 Pyuria D MF98 Abnormal levels of serum electrolytes in the urine E H02340 Absorptive hypercalciuria D MF99 Elevated urine levels of drugs, medicaments and biological substances D MF9A Abnormal urine levels of substances chiefly nonmedicinal as to source D MF9B Abnormal findings on microbiological examination of urine D MF9C Abnormal findings on cytological and histological examination of urine D MF9Y Other specified clinical findings on examination of urine, without diagnosis C MG00 Clinical findings on diagnostic imaging of breast C MG01 Clinical findings on diagnostic imaging of urinary organs C MG02 Results of kidney function studies C MG0Y Other specified symptoms, signs or clinical findings of the genitourinary system B General symptoms, signs or clinical findings C General symptoms D MG20 Cachexia D MG21 Chills D MG22 Fatigue D MG23 Fear of death or dying D MG24 Fear of disease D MG25 Feeling ill D MG26 Fever of other or unknown origin D MG27 Haemorrhage, not elsewhere classified D MG28 Hypothermia, not associated with low environmental temperature D MG29 Oedema D MG2A Ageing associated decline in intrinsic capacity D Pain E MG30 Chronic pain F H01636 Fibromyalgia E MG31 Acute pain E MG3Z Pain, unspecified D MG40 Shock D MG41 Sleep disturbance, not elsewhere classified D MG42 Somnolence, not elsewhere classified D MG43 Symptoms and signs concerning food and fluid intake D MG44 Symptoms peculiar to infancy E H02681 Short stature with nonspecific skeletal abnormalities D MG45 Syncope and collapse D MG46 Systemic inflammatory response syndrome of noninfectious origin D MG47 Toxicosis not further specified D MG48 Unknown and unspecified causes of morbidity D MG49 Hangover D MG4A Multi organ failure D MG4Y Other specified general symptoms C Finding of microorganism resistant to antimicrobial drugs D MG50 Finding of gram negative bacteria resistant to antimicrobial drugs E H00309 Multidrug-resistant Acinetobacter infection E H01422 Carbapenem-resistant bacterial infection E H00313 Multidrug-resistant Pseudomonas aeruginosa infection D MG51 Finding of gram positive bacteria resistant to antimicrobial drugs E H00330 Methicillin-resistant Staphylococcal aureus (MRSA) infection E H00331 Vancomycin-resistant Staphylococcal aureus (VRSA) infection E H01423 Penicillin-resistant Streptococcus pneumoniae infection E H00340 Vancomycin-resistant enterococci infection E H01401 Methicillin-resistant Staphylococcus epidermidis (MRSE) infection D MG52 Finding of bacteria, neither gram negative nor positive, resistant to antimicrobial drugs E H01472 Multidrug-resistant tuberculosis D MG53 Finding of virus resistant to antimicrobial drugs D MG54 Finding of fungus resistant to antimicrobial drugs D MG55 Finding of parasite resistant to antimicrobial drugs D MG56 Finding of microorganism resistant to other multiple antimicrobial drugs D MG5Y Finding of other microorganism resistant to antimicrobial drugs D MG5Z Finding of microorganism resistant to antimicrobial drugs, unspecified C Clinical findings in specimens from other specified organs, systems and tissues D MG60 Abnormal level of enzymes in specimens from other organs, systems and tissues D MG61 Abnormal level of hormones in specimens from other organs, systems and tissues D MG62 Abnormal level of drugs, medicaments and biological substances in specimens from other organs, systems and tissues D MG63 Abnormal level of substances chiefly nonmedicinal as to source in specimens from other organs, systems and tissues D MG64 Abnormal immunological findings in specimens from other organs, systems and tissues D MG65 Abnormal microbiological findings in specimens from other organs, systems and tissues D MG66 Abnormal cytological findings in specimens from other organs, systems and tissues D MG67 Abnormal histological findings in specimens from other organs, systems and tissues D MG6Y Other specified clinical findings in specimens from other specified organs, systems and tissues C Abnormal results, not elsewhere classified D MG70 Abnormal diagnostic imaging results not elsewhere classified D MG71 Abnormal laboratory results, not elsewhere classified D MG72 Abnormal results of function studies of other organs and systems D MG7Y Other specified abnormal results, not elsewhere classified D MG7Z Abnormal results, not elsewhere classified, unspecified C MG9Y Other specified general symptoms, signs or clinical findings B Ill-defined and unknown causes of mortality C MH10 Brain death C MH11 Sudden infant death syndrome D H02174 Sudden infant death with dysgenesis of the testes syndrome C MH12 Other sudden death, cause unknown C MH13 Unattended death C MH14 Other