 01 Certain infectious or parasitic diseases
|
Gastroenteritis or colitis of infectious origin
|
Bacterial intestinal infections
|
1A00 Cholera
|
 H00110 Cholera
|
1A01 Intestinal infection due to other Vibrio
|
H00307 Vibrio parahaemolyticus infection
H00308 Vibrio vulnificus infection
|
1A02 Intestinal infections due to Shigella
|
H00299 Shigellosis
|
1A03 Intestinal infections due to Escherichia coli
|
H00278 Enteropathogenic Escherichia coli (EPEC) infection
H00280 Enterotoxigenic Escherichia coli (ETEC) infection
H01311 Enteroinvasive Escherichia coli (EIEC) infection
H00277 Enterohemorrhagic Escherichia coli (EHEC) infection
H01312 Enteroaggregative Escherichia coli (EAEC) infection
|
1A04 Intestinal infections due to Clostridioides difficile
|
H00338 Pseudomembranous colitis
|
1A05 Intestinal infections due to Yersinia enterocolitica
|
H00298 Yersiniosis
|
1A06 Gastroenteritis due to Campylobacter
|
H00321 Campylobacter infection
|
1A07 Typhoid fever
|
H00111 Typhoid fever
|
1A08 Paratyphoid fever
|
H00112 Paratyphoid fever
|
1A09 Infections due to other Salmonella
|
H00113 Salmonellosis
|
1A0Y Other specified bacterial intestinal infections
|
H01454 Colonic spirochetosis
|
1A0Z Bacterial intestinal infections, unspecified
|
Bacterial foodborne intoxications
|
1A10 Foodborne staphylococcal intoxication
|
H01175 Staphylococcal infection
|
1A11 Botulism
|
H00339 Botulism
|
1A12 Foodborne Clostridium perfringens intoxication
|
H00335 Foodborne Clostridium perfringens intoxication
|
1A13 Foodborne Bacillus cereus intoxication
|
H00329 Foodborne Bacillus cereus intoxication
|
1A1Y Other specified bacterial foodborne intoxications
|
H00300 Enterobacter infection
|
1A1Z Bacterial foodborne intoxications, unspecified
|
Viral intestinal infections
|
1A20 Enteritis due to Adenovirus
|
1A21 Gastroenteritis due to Astrovirus
|
1A22 Gastroenteritis due to Rotavirus
|
H00975 Rotaviral enteritis
|
1A23 Enteritis due to Norovirus
|
H01323 Enteritis due to Norovirus
|
1A24 Intestinal infections due to Cytomegalovirus
|
1A2Y Other specified viral intestinal infections
|
1A2Z Viral intestinal infections, unspecified
|
H01430 Viral gastroenteritis
|
Protozoal intestinal infections
|
1A30 Infections due to Balantidium coli
|
H01087 Balantidiasis
|
1A31 Giardiasis
|
H00362 Giardiasis
|
1A32 Cryptosporidiosis
|
H00356 Cryptosporidiosis
|
1A33 Cystoisosporiasis
|
H02372 Cystoisosporiasis
|
1A34 Sarcocystosis
|
H02373 Sarcocystosis
|
1A35 Blastocystosis
|
H02374 Blastocystosis
|
1A36 Amoebiasis
|
H00360 Amoebiasis
|
1A3Y Other specified protozoal intestinal infections
|
H01089 Dientamoebiasis
|
1A3Z Protozoal intestinal infections, unspecified
|
1A40 Gastroenteritis or colitis without specification of infectious agent
|
Predominantly sexually transmitted infections
|
Syphilis
|
1A60 Congenital syphilis
|
H00354 Syphilis
|
1A61 Early syphilis
|
H00354 Syphilis
|
1A62 Late syphilis
|
H00354 Syphilis
|
1A63 Latent syphilis, unspecified as early or late
|
1A6Z Syphilis, unspecified
|
Gonococcal infection
|
1A70 Gonococcal genitourinary infection
|
H00315 Gonococcal infection
|
1A71 Gonococcal pelviperitonitis
|
H00315 Gonococcal infection
|
1A72 Gonococcal infection of other sites
|
H00315 Gonococcal infection
|
1A73 Disseminated gonococcal infection
|
1A7Z Gonococcal infection, unspecified
|
Sexually transmissible infections due to chlamydia
|
1A80 Chlamydial lymphogranuloma
|
H00348 Lymphogranuloma venereum
|
1A81 Non-ulcerative sexually transmitted chlamydial infection
|
H00347 Chlamydia infection
|
1A8Y Other specified sexually transmissible infections due to chlamydia
|
1A8Z Sexually transmissible infections due to chlamydia, unspecified
|
1A90 Chancroid
|
H00305 Chancroid
|
1A91 Granuloma inguinale
|
H01415 Donovanosis
|
1A92 Trichomoniasis
|
H00812 Trichomoniasis
|
1A93 Sexually transmissible infestations
|
1A94 Anogenital herpes simplex infection
|
H00365 Herpes simplex virus infection
|
1A95 Anogenital warts
|
H01418 Condyloma acuminatum
|
1A9Y Other specified predominantly sexually transmitted infections
|
H00388 Non-chlamydial non-gonococcal urethritis
|
1A9Z Predominantly sexually transmitted infections, unspecified
|
Mycobacterial diseases
|
Tuberculosis
|
1B10 Tuberculosis of the respiratory system
|
H00342 Tuberculosis
|
1B11 Tuberculosis of the nervous system
|
H00342 Tuberculosis
|
1B12 Tuberculosis of other systems and organs
|
H00342 Tuberculosis
|
1B13 Miliary tuberculosis
|
1B14 Latent tuberculosis
|
1B1Y Other specified tuberculosis
|
1B1Z Tuberculosis, unspecified
|
1B20 Leprosy
|
H00344 Leprosy
H01473 Erythema nodosum leprosum
|
1B21 Infections due to non-tuberculous mycobacteria
|
H01458 Nontuberculous mycobacterial infection
H01462 Rapidly growing mycobacteria infection
H02029 Mycobacterium avium complex (MAC) pulmonary disease
H01042 Buruli ulcer
|
1B2Y Other specified mycobacterial diseases
|
1B2Z Mycobacterial diseases, unspecified
|
H01021 Rhodococcus equi infection
H01049 Gordonia bronchialis infection
H01050 Tsukamurella infection
|
Certain staphylococcal or streptococcal diseases
|
Acute rheumatic fever
|
1B40 Acute rheumatic fever without mention of heart involvement
|
1B41 Acute rheumatic fever with heart involvement
|
1B42 Rheumatic chorea
|
H01924 Sydenham chorea
|
1B50 Scarlet fever
|
H01515 Scarlet fever
|
1B51 Streptococcal pharyngitis
|
H00333 Streptococcal infection
H01424 Group A streptococcal pharyngitis
|
1B53 Meningitis due to Streptococcus
|
H00333 Streptococcal infection
H01406 Streptococcus suis infection
|
1B54 Meningitis due to Staphylococcus
|
1B5Y Other specified staphylococcal or streptococcal diseases
|
1B5Z Staphylococcal or streptococcal diseases, unspecified
|
Pyogenic bacterial infections of the skin or subcutaneous tissues
|
1B70 Bacterial cellulitis, erysipelas or lymphangitis
|
H01517 Erysipelas
|
1B71 Necrotising fasciitis
|
H01455 Necrotizing fasciitis
|
1B72 Impetigo
|
1B73 Ecthyma
|
1B74 Superficial bacterial folliculitis
|
1B75 Deep bacterial folliculitis or pyogenic abscess of the skin
|
1B7Y Other specified pyogenic bacterial infection of skin or subcutaneous tissue
|
H01407 Capnocytophaga ochracea infection
|
1B7Z Pyogenic bacterial infection of skin or subcutaneous tissue, unspecified
|
Certain zoonotic bacterial diseases
|
1B90 Rat-bite fevers
|
H01314 Rat-bite fever
|
1B91 Leptospirosis
|
H00355 Leptospirosis
|
1B92 Glanders
|
H00316 Glanders
|
1B93 Plague
|
H00297 Plague
|
1B94 Tularaemia
|
H00312 Tularemia
|
1B95 Brucellosis
|
H00325 Brucellosis
|
1B96 Erysipeloid
|
H01315 Erysipeloid
|
1B97 Anthrax
|
H00328 Anthrax
|
1B98 Cat-scratch disease
|
H00326 Bartonellosis
|
1B99 Pasteurellosis
|
H00306 Pasteurellosis
|
1B9A Extraintestinal yersiniosis
|
H00298 Yersiniosis
|
1B9Z Unspecified zoonotic bacterial disease
|
Other bacterial diseases
|
1C10 Actinomycosis
|
H01325 Actinomycosis
|
1C11 Bartonellosis
|
H00326 Bartonellosis
H00327 Trench fever
|
1C12 Whooping cough
|
H00319 Pertussis
|
1C13 Tetanus
|
H00337 Tetanus
|
1C14 Obstetrical tetanus
|
1C15 Tetanus neonatorum
|
1C16 Gas gangrene
|
H00336 Gas gangrene
|
1C17 Diphtheria
|
H00343 Diphtheria
H01051 Corynebacterium ulcerans infection
|
1C18 Brazilian purpuric fever
|
H01330 Brazilian purpuric fever
|
1C19 Legionellosis
|
H00311 Legionellosis
|
1C1A Listeriosis
|
H00332 Listeriosis
|
1C1B Nocardiosis
|
H00345 Nocardiosis
|
1C1C Meningococcal disease
|
H00314 Meningococcal infection
|
1C1D Yaws
|
H01318 Yaws
|
1C1E Pinta
|
H01530 Pinta
|
1C1F Endemic non-venereal syphilis
|
H01531 Bejel
|
1C1G Lyme borreliosis
|
H00353 Lyme borreliosis
|
1C1H Necrotising ulcerative gingivitis
|
H01440 Acute necrotizing ulcerative gingivitis
|
1C1J Relapsing fever
|
H00427 Relapsing fever
|
Other diseases due to chlamydiae
|
1C20 Chlamydial conjunctivitis
|
1C21 Chlamydial peritonitis
|
1C22 Infections due to Chlamydia psittaci
|
H00350 Psittacosis
|
1C23 Trachoma
|
H00349 Trachoma
|
1C2Y Other specified diseases due to chlamydiae
|
1C2Z Diseases due to chlamydiae, unspecified
|
Rickettsioses
|
1C30 Typhus fever
|
H00322 Epidemic typhus
H00324 Scrub typhus
|
1C31 Spotted fever
|
H00323 Spotted fever
|
1C32 Rickettsialpox
|
H02379 Rickettsialpox
|
1C33 Q fever
|
H00310 Q fever
|
1C3Y Other specified rickettsioses
|
H01140 Sennetsu neorickettsiosis
|
1C3Z Rickettsioses, unspecified
|
1C40 Campylobacteriosis
|
H00321 Campylobacter infection
|
1C41 Bacterial infection of unspecified site
|
H00302 Citrobacter infection
H00303 Serratia infection
H01441 Pseudomonas aeruginosa infection
|
1C42 Melioidosis
|
H00317 Melioidosis
|
1C43 Actinomycetoma
|
H01451 Actinomycetoma
|
1C44 Non-pyogenic bacterial infections of the skin
|
1C45 Toxic shock syndrome
|
H01426 Invasive streptococcal disease
|
1C4Y Other specified bacterial diseases
|
H01335 Photorhabdus asymbiotica infection
H01343 Pantoea ananatis infection
H01446 Propionibacterium acnes infection
|
1C4Z Unspecified bacterial disease
|
Human immunodeficiency virus disease
|
1C60 Human immunodeficiency virus disease associated with tuberculosis
|
1C61 Human immunodeficiency virus disease associated with malaria
|
1C62 Human immunodeficiency virus disease without mention of tuberculosis or malaria
|
H01563 HIV infection
|
Viral infections of the central nervous system
|
1C80 Viral encephalitis, not elsewhere classified
|
H02511 Jamestown Canyon encephalitis
H02512 Cache Valley virus infection
H02536 Infection-induced acute encephalopathy
|
1C81 Acute poliomyelitis
|
H00376 Acute poliomyelitis
|
1C82 Rabies
|
H00377 Rabies
H00378 Lyssavirus infection
|
1C83 Western equine encephalitis
|
H01534 Western equine encephalitis
|
1C84 Eastern equine encephalitis
|
H01535 Eastern equine encephalitis
|
1C85 Japanese encephalitis
|
H01533 Japanese encephalitis
|
1C86 St Louis encephalitis
|
H02166 Saint Louis encephalitis
|
1C87 Rocio viral encephalitis
|
H02171 Rocio viral encephalitis
|
1C88 Murray Valley encephalitis
|
H01536 Murray Valley encephalitis
|
1C8B California encephalitis
|
1C8C Venezuelan equine encephalitis
|
H01547 Venezuelan equine encephalitis
|
1C8D La Crosse encephalitis
|
H01537 La Crosse encephalitis
|
1C8E Viral meningitis, not elsewhere classified
|
H00393 Enterovirus infection
|
1C8F Lymphocytic choriomeningitis
|
H01324 Lymphocytic choriomeningitis
|
1C8G Tick-borne encephalitis
|
H00380 Tick-borne viral encephalitis
|
1C8Y Other specified viral infections of the central nervous system
|
1C8Z Viral infections of the central nervous system, unspecified
|
H00379 Mosquito-borne viral encephalitis
|
Non-viral and unspecified infections of the central nervous system
|
1D00 Infectious encephalitis, not elsewhere classified
|
H01417 Acute encephalitis
|
1D01 Infectious meningitis, not elsewhere classified
|
H00304 Haemophilus influenzae infection
H01313 Escherichia coli meningitis
H01429 Aseptic meningitis
|
1D02 Infectious myelitis, not elsewhere classified
|
1D03 Infectious abscess of the central nervous system
|
1D04 Infectious granulomas of the central nervous system
|
1D05 Infectious cysts of the central nervous system
|
1D0Y Other specified non-viral and unspecified infections of the central nervous system
|
1D0Z Non-viral and unspecified infections of the central nervous system, unspecified
|
Dengue
|
1D20 Dengue without warning signs
|
H00381 Dengue
|
1D21 Dengue with warning signs
|
H00381 Dengue
|
1D22 Severe dengue
|
H00381 Dengue
|
1D2Z Dengue fever, unspecified
|
H00381 Dengue
|
Certain arthropod-borne viral fevers
|
1D40 Chikungunya virus disease
|
H01540 Chikungunya fever
|
1D41 Colorado tick fever
|
H02165 Colorado tick fever
|
1D42 O'nyong-nyong fever
|
H01545 O'nyong-nyong fever
|
1D43 Oropouche virus disease
|
H02163 Oropouche fever
|
1D44 Rift Valley fever
|
H01549 Rift Valley fever
|
1D45 Sandfly fever
|
H02164 Sandfly fever
|
1D46 West Nile virus infection
|
H01548 West Nile fever
|
1D47 Yellow fever
|
H00384 Yellow fever
|
1D48 Zika virus disease
|
H01553 Zika fever
|
1D49 Crimean-Congo haemorrhagic fever
|
H00284 Crimean-Congo hemorrhagic fever
|
1D4A Omsk haemorrhagic fever
|
H00416 Omsk hemorrhagic fever
|
1D4B Kyasanur Forest disease
|
H01322 Kyasanur Forest disease
|
1D4C Alkhurma haemorrhagic fever
|
H01560 Alkhumra hemorrhagic fever
|
1D4D Ross River disease
|
H00397 Ross River fever
|
1D4E Severe fever with thrombocytopenia syndrome
|
H01416 Severe fever with thrombocytopenia syndrome
|
1D4Y Other specified arthropod-borne viral fevers
|
H01546 Mayaro fever
H01550 Bunyamwera fever
H02509 Vesicular stomatitis fever
|
1D4Z Arthropod-borne viral fever, virus unspecified
|
H00382 Mosquito-borne viral fever
H00383 Arthropod-borne viral fever
|
Certain zoonotic viral diseases
|
1D60 Filovirus disease
|
H00283 Ebola disease
H00405 Marburg disease
|
1D61 Arenavirus disease
|
H00385 South American hemorrhagic fever
H02173 Arenaviral hemorrhagic fever
H01541 Argentine hemorrhagic fever
H01542 Bolivian hemorrhagic fever
H00386 Lassa fever
H01543 Venezuelan hemorrhagic fever
H01544 Brazilian hemorrhagic fever
|
1D62 Hantavirus disease
|
H00389 Hemorrhagic fever with renal syndrome
H00390 Hantavirus pulmonary syndrome
|
1D63 Henipavirus encephalitis
|
H00391 Henipavirus infection
H01538 Hendra virus infection
H01539 Nipah virus infection
|
1D64 Middle East respiratory syndrome
|
H01419 Middle East respiratory syndrome
|
1D65 Severe acute respiratory syndrome
|
H00402 Severe acute respiratory syndrome
|
1D6Y Other specified zoonotic viral diseases
|
1D6Z Zoonotic viral disease, virus unspecified
|
Certain other viral diseases
|
1D80 Mumps
|
H00396 Mumps
|
1D81 Infectious mononucleosis
|
H00367 Infectious mononucleosis
|
1D82 Cytomegaloviral disease
|
H00368 Cytomegalovirus infection
|
1D83 Epidemic myalgia
|
H00393 Enterovirus infection
H02413 Epidemic myalgia
|
1D84 Viral conjunctivitis
|
H01320 Epidemic keratoconjunctivitis
H00393 Enterovirus infection
H01421 Acute hemorrhagic conjunctivitis
H01420 Pharyngoconjunctival fever
|
1D85 Viral carditis
|
1D86 Viral haemorrhagic fever, not elsewhere classified
|
Viral infection of unspecified site
|
1D90 Adenovirus infection of unspecified site
|
H00371 Adenovirus infection
|
1D91 Enterovirus infection of unspecified site
|
H00393 Enterovirus infection
|
1D92 Coronavirus infection, unspecified site
|
1D93 Parvovirus infection of unspecified site
|
1D9Y Other viral infections of unspecified site
|
1D9Z Unspecified viral infection of unspecified site
|
1E1Y Other specified viral diseases
|
1E1Z Unspecified viral disease
|
Influenza
|
1E30 Influenza due to identified seasonal influenza virus
|
H00398 Influenza
|
1E31 Influenza due to identified zoonotic or pandemic influenza virus
|
H00399 Avian influenza
|
1E32 Influenza, virus not identified
|
Viral hepatitis
|
1E50 Acute viral hepatitis
|
H02162 Viral hepatitis
H00411 Hepatitis A
H00412 Hepatitis B
H00413 Hepatitis C
H00414 Hepatitis D
H00415 Hepatitis E
|
1E51 Chronic viral hepatitis
|
H02162 Viral hepatitis
H00412 Hepatitis B
H00413 Hepatitis C
H00414 Hepatitis D
H00415 Hepatitis E
|
1E5Z Viral hepatitis, unspecified
|
Viral infections characterised by skin or mucous membrane lesions
|
Infections due to poxvirus
|
1E70 Smallpox
|
H00372 Smallpox
|
1E71 Mpox
|
H00373 Mpox (Monkeypox)
|
1E72 Cowpox
|
H02351 Cowpox
|
1E73 Vaccinia
|
H02352 Vaccinia
|
1E74 Buffalopox
|
1E75 Orf
|
H02354 Orf
|
1E76 Molluscum contagiosum
|
H01052 Molluscum contagiosum
|
1E7Y Other specified infections due to poxvirus
|
1E7Z Infections due to poxvirus, unspecified
|
Human papillomavirus infection of skin or mucous membrane
|
1E80 Common warts
|
1E81 Plane warts
|
1E82 Warts of lips or oral cavity
|
1E83 Wart virus proliferation in immune-deficient states
|
H00842 Epidermodysplasia verruciformis
|
1E8Z Viral warts, not elsewhere classified
|
H00374 Viral wart
|
Varicella zoster virus infections
|
1E90 Varicella
|
H00366 Varicella
|
1E91 Zoster
|
H00366 Varicella
H01624 Postherpetic neuralgia
|
1F00 Herpes simplex infections
|
H00365 Herpes simplex virus infection
H00387 B virus infection
|
1F01 Roseola infantum
|
H00369 Exanthema subitum
|
1F02 Rubella
|
H00395 Rubella
|
1F03 Measles
|
H00394 Measles
|
1F04 Erythema infectiosum
|
H00404 Erythema infectiosum
|
1F05 Picornavirus infections presenting in the skin or mucous membranes
|
H00393 Enterovirus infection
H01327 Herpangina
H01326 Hand, foot and mouth disease
|
1F0Y Other specified viral infections characterised by skin or mucous membrane lesions
|
1F0Z Viral infections characterised by skin or mucous membrane lesions, unspecified
|
Mycoses
|
1F20 Aspergillosis
|
H01328 Aspergillosis
|
1F21 Basidiobolomycosis
|
H01503 Zygomycosis
H02032 Entomophthoramycosis
|
1F22 Blastomycosis
|
H01501 Blastomycosis
|
1F23 Candidosis
|
H00363 Candidiasis
H01109 Chronic mucocutaneous candidiasis
|
1F24 Chromoblastomycosis
|
H01520 Chromomycosis
|
1F25 Coccidioidomycosis
|
H01319 Coccidioidomycosis
|
1F26 Conidiobolomycosis
|
H01503 Zygomycosis
H02032 Entomophthoramycosis
|
1F27 Cryptococcosis
|
H00364 Cryptococcosis
|
1F28 Dermatophytosis
|
H01316 Dermatophytosis
|
1F29 Eumycetoma
|
H02385 Eumycetoma
|
1F2A Histoplasmosis
|
H01062 Histoplasmosis
|
1F2B Lobomycosis
|
H01518 Lobomycosis
|
1F2C Mucormycosis
|
H01503 Zygomycosis
H02033 Mucormycosis
|
1F2D Non-dermatophyte superficial dermatomycoses
|
H01334 Tinea versicolor
H02428 Trichosporonosis
|
1F2E Paracoccidioidomycosis
|
H01329 Paracoccidioidomycosis
|
1F2F Phaeohyphomycosis
|
H02386 Phaeohyphomycosis
|
1F2G Pneumocystosis
|
H01521 Pneumocystis pneumonia
|
1F2H Scedosporiosis
|
H02392 Scedosporiosis
|
1F2J Sporotrichosis
|
H01499 Sporotrichosis
|
1F2K Talaromycosis
|
H02393 Talaromycosis
|
1F2L Emmonsiosis
|
1F2Y Other specified mycoses
|
1F2Z Mycoses, unspecified
|
Parasitic diseases
|
Malaria
|
1F40 Malaria due to Plasmodium falciparum
|
H00361 Malaria
|
1F41 Malaria due to Plasmodium vivax
|
H00361 Malaria
|
1F42 Malaria due to Plasmodium malariae
|
H00361 Malaria
|
1F43 Malaria due to Plasmodium ovale
|
H00361 Malaria
|
1F44 Other parasitologically confirmed malaria
|
1F45 Malaria without parasitological confirmation
|
1F4Z Malaria, unspecified
|
Nonintestinal protozoal diseases
|
1F50 Acanthamoebiasis
|
H02401 Acanthamoebiasis
|
1F51 African trypanosomiasis
|
H00357 African trypanosomiasis
|
1F52 Babesiosis
|
H01060 Babesiosis
|
1F53 Chagas disease
|
H00358 Chagas disease
|
1F54 Leishmaniasis
|
H00359 Leishmaniasis
|
1F55 Naegleriasis
|
H02399 Primary amoebic meningoencephalitis (PAM)
|
1F56 Rhinosporidiosis
|
H02400 Rhinosporidiosis
|
1F57 Toxoplasmosis
|
H00435 Toxoplasmosis
|
1F58 Microsporidiosis
|
H01336 Encephalitozoon infection
|
1F5Z Unspecified protozoal disease
|
Helminthiases
|
Diseases due to nematodes
|
 1F60 Angiostrongyliasis
|
1F61 Anisakiasis
|
1F62 Ascariasis
|
1F63 Capillariasis
|
1F64 Dracunculiasis
|
1F65 Enterobiasis
|
1F66 Filariasis
|
1F67 Gnathostomiasis
|
1F68 Hookworm diseases
|
1F69 Oesophagostomiasis
|
1F6A Onchocerciasis
|
1F6B Strongyloidiasis
|
1F6C Syngamosis
|
1F6D Toxocariasis
|
1F6E Trichinosis
|
1F6F Trichostrongyliasis
|
1F6G Trichuriasis
|
1F6H Uncinariosis
|
1F6Y Other specified diseases due to nematodes
|
1F6Z Diseases due to nematodes, unspecified
|
Diseases due to cestodes
|
1F70 Cysticercosis
|
1F71 Diphyllobothriasis
|
1F72 Dipylidiasis
|
1F73 Echinococcosis
|
1F74 Hymenolepiasis
|
1F75 Sparganosis
|
1F76 Taeniasis
|
1F7Y Other specified diseases due to cestodes
|
1F7Z Diseases due to cestodes, unspecified
|
Diseases due to trematodes
|
1F80 Clonorchiasis
|
1F81 Dicrocoeliasis
|
1F82 Fascioliasis
|
1F83 Fasciolopsiasis
|
1F84 Opisthorchiasis
|
1F85 Paragonimiasis
|
1F86 Schistosomiasis
|
1F8Y Other specified diseases due to trematodes
|
1F8Z Diseases due to trematodes, unspecified
|
1F90 Other and unspecified infestation by parasitic worms
|
1F91 Diphyllobothriasis and sparganosis
|
1F9Z Helminthiases, unspecified
|
H01055 Giant kidney worm infection
|
Infestations by ectoparasites
|
1G00 Pediculosis
|
H01054 Pediculosis
|
1G01 Myiasis
|
H01178 Myiasis
|
1G02 External hirudiniasis
|
1G03 Pthiriasis
|
H02423 Phthiriasis
|
1G04 Scabies
|
H01519 Scabies
|
1G05 Tungiasis
|
H01179 Tungiasis
|
1G06 Cimicosis
|
H02416 Cimicosis
|
1G07 Infestation by mites
|
1G0Y Infestation by other specified ectoparasite
|
1G0Z Infestation by unknown or unspecified ectoparasite
|
H01098 Pentastomiasis
|
1G2Y Other specified parasitic diseases
|
1G2Z Unspecified parasitic diseases
|
Sepsis
|
1G40 Sepsis without septic shock
1G41 Sepsis with septic shock
|
1G60 Certain other disorders of infectious origin
|
Sequelae of infectious diseases
|
1G80 Sequelae of tuberculosis
1G81 Sequelae of trachoma
1G82 Sequelae of leprosy
1G83 Sequelae of poliomyelitis
1G84 Sequelae of viral encephalitis
1G85 Sequelae of diphtheria
1G8Y Sequelae of other specified infectious diseases
|
1H0Z Infection, unspecified
|
|
02 Neoplasms
|
Neoplasms of brain or central nervous system
|
2A00 Primary neoplasms of brain
|
H00042 Glioma
H01692 Subependymal giant cell astrocytoma
H01667 Medulloblastoma
H01007 Choroid plexus papilloma
|
2A01 Primary neoplasms of meninges
|
H01556 Meningioma
|
2A02 Primary neoplasm of spinal cord, cranial nerves or remaining parts of central nervous system
|
H00043 Neuroblastoma
|
2A0Z Other and unspecified neoplasms of brain or central nervous system
|
Neoplasms of haematopoietic or lymphoid tissues
|
Myeloproliferative neoplasms
|
2A20 Non mast cell myeloproliferative neoplasms
|
H00004 Chronic myeloid leukemia
H01605 Myelofibrosis
H01590 Chronic eosinophilic leukemia
H01599 Hypereosinophilic syndrome
H00012 Polycythemia vera
|
2A21 Mastocytosis
|
H01511 Mast-cell leukemia
H02896 Cutaneous mastocytosis
|
2A22 Other and unspecified myeloproliferative neoplasms
|
Myelodysplastic syndromes
|
2A30 Refractory anaemia
|
2A31 Refractory neutropaenia
|
2A32 Refractory thrombocytopenia
|
2A33 Refractory anaemia with ring sideroblasts
|
2A34 Refractory cytopenia with multi-lineage dysplasia
|
2A35 Refractory anaemia with excess of blasts
|
2A36 Myelodysplastic syndrome with isolated del(5q)
|
H01481 Myelodysplastic syndrome
H01484 5q- syndrome
|
2A37 Myelodysplastic syndrome, unclassifiable
|
H01481 Myelodysplastic syndrome
|
2A38 Refractory cytopenia of childhood
|
2A3Y Other specified myelodysplastic syndromes
|
H02835 Congenital myelofibrosis with anemia, neutropenia, developmental delay, and ocular abnormalities
H02878 Monosomy 7 myelodysplasia and leukemia syndrome
|
2A3Z Myelodysplastic syndromes, unspecified
|
H01481 Myelodysplastic syndrome
|
Myelodysplastic and myeloproliferative neoplasms
|
2A40 Chronic myelomonocytic leukaemia
|
H02411 Chronic myelomonocytic leukemia
|
2A41 Atypical chronic myeloid leukaemia, BCR-ABL1-negative
|
H02412 Atypical chronic myeloid leukemia
|
2A42 Juvenile myelomonocytic leukaemia
|
H02541 Juvenile myelomonocytic leukemia
|
2A43 Refractory anaemia with ring sideroblasts associated with marked thrombocytosis
|
2A44 Myeloproliferative and myelodysplastic disease, unclassifiable
|
2A4Y Other specified myelodysplastic and myeloproliferative neoplasms
|
2A4Z Myelodysplastic and myeloproliferative neoplasms, unspecified
|
H02410 Myelodysplastic/myeloproliferative neoplasms
|
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1
|
2A50 Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement
2A51 Myeloid neoplasm associated with PDGFRB rearrangement
2A52 Myeloid or lymphoid neoplasms with FGFR1 abnormalities
2A5Z Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1, unspecified
|
2A60 Acute myeloid leukaemias and related precursor neoplasms
|
H00003 Acute myeloid leukemia
H02542 Acute promyelocytic leukemia
|
2A61 Acute leukaemias of ambiguous lineage
|
Precursor lymphoid neoplasms
|
2A70 Precursor B-lymphoblastic neoplasms
|
H00001 B-cell acute lymphoblastic leukemia
|
2A71 Precursor T-lymphoblastic neoplasms
|
H00002 T-cell acute lymphoblastic leukemia
|
2A7Z Precursor lymphoid neoplasms, unspecified
|
Mature B-cell neoplasms
|
2A80 Follicular lymphoma
|
H01613 Follicular lymphoma
|
2A81 Diffuse large B-cell lymphomas
|
H02424 Primary central nervous system lymphoma
H02434 Diffuse large B-cell lymphoma, not otherwise specified
|
2A82 Mature B-cell neoplasm with leukaemic behaviour
|
H00005 Chronic lymphocytic leukemia
H00006 Hairy cell leukemia
|
2A83 Plasma cell neoplasms
|
H00010 Multiple myeloma
H01461 Crow-Fukase syndrome
|
2A84 Heavy chain diseases or malignant immunoproliferative diseases
|
2A85 Other specified mature B-cell neoplasms or lymphoma
|
H00011 Lymphoplasmacytic lymphoma
H01464 Mantle cell lymphoma
H00008 Burkitt lymphoma