ill-defined and unspecified causes of mortality C MH15 Sudden unexpected death in epilepsy B MH2Y Other specified symptoms, signs or clinical findings, not elsewhere classified # A22 Injury, poisoning or certain other consequences of external causes B Injuries to the head C NA00 Superficial injury of head C NA01 Open wound of head C NA02 Fracture of skull or facial bones C NA03 Dislocation or strain or sprain of joints or ligaments of head C NA04 Injury of cranial nerves C NA05 Injury of blood vessels of head C NA06 Injury of eye or orbit C NA07 Intracranial injury C NA08 Crushing injury of head C NA09 Traumatic amputation of part of head C NA0A Certain specified injuries of head C NA0B Injury of the auricle C NA0C Injury of middle or inner ear C NA0D Injury of teeth or supporting structures C NA0Z Injuries to the head, unspecified B Injuries to the neck C NA20 Superficial injury of neck C NA21 Open wound of neck C NA22 Fracture of neck C NA23 Dislocation or strain or sprain of joints or ligaments at neck level C Injury of nerves or spinal cord at neck level D Injury of spinal cord at neck level E NA30 Concussion or oedema of cervical spinal cord E NA31 Certain specified injuries of cervical spinal cord E NA3Z Injury of cervical spinal cord, unspecified D Injury of nerves at neck level E NA40 Injury of nerve root of cervical spine E NA41 Injury of brachial plexus E NA42 Injury of peripheral nerves of neck E NA43 Injury of cervical sympathetic nerves E NA44 Injury of phrenic nerve E NA4Y Injury of other specified nerves at neck level E NA4Z Injury of nerves at neck level, unspecified C NA60 Injury of blood vessels at neck level C NA61 Injury of muscle, fascia or tendon at neck level C NA62 Crushing injury of neck C NA63 Traumatic amputation at neck level C NA64 Multiple injuries of neck C NA6Y Other specified injuries to the neck C NA6Z Injuries to the neck, unspecified B Injuries to the thorax C NA80 Superficial injury of thorax C NA81 Open wound of thorax C NA82 Fracture of rib, sternum or thoracic spine C NA83 Dislocation or strain or sprain of joints or ligaments of thorax C Injury of nerves or spinal cord at thorax level D Injury of spinal cord at thorax level E NA90 Concussion or oedema of thoracic spinal cord E NA91 Certain specified injuries of thoracic spinal cord E NA9Z Injury of thoracic spinal cord, unspecified D Injury of nerves at thorax level E NB00 Injury of nerve root of thoracic spine E NB01 Injury of peripheral nerves of thorax E NB02 Injury of thoracic sympathetic nerves E NB0Y Injury of other specified nerves at thorax level D NB2Y Other specified injury of nerves or spinal cord at thorax level D NB2Z Injury of nerves or spinal cord at thorax level, unspecified C NB30 Injury of blood vessels of thorax C NB31 Injury of heart C NB32 Injury of other or unspecified intrathoracic organs C NB33 Crushing injury of thorax or traumatic amputation of part of thorax C NB34 Injury of muscle, fascia or tendon at thorax level C NB35 Multiple injuries of thorax C NB3Y Other specified injuries to the thorax C NB3Z Injuries to the thorax, unspecified B Injuries to the abdomen, lower back, lumbar spine or pelvis C NB50 Superficial injury of abdomen, lower back or pelvis C NB51 Open wound of abdomen, lower back or pelvis C NB52 Fracture of lumbar spine or pelvis C NB53 Dislocation or strain or sprain of joints or ligaments of lumbar spine or pelvis C Injury of nerves or lumbar spinal cord at abdomen, lower back or pelvis level D Injury of spinal cord at abdomen, lower back or pelvis level E NB60 Concussion or oedema of lumbar spinal cord E NB61 Concussion or oedema of sacral spinal cord E NB62 Certain specified injuries of lumbar spinal cord E NB63 Certain specified injuries of sacral spinal cord E NB6Z Injury of spinal cord at abdomen, lower back or pelvis level, unspecified D Injury of nerves at abdomen, lower back or pelvis level E NB70 Injury of nerve root of lumbar spine E NB71 Injury of nerve root of sacral spine E NB72 Injury of cauda equina E NB73 Injury of lumbosacral plexus E NB74 Injury of lumbar, sacral or pelvic sympathetic nerves E NB75 Injury of peripheral nerve of abdomen, lower back or pelvis E NB7Y Other specified injury of nerves at abdomen, lower back or pelvis level E NB7Z Injury of nerves at abdomen, lower back or pelvis level, unspecified C NB90 Injury of blood vessels at abdomen, lower back or pelvis level C NB91 Injury of intra-abdominal organs C NB92 Injury of urinary or pelvic organs C NB93 Crushing injury or traumatic amputation of part of abdomen, lower back or pelvis C NB94 Injury of muscle, fascia or tendon of abdomen, lower back or pelvis C NB95 Injury of