|
2A86 B-cell lymphoma, mixed features
|
H02664 Joint contracture, osteochondromas, and B-cell lymphoma
|
2A8Z Mature B-cell neoplasms, unspecified
|
Mature T-cell or NK-cell neoplasms
|
2A90 Mature T-cell lymphoma, specified types, nodal or systemic
|
H01892 Peripheral T cell lymphoma
H00009 Adult T-cell leukemia
H01601 Anaplastic large-cell lymphoma
|
Mature T-cell or NK-cell lymphomas and lymphoproliferative disorders, primary cutaneous specified types
|
2B00 Subcutaneous panniculitis-like T-cell lymphoma
|
2B01 Mycosis fungoides
|
2B02 Sรฉzary syndrome
|
2B03 Primary cutaneous CD30-positive T-cell lymphoproliferative disorders
|
2B0Y Other specified primary cutaneous mature T-cell or NK-cell lymphomas and lymphoproliferative disorders
|
2B0Z Primary cutaneous T-cell lymphoma of undetermined or unspecified type
|
2B2Y Other specified mature T-cell or NK-cell neoplasms
|
2B2Z Mature T-cell or NK-cell neoplasms, unspecified
|
2B30 Hodgkin lymphoma
|
H00007 Hodgkin lymphoma
|
2B31 Histiocytic or dendritic cell neoplasms
|
H01512 Langerhans cell histiocytosis
H02425 Erdheim-Chester disease
|
2B32 Immunodeficiency-associated lymphoproliferative disorders
|
2B33 Malignant haematopoietic neoplasms without further specification
|
H02418 Non-Hodgkin lymphoma
|
2B3Z Neoplasms of haematopoietic or lymphoid tissues, unspecified
|
Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues
|
Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues
|
Malignant mesenchymal neoplasms
|
2B50 Chondrosarcoma, primary site
|
2B51 Osteosarcoma, primary site
|
2B52 Ewing sarcoma, primary site
|
2B53 Fibroblastic or myofibroblastic tumour, primary site
|
2B54 Unclassified pleomorphic sarcoma, primary site
|
2B55 Rhabdomyosarcoma, primary site
|
2B56 Angiosarcoma, primary site
|
2B57 Kaposi sarcoma, primary site
|
2B58 Leiomyosarcoma, primary site
|
2B59 Liposarcoma, primary site
|
2B5A Synovial sarcoma, primary site
|
2B5B Gastrointestinal stromal tumour, primary site
|
2B5C Endometrial stromal sarcoma, primary site
|
2B5D Malignant mixed epithelial mesenchymal tumour, primary site
|
2B5E Malignant nerve sheath tumour of peripheral nerves or autonomic nervous system, primary site
|
2B5F Sarcoma, not elsewhere classified, primary site
|
2B5G Myosarcoma of uterus, part not specified
|
2B5H Well differentiated lipomatous tumour, primary site
|
2B5J Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites
|
2B5K Unspecified malignant soft tissue tumours or sarcomas of bone or articular cartilage of other or unspecified sites
|
2B5Y Other specified malignant mesenchymal neoplasms
|
2B5Z Malignant mesenchymal neoplasm of unspecified type
|
Malignant neoplasms of lip, oral cavity or pharynx
|
2B60 Malignant neoplasms of lip
|
2B61 Malignant neoplasms of base of tongue
|
2B62 Malignant neoplasms of other or unspecified parts of tongue
|
2B63 Malignant neoplasms of gum
|
2B64 Malignant neoplasms of floor of mouth
|
2B65 Malignant neoplasms of palate
|
2B66 Malignant neoplasms of other or unspecified parts of mouth
|
2B67 Malignant neoplasms of parotid gland
|
2B68 Malignant neoplasms of submandibular or sublingual glands
|
2B69 Malignant neoplasms of tonsil
|
2B6A Malignant neoplasms of oropharynx
|
2B6B Malignant neoplasms of nasopharynx
|
2B6C Malignant neoplasms of piriform sinus
|
2B6D Malignant neoplasms of hypopharynx
|
2B6E Malignant neoplasms of other or ill-defined sites in the lip, oral cavity or pharynx
|
2B6Y Other specified malignant neoplasms of lip, oral cavity or pharynx
|
Malignant neoplasms of digestive organs
|
2B70 Malignant neoplasms of oesophagus
|
2B71 Malignant neoplasms of oesophagogastric junction
|
2B72 Malignant neoplasms of stomach
|
Malignant neoplasms of intestine
|
2C10 Malignant neoplasm of pancreas
|
2C11 Malignant neoplasms of other or ill-defined digestive organs
|
2C12 Malignant neoplasms of liver or intrahepatic bile ducts
|
2C13 Malignant neoplasms of gallbladder
|
2C14 Malignant neoplasms of proximal biliary tract, cystic duct
|
2C15 Malignant neoplasms of biliary tract, distal bile duct
|
2C16 Malignant neoplasms of ampulla of Vater
|
2C17 Malignant neoplasms of other or unspecified parts of biliary tract
|
2C18 Malignant neoplasms of perihilar bile duct
|
2C1Z Malignant neoplasms of digestive organs, unspecified
|
Malignant neoplasms of middle ear, respiratory or intrathoracic organs
|
2C20 Malignant neoplasms of nasal cavity
|
2C21 Malignant neoplasms of middle ear
|
2C22 Malignant neoplasms of accessory sinuses
|
2C23 Malignant neoplasms of larynx
|
2C24 Malignant neoplasms of trachea
|
2C25 Malignant neoplasms of bronchus or lung
|
2C26 Malignant neoplasms of the pleura
|
2C27 Malignant neoplasms of thymus
|
2C28 Malignant neoplasms of heart, mediastinum or non-mesothelioma of pleura
|
2C29 Malignant neoplasms of other or ill-defined sites in the respiratory system or intrathoracic organs
|
2C2Y Other specified malignant neoplasms of middle ear, respiratory or intrathoracic organs
|
2C2Z Malignant neoplasms of middle ear, respiratory or intrathoracic organs, unspecified
|
Malignant neoplasms of skin
|
2C30 Melanoma of skin
|
2C31 Squamous cell carcinoma of skin
|
2C32 Basal cell carcinoma of skin
|
2C33 Adnexal carcinoma of skin
|
2C34 Cutaneous neuroendocrine carcinoma
|
2C35 Cutaneous sarcoma
|
2C3Y Other specified malignant neoplasms of skin
|
2C3Z Malignant neoplasm of skin of unknown or unspecified type
|
Malignant neoplasms of peripheral nerves or autonomic nervous system
|
2C40 Malignant neuroepitheliomatous neoplasms of peripheral nerves or autonomic nervous system
2C41 Malignant perineurioma
2C4Y Other specified malignant neoplasms of peripheral nerves and autonomic nervous system
2C4Z Malignant neoplasms of peripheral nerves or autonomic nervous system, unspecified
|
Malignant neoplasms of retroperitoneum, peritoneum or omentum
|
2C50 Malignant neoplasms of retroperitoneum
|
2C51 Malignant neoplasms of peritoneum
|
2C52 Malignant neoplasms of omentum
|
2C53 Malignant neoplasm involving overlapping sites of retroperitoneum, peritoneum or omentum
|
2C5Y Other specified malignant neoplasms of retroperitoneum, peritoneum or omentum
|
2C5Z Malignant neoplasms of retroperitoneum, peritoneum or omentum, unspecified
|
Malignant neoplasms of breast
|
2C60 Carcinoma of breast, specialised type
|
2C61 Invasive carcinoma of breast
|
2C62 Inflammatory carcinoma of breast
|
2C63 Malignant phyllodes tumour of breast
|
2C64 Solid papillary carcinoma of breast with evidence of invasion
|
2C65 Hereditary breast and ovarian cancer syndrome
|
2C6Y Other specified malignant neoplasms of breast
|
2C6Z Malignant neoplasms of breast, unspecified
|
Malignant neoplasms of female genital organs
|
2C70 Malignant neoplasms of vulva
|
2C71 Malignant neoplasms of vagina
|
2C72 Malignant neoplasms of uterine ligament, parametrium, or uterine adnexa
|
2C73 Malignant neoplasms of ovary
|
2C74 Malignant neoplasms of fallopian tube
|
2C75 Malignant neoplasms of placenta
|
2C76 Malignant neoplasms of corpus uteri
|
2C77 Malignant neoplasms of cervix uteri
|
2C78 Malignant neoplasms of uterus, part not specified
|
2C79 Malignant neoplasm involving overlapping sites of female genital organs
|
2C7Y Other specified malignant neoplasms of female genital organs
|
2C7Z Malignant neoplasms of female genital organs, unspecified
|
Malignant neoplasms of male genital organs
|
2C80 Malignant neoplasms of testis
|
2C81 Malignant neoplasms of penis
|
2C82 Malignant neoplasms of prostate
|
2C83 Malignant neoplasms of scrotum
|
2C84 Malignant neoplasms of other specified male genital organs
|
2C8Z Malignant neoplasms of male genital organs, unspecified
|
Malignant neoplasms of urinary tract
|
2C90 Malignant neoplasms of kidney, except renal pelvis
|
2C91 Malignant neoplasms of renal pelvis
|
2C92 Malignant neoplasms of ureter
|
2C93 Malignant neoplasms of urethra or paraurethral gland
|
2C94 Malignant neoplasms of bladder
|
2C95 Malignant neoplasm involving overlapping sites of urinary organs
|
2C9Y Other specified malignant neoplasms of urinary tract
|
2C9Z Malignant neoplasms of urinary tract, unspecified
|
Malignant neoplasms of eye or ocular adnexa
|
2D00 Malignant neoplasm of conjunctiva
|
2D01 Malignant neoplasm of cornea
|
2D02 Malignant neoplasm of retina
|
2D03 Malignant neoplasm of lacrimal apparatus
|
2D04 Malignant neoplasm of orbit
|
2D05 Malignant neoplasm of choroid
|
2D06 Malignant neoplasm of ciliary body
|
2D07 Malignant neoplasm of iris
|
2D0Y Other specified malignant neoplasms of eye and ocular adnexa
|
2D0Z Malignant neoplasms of eye or ocular adnexa, unspecified
|
Malignant neoplasms of endocrine glands
|
2D10 Malignant neoplasms of thyroid gland
|
2D11 Malignant neoplasms of adrenal gland
|
2D12 Malignant neoplasms of other endocrine glands or related structures
|
2D1Z Malignant neoplasms of endocrine glands, unspecified
|
2D3Y Other specified malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues
|
2D3Z Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues, unspecified
|
Malignant neoplasms of ill-defined or unspecified primary sites
|
2D40 Adenocarcinoma of unspecified site
2D41 Unspecified carcinoma of unspecified site
2D42 Malignant neoplasms of ill-defined sites
2D43 Malignant neoplasms of independent, multiple primary sites
2D44 Malignant neoplasm, primary site unknown, so stated
2D4Y Other specified malignant neoplasms of unspecified primary sites
2D4Z Unspecified malignant neoplasms of unspecified sites
|
Malignant neoplasm metastases
|
2D50 Malignant neoplasm metastasis in brain
|
2D51 Malignant neoplasm metastasis in meninges
|
2D52 Malignant neoplasm metastasis in spinal cord, cranial nerves or remaining parts of central nervous system
|
Malignant neoplasm metastasis in lymph nodes
|
2D60 Malignant neoplasm metastasis in lymph node of a single region
|
2D61 Malignant neoplasm metastases in lymph nodes of multiple regions
|
2D6Z Metastatic malignant neoplasm to unspecified lymph node
|
Malignant neoplasm metastasis in thoracic or respiratory organs
|
2D70 Malignant neoplasm metastasis in lung
2D71 Malignant neoplasm metastasis in mediastinum
2D72 Malignant neoplasm metastasis in pleura
2D73 Malignant neoplasm metastasis in upper respiratory tract organs
2D7Y Malignant neoplasm metastasis in other specified thoracic organs
2D7Z Malignant neoplasm metastasis in thoracic or respiratory organs, unspecified
|
Malignant neoplasm metastasis in digestive system
|
2D80 Malignant neoplasm metastasis in liver or intrahepatic bile duct
2D81 Malignant neoplasm metastasis in pancreas
2D82 Malignant neoplasm metastasis in extrahepatic bile ducts
2D83 Malignant neoplasm metastasis in ampulla of Vater
2D84 Malignant neoplasm metastasis in the small intestine
2D85 Malignant neoplasm metastasis in large intestine
2D86 Malignant neoplasm metastasis in anus
2D8Y Malignant neoplasm metastasis in other specified digestive system organ
2D8Z Malignant neoplasm metastasis in unspecified digestive system organ
|
Malignant neoplasm metastasis in retroperitoneum or peritoneum
|
2D90 Malignant neoplasm metastasis in retroperitoneum
2D91 Malignant neoplasm metastasis in peritoneum
|
Malignant neoplasm metastasis in other sites
|
2E00 Malignant neoplasm metastasis in kidney or renal pelvis
2E01 Malignant neoplasm metastasis in bladder
2E02 Malignant neoplasm metastasis in other or unspecified urinary system organs
2E03 Malignant neoplasm metastasis in bone or bone marrow
2E04 Malignant neoplasm metastasis in soft tissue
2E05 Malignant neoplasm metastasis in female reproductive system
2E06 Malignant neoplasm metastasis in male genital organs
2E07 Malignant neoplasm metastasis in adrenal gland
2E08 Metastatic malignant neoplasm involving skin
2E09 Malignant neoplasm metastasis in peripheral nervous system
2E0Y Malignant neoplasm metastasis in other specified sites
|
2E2Z Malignant neoplasm metastasis, unspecified
|
In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues
|
2E60 Carcinoma in situ of oral cavity, oesophagus or stomach
|
2E61 Carcinoma in situ of other or unspecified digestive organs
|
2E62 Carcinoma in situ of middle ear or respiratory system
|
2E63 Melanoma in situ neoplasms
|
2E64 Carcinoma in situ of skin
|
2E65 Carcinoma in situ of breast
|
2E66 Carcinoma in situ of cervix uteri
|
2E67 Carcinoma in situ of other or unspecified genital organs
|
2E68 Carcinoma in situ of bladder
|
2E69 Carcinoma in situ of other or unspecified urinary organs
|
2E6A Carcinoma in situ of the eye or ocular adnexa
|
2E6B Carcinoma in situ of thyroid and other endocrine glands
|
H01558 Parathyroid carcinoma
|
2E6Y Carcinoma in situ of other specified site
|
2E6Z Carcinoma in situ of unspecified site
|
Benign neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues
|
Benign mesenchymal neoplasms
|
2E80 Benign lipomatous neoplasm
|
2E81 Benign vascular neoplasms
|
H01471 Lymphangioma
H01735 Lymphangiomatosis
H01482 Infantile hemangioma
H01875 Infantile hepatic hemangioma
|
2E82 Benign chondrogenic tumours
|
2E83 Benign osteogenic tumours
|
2E84 Benign fibrogenic or myofibrogenic tumour
|
2E85 Benign fibrohistiocytic tumour
|
2E86 Benign smooth muscle or skeletal muscle tumour
|
H01640 Uterine leiomyoma
|
2E87 Benign gastrointestinal stromal tumour
|
2E88 Benign endometrial stromal nodule
|
2E89 Benign mesenchymal tumours of uncertain differentiation
|
2E8A Other mixed or unspecified benign mesenchymal tumours
|
2E8Y Other specified benign mesenchymal neoplasm
|
2E8Z Benign mesenchymal neoplasms, unspecified
|
H00804 Multiple cutaneous and uterine leiomyomata
|
Benign non-mesenchymal neoplasms
|
2E90 Benign neoplasm of lip, oral cavity or pharynx
|
2E91 Benign neoplasm of major salivary glands
|
H02922 Pleomorphic salivary gland adenoma
|
2E92 Benign neoplasm of digestive organs
|
H02538 Paraganglioma
H01025 Familial adenomatous polyposis
H00539 PTEN hamartoma tumor syndrome
H01023 Juvenile polyposis syndrome
H01024 Hereditary mixed polyposis syndrome
H02795 Sessile serrated polyposis cancer syndrome
H02869 Familial hepatic adenomas
|
Benign neoplasm of respiratory or intrathoracic organs
|
2F00 Benign neoplasm of middle ear or respiratory system
|
2F01 Benign neoplasm of intrathoracic organs
|
2F0Y Benign neoplasms of other specified respiratory and intrathoracic organs
|
2F0Z Benign neoplasms of unspecified respiratory and intrathoracic organs
|
2F10 Benign neoplasm of mesothelial tissue
|
Benign cutaneous neoplasms
|
2F20 Benign cutaneous melanocytic neoplasms
|
2F21 Benign keratinocytic acanthomas
|
2F22 Benign neoplasms of epidermal appendages
|
2F23 Benign dermal fibrous or fibrohistiocytic neoplasms
|
2F24 Benign cutaneous neoplasms of neural or nerve sheath origin
|
2F25 Cherry angioma
|
2F26 Lobular capillary haemangioma
|
2F2Y Other specified benign cutaneous neoplasms
|
2F2Z Benign cutaneous neoplasm of unspecified type
|
2F30 Benign neoplasm of breast
|
2F31 Benign non-mesenchymal neoplasms of uterus
|
2F32 Benign neoplasm of ovary
|
2F33 Benign neoplasm of other or unspecified female genital organs
|
2F34 Benign neoplasm of male genital organs
|
2F35 Benign neoplasm of urinary organs
|
H01691 Renal angiomyolipoma
|
2F36 Benign neoplasm of eye or ocular adnexa
|
H01149 Ring dermoid of cornea
|
2F37 Benign neoplasm of endocrine glands
|
H01102 Pituitary adenomas
|
2F3Y Benign non-mesenchymal neoplasms of other specified site
|
2F3Z Benign non-mesenchymal neoplasms of unspecified site
|
2F5Y Other specified benign neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues
|
2F5Z Benign neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues, unspecified
|
Neoplasms of uncertain behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues
|
2F70 Neoplasms of uncertain behaviour of oral cavity or digestive organs
|
2F71 Neoplasms of uncertain behaviour of middle ear, respiratory or intrathoracic organs
|
2F72 Neoplasms of uncertain behaviour of skin
|
2F73 Neoplasms of uncertain behaviour of retroperitoneum
|
2F74 Neoplasms of uncertain behaviour of peritoneum
|
2F75 Neoplasms of uncertain behaviour of breast
|
2F76 Neoplasms of uncertain behaviour of female genital organs
|
2F77 Neoplasms of uncertain behaviour of male genital organs
|
2F78 Neoplasms of uncertain behaviour of urinary organs
|
2F79 Neoplasms of uncertain behaviour of eye or ocular adnexa
|
2F7A Neoplasms of uncertain behaviour of endocrine glands
|
H00247 Multiple endocrine neoplasia syndrome
|
2F7B Neoplasms of uncertain behaviour of bone or articular cartilage
|
2F7C Neoplasms of uncertain behaviour of connective or other soft tissue
|
2F7Y Neoplasms of uncertain behaviour of other specified site
|
H01134 Rhabdoid predisposition syndrome
H02624 Tumor predisposition syndrome
|
2F7Z Neoplasms of uncertain behaviour of unspecified site
|
Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues
|
2F90 Neoplasms of unknown behaviour of oral cavity or digestive organs
2F91 Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs
2F92 Neoplasms of unknown behaviour of skin
2F93 Neoplasms of unknown behaviour of retroperitoneum
2F94 Neoplasms of unknown behaviour of peritoneum
2F95 Neoplasms of unknown behaviour of breast
2F96 Neoplasms of unknown behaviour of female genital organs
2F97 Neoplasms of unknown behaviour of male genital organs
2F98 Neoplasms of unknown behaviour of urinary organs
2F99 Neoplasms of unknown behaviour of eye or ocular adnexa
2F9A Neoplasms of unknown behaviour of endocrine glands
2F9B Neoplasms of unknown behaviour of bone or articular cartilage
2F9C Neoplasms of unknown behaviour of connective or other soft tissue
2F9Y Neoplasms of unknown behaviour of other specified site
2F9Z Neoplasms of unknown behaviour of unspecified site
|
|
03 Diseases of the blood or blood-forming organs
|
Anaemias or other erythrocyte disorders
|
Nutritional or metabolic anaemias
|
3A00 Iron deficiency anaemia
|
H01145 Atransferrinemia
H01196 Hypochromic microcytic anemia
H01278 Iron-refractory iron deficiency anemia
H02206 Aceruloplasminemia
|
3A01 Megaloblastic anaemia due to vitamin B12 deficiency
|
H01277 Vitamin B12 deficiency anaemia
H01190 Transcobalamin II deficiency
|
3A02 Folate deficiency anaemia
|
H01197 Dihydrofolate reductase deficiency
H01262 Formiminotransferase deficiency
H02761 Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia
|
3A03 Other nutritional or metabolic anaemias
|
H00198 Orotic aciduria
|
Haemolytic anaemias
|
Congenital haemolytic anaemia
|
3A10 Hereditary haemolytic anaemia
|
3A1Y Other specified congenital haemolytic anaemia
|
Acquired haemolytic anaemia
|
3A20 Acquired haemolytic anaemia, immune
|
3A21 Acquired haemolytic anaemia, non-immune
|
3A2Z Acquired haemolytic anaemia, unspecified
|
3A4Z Haemolytic anaemias, unspecified
|
3A50 Thalassaemias
|
H00228 Thalassemia
H01752 ATR-X syndrome
|
3A51 Sickle cell disorders or other haemoglobinopathies
|
H00229 Sickle cell disease
|
Pure red cell aplasia
|
3A60 Congenital pure red cell aplasia
|
H00237 Diamond-Blackfan anemia
|
3A61 Acquired pure red cell aplasia
|
H01586 Acquired pure red cell aplasia
|
3A6Z Pure red cell aplasia, unspecified
|
3A70 Aplastic anaemia
|
H01132 Aplastic anemia
H00238 Fanconi anemia
H00439 Shwachman-Diamond syndrome
H00507 Dyskeratosis congenita
H00788 Hoyeraal-Hreidarsson syndrome
H00921 Revesz syndrome
H02524 Ataxia-pancytopenia syndrome
H02529 Bone marrow failure syndrome
H02569 Pulmonary fibrosis and/or bone marrow failure, telomere-related
H02608 Autoinflammatory-pancytopenia syndrome
|
3A71 Anaemia due to chronic disease
|
H01642 Renal anemia
|
3A72 Sideroblastic anaemia
|
H00982 Sideroblastic anemia
H02670 Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay
H00898 Myopathy with lactic acidosis and sideroblastic anaemia
|
3A73 Congenital dyserythropoietic anaemia
|
H00917 Congenital dyserythropoietic anemia
|
Polycythaemia
|
3A80 Congenital polycythaemia
|
H00236 Congenital polycythemia
|
3A81 Acquired polycythaemia
|
3A8Z Polycythaemia, unspecified
|
3A90 Anaemia due to acute disease
|
3A91 Congenital methaemoglobinaemia
|
H00235 Methemoglobinemia
|
3A92 Hereditary methaemoglobinaemia
|
H00235 Methemoglobinemia
|
3A93 Acquired methaemoglobinaemia
|
3A94 Acute posthaemorrhagic anaemia
|
3A9Y Other specified anaemias or erythrocyte disorders
|
H02907 Elevated adenosine triphosphate of erythrocytes
|
3A9Z Anaemias or other erythrocyte disorders, unspecified
|
Coagulation defects, purpura or other haemorrhagic or related conditions
|
Coagulation defects
|
Congenital or constitutional haemorrhagic condition
|
3B10 Hereditary factor VIII deficiency
|
3B11 Hereditary factor IX deficiency
|
3B12 Von Willebrand disease
|
3B13 Haemophilia C
|
3B14 Other inherited coagulation factor deficiency with bleeding tendency
|
3B15 Inherited coagulation factor deficiency without bleeding tendency
|
3B1Z Congenital or constitutional haemorrhagic condition, unspecified
|
Haemorrhagic diseases due to acquired coagulation factor defects
|
3B20 Disseminated intravascular coagulation
|
3B21 Haemorrhagic disorder due to circulating anticoagulants and coagulation factors
|
3B22 Acquired haemophilia
|
3B2Y Other specified haemorrhagic diseases due to acquired coagulation factor defects
|
3B4Z Coagulation defects, unspecified
|
Fibrinolytic defects
|
3B50 Inherited fibrinolytic defects
|
H00983 Alpha-2-plasmin inhibitor (a2-PI) deficiency
H01106 Plasminogen activator inhibitor type 1 deficiency
H01206 Plasminogen deficiency
|
3B51 Acquired fibrinolytic defects
|
3B60 Non-thrombocytopenic purpura
|
3B61 Thrombophilia
|
H00223 Inherited thrombophilia
H01381 Antithrombin III deficiency
|
3B62 Qualitative platelet defects
|
H01235 Bleeding disorder platelet-type
H01108 CD36 deficiency
H02097 Gray platelet syndrome
H00224 Bernard-Soulier syndrome
H00226 Glanzmann thrombasthenia
H01523 Wiskott-Aldrich syndrome
H01162 Scott syndrome
H02093 Platelet-type von Willebrand disease
H02259 Stormorken syndrome
|
3B63 Thrombocytosis
|
H01612 Essential thrombocythemia
|
3B64 Thrombocytopenia
|
H00978 Thrombocytopenia (THC)
H00227 Congenital amegakaryocytic thrombocytopenia
H00233 MYH9-related disease
H00578 Epstein syndrome
H00867 Radioulnar synostosis with amegakaryocytic thrombocytopenia
H01740 Macrothrombocytopenia
H01847 Thrombocytopenia-absent radius syndrome
H02052 Sebastian syndrome
H02053 Fechtner syndrome
H01240 Immune thrombocytopenia
H00225 Thrombotic thrombocytopenic purpura
|
3B65 Thrombotic microangiopathy, not elsewhere classified
|
3B6Y Other specified coagulation defects, purpura or other haemorrhagic or related conditions
|
H02749 Bleeding disorder vascular-type
|
3B6Z Coagulation defects, purpura or other haemorrhagic or related conditions, unspecified
|
Diseases of spleen
|
3B80 Congenital disorders of spleen
3B81 Acquired disorders of spleen
3B8Z Diseases of spleen, unspecified
|
3C0Y Other specified diseases of the blood or blood-forming organs
|
H01013 Adult i phenotype
|
3C0Z Diseases of the blood or blood-forming organs, unspecified
|
|
04 Diseases of the immune system
|
Primary immunodeficiencies
|
4A00 Primary immunodeficiencies due to disorders of innate immunity
|
H01725 Primary immunodeficiency disease
H02525 Disorders of innate immunity
H02620 Autoinflammation with episodic fever and lymphadenopathy
H00098 Chronic granulomatous disease
H01094 Eosinophil peroxidase deficiency
H02024 Neutrophil specific granule deficiency
H02025 Myeloperoxidase deficiency
H00104 Alternative complement pathway component defects
H00102 Classic complement pathway component defects
H00103 Late complement pathway defects
H01006 Hereditary angioedema
H00105 Mannose-binding lectin pathway component defects
H00106 Complement regulatory protein defects
H01136 Carboxypeptidase N deficiency
H02904 Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy
H00089 IFN-gamma/IL-12 axis
H00096 Defects of toll-like receptor signaling
H00721 Pyogenic bacterial infections, recurrent, due to MYD88 deficiency
H00090 NK cell defects
H00097 WHIM syndrome
|
4A01 Primary immunodeficiencies due to disorders of adaptive immunity
|
H01725 Primary immunodeficiency disease
H02526 Disorders of adaptive immunity
H00085 Agammaglobulinemias
H02308 Immunodeficiency-centromeric instability-facial anomalies syndrome
H00086 Immunodeficiency with hyper-IgM
H00088 Common variable immunodeficiency
H00093 Combined immunodeficiency
H00091 T-B+Severe combined immunodeficiency
H00092 T-B-Severe combined immunodeficiency
H01128 Reticular dysgenesis
H01244 T+B+Severe combined immunodeficiencies (SCIDs)