intra-abdominal organ with pelvic organ C NB96 Other multiple injuries of abdomen, lower back or pelvis C NB97 Certain specified injuries of abdomen, lower back or pelvis C NB98 Injury to female genital organ without further specification C NB99 Injury to male genital organ without further specification C NB9Y Other specified injuries to the abdomen, lower back, lumbar spine or pelvis C NB9Z Injuries to the abdomen, lower back, lumbar spine or pelvis, unspecified B Injuries to the shoulder or upper arm C NC10 Superficial injury of shoulder or upper arm C NC11 Open wound of shoulder or upper arm C NC12 Fracture of shoulder or upper arm C NC13 Dislocation or strain or sprain of joints or ligaments of shoulder girdle C NC14 Injury of nerves at shoulder or upper arm level C NC15 Injury of blood vessels at shoulder or upper arm level C NC16 Injury of muscle, fascia, tendon or bursa at shoulder or upper arm level C NC17 Crushing injury of shoulder or upper arm C NC18 Traumatic amputation of shoulder or upper arm C NC19 Multiple injuries of shoulder or upper arm C NC1Y Other specified injuries to the shoulder or upper arm C NC1Z Injuries to the shoulder or upper arm, unspecified B Injuries to the elbow or forearm C NC30 Superficial injury of forearm C NC31 Open wound of forearm C NC32 Fracture of forearm C NC33 Dislocation or strain or sprain of joints or ligaments of elbow C NC34 Injury of nerves at forearm level C NC35 Injury of blood vessels at forearm level C NC36 Injury of muscle, fascia, tendon or bursa at forearm level C NC37 Crushing injury of forearm C NC38 Traumatic amputation of forearm C NC39 Multiple injuries of forearm C NC3Y Other specified injuries to the elbow or forearm C NC3Z Injuries to the elbow or forearm, unspecified B Injuries to the wrist or hand C NC50 Injury to fingernail C NC51 Superficial injury of wrist or hand C NC52 Open wound of wrist or hand C NC53 Fracture at wrist or hand level C NC54 Dislocation or strain or sprain of joints or ligaments at wrist or hand level C NC55 Injury of nerves at wrist or hand level C NC56 Injury of blood vessels at wrist or hand level C NC57 Injury of muscle, fascia or tendon at wrist or hand level C NC58 Crushing injury of wrist or hand C NC59 Traumatic amputation of wrist or hand C NC5A Multiple injuries of wrist or hand C NC5Y Other specified injuries to the wrist or hand C NC5Z Injuries to the wrist or hand, unspecified B Injuries to the hip or thigh C NC70 Superficial injury of hip or thigh C NC71 Open wound of hip or thigh C NC72 Fracture of femur C NC73 Dislocation or strain or sprain of joint or ligaments of hip C NC74 Injury of nerves at hip or thigh level C NC75 Injury of blood vessels at hip or thigh level C NC76 Injury of muscle, fascia, tendon or bursa at hip or thigh level C NC77 Crushing injury of hip or thigh C NC78 Traumatic amputation of hip or thigh C NC79 Multiple injuries of hip or thigh C NC7Y Other specified injuries to the hip or thigh C NC7Z Injuries to the hip or thigh, unspecified B Injuries to the knee or lower leg C NC90 Superficial injury of knee or lower leg C NC91 Open wound of knee or lower leg C NC92 Fracture of lower leg, including ankle C NC93 Dislocation or strain or sprain of joints or ligaments of knee C NC94 Injury of nerves at lower leg level C NC95 Injury of blood vessels at lower leg level C NC96 Injury of muscle, fascia, tendon or bursa at lower leg level C NC97 Crushing injury of lower leg C NC98 Traumatic amputation of lower leg C NC99 Multiple injuries of lower leg C NC9Y Other specified injuries to the knee or lower leg C NC9Z Injuries to the knee or lower leg, unspecified B Injuries to the ankle or foot C ND10 Injury to toenail C ND11 Superficial injury of ankle or foot C ND12 Open wound of ankle or foot C ND13 Fracture of foot, except ankle C ND14 Dislocation or strain or sprain of joints or ligaments at ankle or foot level C ND15 Injury of nerves at ankle or foot level C ND16 Injury of blood vessels at ankle or foot level C ND17 Injury of muscle, fascia or tendon at ankle or foot level C ND18 Crushing injury of ankle or foot C ND19 Traumatic amputation of ankle or foot C ND1A Multiple injuries of ankle or foot C ND1Y Other specified injuries to the ankle or foot C ND1Z Injuries to the ankle or foot, unspecified B Injuries involving multiple body regions C ND30 Superficial injuries involving multiple body regions C ND31 Open wounds involving multiple body regions C ND32 Fractures involving multiple body regions C ND33 Dislocations, strains or sprains involving multiple body regions C ND34 Crushing injuries involving multiple body regions C ND35 Traumatic amputations involving multiple