H02309 Adenosine deaminase deficiency
H02554 Omenn syndrome
H00984 MHC class I deficiency
H01303 Hypercatabolic hypoproteinemia
H00985 MHC class II deficiency
H00087 Other humoral immunodeficiencies
H00924 Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation
H01181 T-cell immunodeficiency congenital alopecia and nail dystrophy
H01387 Activated PI3K-delta syndrome
H02015 LIG4 syndrome
H02133 Vici syndrome
H02585 Roifman-Chitayat syndrome
H01971 IPEX syndrome
H02792 Immune dysregulation, autoimmunity, and autoinflammation
H00108 Autoimmune lymphoproliferative syndromes
H01969 X-linked lymphoproliferative syndrome
H01970 Lymphoproliferative syndrome
H00109 Familial hemophagocytic lymphohistiocytosis
H02491 Immunoskeletal dysplasia with neurodevelopmental abnormalities
H02574 BILU syndrome
H00064 Ataxia telangiectasia
H00094 Immunodeficiency associated with DNA repair defects
H00962 RIDDLE syndrome
H01344 Nijmegen breakage syndrome
H01346 Bloom syndrome
H02014 Ataxia-telangiectasia-like syndrome
H00580 Schimke immunoosseous dysplasia
H01264 Hepatic venoocclusive disease with immunodeficiency
H01968 Hyper-IgE syndrome
|
4A0Y Other specified primary immunodeficiencies
|
H01245 Immunodeficiency without anhidrotic ectodermal dysplasia
|
4A0Z Primary immunodeficiencies, unspecified
|
4A20 Acquired immunodeficiencies
|
H00406 Acquired immunodeficiency syndrome (AIDS)
|
Nonorgan specific systemic autoimmune disorders
|
4A40 Lupus erythematosus
|
H00080 Systemic lupus erythematosus
H01500 Lupus nephritis
|
4A41 Idiopathic inflammatory myopathy
|
H01604 Polymyositis and dermatomyositis
H01229 Inclusion body myopathy 3
H01505 Inclusion body myositis
H02031 Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
|
4A42 Systemic sclerosis
|
H01492 Systemic sclerosis
|
4A43 Overlap or undifferentiated nonorgan specific systemic autoimmune disease
|
H01761 Immunoglobulin G4-related disease
H01502 Sjogren syndrome
H01710 Mixed connective tissue disease
H01693 Eosinophilic fasciitis
H01133 Reynolds syndrome
H01232 Syndromic multisystem autoimmune disease
H02540 Infantile-onset multisystem autoimmune disease
|
4A44 Vasculitis
|
H01698 Giant cell arteritis
H01382 Polyarteritis nodosa
H01718 Kawasaki disease
H02883 Sneddon syndrome
H01625 Buerger disease
H01584 IgA vasculitis
H01767 Henoch-Schonlein purpura nephritis
H01658 Microscopic polyangiitis
H01655 Granulomatosis with polyangiitis
H01468 Eosinophilic granulomatosis with polyangiitis
H01465 Large-vessel vasculitis
|
4A45 Antiphospholipid syndrome
|
H01697 Antiphospholipid syndrome
|
4A4Y Other specified nonorgan specific systemic autoimmune disorders
|
H02537 Autoinflammation, immune dysregulation, and eosinophilia
H02621 X-linked systemic autoinflammatory disease
|
4A4Z Nonorgan specific systemic autoimmune disorders, unspecified
|
Autoinflammatory disorders
|
4A60 Monogenic autoinflammatory syndromes
|
H02588 NLRP1-associated autoinflammation with arthritis and dyskeratosis
H02589 Periodic fever, immunodeficiency, and thrombocytopenia syndrome
H02591 Interleukin-18 binding protein deficiency
H02592 Familial Behcet-like autoinflammatory syndrome
H02593 Chronic mucocutaneous ulceration
H02599 Inherited autoinflammatory disease
H00288 Familial Mediterranean fever
H00282 Cryopyrin associated periodic syndrome
H02159 Familial cold autoinflammatory syndrome
H02555 Muckle-Wells syndrome
H02556 CINCA syndrome
H00912 Tumor necrosis factor receptor-associated periodic syndrome
H00285 Blau syndrome
H00287 Pyogenic sterile arthritis, pyoderma gangrenosum, and acne syndrome
H01743 Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation
H01744 Polyglucosan body myopathy
H02414 Autoinflammation, panniculitis, and dermatosis syndrome
H02467 Neonatal inflammatory skin and bowel disease
H02532 Proteasome-associated autoinflammatory syndrome
H02561 Familial autoinflammatory syndrome with or without immunodeficiency
H02656 X-linked multisystem autoinflammatory disease with immune dysregulation
H02660 Autoinflammation with pulmonary and cutaneous vasculitis
H02672 Systemic autoinflammatory disease with vasculitis
|
4A61 SAPHO syndrome
|
4A62 Behรงet disease
|
H01476 Behcet disease
|
4A6Y Other specified autoinflammatory disorders
|
H01117 Chronic recurrent multifocal osteomyelitis
H01275 Interleukin 1 receptor antagonist deficiency
H01748 NLRC4 inflammasomopathy
H02826 Autoinflammation with episodic fever and immune dysregulation
H02829 Autoinflammation with arthritis and vasculitis
|
4A6Z Autoinflammatory disorders, unspecified
|
Allergic or hypersensitivity conditions
|
4A80 Allergic or hypersensitivity disorders involving the respiratory tract
|
4A81 Allergic or hypersensitivity disorders involving the eye
|
4A82 Allergic or hypersensitivity disorders involving skin or mucous membranes
|
4A83 Allergic or hypersensitivity disorders involving the gastrointestinal tract
|
H01782 Eosinophilic gastrointestinal disorder
|
4A84 Anaphylaxis
|
H01359 Anaphylaxis
|
4A85 Complex allergic or hypersensitivity conditions
|
4A8Y Allergic or hypersensitivity conditions of other specified type
|
4A8Z Allergic or hypersensitivity conditions of unspecified type
|
Immune system disorders involving white cell lineages
|
4B00 Disorders of neutrophil number
|
H00100 Neutropenic disorders
H00939 Darsun syndrome
H01218 P14 deficiency
|
4B01 Disorders of neutrophil function
|
4B02 Eosinopenia
|
4B03 Eosinophilia
|
4B04 Disorders with decreased monocyte counts
|
4B05 Disorders with increased monocyte counts
|
4B06 Acquired lymphopenia
|
4B07 Acquired lymphocytosis
|
4B0Y Other specified immune system disorders involving white cell lineages
|
H00234 Pelger-Huet anomaly
H02051 May-Hegglin anomaly
|
4B0Z Immune system disorders involving white cell lineages, unspecified
|
Certain disorders involving the immune system
|
4B20 Sarcoidosis
|
H01309 Sarcoidosis
|
4B21 Polyclonal hypergammaglobulinaemia
|
4B22 Cryoglobulinaemia
|
4B23 Immune reconstitution inflammatory syndrome
|
4B24 Graft-versus-host disease
|
H00084 Graft-versus-host disease
|
4B2Y Other specified disorders involving the immune system
|
H01479 Castleman disease
H02669 Inflammatory bowel disease, immunodeficiency, and encephalopathy
|
4B40 Diseases of thymus
|
4B4Y Other specified diseases of the immune system
|
4B4Z Diseases of the immune system, unspecified
|
|
05 Endocrine, nutritional or metabolic diseases
|
Endocrine diseases
|
Disorders of the thyroid gland or thyroid hormones system
|
5A00 Hypothyroidism
|
H01186 Abnormal thyroid hormone metabolism
H00251 Thyroid dyshormonogenesis
H00249 Thyroid hormone resistance syndrome
H00250 Congenital nongoitrous hypothyroidism (CHNG)
H00650 Allan-Herndon-Dudley syndrome
H01040 Bamforth-Lazarus syndrome
|
5A01 Nontoxic goitre
|
H02737 Familial multinodular goiter
|
5A02 Thyrotoxicosis
|
H01269 Congenital hyperthyroidism
H01645 Hyperthyroidism
H00082 Graves disease
H02402 Thyroid eye disease
|
5A03 Thyroiditis
|
H01647 Subacute thyroiditis
H00081 Hashimoto thyroiditis
|
5A04 Hypersecretion of calcitonin
|
5A05 Generalised resistance to thyroid hormone
|
5A06 Sick-euthyroid syndrome
|
5A0Y Other specified disorders of the thyroid gland or thyroid hormones system
|
H02893 Euthyroid hyperthyroxinemia
|
5A0Z Disorders of the thyroid gland or thyroid hormones system, unspecified
|
Diabetes mellitus
|
5A10 Type 1 diabetes mellitus
|
H00408 Type 1 diabetes mellitus
H01224 Ketosis-prone diabetes mellitus
|
5A11 Type 2 diabetes mellitus
|
H00409 Type 2 diabetes mellitus
|
5A12 Malnutrition-related diabetes mellitus
|
5A13 Diabetes mellitus, other specified type
|
H00410 Maturity onset diabetes of the young (MODY)
H01228 Insulin-resistant diabetes mellitus with acanthosis nigricans
H00766 Wolcott-Rallison syndrome
H02806 Insulinomatosis and diabetes mellitus syndrome
|
5A14 Diabetes mellitus, type unspecified
|
Acute complications of diabetes mellitus
|
5A20 Diabetic hyperosmolar hyperglycaemic state
5A21 Hypoglycaemia in the context of diabetes mellitus
5A22 Diabetic acidosis
5A23 Diabetic coma
5A24 Uncontrolled or unstable diabetes mellitus
5A2Y Other specified acute complications of diabetes mellitus
|
Other disorders of glucose regulation or pancreatic internal secretion
|
5A40 Intermediate hyperglycaemia
|
5A41 Hypoglycaemia without associated diabetes
|
H01909 Hypoinsulinemic hypoglycemia with hemihypertrophy
|
5A42 Increased secretion of glucagon
|
H02787 Mahvash disease
|
5A43 Abnormal secretion of gastrin
|
H01522 Zollinger-Ellison syndrome
|
5A44 Insulin-resistance syndromes
|
H00419 Congenital generalized lipodystrophy
H00420 Familial partial lipodystrophy
H00719 Leprechaunism
H00942 Rabson-Mendenhall syndrome
H01474 Acquired generalized lipodystrophy
H02384 Abdominal obesity-metabolic syndrome
|
5A45 Persistent hyperinsulinaemic hypoglycaemia of infancy
|
H01267 Familial hyperinsulinemic hypoglycemia
|
5A4Y Other specified disorders of glucose regulation or pancreatic internal secretion
|
H02760 BDV syndrome
|
5A4Z Disorders of glucose regulation or pancreatic internal secretion, unspecified
|
Disorders of the parathyroids or parathyroid hormone system
|
5A50 Hypoparathyroidism
|
H01862 Hypoparathyroidism
H00244 Pseudohypoparathyroidism
|
5A51 Hyperparathyroidism
|
H00246 Primary hyperparathyroidism
H01669 Secondary hyperparathyroidism
H02026 Familial hypocalciuric hypercalcemia
H02030 Neonatal hyperparathyroidism
|
5A5Y Other specified disorders of the parathyroids or parathyroid hormone system
|
5A5Z Disorders of the parathyroids or parathyroid hormone system, unspecified
|
Disorders of the pituitary hormone system
|
5A60 Hyperfunction of pituitary gland
|
H01683 Disorders of antidiuretic hormone (ADH) secretion
H01483 Acromegaly
H01618 Pituitary gigantism
H01864 Excessive secretion of growth hormone
H01388 Hyperprolactinemia
H01682 Syndrome of inappropriate antidiuretic hormone secretion
H01294 Nephrogenic syndrome of inappropriate antidiuresis
H00937 Precocious puberty
H02018 Central precocious puberty
H01701 Pituitary TSH hypersecretion
|
5A61 Hypofunction or certain other specified disorders of pituitary gland
|
H01683 Disorders of antidiuretic hormone (ADH) secretion
H00254 Growth hormone deficiency
H00931 Growth hormone insensitivity with immunodeficiency
H01253 Isolated follicle-stimulating hormone deficiency
H01274 Growth delay due to insulin-like growth factor I resistance
H01700 Hypopituitarism
H01907 Acid-labile subunit deficiency
H01973 Fertile eunuch syndrome
H02035 Isolated growth hormone deficiency
H02036 Combined pituitary hormone deficiency
H02037 Laron syndrome
H02038 X-linked panhypopituitarism
H02039 Kowarski syndrome
H02040 Insulin-like growth factor I deficiency
H01011 Adrenocorticotropic hormone deficiency
H00255 Hypogonadotropic hypogonadism
H01860 Abnormal pituitary gonadotropin secretion
H01699 Isolated TSH deficiency
H02034 Central hypothyroidism and testicular enlargement
H00253 Neurohypophyseal diabetes insipidus
H00854 Wolfram syndrome
H00682 Woodhouse-Sakati syndrome
|
5A6Z Disorders of the pituitary hormone system, unspecified
|
Disorders of the adrenal glands or adrenal hormone system
|
5A70 Cushing syndrome
|
H01431 Cushing syndrome
H00260 Pigmented micronodular adrenocortical disease
H01820 Carney complex
H02049 Bilateral macronodular adrenal hyperplasia
H02879 MIRAGE syndrome
|
5A71 Adrenogenital disorders
|
H01702 Glucocorticoid resistance syndrome
H00216 Congenital adrenal hyperplasia
H02315 Disordered steroidogenesis due to cytochrome P450 oxidoreductase
H01111 Cortisone reductase deficiency
|
5A72 Hyperaldosteronism
|
H00602 Glucocorticoid-remediable aldosteronism (GRA)
H01603 Primary aldosteronism
H00259 Apparent mineralocorticoid excess syndrome
|
5A73 Hypoaldosteronism
|
H00258 Aldosterone synthase deficiency
|
5A74 Adrenocortical insufficiency
|
H01598 Addison disease
H00177 Neonatal adrenoleukodystrophy
H00256 Familial glucocorticoid deficiency
H00257 Achalasia Addisonianism Alacrima syndrome
H02314 Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete
H02316 Adrenal insufficiency, NR5A1 related
H02319 IMAGE syndrome
|
5A75 Adrenomedullary hyperfunction
|
5A76 Certain specified disorders of adrenal gland
|
H01163 Corticosteroid-binding globulin (CBG) deficiency
|
5A7Z Disorders of the adrenal glands or adrenal hormone system, unspecified
|
Disorders of the gonadal hormone system
|
5A80 Ovarian dysfunction
|
H01739 Polycystic ovary syndrome
|
5A81 Testicular dysfunction or testosterone-related disorders
|
H02019 Familial male-limited precocious puberty
H02027 Male hypogonadism
|
5A8Z Disorders of the gonadal hormone system, unspecified
|
Certain disorders of puberty
|
5A90 Disorder of puberty due to oestrogen resistance
|
H02061 Estrogen resistance syndrome
|
5A91 Delayed puberty
|
5A92 Peripheral precocious puberty
|
H00794 Aromatase excess syndrome
H00937 Precocious puberty
|
5A9Y Other disorders of puberty
|
H02020 Aromatase deficiency
|
5A9Z Disorders of puberty, unspecified
|
Polyglandular dysfunction
|
5B00 Autoimmune polyendocrinopathy
|
H01972 Autoimmune polyendocrinopathy syndrome type 1
|
5B01 Polyglandular hyperfunction
|
5B0Y Other specified polyglandular dysfunction
|
5B0Z Polyglandular dysfunction, unspecified
|
Endocrine disorders, not elsewhere classified
|
5B10 Carcinoid syndrome
5B11 Short stature, not elsewhere classified
5B12 Constitutional tall stature
5B1Y Other specified endocrine disorders, not elsewhere classified
|
5B3Y Other specified endocrine diseases
|
H02773 Menstrual cycle-dependent periodic fever
|
5B3Z Endocrine diseases, unspecified
|
Nutritional disorders
|
Undernutrition
|
5B50 Underweight in infants, children or adolescents
|
5B51 Wasting in infants, children or adolescents
|
5B52 Acute malnutrition in infants, children or adolescents
|
5B53 Stunting in infants, children or adolescents
|
5B54 Underweight in adults
|
5B55 Vitamin A deficiency
|
H01266 Hypercarotenemia and vitamin A deficiency
|
5B56 Vitamin C deficiency
|
H01580 Vitamin C deficiency
|
5B57 Vitamin D deficiency
|
H01143 Vitamin D-dependent rickets
|
5B58 Vitamin E deficiency
|
H00981 Ataxia with isolated vitamin E deficiency (AVED)
|
5B59 Vitamin K deficiency
|
5B5A Vitamin B1 deficiency
|
H01566 Beriberi
H01565 Wernicke encephalopathy
|
5B5B Vitamin B2 deficiency
|
H02544 Riboflavin deficiency
|
5B5C Vitamin B3 deficiency
|
H01582 Pellagra
|
5B5D Vitamin B6 deficiency
|
5B5E Folate deficiency
|
5B5F Vitamin B12 deficiency
|
5B5G Biotin deficiency
|
5B5H Pantothenic acid deficiency
|
5B5J Choline deficiency
|
5B5K Mineral deficiencies
|
H01925 Transient neonatal zinc deficiency
|
Sequelae of malnutrition or certain specified nutritional deficiencies
|
5B60 Sequelae of protein-energy malnutrition
5B61 Sequelae of vitamin A deficiency
5B62 Sequelae of vitamin C deficiency
5B63 Sequelae of rickets
5B6Y Other specified sequelae of malnutrition or certain specified nutritional deficiencies
5B6Z Sequelae of malnutrition or certain specified nutritional deficiencies, unspecified
|
5B70 Essential fatty acid deficiency
|
5B71 Protein deficiency
|
5B7Y Other specified undernutrition
|
5B7Z Unspecified undernutrition
|
Overweight, obesity or specific nutrient excesses
|
Overweight or obesity
|
5B80 Overweight or localised adiposity
|
5B81 Obesity
|
Certain specified nutrient excesses
|
5B90 Vitamin excesses
|
5B91 Mineral excesses
|
5B9Y Other specified nutrient excesses
|
5B9Z Certain specified nutrient excesses, unspecified
|
5C1Y Other specified overweight, obesity or specific nutrient excesses
|
5C1Z Overweight, obesity or specific nutrient excesses, unspecified
|
5C3Y Other specified nutritional disorders
|
5C3Z Nutritional disorders, unspecified
|
Metabolic disorders
|
Inborn errors of metabolism
|
5C50 Inborn errors of amino acid or other organic acid metabolism
|
H00167 Phenylketonuria
H02419 Glycine encephalopathy with normal serum glycine
H00163 Alkaptonuria
H00165 Tyrosinemia
H00171 Histidinemia
H01233 Urocanase deficiency
H01583 Hydroxykynureninuria
H02545 Hypertryptophanemia
H00188 Hyperlysinemia
H01242 Saccharopinuria
H02644 Alpha-aminoadipic and alpha-ketoadipic aciduria
H02313 5-Oxoprolinase deficiency
H01079 3-Phosphoglycerate dehydrogenase (3-PGDH) deficiency
H01082 Phosphoserine aminotransferase deficiency
H02116 Phosphoserine phosphatase deficiency
H01003 Dimethylglycine dehydrogenase deficiency
H00191 Nonketotic hyperglycinemia
H02657 Sarcosinemia
H02380 D-glyceric aciduria
H00190 Hyperprolinemia
H00187 Ornithine transcarbamylase deficiency
H00189 Ornithinaemia
H02919 Bachmann-Bupp syndrome
H01398 Primary hyperammonemia (Urea cycle disorders)
H01400 Secondary hyperammonemia
H01028 Argininosuccinic aciduria
H00164 Carbamoyl phosphate synthetase I deficiency
H00186 Hyperargininemia
H00185 Citrullinemia
H01032 N-acetylglutamate synthase deficiency
H01268 Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
H00182 Cystathioninuria
H00183 Homocystinuria
H00184 Hypermethioninemia
H01237 Sulfite oxidase deficiency
H01285 Methylcobalamin deficiency type G
H02311 Molybdenum cofactor deficiency
H02485 Extraoral halitosis due to MTO deficiency
H00172 Maple syrup urine disease
H01076 Beta-ketothiolase deficiency
H01279 Isobutyryl-CoA dehydrogenase deficiency
H02136 Branched-chain ketoacid dehydrogenase kinase deficiency
H02285 Methylmalonate semialdehyde dehydrogenase deficiency
H02546 Hypervalinemia and hyperleucine-isoleucinemia
H01349 Methacrylic aciduria
H00173 Isovaleric acidemia
H00174 Methylmalonic aciduria
H00175 Propionic acidemia
H00180 Holocarboxylase synthetase deficiency
H00181 3-Methylcrotonylglycinuria
H00375 SBCAD deficiency
H00654 Barth syndrome
H00754 3-Methylglutaconic aciduria
H01182 Biotinidase deficiency
H02221 Methylmalonic aciduria and homocystinuria
H02222 Methylmalonic acidemia and hyperhomocysteinemia, cblX type
H00074 Canavan disease
H00178 Glutaric acidemia
H00835 Succinic semialdehyde dehydrogenase deficiency
H01146 Aminoacylase 1 deficiency
H01225 D-2-hydroxyglutaric aciduria
H01280 L-2-hydroxyglutaric aciduria
H01283 Malonyl-CoA decarboxylase deficiency
H02304 Combined D-2- and L-2-hydroxyglutaric aciduria
H02109 Combined malonic and methylmalonic aciduria
H01119 Prolidase deficiency
H01234 Trimethylaminuria
H00923 Congenital systemic glutamine deficiency
H01386 Asparagine synthetase deficiency
H02312 Glutathione synthetase deficiency
H02750 Glutathionuria
H02774 Hypotaurinemic retinal degeneration and cardiomyopathy
H02800 N-acetylaspartate deficiency
H02846 Global developmental delay, progressive ataxia, and elevated glutamine
H02847 CASGID syndrome
|
5C51 Inborn errors of carbohydrate metabolism
|
H01065 Pentosuria
H01135 Ribose 5-phosphate isomerase deficiency
H01189 Transaldolase deficiency
H02439 Short stature, developmental delay, congenital heart defect
H02013 Glycerol kinase deficiency
H00117 Primary hyperoxaluria
H00069 Glycogen storage disease
H00150 Danon disease
H01375 Glucose 6-phosphate dehydrogenase deficiency
H01760 Hepatic glycogen storage disease
H01762 Muscle glycogen storage disease
H01939 Glycogen storage disease type I
H01940 Glycogen storage disease type II
H01941 Glycogen storage disease type III
H01942 Glycogen storage disease type IV
H01943 Glycogen storage disease type V
H01944 Glycogen storage disease type VI
H01945 Glycogen storage disease type VII
H01946 Glycogen storage disease type XI
H01947 Fanconi-Bickel syndrome
H01948 Glycogen storage disease type IX
H01949 Glycogen storage disease type 0b
H01950 Glycogen storage disease type 0a
H01951 Glycogen storage disease type X
H01952 Glycogen storage disease type XII
H01953 Glycogen storage disease type XIII
H01954 Glycogen storage disease type XIV
H01955 Glycogen storage disease type XV
H01956 Glycogen storage disease of heart
H00070 Galactosemia
H02008 Galactose-1P uridylyltransferase deficiency
H02009 Galactokinase deficiency
H02010 Galactose epimerase deficiency
H00071 Hereditary fructose intolerance
H00114 Fructose-1,6-bisphosphatase deficiency
H02567 Sorbitol dehydrogenase deficiency with peripheral neuropathy
|
5C52 Inborn errors of lipid metabolism
|
H01589 Systemic primary carnitine deficiency
H01981 Carnitine palmitoyltransferase I deficiency
H01982 Carnitine palmitoyltransferase II deficiency
H01983 Carnitine-acylcarnitine translocase deficiency
H02596 Disorders of carnitine transport and the carnitine cycle
H00392 VLCAD deficiency
H00488 MCAD deficiency
H00489 LCHAD deficiency
H00525 Disorders of mitochondrial fatty-acid oxidation
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency
H01352 Mitochondrial trifunctional protein deficiency
H01364 3-Hydroxyacyl-CoA dehydrogenase deficiency
H01929 2,4-Dienoyl-CoA reductase deficiency
H01980 SCAD deficiency
H02085 Acyl-CoA dehydrogenase 9 deficiency
H00179 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
H01121 Succinyl CoA:3-oxoacid CoA transferase (SCOT) deficiency
H01123 HMG-CoA synthase deficiency
H00162 Sjogren-Larsson syndrome
H02284 Leukotriene C4 synthase deficiency
H02689 Retinal dystrophy with leukodystrophy
H00161 Smith-Lemli-Opitz syndrome
H00206 Mevalonate kinase deficiency
H00617 Desmosterolosis
H01281 Lathosterolosis
H00151 Cerebrotendinous xanthomatosis
H00624 Progressive familial intrahepatic cholestasis
H00628 Congenital bile acid synthesis defect
H02099 Alpha-methylacyl-CoA racemase deficiency
H00152 Sitosterolemia
H00736 Dorfman-Chanarin syndrome
H01297 Neutral lipid storage disease with myopathy
H02527 Lipid storage myopathy due to FLAD1 deficiency
H02711 Acetyl-CoA carboxylase-alpha deficiency
|
5C53 Inborn errors of energy metabolism
|
H01427 Mitochondrial disease
H01096 Pyruvate kinase deficiency
H00072 Pyruvate dehydrogenase complex deficiency
H01996 Pyruvate dehydrogenase phosphatase deficiency
H01997 Pyruvate dehydrogenase E1-alpha deficiency
H01998 Pyruvate dehydrogenase E1-beta deficiency
H01999 Pyruvate dehydrogenase E2 deficiency
H02000 Dihydrolipoamide dehydrogenase deficiency
H02003 Pyruvate dehydrogenase E3-binding protein deficiency
H00073 Pyruvate carboxylase deficiency
H02197 Mitochondrial pyruvate carrier deficiency
H02438 Hyperglycinemia, lactic acidosis, and seizures
H02520 Phosphoenolpyruvate carboxykinase deficiency
H01022 Diseases of the tricarboxylic acid cycle
H02004 Fumarase deficiency
H02006 Alpha-ketoglutarate dehydrogenase complex deficiency
H02113 Infantile cerebellar-retinal degeneration
H02562 Yoon-Bellen neurodevelopmental syndrome
H00469 Mitochondrial DNA depletion syndrome
H01389 Alpers syndrome
H01390 Mitochondrial neurogastrointestinal encephalomyopathy
H01384 Mitochondrial recessive ataxia syndrome
H00999 Coenzyme Q10 deficiency
H00871 Leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
H01367 Infantile liver failure
H01354 Leigh syndrome
H01369 ATP synthase deficiency
H00473 Mitochondrial complex I deficiency
H00891 Combined oxidative phosphorylation deficiency
H00920 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis
H01201 Jensen syndrome
H01368 Cytochrome c oxidase (COX) deficiency
H01894 Multiple mitochondrial dysfunctions syndrome
H02005 Mitochondrial complex II deficiency
H02007 GRACILE syndrome
H02086 Mitochondrial complex III deficiency
H02779 Riboflavin-responsive exercise intolerance
H01305 Global cerebral hypomyelination
H01348 Mitochondrial phosphate carrier deficiency
H00834 Guanidinoacetate methyltransferase deficiency
H00849 Cerebral creatine deficiency syndrome
H02181 Idiopathic hyperCKemia
H02196 X-linked creatine deficiency syndrome
H01248 Monocarboxylate transporter 1 deficiency
H01900 Encephalopathy due to defective mitochondrial and peroxisomal fission
H02518 Neonatal severe encephalopathy with lactic acidosis and brain abnormalities
H02643 Lipoyltransferase 1 deficiency
H02841 Hydrops, lactic acidosis, and sideroblastic anemia
|
5C54 Inborn errors of glycosylation or other specified protein modification
|
H01486 Multiple congenital anomalies-hypotonia-seizures syndrome
H01487 CHIME syndrome
H00118 Congenital disorders of glycosylation type I
H00119 Congenital disorders of glycosylation type II
H02767 Congenital disorder of deglycosylation
H02900 Kahrizi syndrome
H01188 Tn syndrome
H01193 Familial tumoral calcinosis
H00996 Amish infantile epilepsy syndrome
H01127 PIGM-congenital disorder of glycosylation
H01489 Inherited glycosylphosphatidylinositol deficiencies
H02451 Congenital disorder of glycosylation with defective fucosylation
H02690 Structural heart defects and renal anomalies syndrome
H02815 Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome
|
5C55 Inborn errors of purine, pyrimidine or nucleotide metabolism
|
H00192 Xanthinuria
H00194 Lesch-Nyhan syndrome
H00195 Adenine phosphoribosyltransferase deficiency
H00196 Phosphoribosylpyrophosphate synthetase superactivity
H00197 Adenylosuccinate lyase deficiency
H00964 Poor metabolism of thiopurines
H00966 AICA-ribosiduria
H02011 Familial juvenile hyperuricemic nephropathy
H02237 AMP deaminase deficiency
H00193 Dihydropyrimidine dehydrogenase deficiency
H00199 Dihydropyrimidinase deficiency
H00200 Beta-ureidopropionase deficiency
H00290 Aicardi-Goutieres syndrome
H00878 Cystic leukoencephalopathy without megalencephaly
H02433 Hypomyelination with brainstem and spinal cord involvement and leg spasticity
|
5C56 Lysosomal diseases
|
H01425 Lysosomal storage disease
H00423 Sphingolipidosis
H00124 GM2 gangliosidoses
H00281 GM1 gangliosidosis
H00426 Gangliosidosis
H02016 Tay-Sachs disease
H02017 Sandhoff disease
H00125 Fabry disease
H00127 Metachromatic leukodystrophy
H00272 Multiple sulfatase deficiency
H00126 Gaucher disease
H00136 Niemann-Pick disease type C
H00137 Niemann-Pick disease type A/B
H00138 Farber lipogranulomatosis
H00148 Lysosomal acid lipase deficiency
H00424 Defects in the degradation of sphingomyelin
H01239 Combined SAP deficiency
H02468 Early childhood-onset progressive leukodystrophy
H00149 Neuronal ceroid lipofuscinosis
H02275 Batten disease
H02276 Kufs disease
H02277 Santavuori-Haltia disease
H02278 Jansky-Bielschowsky disease
H02279 Cathepsin D deficiency
H00422 Glycoproteinoses
H00143 Mucolipidosis II
H00144 Mucolipidosis IV
H02130 Mucolipidosis III
H00139 alpha-Mannosidosis
H00140 beta-Mannosidosis
H00141 Fucosidosis
H00142 Sialidosis
H00145 Aspartylglucosaminuria
H00146 Alpha-N-acetylgalactosaminidase deficiency
H00276 Galactosialidosis
H00421 Mucopolysaccharidosis
H00128 Mucopolysaccharidosis type I
H00129 Mucopolysaccharidosis type II
H00123 Mucopolysaccharidosis type IV
H00131 Mucopolysaccharidosis type VI
H00130 Mucopolysaccharidosis type III
H00132 Mucopolysaccharidosis type VII
H00133 Mucopolysaccharidosis type IX
H02205 Mucopolysaccharidosis-plus syndrome
H02729 Ain-Naz type of dysostosis multiplex
H00147 Sialuria
H00273 Pycnodysostosis
H00274 Papillon-Lefevre syndrome
H00425 Lysosomal cysteine protease deficiencies
H02128 Defects in lysosomal trafficking
|
5C57 Peroxisomal diseases
|
H00177 Neonatal adrenoleukodystrophy
H00205 Peroxisome biogenesis disorder
H00207 Rhizomelic chondrodysplasia punctata
H01342 Zellweger syndrome
H02100 Peroxisomal fatty acyl-CoA reductase 1 disorder
H00075 Refsum disease
H00176 Adrenoleukodystrophy
H00407 Peroxisomal beta-oxidation enzyme deficiency
H00874 Leukoencephalopathy with dystonia and motor neuropathy
H02096 Peroxisomal acyl-CoA oxidase deficiency
H02098 D-bifunctional protein deficiency
H02099 Alpha-methylacyl-CoA racemase deficiency
H00203 Acatalasemia
|
5C58 Inborn errors of porphyrin or heme metabolism
|
H02025 Myeloperoxidase deficiency
H00208 Hyperbilirubinemia
H02054 Crigler-Najjar syndrome
H02055 Gilbert syndrome
H02056 Dubin-Johnson syndrome
H00624 Progressive familial intrahepatic cholestasis
H02192 Benign recurrent intrahepatic cholestasis
H00950 Arthrogryposis, renal dysfunction, and cholestasis
H01936 Hyperbiliverdinemia
H02057 Rotor syndrome
H01763 Porphyria
H00202 Hepatic porphyria
H00201 Erythropoietic porphyria
|
5C59 Inborn errors of neurotransmitter metabolism
|
H01005 Dopamine beta-hydroxylase deficiency
H01161 Aromatic L-amino acid decarboxylase deficiency
H02597 Sepiapterin reductase deficiency
H00548 Brunner syndrome
H01257 GABA-transaminase deficiency
H02432 Butyrylcholinesterase deficiency
|
5C5A Alpha-1-antitrypsin deficiency
|
H01103 Alpha-1-antitrypsin deficiency
|
5C5Y Other specified inborn errors of metabolism
|
H00967 Adiponectin deficiency
H01567 Thiamine pyrophosphokinase deficiency
H02441 HUPRA syndrome
H02727 Triokinase and FMN cyclase deficiency syndrome
|
5C5Z Inborn errors of metabolism, unspecified
|
Disorders of metabolite absorption or transport
|
5C60 Disorders of amino acid absorption or transport
|
H00692 Lowe syndrome
H00275 Cystinosis
H00901 Cystinuria
H00843 Hartnup disorder
H00899 Lysinuric protein intolerance
H00905 Iminoglycinuria
H00911 Dicarboxylic aminoaciduria
H01304 Hyperglycinuria
H02754 Acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate
|
5C61 Disorders of carbohydrate absorption or transport
|
H00115 Congenital sucrase-isomaltase deficiency
H02090 Trehalase deficiency
H00836 GLUT1 deficiency syndrome
H01126 Familial renal glucosuria
H02575 Lactose intolerance, adult type
H00116 Congenital lactase deficiency
H01261 Congenital glucose-galactose malabsorption
|
5C62 Disorders of lipid absorption or transport
|
H02330 Pancreatic lipase deficiency
|
5C63 Disorders of vitamin or non-protein cofactor absorption or transport
|
H01252 Hereditary folate malabsorption
H01262 Formiminotransferase deficiency
H01295 Neurodegeneration due to cerebral folate transport deficiency
H02761 Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia
H00214 Hypophosphatemic rickets
H02139 Autosomal recessive hypophosphatemic rickets
H02141 Autosomal dominant hypophosphatemic rickets
H02142 X-linked recessive hypophosphatemic rickets
H02143 X-linked dominant hypophosphatemic rickets
H00990 Microcephaly, Amish type
H01124 Pyridoxamine-5'-phosphate oxidase (PNPO) deficiency
H01183 Thiamine-responsive megaloblastic anemia
H01231 Biotin-thiamine-responsive basal ganglia disease
H02662 Sulfide quinone oxidoreductase deficiency
H02671 Sodium-dependent multivitamin transporter deficiency
H02699 Folate-responsive megaloblastic anemia
H02832 Thiamine metabolism dysfunction syndrome
|
5C64 Disorders of mineral absorption or transport
|
H02736 Neurodegeneration and seizures due to copper transport defect
H00210 Wilson disease
H00209 Menkes syndrome
H00833 Neurodegeneration with brain iron accumulation
H02207 Kufor-Rakeb syndrome
H02208 Pantothenate kinase-associated neurodegeneration
H02209 HARP syndrome
H00211 Hemochromatosis
H00212 Acrodermatitis enteropathica
H02550 Birk-Landau-Perez syndrome
H00213 Hypophosphatasia
H01113 Acid phosphatase deficiency
H02138 Hereditary hypophophatemic rickets with hypercalciuria
H00240 Gitelman syndrome
H01210 Hypomagnesemia
H00245 Calcium sensing receptor (CASR) related disease
H01371 Hypercalcemia infantile
H01938 Hypermanganesemia with dystonia
|
5C6Y Other specified disorders of metabolite absorption or transport
|
5C6Z Disorders of metabolite absorption or transport, unspecified
|
Disorders of fluid, electrolyte or acid-base balance
|
5C70 Volume depletion
|
5C71 Hyperosmolality or hypernatraemia
|
5C72 Hypo-osmolality or hyponatraemia
|
5C73 Acidosis
|
5C74 Alkalosis
|
5C75 Mixed disorder of acid-base balance
|
5C76 Hyperkalaemia
|
5C77 Hypokalaemia
|
H02790 Hypokalemic tubulopathy and deafness
|
5C78 Fluid overload
|
5C7Y Other specified disorders of fluid, electrolyte or acid-base balance
|
5C7Z Disorders of fluid, electrolyte or acid-base balance, unspecified
|
Disorders of lipoprotein metabolism or certain specified lipidaemias
|
5C80 Hyperlipoproteinaemia
|
H01101 Combined lipase deficiency
H01635 Hyperlipidemia
H00155 Familial hypercholesterolemia
H01383 Hyperlipoproteinemia type IIa
H01918 Familial autosomal recessive hypercholesterolemia
H00154 Hyperlipoproteinemia, type I
H00157 Hyperlipoproteinemia, type V
H01637 Hypertriglyceridemia
H01784 Primary hyperchylomicronemia
H02731 Transient infantile hypertriglyceridemia
H00153 Familial combined hyperlipidemia
H00156 Hyperlipoproteinemia, type III
H01199 Hyperalphalipoproteinemia
H02329 Hepatic lipase deficiency
|
5C81 Hypolipoproteinaemia
|
H00159 Tangier disease
H00930 Hypoalphalipoproteinemia
H00160 Abetalipoproteinemia
H00927 Chylomicron retention disease
H01270 Familial hypobetalipoproteinemia
H00158 Lecithin:cholesterol acyltransferase deficiency
|
5C8Y Other specified disorders of lipoprotein metabolism or lipidaemias
|
5C8Z Unspecified disorders of lipoprotein metabolism or lipidaemias
|
5C90 Metabolic or transporter liver disease
|
Other metabolic disorders
|
5D00 Amyloidosis
|
H01185 Cerebral amyloid angiopathy
H01217 Primary localized cutaneous amyloidosis
H02499 AL amyloidosis
H00845 Familial amyloidosis
H02484 X-linked reticulate pigmentary disorder with systemic manifestations
H02322 Amyloidosis, Finnish type
|
5D01 Tumour lysis syndrome
|
5D0Y Other specified metabolic disorders
|
H00248 Analbuminemia
|
5D2Z Metabolic disorders, unspecified
|
Postprocedural endocrine or metabolic disorders
|
5D40 Postprocedural hypothyroidism
5D41 Postprocedural hypoinsulinaemia
5D42 Postprocedural hypoparathyroidism
5D43 Postprocedural hypopituitarism
5D44 Postprocedural ovarian failure
5D45 Postprocedural testicular hypofunction
5D46 Postprocedural adrenocortical hypofunction
|
|
06 Mental, behavioural or neurodevelopmental disorders
|
Neurodevelopmental disorders
|
6A00 Disorders of intellectual development
|
H00480 X-linked intellectual developmental disorder
H00658 X-linked syndromic intellectual developmental disorder
H00768 Autosomal recessive intellectual developmental disorder
H00773 Autosomal dominant intellectual developmental disorder
H01306 FRA12A mental retardation
H01911 Syndromic autosomal recessive mental retardation
H02778 Global developmental delay with or without impaired intellectual development
H02784 Global developmental delay with speech and behavioral abnormalities
|
6A01 Developmental speech or language disorders
|
H00902 Speech-language disorder 1
H02897 Familial persistent stuttering
|
6A02 Autism spectrum disorder
|
H02111 Autism
H01882 Asperger syndrome
H02371 Intellectual developmental disorder with autism and speech delay
H02507 Pilarowski-Bjornsson syndrome
|
6A03 Developmental learning disorder
|
6A04 Developmental motor coordination disorder
|
6A05 Attention deficit hyperactivity disorder
|
H01895 Attention deficit hyperactivity disorder (ADHD)
|
6A06 Stereotyped movement disorder
|
6A0Y Other specified neurodevelopmental disorders
|
H02387 Snijders Blok-Fisher syndrome
H02490 Gabriele-de Vries syndrome
H02521 Diets-Jongmans syndrome
H02571 Neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities
H02692 Usmani-Riazuddin syndrome
H02705 Neurodevelopmental disorder with glutamatergic synapse dysfunction
H02865 Neurodevelopmental disorder with or without hyperkinetic movements and seizures
|
6A0Z Neurodevelopmental disorders, unspecified
|
Schizophrenia or other primary psychotic disorders
|
6A20 Schizophrenia
|
H01649 Schizophrenia
|
6A21 Schizoaffective disorder
|
6A22 Schizotypal disorder
|
6A23 Acute and transient psychotic disorder
|
6A24 Delusional disorder
|
6A25 Symptomatic manifestations of primary psychotic disorders
|
6A2Y Other specified primary psychotic disorder
|
6A2Z Schizophrenia or other primary psychotic disorders, unspecified
|
Catatonia
|
6A40 Catatonia associated with another mental disorder
6A41 Catatonia induced by substances or medications
6A4Z Catatonia, unspecified
|
Mood disorders
|
Bipolar or related disorders
|
6A60 Bipolar type I disorder
|
H01653 Bipolar disorder
|
6A61 Bipolar type II disorder
|
H01653 Bipolar disorder
|
6A62 Cyclothymic disorder
|
6A6Y Other specified bipolar or related disorders
|
6A6Z Bipolar or related disorders, unspecified
|
Depressive disorders
|
6A70 Single episode depressive disorder
|
H01646 Major depressive disorder
|
6A71 Recurrent depressive disorder
|
H01646 Major depressive disorder
|
6A72 Dysthymic disorder
|
6A73 Mixed depressive and anxiety disorder
|
6A7Y Other specified depressive disorders
|
6A7Z Depressive disorders, unspecified
|
6A80 Symptomatic and course presentations for mood episodes in mood disorders
|
6A8Y Other specified mood disorders
|
6A8Z Mood disorders, unspecified
|
Anxiety or fear-related disorders
|
6B00 Generalised anxiety disorder
|
H01662 Generalized anxiety disorder
|
6B01 Panic disorder
|
H01664 Panic disorder
|
6B02 Agoraphobia
|
6B03 Specific phobia
|
6B04 Social anxiety disorder
|
H01670 Social anxiety disorder
|
6B05 Separation anxiety disorder
|
6B06 Selective mutism
|
6B0Y Other specified anxiety or fear-related disorders
|
6B0Z Anxiety or fear-related disorders, unspecified
|
Obsessive-compulsive or related disorders
|
6B20 Obsessive-compulsive disorder
|
H01450 Obsessive-compulsive disorder
|
6B21 Body dysmorphic disorder
|
H01447 Body dysmorphic disorder
|
6B22 Olfactory reference disorder
|
6B23 Hypochondriasis
|
6B24 Hoarding disorder
|
H01448 Hoarding disorder
|
6B25 Body-focused repetitive behaviour disorders
|
H00864 Trichotillomania
H01449 Excoriation disorder
|
6B2Y Other specified obsessive-compulsive or related disorders
|
6B2Z Obsessive-compulsive or related disorders, unspecified
|
H01453 Obsessive-Compulsive and Related Disorder
|
Disorders specifically associated with stress
|
6B40 Post traumatic stress disorder
6B41 Complex post traumatic stress disorder
6B42 Prolonged grief disorder
6B43 Adjustment disorder
6B44 Reactive attachment disorder
6B45 Disinhibited social engagement disorder
6B4Y Other specified disorders specifically associated with stress
6B4Z Disorders specifically associated with stress, unspecified
|
Dissociative disorders
|
6B60 Dissociative neurological symptom disorder
6B61 Dissociative amnesia
6B62 Trance disorder
6B63 Possession trance disorder
6B64 Dissociative identity disorder
6B65 Partial dissociative identity disorder
6B66 Depersonalization-derealization disorder
6B6Y Other specified dissociative disorders
6B6Z Dissociative disorders, unspecified
|
Feeding or eating disorders
|
6B80 Anorexia Nervosa
|
6B81 Bulimia Nervosa
|
6B82 Binge eating disorder
|
6B83 Avoidant-restrictive food intake disorder
|
6B84 Pica
|
6B85 Rumination-regurgitation disorder
|
6B8Y Other specified feeding or eating disorders
|
H01703 Eating Disorders
|
6B8Z Feeding or eating disorders, unspecified
|
Elimination disorders
|
6C00 Enuresis
6C01 Encopresis
6C0Z Elimination disorders, unspecified
|
Disorders of bodily distress or bodily experience
|
6C20 Bodily distress disorder
6C21 Body integrity dysphoria
6C2Y Other specified disorders of bodily distress or bodily experience
6C2Z Disorders of bodily distress or bodily experience, unspecified
|
Disorders due to substance use or addictive behaviours
|
Disorders due to substance use
|
6C40 Disorders due to use of alcohol
|
H01611 Alcohol dependence
H01071 Acute alcohol sensitivity
|
6C41 Disorders due to use of cannabis
|
6C42 Disorders due to use of synthetic cannabinoids
|
6C43 Disorders due to use of opioids
|
6C44 Disorders due to use of sedatives, hypnotics or anxiolytics
|
6C45 Disorders due to use of cocaine
|
6C46 Disorders due to use of stimulants including amphetamines, methamphetamine or methcathinone
|
6C47 Disorders due to use of synthetic cathinones
|
6C48 Disorders due to use of caffeine
|
6C49 Disorders due to use of hallucinogens
|
6C4A Disorders due to use of nicotine
|
6C4B Disorders due to use of volatile inhalants
|
6C4C Disorders due to use of MDMA or related drugs, including MDA
|
6C4D Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP]
|
6C4E Disorders due to use of other specified psychoactive substances, including medications
|
6C4F Disorders due to use of multiple specified psychoactive substances, including medications
|
6C4G Disorders due to use of unknown or unspecified psychoactive substances
|
6C4H Disorders due to use of non-psychoactive substances
|
6C4Y Other specified disorders due to substance use
|
6C4Z Disorders due to substance use, unspecified
|
Disorders due to addictive behaviours
|
6C50 Gambling disorder
6C51 Gaming disorder
6C5Y Other specified disorders due to addictive behaviours
6C5Z Disorders due to addictive behaviours, unspecified
|
Impulse control disorders
|
6C70 Pyromania
6C71 Kleptomania
6C72 Compulsive sexual behaviour disorder
6C73 Intermittent explosive disorder
6C7Y Other specified impulse control disorders
6C7Z Impulse control disorders, unspecified
|
Disruptive behaviour or dissocial disorders
|
6C90 Oppositional defiant disorder
6C91 Conduct-dissocial disorder
6C9Y Other specified disruptive behaviour or dissocial disorders
6C9Z Disruptive behaviour or dissocial disorders, unspecified
|
Personality disorders and related traits
|
6D10 Personality disorder
6D11 Prominent personality traits or patterns
|
Paraphilic disorders
|
6D30 Exhibitionistic disorder
6D31 Voyeuristic disorder
6D32 Pedophilic disorder
6D33 Coercive sexual sadism disorder
6D34 Frotteuristic disorder
6D35 Other paraphilic disorder involving non-consenting individuals
6D36 Paraphilic disorder involving solitary behaviour or consenting individuals
6D3Z Paraphilic disorders, unspecified
|
Factitious disorders
|
6D50 Factitious disorder imposed on self
6D51 Factitious disorder imposed on another
6D5Z Factitious disorders, unspecified
|
Neurocognitive disorders
|
6D70 Delirium
|
6D71 Mild neurocognitive disorder
|
6D72 Amnestic disorder
|
Dementia
|
6D80 Dementia due to Alzheimer disease
6D81 Dementia due to cerebrovascular disease
6D82 Dementia due to Lewy body disease
6D83 Frontotemporal dementia
6D84 Dementia due to psychoactive substances including medications
6D85 Dementia due to diseases classified elsewhere
6D86 Behavioural or psychological disturbances in dementia
6D8Y Dementia, other specified cause
6D8Z Dementia, unknown or unspecified cause
|
6E0Y Other specified neurocognitive disorders
|
6E0Z Neurocognitive disorders, unspecified
|
Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium
|
6E20 Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms
6E21 Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, with psychotic symptoms
6E2Z Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, unspecified
|
6E40 Psychological or behavioural factors affecting disorders or diseases classified elsewhere
|
Secondary mental or behavioural syndromes associated with disorders or diseases classified elsewhere
|
6E60 Secondary neurodevelopmental syndrome
6E61 Secondary psychotic syndrome
6E62 Secondary mood syndrome
6E63 Secondary anxiety syndrome
6E64 Secondary obsessive-compulsive or related syndrome
6E65 Secondary dissociative syndrome
6E66 Secondary impulse control syndrome
6E67 Secondary neurocognitive syndrome
6E68 Secondary personality change
6E69 Secondary catatonia syndrome
6E6Y Other specified secondary mental or behavioural syndrome
6E6Z Secondary mental or behavioural syndrome, unspecified
|
6E8Y Other specified mental, behavioural or neurodevelopmental disorders
|
6E8Z Mental, behavioural or neurodevelopmental disorders, unspecified
|
|
07 Sleep-wake disorders
|
Insomnia disorders
|
7A00 Chronic insomnia
|
H01609 Insomnia
|
7A01 Short-term insomnia
|
H01609 Insomnia
|
7A0Z Insomnia disorders, unspecified
|
Hypersomnolence disorders
|
7A20 Narcolepsy
|
H01293 Narcolepsy
|
7A21 Idiopathic hypersomnia
|
7A22 Kleine-Levin syndrome
|
7A23 Hypersomnia due to a medical condition
|
7A24 Hypersomnia due to a medication or substance
|
7A25 Hypersomnia associated with a mental disorder
|
7A26 Insufficient sleep syndrome
|
7A2Y Other specified hypersomnolence disorders
|
7A2Z Hypersomnolence disorders, unspecified
|
Sleep-related breathing disorders
|
7A40 Central sleep apnoeas
|
7A41 Obstructive sleep apnoea
|
7A42 Sleep-related hypoventilation or hypoxemia disorders
|
H01727 Primary alveolar hypoventilation syndrome
H01729 Premature ventricular complexes
H01715 Obesity hypoventilation syndrome
H00916 Congenital central hypoventilation syndrome
|
7A4Y Other specified sleep-related breathing disorders
|
7A4Z Sleep-related breathing disorders, unspecified
|
Circadian rhythm sleep-wake disorders
|
7A60 Delayed sleep-wake phase disorder
|
H00689 Delayed sleep phase disorder
|
7A61 Advanced sleep-wake phase disorder
|
H00688 Familial advanced sleep phase syndrome
|
7A62 Irregular sleep-wake rhythm disorder
|
7A63 Non-24 hour sleep-wake rhythm disorder
|
7A64 Circadian rhythm sleep-wake disorder, shift work type
|
7A65 Circadian rhythm sleep-wake disorder, jet lag type
|
7A6Z Circadian rhythm sleep-wake disorders, unspecified
|
H02849 Familial natural short sleep
|
Sleep-related movement disorders
|
7A80 Restless legs syndrome
|
H01597 Restless legs syndrome
|
7A81 Periodic limb movement disorder
|
7A82 Sleep-related leg cramps
|
7A83 Sleep-related bruxism
|
7A84 Sleep-related rhythmic movement disorder
|
7A85 Benign sleep myoclonus of infancy
|
7A86 Propriospinal myoclonus at sleep onset
|
7A87 Sleep-related movement disorder due to a medical condition
|
7A88 Sleep-related movement disorder due to a medication or substance
|
7A8Y Other specified sleep-related movement disorders
|
7A8Z Sleep-related movement disorders, unspecified
|
Parasomnia disorders
|
7B00 Disorders of arousal from non-REM sleep
7B01 Parasomnias related to REM sleep
7B02 Other parasomnias
7B0Y Other specified parasomnia disorders
7B0Z Parasomnia disorders, unspecified
|
7B2Y Other specified sleep-wake disorders
|
7B2Z Sleep-wake disorders, unspecified
|
|
08 Diseases of the nervous system
|
Movement disorders
|
8A00 Parkinsonism
|
H01600 Parkinsonian syndrome
H00057 Parkinson disease
H00077 Progressive supranuclear palsy
H00879 Perry syndrome
H01574 Familial idiopathic basal ganglia calcification
|
8A01 Choreiform disorders
|
H00860 Benign hereditary chorea
H00059 Huntington disease
H01243 Huntington disease-like syndrome
H00060 Dentatorubropallidoluysian atrophy (DRPLA)
H00655 McLeod syndrome
H00832 Core neuroacanthocytosis syndromes
H01779 Neuroferritinopathy
H02367 Chorea, childhood-onset, with psychomotor retardation
H02809 Early-onset neurodegeneration with choreoathetoid movements and microcytic anemia
|
8A02 Dystonic disorders
|
H00831 Primary dystonia
H01255 Juvenile-onset dystonia
H01608 Cervical dystonia
H02706 Early-onset dystonia and/or spastic paraplegia
H02557 Dopa-responsive dystonia
H00989 Mohr-Tranebjaerg syndrome
H02676 Infantile-onset parkinsonism-dystonia
|
8A03 Ataxic disorders
|
H01616 Spinocerebellar degeneration
H00067 Friedreich ataxia
H00749 Episodic ataxias
H00063 Spinocerebellar ataxia (SCA)
H01478 Machado-Joseph disease
H01891 Autosomal recessive spinocerebellar ataxias
H02573 Autosomal recessive spinocerebellar ataxias with axonal neuropathy
H00848 Ataxia with ocular apraxia
H01036 Posterior column ataxia with retinitis pigmentosa
H01038 Cerebellar ataxia cayman type
H01170 Autosomal recessive spastic ataxia of Charlevoix-Saguenay
H01204 Cerebellar ataxia, mental retardation (MR), and dysequilibrium syndrome (CAMRQ)
H01432 Choreoacanthocytosis
H02101 Autosomal dominant sensory ataxia
H02140 Boucher-Neuhauser syndrome
H02144 Gordon Holmes syndrome
H02273 Nonprogressive cerebellar ataxia with mental retardation
H02552 Ataxia, intention tremor, and hypotonia syndrome
|
8A04 Disorders associated with tremor
|
H01577 Essential tremor
|
8A05 Tic disorders
|
H00862 Tourette syndrome
|
8A06 Myoclonic disorders
|
H02789 Familial myoclonus
H02819 Neonatal intractable myoclonus
|
8A07 Certain specified movement disorder
|
H01287 Congenital mirror movements
H01528 Neuroleptic malignant syndrome
|
8A0Y Other specified movement disorders
|
H01570 Autosomal dominant striatal degeneration
H02820 Progressive encephalopathy with amyotrophy and optic atrophy
|
8A0Z Movement disorders, unspecified
|
Disorders with neurocognitive impairment as a major feature
|
8A20 Alzheimer disease
|
H00056 Alzheimer disease
|
8A21 Progressive focal atrophies
|
8A22 Lewy body disease
|
H00066 Lewy body dementia (LBD)
|
8A23 Frontotemporal lobar degeneration
|
H00078 Frontotemporal lobar degeneration
|
8A2Y Other specified disorders with neurocognitive impairment as a major feature
|
H00290 Aicardi-Goutieres syndrome
|
8A2Z Disorders with neurocognitive impairment as a major feature, unspecified
|
Multiple sclerosis or other white matter disorders
|
8A40 Multiple sclerosis
|
H01490 Multiple sclerosis
|
8A41 Isolated demyelinating syndromes of the central nervous system
|
8A42 Acute disseminated encephalomyelitis
|
8A43 Neuromyelitis optica
|
H01491 Neuromyelitis optica
|
8A44 Leukodystrophies
|
H02598 Progressive leukoencephalopathy
H00176 Adrenoleukodystrophy
H00065 Alexander disease
H00438 Nasu-Hakola disease
H00679 Hypomyelinating leukodystrophy
H00869 Leukoencephalopathy with vanishing white matter
H00875 Megaloencephalic leukoencephalopathy with subcortical cysts
H01230 Adult-onset autosomal dominant leukodystrophy
H01807 Hereditary diffuse leukoencephalopathy with spheroids
H02200 Leukoencephalopathy, progressive, with ovarian failure
H02377 Leukodystrophy and acquired microcephaly with or without dystonia