body regions C ND36 Other injuries involving multiple body regions, not elsewhere classified C ND37 Unspecified multiple injuries B Injuries to unspecified part of trunk, limb or body region C ND50 Fracture of spine, level unspecified C ND51 Other injuries of spine or trunk, level unspecified C ND52 Fracture of arm, level unspecified C ND53 Other injuries of arm, level unspecified C ND54 Fracture of leg, level unspecified C ND55 Other injuries of leg, level unspecified C ND56 Injury of unspecified body region C ND57 Secondary effect of trauma C ND5Y Other specified injuries to unspecified part of trunk, limb or body region C ND5Z Injuries to unspecified part of trunk, limb or body region, unspecified B Effects of foreign body entering through natural orifice C ND70 Foreign body on external eye C ND71 Foreign body in ear C ND72 Foreign body in respiratory tract C ND73 Foreign body in alimentary tract C ND74 Foreign body in genitourinary tract C ND7Z Effects of foreign body entering through natural orifice, unspecified B Burns C Burns of external body surface, specified by site D ND90 Burn of head or neck except face D ND91 Burn of face except eye or ocular adnexa D ND92 Burn of trunk except perineum or genitalia D ND93 Burn of perineum or genitalia D ND94 Burn of shoulder or arm, except wrist or hand D ND95 Burn of wrist or hand D ND96 Burn of hip or leg, except ankle or foot D ND97 Burn of ankle or foot D ND99 Acute skin injury due to skin contact with corrosive substance D ND9Y Burns of external body surface, other specified site D ND9Z Burns of external body surface, unspecified site C Burns of eye or internal organs D NE00 Burn of eye or ocular adnexa D NE01 Burn of respiratory tract D NE02 Burn of other internal organs D NE0Z Burns of unspecified internal organ C Burns of multiple or unspecified body regions D NE10 Burns of multiple body regions D NE11 Burn of unspecified body region C NE2Z Burns, unspecified B Frostbite C NE40 Superficial frostbite C NE41 Frostbite with tissue necrosis C NE42 Frostbite involving multiple body regions C NE4Z Frostbite, unspecified B Harmful effects of substances C NE60 Harmful effects of drugs, medicaments or biological substances, not elsewhere classified C NE61 Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified C NE6Z Harmful effects of unspecified substance B Injury or harm arising from surgical or medical care, not elsewhere classified C NE80 Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified C NE81 Injury or harm arising from a procedure, not elsewhere classified C NE82 Dysfunction or complication of pacemaker, pacemaker lead or implantable cardioverter defibrillator, not elsewhere classified C NE83 Injury or harm arising from other device, implant or graft, not elsewhere classified C NE84 Failure or rejection of transplanted organs or tissues D H00083 Allograft rejection C NE85 Complications peculiar to reattachment or amputation C NE86 Malignant hyperthermia due to anaesthesia C NE87 Failed or difficult intubation C NE88 Drug toxicity associated with harm in surgical or medical care, not elsewhere classified C NE89 Awareness under general anaesthesia C NE8Y Other specified injury or harm arising from surgical or medical care, not elsewhere classified C NE8Z Injury or harm arising from surgical or medical care, not elsewhere classified, unspecified B Other or unspecified effects of external causes C NF00 Effects of radiation, not elsewhere classified C NF01 Effects of heat C NF02 Hypothermia C NF03 Other effects of reduced temperature D H01643 Chilblains C NF04 Effects of air pressure or water pressure C NF05 Asphyxiation C NF06 Effects of strenuous physical exercise C NF07 Effects of other deprivation C NF08 Effects of certain specified external causes C NF09 Adverse effects, not elsewhere classified C NF0A Certain early complications of trauma, not elsewhere classified C NF0Y Other specified effects of external causes C NF0Z Unspecified effects of external causes B NF2Y Other specified injury, poisoning or certain other consequences of external causes B NF2Z Unspecified injury, poisoning or certain other consequences of external causes # A25 Codes for special purposes B International provisional assignment of new diseases of uncertain aetiology and emergency use C RA01 COVID-19 D H02398 COVID-19 C RA02 Post COVID-19 condition C RA03 Multisystem inflammatory syndrome associated with COVID-19 B National provisional assignment of new diseases of uncertain aetiology ! #
#[ DISEASE | BRITE | KEGG2 | KEGG ]
#Last updated: April 23, 2024 #
ICD-11 by World Health Organization #

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