H02788 Childhood-onset remitting leukodystrophy
H00135 Krabbe disease
|
8A45 Secondary white matter disorders
|
H01724 HTLV1-associated myelopathy
H01696 Subacute sclerosing panencephalitis
H00370 Progressive multifocal leukoencephalopathy
|
8A46 Central demyelination of corpus callosum
|
8A4Y Other specified multiple sclerosis or other white matter disorders
|
H02457 Developmental delay, leukoencephalopathy, and neurologic decompensation
|
8A4Z Multiple sclerosis or other white matter disorders, unspecified
|
Epilepsy or seizures
|
8A60 Epilepsy due to structural or metabolic conditions or diseases
|
H02770 Early-onset seizures with neurodegeneration and brain calcifications
H01826 Mesial temporal lobe epilepsy with hippocampal sclerosis
|
8A61 Genetic or presumed genetic syndromes primarily expressed as epilepsy
|
H00577 Symptomatic generalized epilepsies
H00808 Idiopathic generalized epilepsies
H02889 X-linked epilepsy-2 with or without impaired intellectual development and dysmorphic features
H01247 Pyridoxine-dependent epilepsy
H01819 Early myoclonic encephalopathy
H02250 Early-onset vitamin B6-dependent epilepsy
H02696 Early-onset epilepsy
H00806 Benign familial neonatal seizure
H01818 Dravet syndrome
H01815 Malignant migrating partial seizures in infancy
H01775 PCDH19-related epilepsy syndrome
H02212 Familial infantile myoclonic epilepsy
H02215 Childhood absence epilepsy
H01823 Myoclonic-astatic epilepsy
H01822 Epilepsy with myoclonic absence
H01258 Generalized epilepsy and paroxysmal dyskinesia
H02361 Myoclonic-atonic epilepsy
H02564 Generalized epilepsy with febrile seizures plus
H02217 Juvenile myoclonic epilepsy
H02216 Juvenile absence epilepsy
H02213 Familial adult myoclonic epilepsy
H00809 Familial epilepsy temporal lobe (ETL)
H00810 Progressive myoclonic epilepsy
H01212 Familial encephalopathy with neuroserpin inclusion bodies
H01994 Myoclonic epilepsy of Lafora
H01995 Unverricht-Lundborg disease
H00807 Nocturnal frontal lobe epilepsy
H00836 GLUT1 deficiency syndrome
H02214 Familial focal epilepsy with variable foci
|
8A62 Epileptic encephalopathies
|
H01460 West syndrome
H01813 Lennox-Gastaut syndrome
H01514 Landau-Kleffner syndrome
H00606 Early infantile epileptic encephalopathy
H01808 Hemiconvulsion-hemiplegia-epilepsy syndrome
H01812 Rasmussen encephalitis
H01827 Rolandic epilepsy, mental retardation, and speech dyspraxia
H01829 Acute encephalitis with refractory repetitive partial seizures
H02150 Infantile or early childhood epileptic encephalopathy
H02360 Epileptic encephalopathy, childhood-onset
H02472 Early-onset progressive encephalopathy
|
8A63 Seizure due to acute causes
|
H00783 Febrile seizures
|
8A64 Single seizure due to remote causes
|
8A65 Single unprovoked seizure
|
8A66 Status epilepticus
|
8A67 Acute repetitive seizures
|
8A68 Types of seizures
|
8A6Y Other specified epilepsy or seizures
|
8A6Z Epilepsy or seizures, unspecified
|
Headache disorders
|
8A80 Migraine
|
H00775 Hemiplegic migraine
H02362 Benign familial infantile seizure
|
8A81 Tension-type headache
|
8A82 Trigeminal autonomic cephalalgias
|
H01588 Cluster headache
|
8A83 Other primary headache disorder
|
8A84 Secondary headache
|
8A85 Painful cranial neuropathies or other facial pains
|
8A8Y Other specified headache disorders
|
8A8Z Headache disorders, unspecified
|
Cerebrovascular diseases
|
Intracranial haemorrhage
|
8B00 Intracerebral haemorrhage
8B01 Subarachnoid haemorrhage
8B02 Nontraumatic subdural haemorrhage
8B03 Nontraumatic epidural haemorrhage
8B0Z Intracranial haemorrhage, unspecified
|
Cerebral ischaemia
|
8B10 Transient ischaemic attack
8B11 Cerebral ischaemic stroke
8B1Y Other specified cerebral ischaemia
8B1Z Cerebral ischaemia, unspecified
|
8B20 Stroke not known if ischaemic or haemorrhagic
|
8B21 Cerebrovascular disease with no acute cerebral symptom
|
8B22 Certain specified cerebrovascular diseases
|
H01184 Familial dementia
H02845 Arteriovenous malformations of the brain
H00534 Cerebral cavernous malformation
H01396 Moyamoya disease
H00536 Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)
H01757 Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
H00877 Brain small vessel disease
H02718 Autosomal dominant pontine microangiopathy and leukoencephalopathy
|
8B23 Cerebrovascular abnormalities
|
8B24 Hypoxic-ischaemic encephalopathy
|
8B25 Late effects of cerebrovascular disease
|
8B26 Vascular syndromes of brain in cerebrovascular diseases
|
H01120 Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
|
8B2Z Cerebrovascular diseases, unspecified
|
Spinal cord disorders excluding trauma
|
8B40 Cauda equina syndrome
|
8B41 Myelitis
|
H01863 Atopic myelitis
|
8B42 Myelopathy
|
8B43 Non-compressive vascular myelopathies
|
8B44 Degenerative myelopathic disorders
|
H00266 Hereditary spastic paraplegia
H01351 Spastic ataxia
H02114 Spastic paraplegia, optic atrophy, and neuropathy
H02293 Spastic paraplegia-psychomotor retardation-seizures syndrome
H02178 MASA syndrome
H01172 Infantile-onset ascending hereditary spastic paralysis
H02777 Spastic paraplegia, intellectual disability, nystagmus, and obesity
|
8B4Y Other specified spinal cord disorders excluding trauma
|
8B4Z Spinal cord disorders excluding trauma, unspecified
|
Motor neuron diseases or related disorders
|
8B60 Motor neuron disease
|
H00058 Amyotrophic lateral sclerosis (ALS)
H00970 Juvenile primary lateral sclerosis
H02342 Frontotemporal dementia and amyotrophic lateral sclerosis
H00841 Infantile progressive bulbar palsy
|
8B61 Spinal muscular atrophy
|
H00455 Spinal muscular atrophy
H00062 Spinal and bulbar muscular atrophy (SBMA)
H00524 Scapuloperoneal spinal muscular atrophy
H00856 Distal hereditary motor neuropathies
H02238 Spinal muscular atrophy with congenital bone fractures
|
8B62 Post polio progressive muscular atrophy
|
8B6Y Other specified motor neuron diseases or related disorders
|
8B6Z Motor neuron diseases or related disorders, unspecified
|
Disorders of nerve root, plexus or peripheral nerves
|
Disorders of cranial nerves
|
8B80 Disorders of olfactory nerve
|
8B81 Disorders of vestibulocochlear nerve
|
8B82 Disorders of trigeminal nerve
|
8B83 Disorders of spinal accessory nerve
|
8B84 Disorders of hypoglossal nerve
|
8B85 Disorders of multiple cranial nerves
|
8B86 Disorders of vagus nerve
|
8B87 Disorders of glossopharyngeal nerve
|
8B88 Disorders of facial nerve
|
8B8Y Other specified disorders of cranial nerves
|
H02594 Congenital facial palsy with ptosis and velopharyngeal dysfunction
|
8B8Z Disorders of cranial nerves, unspecified
|
Nerve root or plexus disorders
|
8B90 Nerve root and plexus compressions
8B91 Brachial plexus disorders
8B92 Lumbosacral plexus disorders
8B93 Radiculopathy
8B94 Diabetic radiculoplexoneuropathy
8B95 Secondary brachial plexus lesion due to certain specified disorders
8B9Y Other specified nerve root or plexus disorders
8B9Z Nerve root or plexus disorders, unspecified
|
Polyneuropathy
|
8C00 Idiopathic progressive neuropathy
|
8C01 Inflammatory polyneuropathy
|
H01436 Guillain-Barre syndrome
H01689 Fisher syndrome
H01842 Bickerstaff brainstem encephalitis
H01527 Chronic inflammatory demyelinating polyradiculoneuropathy
|
8C03 Other secondary polyneuropathy
|
H01459 Diabetic neuropathy
H02559 Microvascular complications of diabetes
|
8C0Y Other specified polyneuropathy
|
8C0Z Polyneuropathy, unspecified
|
Mononeuropathy
|
8C10 Mononeuropathies of upper limb
|
H00798 Familial carpal tunnel syndrome
|
8C11 Mononeuropathies of lower limb
|
8C12 Certain specified mononeuropathies
|
8C1Y Mononeuropathy of other specified site
|
8C1Z Mononeuropathy of unspecified site
|
Hereditary neuropathy
|
8C20 Hereditary motor and sensory neuropathy
|
H00264 Charcot-Marie-Tooth disease
H02357 Congenital hypomyelinating neuropathy
H01131 Hereditary neuralgic amyotrophy
H01155 Roussy-Levy syndrome
H01296 Hereditary neuropathy with liability to pressure palsies
H02344 Cowchock syndrome
H02345 Autosomal recessive peripheral neuropathy (PNRIID)
H02359 Dejerine-Sottas disease
H02649 Autosomal dominant slowed nerve conduction velocity
H02817 Peripheral neuropathy, myopathy, hoarseness, and hearing loss
|
8C21 Hereditary sensory or autonomic neuropathy
|
H00265 Hereditary sensory and autonomic neuropathy
H02580 Hereditary sensory neuropathy with spastic paraplegia
H01987 Familial dysautonomia
H01836 Congenital pain insensitivity with anhidrosis
H00774 Congenital insensitivity to pain
H00935 Cold-induced sweating syndrome
|
8C2Y Other specified hereditary neuropathy
|
H01259 Giant axonal neuropathy
|
8C2Z Hereditary neuropathy, unspecified
|
8C4Y Other specified disorders of nerve root, plexus or peripheral nerves
|
H02908 Mitchell syndrome
|
8C4Z Disorders of nerve root, plexus or peripheral nerves, unspecified
|
Diseases of neuromuscular junction or muscle
|
Myasthenia gravis or certain specified neuromuscular junction disorders
|
8C60 Myasthenia gravis
|
H01594 Myasthenia gravis
|
8C61 Congenital myasthenic syndromes
|
H00770 Congenital myasthenic syndrome
|
8C62 Lambert-Eaton syndrome
|
H01596 Lambert-Eaton myasthenic syndrome
|
8C6Y Other specified myasthenia gravis and neuromuscular junction disorders
|
8C6Z Unspecified myasthenia gravis or neuromuscular junction disorders
|
Primary disorders of muscles
|
8C70 Muscular dystrophy
|
H00562 Dystrophinopathies
H01964 Becker muscular dystrophy
H01963 Duchenne muscular dystrophy
H00563 Emery-Dreifuss muscular dystrophy
H00591 Facioscapulohumeral muscular dystrophy
H00565 Sarcoglycanopathies
H00593 Limb-girdle muscular dystrophy
H00567 Limb-girdle muscular dystrophy 1C
H00592 Calpainopathy
H01959 Muscular dystrophy-dystroglycanopathy type C
H01962 Congenital muscular dystrophy type 1D
H01974 Limb-girdle muscular dystrophy 2B
H00656 Scapuloperoneal myopathy
H00120 Muscular dystrophy-dystroglycanopathy type A
H00590 Congenital muscular dystrophies (CMD/MDC)
H01284 Marinesco-Sjogren syndrome
H01340 Bethlem myopathy
H01341 Collagen VI myopathy
H01778 Ullrich disease
H01957 Fukuyama congenital muscular dystrophy
H01958 Merosin-deficient congenital muscular dystrophy
H01960 Muscular dystrophy-dystroglycanopathy type B
H01961 Congenital muscular dystrophy type 1C
H02307 Muscular dystrophy-dystroglycanopathy
H00697 X-linked myopathy with postural muscle atrophy
H02721 Scapulohumeroperoneal myopathy
|
8C71 Myotonic disorders
|
H00568 Myotonic dystrophy
H01777 Schwartz-Jampel syndrome
H00705 Myotonia congenita
H00744 Potassium-aggravated myotonia
H01804 Isaacs syndrome
H02390 Autosomal recessive neuromyotonia and axonal neuropathy
H01780 Non-dystrophic myotonia
H02179 Rippling muscle disease
|
8C72 Congenital myopathies
|
H01810 Congenital myopathy
H02805 Sarcoplasmic body myopathy
H00698 Nemaline myopathy
H00702 Cap myopathy
H00700 Centronuclear myopathy
H00699 Central core disease
H00703 Myosin storage myopathy
H01291 Spheroid body myopathy
H01310 Multi-minicore disease
H01338 Myosclerosis
H02678 External ophthalmoplegia with rib and vertebral anomalies
H00701 Congenital fiber type disproportion
H00657 Reducing body myopathy
H01781 Autophagic vacuolar myopathy
H02084 Native American myopathy
H02258 Tubular aggregate myopathy
H02320 Vacuolar myopathy with CASQ1 aggregates
H02321 Early-onset myopathy, areflexia, respiratory distress, and dysphagia
H02791 Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis
|
8C73 Mitochondrial myopathies
|
H01363 NARP syndrome
H00068 Leber hereditary optic atrophy
H01200 Fatal infantile cardioencephalomyopathy
H01347 MELAS syndrome
H01356 Myoclonic Epilepsy and Ragged-Red Fiber Disease
H01365 Leber hereditary optic neuropathy and dystonia
H02201 Mitochondrial myopathy with lactic acidosis
H02447 Myopathy with extrapyramidal signs
H02448 Harel-Yoon syndrome
H02684 Mitochondrial progressive myopathy with congenital cataract and developmental delay
H02701 Recurrent metabolic crises with variable encephalomyopathic features
H02704 Mitochondrial myopathy and ataxia
H02771 Episodic mitochondrial myopathy with or without optic atrophy and reversible leukoencephalopathy
H02866 Hereditary myopathy with lactic acidosis
|
8C74 Periodic paralyses or disorders of muscle membrane excitability
|
H00743 Paramyotonia congenita
H00215 Periodic paralysis
H00746 Hypokalemic periodic paralysis
H00745 Hyperkalemic periodic paralysis
H00747 Thyrotoxic hypokalemic periodic paralysis
H00748 Andersen-Tawil syndrome
|
8C75 Distal myopathies
|
H00566 Distal myopathy with anterior tibial onset
H00594 Distal myopathy
H00596 Nonaka myopathy (NM)
H01965 Miyoshi muscular dystrophy
H01975 Welander distal myopathy
H01976 Tibial muscular dystrophy
H01977 Laing distal myopathy
H02182 Distal myopathy, Tateyama type
H02586 Distal myopathy with rimmed vacuoles
H02783 Myopathy with rimmed ubiquitin-positive autophagic vacuolation
|
8C76 Myofibrillar myopathy
|
H00595 Myofibrillar myopathies
|
8C77 Ocular myopathy
|
8C78 Malignant hyperthermia or hyperpyrexia
|
H02646 Malignant hyperthermia
|
8C7Y Other specified primary disorders of muscles
|
H01129 Brody myopathy
|
8C7Z Primary disorders of muscles, unspecified
|
Secondary myopathies
|
8C80 Drug-induced myopathy
8C81 Autoimmune myopathy
8C82 Myopathy in certain specified infectious or parasitic disease
8C83 Myopathy in certain specified endocrine disease
8C84 Secondary rhabdomyolysis
8C8Y Other specified secondary myopathies
8C8Z Secondary myopathies, unspecified
|
8D0Y Other specified diseases of neuromuscular junction or muscle
|
8D0Z Diseases of neuromuscular junction or muscle, unspecified
|
Cerebral palsy
|
8D20 Spastic cerebral palsy
|
H01097 Spastic quadriplegic cerebral palsy
|
8D21 Dyskinetic cerebral palsy
|
8D22 Ataxic cerebral palsy
|
8D23 Worster-Drought syndrome
|
H01837 Congenital suprabulbar paresis
|
8D2Y Other specified cerebral palsy
|
8D2Z Cerebral palsy, unspecified
|
Nutritional or toxic disorders of the nervous system
|
8D40 Neurological disorders due to nutrient deficiency
|
8D41 Neurological disorders due to an excess of micro or macro nutrients
|
8D42 Neurological disorders due to overweight or obesity in adults or children
|
8D43 Neurological disorders due to toxicity
|
H01578 Subacute myelo-optico-neuropathy (SMON)
|
8D44 Alcohol-related neurological disorders
|
8D4Y Other specified nutritional or toxic disorders of the nervous system
|
8D4Z Nutritional or toxic disorders of the nervous system, unspecified
|
Disorders of cerebrospinal fluid pressure or flow
|
8D60 Increased intracranial pressure
|
8D61 Intracranial hypotension
|
8D62 Cerebrospinal fluid rhinorrhoea
|
8D63 Cerebrospinal fluid otorrhoea
|
8D64 Hydrocephalus
|
H01676 Normal pressure hydrocephalus
|
8D65 Cerebrospinal fluid fistula
|
8D66 Syringomyelia or syringobulbia
|
H01675 Syringomyelia
|
8D67 Intracranial arachnoid cyst
|
8D68 Porencephalic cyst
|
8D6Y Other specified disorders of cerebrospinal fluid pressure or flow
|
8D6Z Disorders of cerebrospinal fluid pressure or flow, unspecified
|
Disorders of autonomic nervous system
|
8D80 Congenital malformations of the autonomic nervous system
|
8D81 Inherited autonomic nervous system disorders
|
8D82 Autoimmune disorders involving the autonomic nervous system
|
8D83 Autonomic nervous system disorder due to infection
|
8D84 Pure autonomic nervous system failure
|
8D85 Autonomic nervous system disorder due to substances
|
8D86 Autonomic nervous system hyperactivity
|
8D87 Autonomic nervous system disorder due to certain specified neurodegenerative disorder
|
H01614 Multiple system atrophy
H01177 Infantile bilateral striatal necrosis
H02802 Childhood-onset striatonigral degeneration
|
8D88 Autonomic neuropathies
|
8D89 Disorders of orthostatic tolerance
|
H01031 Orthostatic intolerance
|
8D8A Focal or segmental autonomic disorders
|
8D8B Disorders affecting autonomic synaptic neurotransmission
|
8D8C Autonomic dysreflexia
|
8D8D Hypoglycaemia unawareness
|
8D8Y Other specified disorders of autonomic nervous system
|
8D8Z Disorders of autonomic nervous system, unspecified
|
Human prion diseases
|
8E00 Sporadic Creutzfeldt-Jakob Disease
|
H00061 Prion disease
|
8E01 Acquired prion disease
|
H00061 Prion disease
|
8E02 Genetic prion diseases
|
H00061 Prion disease
|
8E03 Variably protease sensitive prionopathy
|
H00061 Prion disease
|
8E0Y Other specified human prion diseases
|
H00061 Prion disease
|
8E0Z Human prion diseases, unspecified
|
Disorders of consciousness
|
8E20 Persistent vegetative state
8E21 Permanent vegetative state
8E22 Minimally conscious state
8E2Y Other specified disorders of consciousness
8E2Z Disorders of consciousness, unspecified
|
Other disorders of the nervous system
|
8E40 Disorders of the meninges excluding infection
|
H01668 Neoplastic meningitis
|
8E41 Pachymeningitis
|
8E42 Superficial siderosis of the nervous system
|
H01846 Superficial siderosis
|
8E43 Pain disorders
|
H01638 Neuropathic pain
H00772 Paroxysmal extreme pain disorder
H01391 Familial episodic pain syndrome
|
8E44 Post anoxic brain damage
|
8E45 Locked-in syndrome
|
8E46 Reye syndrome
|
8E47 Encephalopathy, not elsewhere classified
|
H01841 Acute encephalopathy with biphasic seizures and late reduced diffusion
H02261 PEBAT
H02262 PEBEL
H02831 Acute transient encephalopathy
|
8E48 Encephalitis, not elsewhere classified
|
8E49 Postviral fatigue syndrome
|
8E4A Paraneoplastic or autoimmune disorders of the nervous system
|
H01452 Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
|
8E4Y Other specified disorders of the nervous system
|
H02473 Leukoencephalopathy, brain calcifications, and cysts
H02476 Childhood-onset neurodegeneration with brain atrophy
H02489 Mild encephalopathy with reversible myelin vacuolization
H02572 Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
H02738 Childhood-onset neurodegeneration with cerebellar atrophy
H02739 Childhood-onset neurodegeneration with ataxia, tremor, optic atrophy, and cognitive decline
H02740 Childhood-onset neurodegeneration with hypotonia, respiratory insufficiency, and brain imaging abnormalities
H02741 Childhood-onset neurodegeneration with cerebellar ataxia and cognitive decline
|
Postprocedural disorders of the nervous system
|
8E60 Post ventricular shunting leak
8E61 Post radiation injury of the nervous system
8E62 Postprocedural meningitis
8E63 Post pump encephalopathy
8E64 Multifocal cerebral infarctions
8E66 Intracranial hypotension due to lumbar puncture
|
8E7Y Other specified diseases of the nervous system
|
8E7Z Diseases of the nervous system, unspecified
|
|
09 Diseases of the visual system
|
Disorders of the ocular adnexa or orbit
|
Disorders of eyelid or peri-ocular area
|
9A00 Congenital malposition of eyelids
|
9A01 Infectious disorders of eyelid
|
H01644 Blepharitis
|
9A02 Inflammatory disorders of eyelid
|
H01644 Blepharitis
|
9A03 Acquired malposition of eyelid
|
9A04 Acquired disorders of eyelashes
|
9A05 Movement disorders of eyelid
|
9A06 Certain specified disorders of eyelid
|
9A0Y Other specified disorders of eyelid or peri-ocular area
|
9A0Z Disorders of eyelid or peri-ocular area, unspecified
|
Disorders of lacrimal apparatus
|
9A10 Disorders of lacrimal gland
9A11 Disorders of lacrimal drainage system
9A1Y Other specified disorders of lacrimal apparatus
9A1Z Disorders of lacrimal apparatus, unspecified
|
Disorders of orbit
|
9A20 Displacement of eyeball
9A21 Orbital infection
9A22 Orbital inflammation
9A23 Orbital cyst
9A24 Bony deformity of orbit
9A25 Soft tissue deformity of orbit
9A26 Combined bony and soft tissue deformity of orbit
9A2Y Other specified disorders of orbit
9A2Z Disorders of orbit, unspecified
|
9A4Y Other specified disorders of the ocular adnexa or orbit
|
9A4Z Disorders of the ocular adnexa or orbit, unspecified
|
Disorders of the eyeball anterior segment
|
Disorders of conjunctiva
|
9A60 Conjunctivitis
|
H01366 Bacterial conjunctivitis
|
9A61 Certain specified disorders of conjunctiva
|
9A62 Mucous membrane pemphigoid with ocular involvement
|
9A6Y Other specified disorders of conjunctiva
|
9A6Z Disorders of conjunctiva, unspecified
|
Disorders of the cornea
|
9A70 Hereditary corneal dystrophies
|
H00960 Fuchs corneal dystrophy
H00963 Congenital hereditary endothelial dystrophy
H00726 Meesmann corneal dystrophy
H00951 Reis-Bucklers corneal dystrophy
H00952 Thiel-Behnke dystrophies
H00953 Gelatinous drop-like corneal dystrophy
H00954 Macular corneal dystrophy
H00955 Granular corneal dystrophies
H00956 Lattice corneal dystrophies
H00957 Fleck corneal dystrophy
H00958 Congenital stromal corneal dystrophy
H00959 Schnyder corneal dystrophy
H01221 Epithelial basement membrane corneal dystrophy
H02822 Lisch epithelial corneal dystrophy
H02867 Epithelial recurrent erosion dystrophy
|
9A71 Infectious keratitis
|
9A72 Traumatic keratitis
|
9A73 Exposure keratitis
|
9A74 Neurotrophic keratitis
|
9A75 Autoimmune keratitis
|
9A76 Corneal ulcer
|
9A77 Corneal scars or opacities
|
9A78 Certain specified disorders of cornea
|
H00789 Keratoconus
H02426 EDICT syndrome
|
9A79 Keratoconjunctivitis sicca
|
H01641 Dry eye disease
|
9A7Y Other specified disorders of the cornea
|
H01273 Autosomal dominant keratitis
H02923 Keratoendotheliitis fugax hereditaria
|
9A7Z Disorders of the cornea, unspecified
|
Disorders of the anterior chamber
|
9A80 Hyphaema
9A81 Parasites in the anterior chamber of the eye
9A82 Cyst in the anterior chamber of the eye
9A83 Flat anterior chamber hypotony of eye
9A8Y Other specified disorders of the anterior chamber
9A8Z Disorders of the anterior chamber, unspecified
|
Disorders of the anterior uvea
|
9A90 Degeneration of iris or ciliary body
9A91 Cyst of iris or ciliary body
9A92 Persistent pupillary membranes
9A93 Adhesions or disruptions of iris or ciliary body
9A94 Certain specified disorders of iris or ciliary body
9A96 Anterior uveitis
9A9Y Other specified disorders of the anterior uvea
9A9Z Disorders of the anterior uvea, unspecified
|
Functional disorders of the pupil
|
9B00 Disorders of the afferent pupillary system
9B01 Disorders of the efferent pupillary system
9B02 Light-near dissociations
9B0Y Other specified functional disorders of the pupil
9B0Z Functional disorders of the pupil, unspecified
|
Disorders of lens
|
9B10 Cataract
|
H01202 Cataract
H02204 Hereditary hyperferritinaemia-cataract syndrome
|
9B11 Certain specified disorders of lens
|
9B1Z Disorders of lens, unspecified
|
9B3Y Other specified disorders of the eyeball anterior segment
|
9B3Z Disorders of the eyeball anterior segment, unspecified
|
Disorders of the eyeball posterior segment
|
Disorders of sclera
|
9B50 Episcleritis
9B51 Scleritis
9B52 Scleral staphyloma
9B5Y Other specified disorders of sclera
9B5Z Disorders of sclera, unspecified
|
Disorders of the choroid
|
9B60 Choroidal degeneration
|
9B61 Choroidal dystrophy
|
H00732 Sorsby fundus dystrophy
H01116 Choroideremia
H01768 Central areolar choroidal dystrophy
H01880 Autosomal recessive microcephaly and chorioretinopathy
H02107 Bietti crystalline corneoretinal dystrophy
|
9B62 Chorioretinal scars
|
9B63 Choroidal haemorrhage or rupture
|
9B64 Choroidal detachment
|
9B65 Choroiditis
|
9B66 Intermediate choroiditis
|
9B6Y Other specified disorders of the choroid
|
9B6Z Disorders of the choroid, unspecified
|
Disorders of the retina
|
9B70 Inherited retinal dystrophies
|
H00481 Cone-rod dystrophy and cone dystrophy
H00527 Retinitis pigmentosa
H00814 Vitelliform macular dystrophy
H00819 Stargardt disease
H00825 Familial flecked retina syndrome
H00837 Leber congenital amaurosis
H00971 Achromatopsia
H00974 Blue cone monochromacy
H01009 Newfoundland rod-cone dystrophy
H01130 Late-onset retinal degeneration
H01770 Macular dystrophy
H01890 Pattern dystrophies of the retinal pigment epithelium
H02075 Enhanced S-cone syndrome
H02077 Snowflake vitreoretinal degeneration
H02078 Vitreoretinochoroidopathy
H02108 Basal laminar drusen
H02110 Doyne honeycomb retinal dystrophy
H02288 Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities
H02289 Retinal dystrophy with or without extraocular anomalies
H02290 Retinal dystrophy and iris coloboma with or without congenital cataract
H02291 Retinal dystrophy, iris coloboma, and comedogenic acne syndrome
H02341 Goldmann-Favre syndrome
H02440 Fleck retina, familial benign
H02898 Behr syndrome
H02899 Impaired intellectual development, truncal obesity, retinal dystrophy, and micropenis syndrome
H02914 Retinal dystrophy with or without macular staphyloma
|
9B71 Retinopathy
|
H01457 Diabetic retinopathy
H02559 Microvascular complications of diabetes
|
9B72 Inflammatory diseases of the retina
|
9B73 Retinal detachments or breaks
|
H01766 Juvenile retinoschisis
|
9B74 Retinal vascular occlusions
|
9B75 Macular disorders
|
H00821 Age-related macular degeneration
H01480 Idiopathic macular hole
H01010 Occult macular dystrophy
H01651 Macular edema
|
9B76 Degenerative high myopia
|
9B77 Eales disease
|
9B78 Certain specified retinal disorders
|
H01000 Retinal vasculopathy with cerebral leukodystrophy
H02251 Cerebroretinal microangiopathy with calcifications and cysts
H01798 Autosomal dominant neovascular inflammatory vitreoretinopathy
H01180 Sveinsson chorioretinal atrophy (SCRA)
|
9B7Y Other specified disorders of the retina
|
H00690 Aland Island eye disease
H01088 Pigmented paravenous chorioretinal atrophy
H02469 Cone-rod synaptic disorder
H02642 Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
|
9B7Z Disorders of the retina, unspecified
|
Disorders of the vitreous body
|
9B80 Inherited vitreoretinal disorders
|
H00805 Vitreoretinal degeneration
H02073 Wagner syndrome
|
9B81 Posterior vitreous detachment
|
9B82 Vitreous prolapse
|
9B83 Vitreous haemorrhage
|
9B84 Vitreous opacities, membranes or strands
|
9B8Y Other specified disorders of the vitreous body
|
9B8Z Disorders of the vitreous body, unspecified
|
9C0Y Other specified disorders of the eyeball posterior segment
|
9C0Z Disorders of the eyeball posterior segment, unspecified
|
Disorders of the eyeball affecting both anterior and posterior segments
|
9C20 Panuveitis
|
9C21 Endophthalmitis
|
9C22 Eyeball deformity
|
H02775 Visual impairment and progressive phthisis bulbi
|
9C2Y Other specified disorders of the eyeball affecting both anterior and posterior segments
|
9C2Z Disorders of the eyeball affecting both anterior and posterior segments, unspecified
|
Disorders of the visual pathways or centres
|
9C40 Disorder of the optic nerve
|
H01719 Optic neuropathy
H01717 Optic neuritis
H00068 Leber hereditary optic atrophy
H01020 Optic atrophy
H01365 Leber hereditary optic neuropathy and dystonia
H01378 Bosch-Boonstra optic atrophy syndrome
|
9C41 Disorder of optic chiasm
|
9C42 Disorder of post chiasmal visual pathways
|
9C43 Disorder of visual cortex
|
9C44 Disorder of higher visual centres
|
9C4Y Other specified disorders of the visual pathways or centres
|
9C4Z Disorders of the visual pathways or centres, unspecified
|
Glaucoma or glaucoma suspect
|
9C60 Glaucoma suspect
|
9C61 Glaucoma
|
H02877 Glaucoma
H00612 Primary open angle glaucoma
H01203 Primary congenital glaucoma
|
9C6Y Other specified glaucoma or glaucoma suspect
|
9C6Z Glaucoma or glaucoma suspect, unspecified
|
Strabismus or ocular motility disorders
|
9C80 Non paralytic strabismus
|
9C81 Ocular motor nerve palsies
|
H02814 Oculomotor-abducens synkinesis
|
9C82 Disorders of extraocular muscles
|
H01118 Progressive external ophthalmoplegia
H01355 Kearns-Sayre syndrome
H01395 Autosomal recessive progressive external ophthalmoplegia
H00704 Oculopharyngeal muscular dystrophy
H02513 Oculopharyngodistal myopathy
H00633 Duane retraction syndrome
H00838 Congenital fibrosis of the extraocular muscles
H02151 Hereditary congenital facial paresis
H02693 Congenital cranial dysinnervation disorder with absent corneal reflex and developmental delay
|
9C83 Disorders of binocular movement
|
H02450 Horizontal gaze palsy with progressive scoliosis
|
9C84 Nystagmus
|
H00776 Congenital motor nystagmus (CMN)
|
9C85 Certain specified irregular eye movements
|
9C8Y Other specified strabismus or ocular motility disorders
|
9C8Z Strabismus or ocular motility disorders, unspecified
|
Disorders of refraction or accommodation
|
9D00 Disorders of refraction
|
H02041 Myopia
|
9D01 Disorders of accommodation
|
9D0Y Other specified disorders of refraction or accommodation
|
9D0Z Disorders of refraction or accommodation, unspecified
|
Postprocedural disorders of eye or ocular adnexa
|
9D20 Bullous aphakic keratopathy following cataract surgery
9D21 Cataract lens fragments in eye following cataract surgery
9D22 Chorioretinal scars after surgery for detachment
9D23 Conjunctival blebitis after glaucoma surgery
9D24 Complications with glaucoma drainage devices
9D25 Glaucoma due to ocular surgery or laser
|
Impairment of visual functions
|
9D41 Impairment of visual field
|
9D42 Patterns of visual field impairment
|
9D43 Impairment of contrast vision
|
9D44 Impairment of colour vision
|
H00971 Achromatopsia
H00976 Colorblindness
|
9D45 Impairment of light sensitivity
|
H00787 Congenital stationary night blindness
|
9D46 Impairment of binocular functions
|
Subjective visual experiences
|
9D50 Visual discomfort
9D51 Transient visual loss
9D52 Hemifield losses
9D53 Entoptic phenomena
9D54 Visual illusions
9D55 Nonorganic visual loss
9D56 Visual release hallucinations
9D5Y Other specified subjective visual experiences
9D5Z Subjective visual experiences, unspecified
|
9D7Y Other specified impairment of visual functions
|
H00973 Bradyopsia
|
9D7Z Impairment of visual functions, unspecified
|
Vision impairment
|
9D90 Vision impairment including blindness
9D92 Specific vision dysfunctions
9D93 Complex vision-related dysfunctions
9D94 Impairment of presenting visual acuity
9D95 Impairment of best corrected visual acuity
9D96 Impairment of uncorrected visual acuity
9D9Y Other specified vision impairment
9D9Z Vision impairment, unspecified
|
9E1Y Other specified diseases of the visual system
|
H00169 Ocular albinism
|
9E1Z Diseases of the visual system, unspecified
|
|
10 Diseases of the ear or mastoid process
|
Diseases of external ear
|
Infectious diseases of external ear
|
AA00 Abscess of external ear
AA01 Cellulitis of external ear
AA02 Malignant otitis externa
AA03 Otomycosis
AA04 Perichondritis of external ear
AA0Y Other specified infectious diseases of external ear
AA0Z Infectious diseases of external ear, unspecified
|
Otitis externa
|
Noninfectious inflammation of external ear
|
AA10 Seborrhoeic otitis externa
AA11 Acute noninfectious otitis externa
AA12 Chondrodermatitis nodularis
AA13 Chronic otitis externa
AA1Y Other specified noninfectious inflammation of external ear
AA1Z Noninfectious inflammation of external ear, unspecified
|
AA3Y Other specified otitis externa
|
AA3Z Otitis externa, unspecified
|
Noninflammatory disorders of the external ear
|
AA40 Acquired deformity of external auditory canal
AA41 Acquired deformity of pinna
AA42 Impacted cerumen
AA4Y Other specified noninflammatory disorders of the external ear
AA4Z Noninflammatory disorders of the external ear, unspecified
|
AA6Z Diseases of external ear, unspecified
|
Diseases of middle ear or mastoid
|
Otitis media
|
Nonsuppurative otitis media
|
AA80 Acute serous or mucoid otitis media
AA81 Acute nonserous nonsuppurative otitis media
AA82 Chronic serous or mucoid otitis media
AA83 Noninfected otitis media with effusion
AA8Z Nonsuppurative otitis media, unspecified
|
Suppurative otitis media
|
AA90 Acute suppurative otitis media
AA91 Chronic suppurative otitis media
AA9Z Suppurative otitis media, unspecified whether acute or chronic
|
AB00 Acute otitis media
|
AB01 Chronic otitis media
|
AB0Y Other specified otitis media
|
AB0Z Otitis media, unspecified
|
AB10 Disorders of Eustachian tube
|
AB11 Mastoiditis or related conditions
|
AB12 Cholesteatoma of middle ear
|
AB13 Perforation of tympanic membrane
|
AB14 Acute myringitis
|
AB15 Chronic myringitis
|
AB16 Tympanosclerosis
|
AB17 Adhesive middle ear disease
|
AB18 Discontinuity or dislocation of ear ossicles
|
AB19 Acquired abnormalities of ear ossicles not related to discontinuity or dislocation
|
AB1A Polyp of middle ear
|
AB1B Middle ear cicatrix
|
AB1Y Other specified diseases of middle ear or mastoid
|
AB1Z Diseases of middle ear or mastoid, unspecified
|
Diseases of inner ear
|
AB30 Acute vestibular syndrome
|
AB31 Episodic vestibular syndrome
|
H01495 Meniere disease
H01706 Delayed endolymphatic hydrops
|
AB32 Chronic vestibular syndrome
|
AB33 Otosclerosis
|
H02828 Otosclerosis
|
AB34 Disorders of vestibular function
|
AB35 Labyrinthine fistula
|
AB36 Labyrinthine dysfunction
|
AB37 Noise effects on inner ear
|
AB3Y Other specified diseases of inner ear
|
AB3Z Diseases of inner ear, unspecified
|
Disorders with hearing impairment
|
AB50 Congenital hearing impairment
|
H00604 Deafness, autosomal dominant
H00605 Deafness, autosomal recessive
H01209 Deafness, X-linked
H02336 Deafness, Y-linked
H02636 Sinoatrial node dysfunction and deafness
|
AB51 Acquired hearing impairment
|
H01704 Sudden sensorineural hearing loss
H01705 Bilateral sudden sensorineural hearing loss
|
AB52 Deafness not otherwise specified
|
AB53 Ototoxic hearing loss
|
AB54 Presbycusis
|
AB55 Sudden idiopathic hearing loss
|
AB56 Hereditary hearing loss
|
AB57 Auditory synaptopathy or neuropathy
|
H02339 Auditory neuropathy
|
AB5Y Other specified disorders with hearing impairment
|
AB5Z Disorders with hearing impairment, unspecified
|
Disorders of ear, not elsewhere classified
|
AB70 Otalgia or effusion of ear
AB71 Degenerative or vascular disorders of ear
AB72 Disorders of acoustic nerve
AB73 Atrophy ear
AB7Y Other specified disorders of ear, not elsewhere classified
|
Postprocedural disorders of ear or mastoid process
|
AB90 Recurrent cholesteatoma of postmastoidectomy cavity
AB91 Mucosal cyst of postmastoidectomy cavity
AB92 Granulation of postmastoidectomy cavity
AB93 Chronic inflammation of postmastoidectomy cavity
|
AC0Y Other specified diseases of the ear or mastoid process
|
AC0Z Diseases of the ear or mastoid process, unspecified
|
|
11 Diseases of the circulatory system
|
Hypertensive diseases
|
BA00 Essential hypertension
|
H01633 High blood pressure
|
BA01 Hypertensive heart disease
|
BA02 Hypertensive renal disease
|
BA03 Hypertensive crisis
|
BA04 Secondary hypertension
|
H00242 Liddle syndrome
H00603 Hypertension exacerbated in pregnancy
|
Hypotension
|
BA20 Idiopathic hypotension
|
BA21 Orthostatic hypotension
|
H02751 Orthostatic hypotension
|
BA2Y Other specified hypotension
|
BA2Z Hypotension, unspecified
|
Ischaemic heart diseases
|
Acute ischaemic heart disease
|
BA40 Angina pectoris
|
H01632 Angina pectoris
|
BA41 Acute myocardial infarction
|
H01730 Myocardial infarction
|
BA42 Subsequent myocardial infarction
|
BA43 Coronary thrombosis not resulting in myocardial infarction
|
BA4Z Acute ischaemic heart disease, unspecified
|
Chronic ischaemic heart disease
|
BA50 Old myocardial infarction
BA51 Ischaemic cardiomyopathy
BA52 Coronary atherosclerosis
BA5Y Other specified chronic ischaemic heart disease
BA5Z Chronic ischaemic heart disease, unspecified
|
BA60 Certain current complications following acute myocardial infarction
|
BA6Z Ischaemic heart diseases, unspecified
|
Diseases of coronary artery
|
BA81 Coronary artery aneurysm
|
BA82 Coronary artery dissection
|
BA83 Coronary artery fistula, acquired
|
BA84 Chronic total occlusion of coronary artery
|
BA85 Coronary vasospastic disease
|
BA86 Coronary microvascular disease
|
BA8Y Other specified diseases of coronary artery
|
BA8Z Diseases of coronary artery, unspecified
|
H01742 Coronary artery disease
|
Pulmonary heart disease or diseases of pulmonary circulation
|
BB00 Pulmonary thromboembolism
|
BB01 Pulmonary hypertension
|
H01619 Primary pulmonary hypertension
H01621 Pulmonary arterial hypertension
H01866 Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis
H01622 Chronic thromboembolic pulmonary hypertension
|
BB02 Certain specified diseases of pulmonary vessels
|
BB03 Acquired pulmonary venous abnormality
|
BB0Y Other specified pulmonary heart disease or diseases of pulmonary circulation
|
BB0Z Pulmonary heart disease or diseases of pulmonary circulation, unspecified
|
Pericarditis
|
BB20 Acute pericarditis
BB21 Chronic rheumatic pericarditis
BB22 Constrictive pericarditis
BB23 Cardiac tamponade
BB24 Haemopericardium
BB25 Pericardial effusion
BB2Y Other specified pericarditis
BB2Z Pericarditis, unspecified
|
Acute or subacute endocarditis
|
BB40 Acute or subacute infectious endocarditis
BB41 Myoendocarditis
BB42 Periendocarditis
BB4Y Other specified acute or subacute endocarditis
BB4Z Acute or subacute endocarditis, unspecified
|
Heart valve diseases
|
Mitral valve disease
|
BB60 Mitral valve stenosis
|
BB61 Mitral valve insufficiency
|
BB62 Mitral valve prolapse
|
H01868 Mitral valve prolapse
|
BB63 Mitral valve stenosis with insufficiency
|
BB64 Mitral valvar abscess
|
BB65 Mitral valve rupture
|
BB6Y Other specified mitral valve disease
|
BB6Z Mitral valve disease, unspecified
|
Aortic valve disease
|
BB70 Aortic valve stenosis
BB71 Aortic valve insufficiency
BB72 Aortic valve stenosis with insufficiency
BB73 Aortic valvar abscess
BB74 Aortic valvar prolapse
BB7Y Other specified aortic valve disease
BB7Z Aortic valve disease, unspecified
|
Tricuspid valve disease
|
BB80 Tricuspid valve stenosis
BB81 Tricuspid valve insufficiency
BB82 Tricuspid valve stenosis with insufficiency
BB83 Tricuspid valvular abscess
BB84 Tricuspid valve rupture
BB8Y Other specified tricuspid valve disease
BB8Z Tricuspid valve disease, unspecified
|
Pulmonary valve disease
|
BB90 Pulmonary valve stenosis
BB91 Pulmonary valve insufficiency
BB92 Pulmonary valve stenosis with insufficiency
BB93 Pulmonary valvar abscess
BB9Y Other specified pulmonary valve disease
BB9Z Pulmonary valve disease, unspecified
|
BC00 Multiple valve disease
|
BC01 Prosthetic valve disease
|
BC02 Acquired abnormality of congenitally malformed valve
|
BC0Z Heart valve diseases, unspecified
|
H00334 Bacterial endocarditis
|
BC20 Chronic rheumatic heart diseases, not elsewhere classified
|
Diseases of the myocardium or cardiac chambers
|
BC40 Acquired atrial abnormality
|
BC41 Acquired ventricular abnormality
|
BC42 Myocarditis
|
H00295 Viral myocarditis
|
BC43 Cardiomyopathy
|
H00294 Dilated cardiomyopathy
H02697 Long-Olsen-Distelmaier syndrome
H00292 Hypertrophic cardiomyopathy
H01219 Restrictive cardiomyopathy
H00293 Arrhythmogenic right ventricular cardiomyopathy
H00669 Naxos disease
H02094 Carvajal syndrome
H02498 Diabetic cardiomyopathy
H02683 Arrhythmogenic cardiomyopathy with variable ectodermal abnormalities
|
BC44 Noncompaction cardiomyopathy
|
H01216 Left ventricular noncompaction
|
BC45 Cardiomegaly
|
BC46 Intracardiac thrombosis
|
BC4Y Other specified diseases of the myocardium or cardiac chambers
|
BC4Z Diseases of the myocardium or cardiac chambers, unspecified
|
Cardiac arrhythmia
|
BC60 Atrial premature depolarization
|
BC61 Junctional premature depolarization
|
BC62 Accessory pathway
|
BC63 Conduction disorders
|
H01263 Progressive cardiac conduction defect (PCCD)
H02125 Cardiac conduction disease with or without dilated cardiomyopathy
|
BC64 Sudden arrhythmic death syndrome
|
BC65 Cardiac arrhythmia associated with genetic disorder
|
H00720 Long QT syndrome
H00748 Andersen-Tawil syndrome
H02091 Jervell and Lange-Nielsen syndrome
H00728 Brugada syndrome
H00725 Short QT syndrome
H00730 Familial idiopathic ventricular fibrillation
H01019 Catecholaminergic polymorphic ventricular tachycardia
H02122 Chronic atrial and intestinal dysrhythmia
H02895 Lodder-Merla syndrome
|
Ventricular rhythm disturbance
|
BC70 Ventricular premature depolarization
|
BC71 Ventricular tachyarrhythmia
|
H02269 Familial ventricular tachycardia
|
BC7Y Other specified ventricular rhythm disturbance
|
H02848 Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome
|
BC7Z Ventricular rhythm disturbance, unspecified
|
Supraventricular rhythm disturbance
|
BC80 Supraventricular bradyarrhythmia
|
H02636 Sinoatrial node dysfunction and deafness
H00729 Sick sinus syndrome
H02674 Atrial standstill
|
BC81 Supraventricular tachyarrhythmia
|
H00731 Atrial fibrillation
H01154 Wolff-Parkinson-White (WPW) syndrome
|
BC8Y Other specified supraventricular rhythm disturbance
|
BC8Z Supraventricular rhythm disturbance, unspecified
|
BC90 Rhythm disturbance at level of atrioventricular junction
|
BC91 Pacemaker or implantable cardioverter defibrillator battery at end of battery life
|
BC9Y Other specified cardiac arrhythmia
|
BC9Z Cardiac arrhythmia, unspecified
|
Heart failure
|
BD10 Congestive heart failure
|
BD11 Left ventricular failure
|
BD12 High output syndromes
|
BD13 Right ventricular failure
|
BD14 Biventricular failure
|
BD1Y Other specified heart failure
|
H01631 Acute heart failure
|
BD1Z Heart failure, unspecified
|
Diseases of arteries or arterioles
|
BD30 Acute arterial occlusion
|
Chronic arterial occlusive disease
|
BD40 Atherosclerotic chronic arterial occlusive disease
|
H01626 Arteriosclerosis obliterans
H01629 Chronic arterial occlusive disease
H02505 Atherosclerosis
|
BD41 Non-atherosclerotic chronic arterial occlusive disease
|
H01629 Chronic arterial occlusive disease
H02719 Multifocal fibromuscular dysplasia
|
BD42 Raynaud phenomenon
|
H01620 Raynaud syndrome
H01629 Chronic arterial occlusive disease
|
BD4Y Other specified chronic arterial occlusive disease
|
BD4Z Chronic arterial occlusive disease, unspecified
|
BD50 Aortic aneurysm or dissection
|
H00801 Familial thoracic aortic aneurysm and dissection
|
BD51 Arterial aneurysm or dissection, excluding aorta
|
BD52 Certain specified disorders of arteries or arterioles
|
H00824 Calcification of joints and arteries
H01002 Generalized arterial calcification of infancy
|
BD53 Secondary disorders of arteries and arterioles
|
BD54 Diabetic foot ulcer
|
BD55 Asymptomatic stenosis of intracranial or extracranial artery
|
BD56 Asymptomatic occlusion of intracranial or extracranial artery
|
BD5Y Other specified diseases of arteries or arterioles
|
BD5Z Diseases of arteries or arterioles, unspecified
|
Diseases of veins
|
BD70 Superficial thrombophlebitis
|
BD71 Deep vein thrombosis
|
H01723 Deep vein thrombosis
|
BD72 Venous thromboembolism
|
BD73 Acquired systemic vein abnormality
|
BD74 Chronic peripheral venous insufficiency of lower extremities
|
BD75 Venous varicosities of sites other than lower extremity
|
BD7Y Other specified diseases of veins
|
BD7Z Diseases of veins, unspecified
|
Disorders of lymphatic vessels or lymph nodes
|
BD90 Lymphadenitis
|
H01397 Tick-borne lymphadenopathy
|
BD91 Lymphangitis
|
BD92 Lymphangiectasia
|
BD93 Lymphoedema
|
H00535 Lymphatic malformation
H01017 Choanal atresia and lymphedema
H02167 Lymphedema-distichiasis syndrome
H02168 Hypotrichosis-lymphedema-telangiectasia syndrome
H02169 Hennekam lymphangiectasia-lymphedema syndrome
|
BD9Y Other specified disorders of lymphatic vessels or lymph nodes
|
BD9Z Disorders of lymphatic vessels or lymph nodes, unspecified
|
Postprocedural disorders of circulatory system
|
BE10 Postcardiotomy syndrome
BE11 Other functional disturbances following cardiac surgery
BE12 Postprocedural valve disorders
BE13 Postprocedural true or false aortic aneurysm
BE14 Postprocedural disorder of circulatory system following repair of congenital heart or great vessel anomaly
BE15 Postprocedural pulmonary arterial tree disorder
BE16 Postprocedural pulmonary venous disorder
BE17 Postprocedural residual or recurrent interatrial communication
BE19 Postprocedural ventricular abnormality
BE1A Cardiac transplant associated coronary allograft vasculopathy
BE1B Lymphoedema due to surgery or radiotherapy
BE1C Inferior caval vein obstruction due to foreign body
BE1D Superior caval vein obstruction due to foreign body
BE1E Postprocedural right atrial complication
BE1F Postprocedural left atrial complication
|
BE2Y Other specified diseases of the circulatory system
|
BE2Z Diseases of the circulatory system, unspecified
|
|
12 Diseases of the respiratory system
|
Upper respiratory tract disorders
|
CA00 Acute nasopharyngitis
|
H02442 Common cold
|
CA01 Acute sinusitis
|
CA02 Acute pharyngitis
|
CA03 Acute tonsillitis
|
CA04 Acute laryngopharyngitis
|
CA05 Acute laryngitis or tracheitis
|
CA06 Acute obstructive laryngitis or epiglottitis
|
CA07 Acute upper respiratory infections of multiple and unspecified sites
|
CA08 Vasomotor or allergic rhinitis
|
H01360 Allergic rhinitis
|
CA09 Chronic rhinitis, nasopharyngitis or pharyngitis
|
CA0A Chronic rhinosinusitis
|
H01765 Eosinophilic sinusitis
|
CA0B Silent sinus syndrome
|
CA0C Cyst or mucocele of nose or nasal sinus
|
CA0D Deviated nasal septum
|
CA0E Hypertrophy of nasal turbinates
|
CA0F Chronic diseases of tonsils or adenoids
|
CA0G Chronic laryngitis or laryngotracheitis
|
CA0H Diseases of vocal cords or larynx, not elsewhere classified
|
CA0J Nasal polyp
|
CA0K Abscess of upper respiratory tract
|
CA0Y Other specified upper respiratory tract disorders
|
CA0Z Upper respiratory tract disorders, unspecified
|
Certain lower respiratory tract diseases
|
CA20 Bronchitis
|
CA21 Emphysema
|
CA22 Chronic obstructive pulmonary disease
|
H01714 Chronic obstructive pulmonary disease (COPD)
H01873 Obliterative bronchiolitis
|
CA23 Asthma
|
H00079 Asthma
H01191 Asthma with nasal polyps and aspirin intolerance
|
CA24 Bronchiectasis
|
H00892 Bronchiectasis with or without elevated sweat chloride
H02836 Bronchiectasis and nasal polyposis
|
CA25 Cystic fibrosis
|
H00218 Cystic fibrosis
|
CA26 Chronic bronchiolitis
|
H01873 Obliterative bronchiolitis
H01713 Diffuse panbronchiolitis
|
CA27 Tracheobronchitis
|
CA2Y Other specified lower respiratory tract disease
|
H02757 Recurrent respiratory infections and failure to thrive with or without diarrhea
|
CA2Z Lower respiratory tract disease, unspecified
|
Lung infections
|
CA40 Pneumonia
|
H00351 Chlamydial pneumonia
H00304 Haemophilus influenzae infection
H00301 Klebsiella infection
H00341 Mycoplasma pneumonia
H01441 Pseudomonas aeruginosa infection
H00333 Streptococcal infection
H01321 Pneumococcal disease
H00401 Respiratory syncytial virus infection
H00400 Parainfluenza infection
H01063 Human metapneumovirus infection
H01521 Pneumocystis pneumonia
|
CA41 Acute bronchiolitis
|
H00401 Respiratory syncytial virus infection
|
CA42 Acute bronchitis
|
H00341 Mycoplasma pneumonia
H00401 Respiratory syncytial virus infection
H00400 Parainfluenza infection
H00304 Haemophilus influenzae infection
|
CA43 Abscess of lung or mediastinum
|
CA44 Pyothorax
|
CA45 Respiratory infections, not elsewhere classified
|
CA4Y Other specified lung infections
|
CA4Z Lung infections, unspecified
|
Lung diseases due to external agents
|
CA60 Pneumoconiosis
|
Pneumonitis
|
CA70 Hypersensitivity pneumonitis due to organic dust
|
H00346 Extrinsic allergic alveolitis
H01411 Saccharomonospora viridis infection
|
CA71 Pneumonitis due to solids and liquids
|
CA72 Mendelson syndrome
|
CA7Y Other specified pneumonitis
|
CA7Z Pneumonitis, unspecified
|
CA80 Airway disease due to specific organic dust
|
CA81 Respiratory conditions due to inhalation of chemicals, gases, fumes or vapours
|
CA82 Respiratory conditions due to other external agents
|
CA8Y Other specified lung diseases due to external agents
|
CA8Z Lung diseases due to external agents, unspecified
|
Respiratory diseases principally affecting the lung interstitium
|
CB00 Acute respiratory distress syndrome
|
CB01 Pulmonary oedema
|
CB02 Pulmonary eosinophilia
|
CB03 Idiopathic interstitial pneumonitis
|
H01716 Idiopathic interstitial pneumonias
H01299 Idiopathic pulmonary fibrosis
|
CB04 Primary interstitial lung diseases specific to infancy or childhood
|
H00830 Alveolar capillary dysplasia with misalignment of pulmonary veins
H00217 Pulmonary alveolar proteinosis
H01122 Congenital pulmonary alveolar proteinosis
H02124 Interstitial lung and liver disease
H00913 Brain-lung-thyroid syndrome
|
CB05 Interstitial lung diseases associated with systemic diseases
|
H02466 Rajab interstitial lung disease with brain calcification
|
CB06 Pulmonary alveolar microlithiasis
|
H01298 Pulmonary alveolar microlithiasis
|
CB07 Lymphangioleiomyomatosis
|
H00896 Lymphangioleiomyomatosis
|
CB0Y Other specified respiratory diseases principally affecting the lung interstitium
|
CB0Z Respiratory diseases principally affecting the lung interstitium, unspecified
|
Pleural, diaphragm or mediastinal disorders
|
CB20 Pleural plaque
|
CB21 Pneumothorax
|
H01110 Pneumothorax
|
CB22 Diseases of mediastinum, not elsewhere classified
|
CB23 Disorders of diaphragm
|
CB24 Chylous effusion
|
CB25 Fibrothorax
|
CB26 Haemothorax
|
CB27 Pleural effusion
|
CB2Y Other specified pleural, diaphragm or mediastinal disorders
|
CB2Z Pleural, diaphragm or mediastinal disorders, unspecified
|
CB40 Certain diseases of the respiratory system
|
CB41 Respiratory failure
|
Postprocedural disorders of the respiratory system
|
CB60 Tracheostomy malfunction
CB61 Chronic pulmonary insufficiency following surgery
CB62 Postprocedural subglottic stenosis
CB63 Postprocedural stenosis of the trachea
CB64 Transfusion related acute lung injury
|
CB7Z Diseases of the respiratory system, unspecified
|
|
13 Diseases of the digestive system
|
Diseases or disorders of orofacial complex
|
DA00 Disorders of lips
|
DA01 Disorders of oral mucosa
|
H02648 Acantholytic blistering of the oral and laryngeal mucosa
|
DA02 Miscellaneous specified disorders of lips or oral mucosa
|
H00724 White sponge nevus
|
DA03 Diseases of tongue
|
DA04 Diseases of salivary glands
|
DA05 Cysts of oral or facial-neck region
|
DA06 Certain specified diseases of jaws
|
DA07 Disorders of tooth development or eruption
|
H00680 Primary failure of tooth eruption
|
DA08 Diseases of hard tissues of teeth
|
H01331 Dental caries
|
DA09 Diseases of pulp or periapical tissues
|
DA0A Certain specified disorders of teeth or supporting structures
|
DA0B Gingival diseases
|
DA0C Periodontal disease
|
H01408 Periodontal disease
H02050 Prepubertal periodontitis
H01317 Aggressive periodontitis
|
DA0D Certain specified disorders of gingiva or edentulous alveolar ridge
|
H01250 Hereditary gingival fibromatosis
|
DA0E Dentofacial anomalies
|
DA0F Sensory disturbances affecting orofacial complex
|
DA0Y Other specified diseases or disorders of orofacial complex
|
DA0Z Diseases or disorders of orofacial complex, unspecified
|
H01407 Capnocytophaga ochracea infection
|
Diseases of oesophagus
|
DA20 Acquired anatomical alterations of the oesophagus
|
DA21 Motility disorders of oesophagus
|
DA22 Gastro-oesophageal reflux disease
|
H01602 Gastroesophageal reflux disease
|
DA23 Columnar metaplastic epithelium of the oesophagus
|
H01901 Barrett esophagus
|
DA24 Oesophagitis
|
H01361 Eosinophilic esophagitis
|
DA25 Oesophageal ulcer
|
DA26 Vascular disorders of the oesophagus
|
DA2Y Other specified diseases of oesophagus
|
DA2Z Diseases of oesophagus, unspecified
|
Diseases of the stomach or the duodenum
|
Diseases of stomach
|
DA40 Acquired anatomical alterations of the stomach
DA41 Gastroduodenal motor or secretory disorders
DA42 Gastritis
DA43 Vascular disorders of the stomach
DA44 Gastric polyp
DA4Y Other specified diseases of stomach
DA4Z Diseases of stomach, unspecified
|
Diseases of duodenum
|
DA50 Acquired anatomical alterations of the duodenum
|
DA51 Duodenitis
|
H00320 Helicobacter pylori infection
|
DA52 Vascular disorders of the duodenum
|
DA53 Duodenal polyp
|
DA5Y Other specified diseases of duodenum
|
DA5Z Diseases of duodenum, unspecified
|
Ulcer of stomach or duodenum
|
DA60 Gastric ulcer
|
H01634 Peptic ulcer
H00320 Helicobacter pylori infection
H02504 Gastrointestinal ulceration, recurrent, with dysfunctional platelets
|
DA61 Peptic ulcer, site unspecified
|
H01634 Peptic ulcer
|
DA62 Anastomotic ulcer
|
H01634 Peptic ulcer
H00320 Helicobacter pylori infection
|
DA63 Duodenal ulcer
|
H01634 Peptic ulcer
H00320 Helicobacter pylori infection
|
DA7Z Diseases of the stomach or the duodenum, unspecified
|
Diseases of small intestine
|
DA90 Nonstructural developmental anomalies of small intestine
|
H01805 Tricho-hepato-enteric syndrome
H01276 Chronic idiopathic intestinal pseudo-obstruction
H02553 Visceral myopathy
|
DA91 Obstruction of small intestine
|
DA92 Other acquired anatomical alterations of small intestine
|
DA93 Motility disorders of small intestine
|
DA94 Noninfectious enteritis or ulcer of small intestine
|
H01853 Chronic nonspecific multiple ulcers of the small intestine
|
DA95 Coeliac disease
|
H02123 Celiac disease
|
DA96 Intestinal malabsorption or protein-losing enteropathy
|
H00352 Whipple disease
H00988 Enterokinase deficiency
H01016 Primary bile acid malabsorption
H01935 Familial hypercholanemia
|
DA97 Certain vascular disorders of small intestine
|
DA98 Polyps of small intestine
|
DA9Y Other specified diseases of small intestine
|
DA9Z Diseases of small intestine, unspecified
|
Diseases of appendix
|
DB10 Appendicitis
DB11 Certain specified diseases of appendix
DB1Y Other specified diseases of appendix
DB1Z Diseases of appendix, unspecified
|
Diseases of large intestine
|
DB30 Obstruction of large intestine
|
DB31 Other acquired anatomical alterations of large intestine
|
DB32 Motility disorders of large intestine
|
H01871 Isolated hypoganglionosis
|
DB33 Certain noninfectious colitis or proctitis
|
DB34 Certain vascular disorders of large intestine
|
DB35 Polyp of large intestine
|
DB36 Certain infections of the large intestine
|
DB3Y Other specified diseases of large intestine
|
DB3Z Diseases of large intestine, unspecified
|
Diseases of anal canal
|
Acquired anatomical alterations of the anal canal
|
DB50 Fissure or fistula of anal regions
DB51 Stenosis of anal canal
DB52 Ulcer of anus
DB53 Anal prolapse
DB5Y Other specified acquired anatomical alterations of the anal canal
DB5Z Acquired anatomical alterations of the anal canal, unspecified
|
Haemorrhoids or perianal venous conditions
|
DB60 Haemorrhoids
DB61 Perianal venous thrombosis
DB62 Residual haemorrhoidal skin tags
DB6Y Other specified haemorrhoids or perianal venous conditions
DB6Z Haemorrhoids or perianal venous conditions, unspecified
|
DB70 Infections of the anal region
|
DB71 Anal polyp
|
DB72 Certain specified diseases of anal canal
|
DB7Y Other specified diseases of anal canal
|
DB7Z Diseases of anal canal, unspecified
|
Diseases of liver
|
DB90 Infectious liver disease
|
DB91 Acute or subacute hepatic failure
|
H01712 Fulminant hepatic failure
|
DB92 Non-alcoholic fatty liver disease
|
H01333 Non-alcoholic fatty liver disease
|
DB93 Hepatic fibrosis or cirrhosis
|
H02194 North American Indian childhood cirrhosis
H02225 Familial cirrhosis
|
DB94 Alcoholic liver disease
|
H02516 Alcoholic liver disease
|
DB95 Drug-induced or toxic liver disease
|
DB96 Autoimmune liver disease
|
H01685 Autoimmune hepatitis
H01467 Primary biliary cholangitis
H01684 Primary sclerosing cholangitis
H00742 Neonatal ichthyosis-sclerosing cholangitis (NISCH) syndrome
|
DB97 Certain specified inflammatory liver diseases
|
DB98 Vascular disorders of the liver
|
H01687 Extrahepatic portal vein obstruction
H01433 Budd-Chiari syndrome
H01686 Idiopathic portal hypertension
|
DB99 Certain specified diseases of liver
|
H00545 Polycystic liver disease
H01506 Hepatic encephalopathy
|
DB9Z Diseases of liver, unspecified
|
Diseases of gallbladder or biliary tract
|
DC10 Acquired anatomical alterations of gallbladder or bile ducts
|
DC11 Cholelithiasis
|
H01213 Gallbladder disease
H01679 Intrahepatic lithiasis
|
DC12 Cholecystitis
|
H01213 Gallbladder disease
|
DC13 Cholangitis
|
DC14 Certain specified biliary diseases
|
DC1Y Other specified diseases of gallbladder or biliary tract
|
DC1Z Diseases of gallbladder or biliary tract, unspecified
|
Diseases of pancreas
|
DC30 Cystic diseases of the pancreas
|
DC31 Acute pancreatitis
|
H01681 Acute pancreatitis
|
DC32 Chronic pancreatitis
|
H01680 Chronic pancreatitis
H00933 Hereditary pancreatitis
H00932 Tropical calcific pancreatitis
|
DC33 Autoimmune pancreatitis
|
DC34 Obstructive pancreatitis
|
DC35 Certain specified diseases of pancreas
|
DC3Y Other specified diseases of pancreas
|
DC3Z Diseases of pancreas, unspecified
|
Diseases of peritoneum
|
DC50 Peritonitis
DC51 Certain specified disorders of peritoneum or retroperitoneum
DC5Z Diseases of peritoneum, unspecified
|
Diverticular disease of intestine
|
Diverticular disease of small intestine
|
DC70 Diverticulitis of small intestine
DC71 Diverticulosis of small intestine
DC72 Diverticulum of small intestine
|
Diverticular disease of large intestine
|
DC80 Diverticulitis of large intestine
DC81 Diverticulosis of large intestine
DC82 Diverticulum of large intestine
|
Diverticular disease of intestine of overlapping sites
|
DC90 Diverticular disease of small and large intestine
|
Diverticular disease of unspecified part of intestine
|
DD00 Diverticulitis of unspecified part of intestine
DD01 Diverticulosis of unspecified part of intestine
DD02 Diverticulum of unspecified part of intestine
|
DD1Z Diverticular disease of intestine, unspecified
|
Ischaemic vascular disorders of intestine
|
DD30 Acute vascular disorders of intestine
DD31 Chronic vascular disorders of intestine
DD3Y Other specified ischaemic vascular disorders of intestine
DD3Z Ischaemic vascular disorders of intestine, unspecified
|
Hernias
|
DD50 Non-abdominal wall hernia
DD51 Inguinal hernia
DD52 Femoral hernia
DD53 Umbilical hernia
DD54 Paraumbilical hernia
DD55 Epigastric hernia
DD56 Incisional hernia
DD57 Parastomal hernia
DD5Y Other specified hernias
DD5Z Hernias, unspecified
|
Inflammatory bowel diseases
|
DD70 Crohn disease
|
H00286 Crohn disease
H01227 Inflammatory bowel disease (IBD)
|
DD71 Ulcerative colitis
|
H01227 Inflammatory bowel disease (IBD)
H01466 Ulcerative colitis
|
DD72 Indeterminate colitis
|
H01227 Inflammatory bowel disease (IBD)
|
DD7Y Other specified inflammatory bowel diseases
|
DD7Z Inflammatory bowel diseases, unspecified
|
Functional gastrointestinal disorders
|
DD90 Functional oesophageal or gastroduodenal disorders
|
DD91 Irritable bowel syndrome or certain specified functional bowel disorders
|
H01615 Irritable bowel syndrome
|
DD92 Functional anorectal disorders
|
DD93 Functional digestive disorders of infants, toddlers or children
|
DD94 Functional gallbladder disorder
|
DD95 Functional sphincter of Oddi disorder
|
DD9Y Other specified functional gastrointestinal disorders
|
H02810 Intestinal dysmotility syndrome
|
DD9Z Functional gastrointestinal disorders, unspecified
|
Postprocedural disorders of digestive system
|
DE10 Vomiting following gastrointestinal surgery
DE11 Dumping syndrome
DE12 Malfunction or complication of external stoma of digestive organs
DE13 Postsurgical malabsorption, not elsewhere classified
|
DE2Y Other specified diseases of the digestive system
|
DE2Z Diseases of the digestive system, unspecified
|
|
14 Diseases of the skin
|
Certain skin disorders attributable to infection or infestation
|
Certain skin disorders attributable to viral infection
|
Viral exanthems
|
EA00 Viral exanthem due to unknown or unspecified agent
EA0Y Viral exanthem due to other specified virus
|
Certain dermatoses with suspected viral aetiology
|
EA10 Pityriasis rosea
|
EA11 Papular purpuric gloves and socks syndrome
|
EA12 Infantile papular acrodermatitis
|
Dermatoses from distant or systemic viral infection
|
EA20 Necrolytic acral erythema
|
EA3Z Unspecified skin disorder attributable to viral infection
|
Certain skin disorders attributable to bacterial infection
|
Predominantly tropical or subtropical bacterial infections affecting skin
|
EA40 Tropical phagedaenic ulcer
|
EA50 Toxin-mediated cutaneous reactions to distant or systemic bacterial infection
|
EA51 Skin complications of BCG immunisation
|
EA5Y Cutaneous involvement by other specified bacterial infection
|
EA5Z Cutaneous involvement by unspecified bacterial infection
|
EA60 Certain skin disorders attributable to fungal infection
|
EA6Y Cutaneous involvement by other specified infection or infestation
|
Inflammatory dermatoses
|
Dermatitis and eczema
|
EA80 Atopic eczema
|
H01358 Atopic dermatitis
|
EA81 Seborrhoeic dermatitis and related conditions
|
H00795 Seborrhea-like dermatitis with psoriasiform element
H01652 Seborrheic dermatitis
|
EA82 Nummular dermatitis
|
EA83 Lichen simplex or lichenification
|
EA84 Asteatotic eczema
|
EA85 Dermatitis or eczema of hands and feet
|
EA86 Dermatitis and eczema of lower legs
|
EA87 Dermatitis or eczema of anogenital region
|
EA88 Miscellaneous specified eczematous dermatoses
|
EA89 Generalised eczematous dermatitis of unspecified type
|
EA8Y Other specified eczematous dermatosis
|
EA8Z Dermatitis or eczema, unspecified
|
Papulosquamous dermatoses
|
EA90 Psoriasis
|
H01656 Psoriasis
H01663 Pustular psoriasis
|
EA91 Lichen planus
|
H01654 Lichen planus
|
EA92 Lichenoid dermatoses
|
EA93 Pityriasis lichenoides
|
EA94 Pityriasis rubra pilaris
|
H01659 Pityriasis rubra pilaris
|
EA95 Small plaque parapsoriasis
|
Urticaria, angioedema and other urticarial disorders
|
EB00 Spontaneous urticaria
|
EB01 Inducible urticaria and angioedema
|
H01799 Vibratory urticaria
|
EB02 Cholinergic urticaria and related conditions
|
EB03 Syndromes with urticarial reactions or angioedema
|
EB04 Idiopathic angioedema
|
EB05 Urticaria of unspecified type
|
EB0Y Other specified urticarial disorders
|
Inflammatory erythemas and other reactive inflammatory dermatoses
|
EB10 Diffuse inflammatory erythemas
|
EB11 Annular erythema
|
EB12 Erythema multiforme
|
H01695 Erythema multiforme
|
EB13 Stevens-Johnson syndrome or toxic epidermal necrolysis
|
H01694 Stevens-Johnson syndrome
|
Neutrophilic dermatoses
|
EB20 Acute febrile neutrophilic dermatosis
|
EB21 Pyoderma gangrenosum
|
EB2Y Other specified neutrophilic dermatoses
|
EB30 Eosinophilic cellulitis
|
EB31 Erythema nodosum
|
H01473 Erythema nodosum leprosum
|
Immunobullous diseases of the skin
|
EB40 Pemphigus
|
H01648 Pemphigus
|
EB41 Pemphigoid
|
H01650 Pemphigoid
|
EB42 Linear IgA bullous dermatosis
|
EB43 Epidermolysis bullosa acquisita
|
EB44 Dermatitis herpetiformis
|
H01362 Dermatitis herpetiformis
|
EB4Y Other specified immunobullous disorder
|
Cutaneous lupus erythematosus
|
EB50 Subacute cutaneous lupus erythematosus
|
H01595 Cutaneous lupus erythematosus
|
EB51 Chronic cutaneous lupus erythematosus
|
H01595 Cutaneous lupus erythematosus
|
EB5Z Cutaneous lupus erythematosus of unspecified type
|
Scarring or sclerosing inflammatory dermatoses
|
EB60 Lichen sclerosus
|
H01690 Lichen sclerosus et atrophicus
|
EB61 Morphoea
|
H01493 Localized Scleroderma
|
EB7Y Other specified inflammatory dermatoses
|
Metabolic and nutritional disorders affecting the skin
|
EB90 Dermatoses resulting from disturbed metabolic processes
|
H01661 Xanthoma
|
EB9Y Other specified metabolic and nutritional disorders affecting the skin
|
Genetic and developmental disorders affecting the skin
|
Genetic syndromes affecting the skin
|
EC10 Genetic syndromes with poikiloderma
|
H00793 Poikiloderma with neutropenia
H01906 Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis
|
EC1Y Other specified genetic syndromes affecting the skin
|
EC20 Genetic disorders of keratinisation
|
H01771 Congenital ichthyosis
H00735 Ichthyosis vulgaris
H00134 X-linked ichthyosis
H00733 Harlequin ichthyosis
H00734 Autosomal recessive congenital ichthyosis
H00691 Bullous congenital ichthyosiform erythroderma (BCIE)
H00693 Ichthyosis bullosa of Siemens
H00707 Ichthyosis hystrix
H02265 Annular epidermolytic ichthyosis
H00710 Erythrokeratodermia variabilis
H00738 Ichthyosis with confetti
H00790 Keratosis linearis with ichthyosis congenita and sclerosing keratoderma
H02449 Autosomal dominant lamellar ichthyosis
H00737 Peeling skin syndrome
H00715 Darier disease
H00844 Familial benign chronic pemphigus
H00716 Palmoplantar keratoderma with deafness
H00274 Papillon-Lefevre syndrome
H00695 Mal de Meleda
H00714 Vohwinkel syndrome
H00722 Epidermolytic palmoplantar keratoderma
H00723 Non-epidermolytic palmoplantar keratoderma
H02264 Palmoplantar keratoderma, Nagashima type
H02266 Palmoplantar keratoderma, Bothnian type
H02517 Olmsted syndrome
H02915 Huriez syndrome
H02920 Keratolytic winter erythema
H00717 Striate palmoplantar keratoderma
H02263 Focal nonepidermolytic palmoplantar keratoderma
H02702 Tylosis with esophageal cancer
H01404 Punctate palmoplantar keratoderma
H00755 Acrokeratosis verruciformis
H01394 Cole disease
|
EC21 Genetic defects of hair or hair growth
|
H00667 Woolly hair
H00670 Monilethrix
H01796 Uncombable hair syndrome
H00820 Bjornstad syndrome
H00866 Trichothiodystrophy
H00893 Cardiomyopathy, dilated, with woolly hair and keratoderma
H00780 Atrichia with papular lesions
H00784 Localized autosomal recessive hypotrichosis
H00786 Hypotrichosis
H00858 Marie-Unna hereditary hypotrichosis
H00782 Hypotrichosis and recurrent skin vesicles
|
EC22 Genetic defects of nails or nail growth
|
H00683 Anonychia congenita
H01307 Nonsyndromic congenital nail disorder
|
EC23 Genetic disorders of skin pigmentation
|
H00884 Familial progressive hyperpigmentation
H00944 Dowling-Degos disease
H02188 Watson syndrome
H00166 Hermansky-Pudlak syndrome
H00168 Oculocutaneous albinism
H02021 Chediak-Higashi syndrome
H00170 Piebaldism
H00759 Waardenburg syndrome
H00885 Hypomelanosis of Ito
H01187 Tietz syndrome
H02022 Griscelli syndrome
H00880 Dyschromatosis symmetrica hereditaria
H02350 Dyschromatosis universalis hereditaria
H02665 Reticulate acropigmentation of Kitamura
|
Genetically-determined epidermolysis bullosa
|
EC30 Epidermolysis bullosa simplex
|
H00584 Epidermolysis bullosa simplex
H00585 Epidermolysis bullosa, hemidesmosomal
H00644 Ectodermal dysplasia/skin fragility syndrome
|
EC31 Junctional epidermolysis bullosa
|
H00586 Epidermolysis bullosa, junctional
|
EC32 Dystrophic epidermolysis bullosa
|
H00587 Epidermolysis bullosa, dystrophica
H00763 Transient bullous dermolysis of the newborn
|
EC33 Syndromic epidermolysis bullosa
|
H00588 Kindler syndrome
|
EC3Z Epidermolysis bullosa
|
H00813 Laryngo onycho cutaneous syndrome
H01737 Epidermolysis bullosa
|
Genetic disorders affecting dermal collagen, elastin or other matrix proteins
|
EC40 Pseudoxanthoma elasticum
|
H00560 Pseudoxanthoma elasticum
|
EC4Y Other specified genetic disorders affecting dermal matrix proteins
|
Specified developmental anomalies affecting the skin
|
EC50 Developmental anomalies of the umbilicus
EC5Y Other specified developmental anomalies affecting the skin
|
EC7Y Other specified genetic and developmental disorders affecting the skin
|
Sensory and psychological disorders affecting the skin
|
Disturbances of cutaneous sensation
|
EC90 Pruritus
EC91 Prurigo
EC92 Mucocutaneous or cutaneous pain syndromes
EC9Y Other specified disturbances of cutaneous sensation
|
Mental conditions affecting the skin
|
Self-inflicted skin disorders
|
ED00 Artefactual skin disorder
ED01 Simulated skin disease
ED02 Painful bruising syndrome
ED0Y Other specified self-inflicted skin disorders
|
ED2Y Other specified mental conditions affecting the skin
|
Neurological conditions affecting the skin
|
ED30 Neuropathic skin damage
ED31 Burning feet syndrome
ED3Y Cutaneous involvement in other specified neurological condition
|
Skin disorders involving specific cutaneous structures
|
Disorders of the epidermis and epidermal appendages
|
Disorders of epidermal keratinisation
|
ED50 Ichthyoses
|
ED51 Diffuse epidermal hyperkeratosis and acanthosis
|
ED52 Porokeratoses
|
ED53 Skin peeling
|
ED54 Xerosis cutis or asteatosis
|
ED55 Palmoplantar keratodermas
|
ED56 Keratosis pilaris
|
ED5Y Other specified disorders of epidermal keratinisation
|
Disorders of skin colour
|
ED60 Acquired hypermelanosis
|
ED61 Acquired melanotic macules or lentigines
|
ED62 Endogenous non-melanin pigmentation
|
ED63 Acquired hypomelanotic disorders
|
ED64 Abnormal skin pigmentation
|
ED6Y Other specified disorders of skin pigmentation
|
Disorders of hair
|
ED70 Alopecia or hair loss
|
ED71 Hypertrichosis
|
ED72 Hirsutism and syndromes with hirsutism
|
ED73 Acquired disorders of the hair shaft
|
ED7Y Other specified disorders of hair
|
Disorders of the hair follicle
|
Acne and related disorders
|
ED90 Rosacea and related disorders
|
ED91 Disorders of the sebaceous gland
|
ED92 Disorders involving the apocrine follicular unit
|
ED9Y Other specified disorders involving the hair follicle
|
Disorders of eccrine sweat glands or sweating
|
EE00 Hyperhidrosis
|
EE01 Hypohidrosis
|
EE02 Miliaria
|
EE0Y Other specified disorders of eccrine sweat glands or sweating
|
Disorders of the nail or perionychium
|
EE10 Acquired deformities of the nail plate
EE11 Acquired abnormalities of nail colour
EE12 Infections of the nail or perionychium
EE13 Certain disorders affecting the nails or perionychium
EE1Y Other specified disorders of the nail or perionychium
EE1Z Disorders of the nail or perionychium, unspecified
|
Disorders of epidermal integrity
|
EE20 Acute cutaneous distension syndrome
EE21 Epidermal fragility
|
Disorders of the dermis and subcutis
|
Disorders of cutaneous connective tissue
|
EE40 Atrophy or degeneration of dermal or subcutaneous connective tissue
|
EE41 Abnormalities of dermal elastin
|
Poikiloderma
|
Fibromatoses and keloids
|
EE70 Perforating dermatoses
|
EE7Y Other specified disorders of cutaneous connective tissue
|
Histiocytic-granulomatous disorders of the skin
|
EE80 Necrobiotic granulomatous skin disorders
EE81 Dermal dendrocyte, Class IIa histiocytoses
EE8Y Other specified histiocytic and granulomatous disorders of the skin
|
Benign dermal lymphocytic or lymphoplasmacytic infiltrations or proliferations
|
EE90 Benign lymphocytic infiltration of the skin
EE91 Lymphocytoma cutis
|
Disorders of subcutaneous fat
|
EF00 Panniculitis
|
EF01 Lipoatrophy or lipodystrophy
|
EF02 Certain noninflammatory disorders of subcutaneous fat
|
EF0Y Other specified disorders of subcutaneous fat
|
Disorders of cutaneous blood and lymphatic vessels
|
Malformations involving cutaneous blood vessels
|
EF20 Acquired malformations of cutaneous blood vessels
EF2Z Cutaneous vascular malformation, unspecified
|
Purpura or bruising
|
EF30 Purpura or bruising due to disorders of coagulation
EF31 Traumatic purpura
EF3Y Other specified purpura
EF3Z Purpura of unspecified aetiology
|
EF40 Vasculitis or capillaritis involving the skin
|
Dermatoses attributable to hyperviscosity or microvascular occlusion
|
EF50 Livedoid vasculopathy
EF5Y Other specified dermatoses attributable to hyperviscosity or microvascular occlusion
|
Dermatoses resulting from vascular insufficiency
|
EF60 Ischaemic ulceration of skin
|
Dermatoses due to venous disease
|
EF9Y Other specified dermatoses resulting from vascular insufficiency
|
Functional vascular disorders of the skin
|
EG00 Vasodilatation of extremities
|
EG01 Vasoconstriction of extremities
|
EG02 Flushing disorders
|
Skin disorders involving certain specific body regions
|
Skin disorders involving the head and neck
|
EG30 Skin disorders localised to the scalp
|
H01446 Propionibacterium acnes infection
|
Disorders of the external ear involving the skin
|
Inflammatory disorders of the external ear
|
Skin disorders involving the genital and perianal regions
|
Dermatoses of the anus, perianal area or perineum
|
EG60 Anal pruritus
EG61 Infections of the anus or perianal skin
EG62 Inflammatory dermatoses of the perianal area
EG63 Sacrococcygeal pilonidal disease
|
EG7Y Other specified skin disorders involving the genital and perianal regions
|
EG9Y Skin disorders involving other specific body regions
|
EG9Z Skin disorders involving certain specific body regions, unspecified
|
Skin disorders associated with pregnancy, the neonatal period and infancy
|
Skin disorders specific to the perinatal or neonatal period
|
Neonatal skin infection
|
EH10 Neonatal viral infections involving the skin
EH11 Neonatal pyogenic skin infections
EH12 Neonatal fungal infections involving the skin
EH1Z Neonatal skin infection, unspecified
|
EH3Y Other specified skin disorders specific to the perinatal or neonatal period
|
EH40 Dermatoses of infancy
|
Adverse cutaneous reactions to medication
|
Drug eruptions
|
EH60 Exanthematic drug eruption
EH61 Drug-induced urticaria, angioedema and anaphylaxis
EH62 Lichenoid drug eruption
EH63 Stevens-Johnson syndrome and toxic epidermal necrolysis due to drug
EH64 Drug-induced erythroderma
EH65 DRESS syndrome
EH66 Fixed drug eruption
EH67 Acne or acneform reactions attributable to drugs
EH6Y Drug eruption of other specified type
EH6Z Drug eruption of unspecified type
|
EH70 Pigmentary abnormalities of skin due to drug
|
EH71 Dermatoses precipitated by drug therapy
|
EH72 Drug-induced hair abnormalities
|
EH73 Drug-induced nail abnormalities
|
EH74 Drug-induced oral conditions
|
EH75 Photosensitivity due to drug
|
EH76 Dermatoses associated with specific classes of medication
|
EH77 Localised adverse cutaneous reactions to administration of drug
|
EH78 Adverse cutaneous reactions to herbal, homoeopathic or other alternative therapies
|
EH7Y Other specified adverse cutaneous reactions to medication
|
EH7Z Unspecified adverse cutaneous reactions to medication
|
Skin disorders provoked by external factors
|
EH90 Pressure ulceration
|
EH92 Dermatoses provoked by friction or mechanical stress
|
EH93 Dermatoses due to foreign bodies
|
EH94 Scar of skin, not elsewhere classified
|
Dermatoses provoked or exacerbated by exposure to cold
|
EJ0Y Other specified dermatoses provoked or exacerbated by exposure to cold
|
Dermatoses provoked by heat or electricity
|
EJ10 Erythema ab igne
EJ1Y Other specified dermatoses provoked by heat or electricity
|
Dermatoses provoked by light or UV radiation
|
Chronic effects of ultraviolet radiation on the skin
|
EJ20 Photoaging of the skin
EJ2Y Other specified chronic effects of ultraviolet radiation on the skin
|
EJ30 Autoimmune or other photodermatoses
|
Acute effects of ultraviolet radiation on normal skin
|
EJ40 Sunburn
EJ41 Burn from exposure to artificial source of ultraviolet radiation
EJ4Z Acute effects of ultraviolet radiation on normal skin, unspecified
|
EJ6Y Other specified dermatoses provoked by light or UV radiation
|
H02131 UV-sensitive syndrome
|
Dermatoses due to ionizing radiation
|
EJ71 Chronic effects of ionizing radiation on the skin
EJ7Z Dermatoses due to ionizing radiation, unspecified
|
EK00 Allergic contact dermatitis
|
H01357 Allergic contact dermatitis
|
EK01 Photo-allergic contact dermatitis
|
EK02 Irritant contact dermatitis
|
EK10 Allergic contact urticaria
|
EK11 Protein contact dermatitis
|
EK12 Allergic contact sensitisation
|
Phototoxic reactions to skin contact with photoactive agents
|
EK20 Phototoxic reaction to fragrance or cosmetics
EK2Y Phototoxic reaction to skin contact with other specified photoactive agent
EK2Z Phototoxic dermatitis, unspecified
|
EK50 Cutaneous reactions to venomous or noxious animals
|
EK5Y Other specified skin disorders provoked by external factors
|
Benign proliferations, neoplasms and cysts of the skin
|
EK70 Cutaneous cysts
EK71 Skin tags or polyps
|
Disorders of the skin of uncertain or unpredictable malignant potential
|
EK90 Actinic keratosis and other discrete epidermal dysplasias
|
H02429 Actinic keratosis
|
EK91 Dermatoses which may presage cutaneous lymphoma
|
EK92 Histiocytoses of uncertain malignant potential
|
H01168 Sea-blue histiocyte disease
|
Cutaneous markers of internal disorders
|
Cutaneous markers of internal malignancy
|
EL10 Paraneoplastic syndromes involving skin
EL1Y Other specified cutaneous markers of internal malignancy
|
EL3Y Other specified cutaneous markers of internal disorders
|
Postprocedural disorders of the skin
|
EL50 Unsatisfactory surgical scar of skin
|
EL51 Cutaneous flap necrosis
|
EL52 Myocutaneous flap necrosis
|
EL53 Skin graft failure
|
EL54 Composite graft failure
|
Adverse cutaneous effects of therapeutic ionizing irradiation
|
EL60 Acute radiodermatitis following radiotherapy
EL61 Chronic radiodermatitis following radiotherapy
EL63 Radionecrosis of skin due to therapeutic ionizing irradiation
|
Complications of cutaneous cosmetic procedures
|
EL73 Unsatisfactory outcome from cutaneous cosmetic surgical procedure
|
EL80 Adverse cutaneous effects of diagnostic procedures
|
EM0Y Other specified diseases of the skin
|
EM0Z Skin disease of unspecified nature
|
|
15 Diseases of the musculoskeletal system or connective tissue
|
Arthropathies
|
Osteoarthritis
|
FA00 Osteoarthritis of hip
FA01 Osteoarthritis of knee
FA02 Osteoarthritis of wrist or hand
FA03 Osteoarthritis of other specified joint
FA04 Oligoosteoarthritis
FA05 Polyosteoarthritis
FA0Z Osteoarthritis, unspecified
|
Infection related arthropathies
|
FA10 Direct infections of joint
|
H01442 Septic arthritis
|
FA11 Reactive arthropathies
|
FA12 Postinfectious arthropathies
|
FA13 Infectious spondyloarthritis
|
FA1Y Other specified infection related arthropathies
|
FA1Z Infection related arthropathies, unspecified
|
Inflammatory arthropathies
|
FA20 Rheumatoid arthritis
|
H00630 Rheumatoid arthritis
|
FA21 Psoriatic arthritis
|
FA22 Polymyalgia rheumatica
|
H01606 Polymyalgia rheumatica
|
FA23 Adult-onset Still disease
|
H01516 Adult onset Still disease
|
FA24 Juvenile idiopathic arthritis
|
H01672 Juvenile idiopathic arthritis
|
FA25 Gout
|
H01532 Gout
|
FA26 Certain specified crystal arthropathies
|
H01236 Familial articular chondrocalcinosis
|
FA27 Certain specified inflammatory arthropathies
|
H01507 Seronegative arthritis
|
FA2Z Inflammatory arthropathies, unspecified
|
Certain specified joint disorders or deformities of limbs
|
FA30 Acquired deformities of fingers or toes
FA31 Other acquired deformities of limbs
FA32 Disorders of patella
FA33 Internal derangement of knee
FA34 Certain specified joint derangements
FA35 Wear of articular bearing surface of joint prosthesis
FA36 Effusion of joint
FA37 Certain joint disorders, not elsewhere classified
FA38 Arthropathy in diseases classified elsewhere
FA3Z Unspecified joint disorders and deformities of limbs
|
FA5Y Other specified arthropathies
|
FA5Z Arthropathies, unspecified
|
Conditions associated with the spine
|
Structural disorders of spine
|
FA70 Spinal deformities
|
FA71 Torticollis
|
FA72 Disorders of vertebra
|
H01708 Diffuse idiopathic skeletal hyperostosis
|
FA7Y Other specified structural disorders of spine
|
FA7Z Structural disorders of spine, unspecified
|
Degenerative condition of spine
|
FA80 Intervertebral disc degeneration
|
H02539 Intervertebral disc disease
|
FA81 Spondylolysis
|
FA82 Spinal stenosis
|
H01711 Spinal stenosis
|
FA83 Ossification of spinal ligaments
|
H00431 Ossification of the posterior longitudinal ligament of spine
H01707 Ossified ligamentum flavum
|
FA84 Spondylolisthesis
|
FA85 Spinal endplate defects
|
FA8Y Other specified degenerative condition of spine
|
FA8Z Degenerative condition of spine, unspecified
|
Inflammation of spine
|
FA90 Infection of vertebra
|
FA91 Infection of intervertebral disc
|
FA92 Inflammatory spondyloarthritis
|
H01674 Ankylosing spondylitis
|
FA9Y Other specified inflammation of spine
|
FA9Z Inflammation of spine, unspecified
|
Spondylopathies
|
FB00 Ankylosis of spinal joint
FB0Y Other specified spondylopathies
FB0Z Spondylopathies, unspecified
|
FB10 Spinal instabilities
|
FB1Y Other specified conditions associated with the spine
|
FB1Z Conditions associated with the spine, unspecified
|
Soft tissue disorders
|
Disorders of muscles
|
FB30 Infectious myositis
|
FB31 Calcification or ossification of muscle
|
H00441 Progressive osseous heteroplasia
H00430 Fibrodysplasia ossificans progressiva
|
FB32 Certain specified disorders of muscle
|
H02452 Muscle hypertrophy
|
FB33 Secondary disorders of muscle
|
FB3Z Disorders of muscles, unspecified
|
Disorders of synovium or tendon
|
FB40 Tenosynovitis
FB41 Spontaneous rupture of synovium or tendon
FB42 Certain specified disorders of synovium or tendon
FB43 Secondary disorders of synovium or tendon
FB4Y Other specified disorders of synovium or tendon
FB4Z Disorders of synovium or tendon, unspecified
|
Miscellaneous specified soft tissue disorders
|
FB50 Bursitis
FB51 Fibroblastic disorders
FB52 Soft tissue disorders in diseases classified elsewhere
FB53 Shoulder lesions
FB54 Enthesopathies of lower limb
FB55 Certain specified enthesopathies
FB56 Specified soft tissue disorders, not elsewhere classified
|
FB6Z Soft tissue disorders, unspecified
|
Osteopathies or chondropathies
|
FB80 Certain specified disorders of bone density or structure
|
H00501 Fibrous dysplasia, polyostotic
H01774 Hyperostosis corticalis generalisata
H02609 Craniodiaphyseal dysplasia
H02909 Hyperostosis cranialis interna
|
FB81 Osteonecrosis
|
H01709 Glucocorticoid-induced osteonecrosis
|
FB82 Chondropathies
|
H00448 Familial osteochondritis dissecans
H01526 Legg-Calve-Perthes Disease
H01529 Avascular necrosis of femoral head
H01758 Relapsing polychondritis
|
FB83 Low bone mass disorders
|
H01593 Osteoporosis
|
FB84 Osteomyelitis or osteitis
|
FB85 Paget disease of bone
|
H00437 Paget disease of bone
|
FB86 Disorders associated with bone growth
|
H00457 Primary hypertrophic osteoarthropathy
H00472 Torg syndrome
H00614 Hyaline fibromatosis syndrome
H00623 Hajdu-Cheney syndrome
H01865 Multicentric carpotarsal osteolysis syndrome
H02042 Familial expansile osteolysis
H02089 Winchester syndrome
|
FB8Y Other specified osteopathies or chondropathies
|
FB8Z Osteopathies or chondropathies, unspecified
|
FC00 Certain specified acquired deformities of musculoskeletal system or connective tissue, not elsewhere classified
|
FC01 Postprocedural disorders of the musculoskeletal system
|
FC0Y Other specified diseases of the musculoskeletal system or connective tissue
|
FC0Z Diseases of the musculoskeletal system or connective tissue, unspecified
|
|
16 Diseases of the genitourinary system
|
Diseases of the female genital system
|
Inflammatory disorders of the female genital tract
|
GA00 Vulvitis
GA01 Inflammatory disorders of the uterus, except cervix
GA02 Vaginitis
GA03 Diseases of Bartholin gland
GA04 Cervicitis
GA05 Female pelvic inflammatory diseases
GA06 Pelvic peritoneal adhesions of unknown or combined origin
GA07 Salpingitis and oophoritis
GA0Z Inflammatory disorders of the female genital tract, unspecified
|
GA10 Endometriosis
|
H01639 Endometriosis
|
GA11 Adenomyosis
|
Noninflammatory disorders of female genital tract
|
GA12 Dyspareunia
GA13 Acquired abnormalities of vulva or perineum
GA14 Acquired abnormalities of vagina
GA15 Acquired abnormalities of cervix uteri
GA16 Acquired abnormalities of uterus, except cervix
GA17 Acquired abnormalities of fallopian tube
GA18 Acquired abnormalities of ovary
GA19 Acquired abnormalities of broad ligament
GA1Y Other specified noninflammatory disorders of female genital tract
GA1Z Noninflammatory disorders of female genital tract, unspecified
|
Abnormal uterine or vaginal bleeding
|
GA20 Menstrual cycle bleeding disorders
GA21 Nonmenstrual bleeding disorders
GA22 Excessive menstruation with irregular cycle
GA23 Anovulatory bleeding
GA2Y Other specified abnormal uterine or vaginal bleeding
GA2Z Abnormal uterine or vaginal bleeding, unspecified
|
GA30 Menopausal or certain specified perimenopausal disorders
|
H00627 Premature ovarian failure
|
GA31 Female infertility
|
H01897 Oocyte/zygote/embryo maturation arrest
H02335 Preimplantation embryonic lethality
|
GA32 Complications associated with medically assisted reproduction
|
H01039 Ovarian hyperstimulation syndrome
|
GA33 Recurrent pregnancy loss
|
GA34 Female pelvic pain associated with genital organs or menstrual cycle
|
Dermatoses of female genitalia
|
GA40 Inflammatory dermatoses of the vulva
GA41 Ulcerative or erosive disorders of the vulva
GA42 Sensory disturbance of the vulva
GA4Y Other specified dermatoses of female genitalia
|
GA6Y Other specified diseases of the female genital system
|
GA6Z Diseases of the female genital system, unspecified
|
Diseases of the male genital system
|
Dermatoses of male genitalia
|
GA80 Ulcerative disorders of the penis or scrotum
GA81 Miscellaneous dermatoses of male genitalia
|
Diseases of prostate
|
GA90 Hyperplasia of prostate
GA91 Inflammatory and other diseases of prostate
|
GB00 Hydrocele or spermatocele
|
GB01 Torsion of testis, epididymis or appendices
|
GB02 Orchitis or epididymitis
|
GB03 Atrophy of testis
|
GB04 Male infertility
|
H00890 Azoospermia
H01208 Globozoospermia
H01282 Spermatogenic failure
H02534 Y-linked spermatogenic failure
|
GB05 Redundant prepuce, phimosis or paraphimosis
|
GB06 Certain specified disorders of penis
|
GB07 Inflammatory disorders of male genital organs, not elsewhere classified
|
GB08 Vascular disorders of male genital organs
|
GB0Y Other specified diseases of the male genital system
|
GB0Z Diseases of the male genital system, unspecified
|
Disorders of breast
|
GB20 Benign breast disease
GB21 Inflammatory disorders of breast
GB22 Hypertrophy of breast
GB23 Certain specified disorders of breast
GB2Z Disorders of breast, unspecified
|
Diseases of the urinary system
|
Glomerular diseases
|
GB40 Nephritic syndrome
|
H01688 Rapidly progressive glomerulonephritis
|
GB41 Nephrotic syndrome
|
H00576 Pierson syndrome
H01657 Nephrotic syndrome
H01722 Galloway-Mowat syndrome
|
GB42 Persistent proteinuria or albuminuria
|
GB4Y Other specified glomerular diseases
|
H00582 Benign familial hematuria
|
GB4Z Glomerular diseases, unspecified
|
Renal tubulo-interstitial diseases
|
GB50 Acute tubulo-interstitial nephritis
|
GB51 Acute pyelonephritis
|
GB52 Acute tubular necrosis
|
GB53 Acute renal papillary necrosis
|
GB54 Tubulo-interstitial nephritis, not specified as acute or chronic
|
GB55 Chronic tubulo-interstitial nephritis
|
H02577 Karyomegalic interstitial nephritis
|
GB56 Obstructive or reflux nephropathy
|
H01037 Vesicoureteral reflux
|
GB57 Nephrocalcinosis
|
GB58 Pyonephrosis
|
GB59 Renal or perinephric abscess
|
GB5Y Other specified renal tubulo-interstitial diseases
|
GB5Z Renal tubulo-interstitial diseases, unspecified
|
Kidney failure
|
GB60 Acute kidney failure
|
GB61 Chronic kidney disease
|
H01456 Diabetic nephropathy
H02559 Microvascular complications of diabetes
|
GB6Z Kidney failure, unspecified
|
Urolithiasis
|
GB70 Calculus of upper urinary tract
|
H02145 Calcium oxalate nephrolithiasis
H02626 Kalamiella piersonii infection
|
GB71 Calculus of lower urinary tract
|
GB7Z Urolithiasis, unspecified
|
Cystic or dysplastic kidney disease
|
GB80 Nonfamilial nongenetic cystic kidney disease
|
GB81 Autosomal dominant polycystic kidney disease
|
H00542 Polycystic kidney disease
|
GB82 Autosomal dominant tubulointerstitial disease
|
H00541 Autosomal dominant tubulointerstitial kidney disease
H02012 Medullary cystic kidney disease
|
GB83 Nephronophthisis
|
H00537 Nephronophthisis
H00538 Senior-Loken syndrome
|
GB8Y Other specified cystic or dysplastic kidney disease
|
H00542 Polycystic kidney disease
|
GB8Z Cystic or dysplastic kidney disease, unspecified
|
GB90 Certain specified disorders of kidney or ureter
|
H01198 Fanconi renotubular syndrome
H00239 Bartter syndrome
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3)
H00243 Hyperkalemic distal renal tubular acidosis (RTA type 4)
H00428 Distal renal tubular acidosis (RTA type 1)
H00429 Proximal renal tubular acidosis (RTA type 2)
H02310 Renal tubular acidosis
H00888 Nephrolithiasis/osteoporosis, hypophosphatemic
H00252 Congenital nephrogenic diabetes insipidus
H00694 Dent disease
H00948 Renal hypouricemia
H02147 X-linked recessive nephrolithiasis with renal failure
H02148 Low molecular weight proteinuria with hypercalciuria and nephrocalcinosis
H02149 X-linked hypercalciuric nephrolithiasis
|
Certain specified diseases of urinary system
|
GC00 Cystitis
|
H01551 Interstitial cystitis
|
GC01 Other disorders of bladder
|
GC02 Urethritis and urethral syndrome
|
GC03 Urethral stricture
|
GC04 Fistula of the genitourinary tract
|
GC05 Prolapsed urethral mucosa
|
GC06 Urethral diverticulum
|
GC07 Urethral caruncle
|
GC08 Urinary tract infection, site not specified
|
H01176 Uncomplicated urinary tract infection
H00279 Uropathogenic Escherichia coli (UPEC) infection
H01339 Asymptomatic bacteriuria
|
GC0Y Other diseases of urinary system
|
GC2Z Diseases of the urinary system, unspecified
|
Other conditions of the genitourinary system
|
Female pelvic floor dysfunction
|
GC40 Pelvic organ prolapse
GC41 Anorectal dysfunction associated with pelvic organ prolapse
GC42 Sexual dysfunction associated with pelvic organ prolapse
GC4Z Female pelvic floor dysfunction, unspecified
|
GC50 Functional bladder disorders, not otherwise specified
|
GC51 Female Genital Mutilation
|
Postprocedural disorders of genitourinary system
|
GC70 Postoperative adhesions of vagina
GC71 Prolapse of vaginal vault after hysterectomy
GC72 Postprocedural urethral stricture
GC73 Postprocedural pelvic peritoneal adhesions
GC74 Malfunction or complication of external stoma of urinary tract
GC75 Malfunction of the afferent segment of a continent urinary pouch
GC76 Malfunction of the efferent segment of a continent urinary pouch
GC77 Postprocedural nonmenstrual uterine bleeding
GC78 Postprocedural acute female pelvic inflammatory disease
GC79 Disorders of breast reduction
GC7A Disorders of breast augmentation
GC7B Postinterventional ischemia or infarction of kidney
|
GC8Y Other specified diseases of the genitourinary system
|
GC8Z Diseases of the genitourinary system, unspecified
|
|
17 Conditions related to sexual health
|
Sexual dysfunctions
|
HA00 Hypoactive sexual desire dysfunction
HA01 Sexual arousal dysfunctions
HA02 Orgasmic dysfunctions
HA03 Ejaculatory dysfunctions
HA0Y Other specified sexual dysfunctions
HA0Z Sexual dysfunctions, unspecified
|
Sexual pain disorders
|
HA20 Sexual pain-penetration disorder
HA2Y Other specified sexual pain disorders
HA2Z Sexual pain disorders, unspecified
|
HA40 Aetiological considerations in sexual dysfunctions and sexual pain disorders
|
Gender incongruence
|
HA60 Gender incongruence of adolescence or adulthood
HA61 Gender incongruence of childhood
HA6Z Gender incongruence, unspecified
|
HA8Y Other specified conditions related to sexual health
|
HA8Z Conditions related to sexual health, unspecified
|
|
18 Pregnancy, childbirth or the puerperium
|
Abortive outcome of pregnancy
|
JA00 Abortion
|
JA01 Ectopic pregnancy
|
JA02 Molar pregnancy
|
H00289 Recurrent hydatidiform moles
|
JA03 Missed abortion
|
JA04 Blighted ovum or nonhydatidiform mole
|
JA05 Complications following abortion, ectopic or molar pregnancy
|
JA0Z Abortive outcome of pregnancy, unspecified
|
Oedema, proteinuria, or hypertensive disorders in pregnancy, childbirth, or the puerperium
|
JA20 Pre-existing hypertension complicating pregnancy, childbirth or the puerperium
JA21 Pre-eclampsia superimposed on chronic hypertension
JA22 Gestational oedema or proteinuria without hypertension
JA23 Gestational hypertension
JA24 Pre-eclampsia
JA25 Eclampsia
JA2Z Oedema, proteinuria, or hypertensive disorders in pregnancy, childbirth, or the puerperium, unspecified
|
Obstetric haemorrhage
|
JA40 Haemorrhage in early pregnancy
JA41 Antepartum haemorrhage
JA42 Intrapartum haemorrhage
JA43 Postpartum haemorrhage
JA4Z Obstetric haemorrhage, unspecified
|
Certain specified maternal disorders predominantly related to pregnancy
|
JA60 Excessive vomiting in pregnancy
|
JA61 Venous complications in pregnancy
|
JA62 Infections of genitourinary tract in pregnancy
|
JA63 Diabetes mellitus in pregnancy
|
JA64 Malnutrition in pregnancy
|
JA65 Maternal care for other conditions predominantly related to pregnancy
|
H02193 Intrahepatic cholestasis of pregnancy
|
JA66 Clinical findings on antenatal screening of mother
|
JA67 Complications of anaesthesia during pregnancy
|
JA6Z Maternal disorders predominantly related to pregnancy, unspecified
|
Maternal care related to the fetus, amniotic cavity or possible delivery problems
|
JA80 Maternal care related to multiple gestation
JA81 Maternal care related to complications specific to multiple gestation
JA82 Maternal care for known or suspected malpresentation of fetus
JA83 Maternal care for known or suspected disproportion
JA84 Maternal care for known or suspected abnormality of pelvic organs
JA85 Maternal care for known or suspected fetal abnormality or damage
JA86 Maternal care for other known or suspected fetal problems
JA87 Maternal care related to polyhydramnios
JA88 Maternal care related to certain specified disorders of amniotic fluid or membranes
JA89 Maternal care related to premature rupture of membranes
JA8A Maternal care related to placental disorders
JA8B Maternal care related to placenta praevia or low lying placenta
JA8C Maternal care related to premature separation of placenta
JA8D Maternal care related to false labour
JA8E Maternal care related to prolonged pregnancy
JA8Y Maternal care related to other specified fetus, amniotic cavity or possible delivery problems
JA8Z Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems
|
Complications of labour or delivery
|
JB00 Preterm labour or delivery
JB01 Failed induction of labour
JB02 Abnormalities of forces of labour
JB03 Long labour
JB04 Obstructed labour due to malposition or malpresentation of fetus
JB05 Obstructed labour due to maternal pelvic abnormality
JB06 Obstructed labour due to other causes
JB07 Labour or delivery complicated by fetal distress
JB08 Labour or delivery complicated by umbilical cord complications
JB09 Perineal laceration during delivery
JB0A Certain specified obstetric trauma
JB0B Retained placenta or membranes, without haemorrhage
JB0C Complications of anaesthesia during labour or delivery
JB0D Certain specified complications of labour or delivery, not elsewhere classified
JB0Y Other specified complications of labour or delivery
JB0Z Complications of labour or delivery, unspecified
|
Delivery
|
JB20 Single spontaneous delivery
JB21 Single delivery by forceps or vacuum extractor
JB22 Single delivery by caesarean section
JB23 Other assisted single delivery
JB24 Multiple delivery
JB2Z Delivery, unspecified
|
Complications predominantly related to the puerperium
|
JB40 Infections in the puerperium
|
JB41 Venous complications in the puerperium
|
JB42 Obstetric embolism
|
JB43 Complications of anaesthesia during the puerperium
|
JB44 Certain specified complications of the puerperium
|
JB45 Infections of breast associated with childbirth
|
JB46 Certain specified disorders of breast or lactation associated with childbirth
|
H01607 Galactorrhea
|
JB4Z Complications predominantly related to the puerperium, unspecified
|
Certain obstetric conditions, not elsewhere classified
|
JB60 Obstetric death of unspecified cause
JB61 Death from any obstetric cause occurring more than 42 days but less than one year after delivery
JB62 Death from sequelae of obstetric causes
JB63 Maternal infectious diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium
JB64 Certain maternal diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium
JB65 Sequelae of complication of pregnancy, childbirth or the puerperium
JB6Y Other specified obstetric conditions, not elsewhere classified
JB6Z Unspecified obstetric condition
|
|
19 Certain conditions originating in the perinatal period
|
Fetus or newborn affected by maternal factors or by complications of pregnancy, labour or delivery
|
KA00 Fetus or newborn affected by maternal conditions that may be unrelated to present pregnancy
KA01 Fetus or newborn affected by maternal complications of pregnancy
KA02 Fetus or newborn affected by complications of placenta
KA03 Fetus or newborn affected by complications of umbilical cord
KA04 Fetus or newborn affected by other abnormalities of membranes
KA05 Fetus or newborn affected by certain complications of labour or delivery
KA06 Fetus or newborn affected by noxious influences transmitted via placenta or breast milk
KA07 Neonatal dermatoses due to maternal antibodies
KA0Z Fetus or newborn affected by unspecified maternal factors or by complications of pregnancy, labour or delivery
|
Disorders of newborn related to length of gestation or fetal growth
|
KA20 Disorders of newborn related to slow fetal growth or fetal malnutrition
KA21 Disorders of newborn related to short gestation or low birth weight, not elsewhere classified
KA22 Disorders of newborn related to long gestation or high birth weight
KA2Y Other specified disorders of newborn related to length of gestation or fetal growth
KA2Z Disorders of newborn related to length of gestation or fetal growth, unspecified
|
Birth injury
|
KA40 Birth injury to central nervous system
KA41 Birth injury to eye
KA42 Birth injury to scalp
KA43 Birth injury to skin or soft tissues
KA44 Birth injury to peripheral nervous system
KA45 Birth injury to skeleton
KA46 Birth injury to other organs
KA4Z Birth injury, unspecified
|
Infections of the fetus or newborn
|
KA60 Sepsis of fetus or newborn
KA61 Other bacterial infections of the fetus or newborn
KA62 Viral infection in the fetus or newborn
KA63 Fungal infection of fetus or newborn
KA64 Parasitic diseases in the fetus or newborn
KA65 Neonatal infections of certain specified sites
KA6Y Other specified infections of the fetus or newborn
KA6Z Infections of the fetus or newborn, unspecified
|
Haemorrhagic or haematological disorders of fetus or newborn
|
KA80 Fetal blood loss
|
KA81 Umbilical haemorrhage of newborn
|
KA82 Intracranial nontraumatic haemorrhage of fetus or newborn
|
KA83 Certain specified neonatal haemorrhages
|
KA84 Haemolytic disease of fetus or newborn
|
H02799 Rh-induced hemolytic disease of the fetus and newborn
|
KA85 Hydrops fetalis due to haemolytic disease
|
KA86 Neonatal kernicterus
|
KA87 Neonatal hyperbilirubinaemia
|
H02152 Transient familial neonatal hyperbilirubinemia
|
KA88 Disseminated intravascular coagulation of fetus or newborn
|
KA89 Transient neonatal thrombocytopaenia
|
KA8A Polycythaemia neonatorum
|
KA8B Anaemia of prematurity
|
KA8C Congenital hypoplastic anaemia
|
KA8D Transient neonatal neutropaenia
|
KA8E Alloimmune neonatal neutropaenia
|
KA8F Neonatal vitamin K deficiency
|
KA8Y Other specified haemorrhagic or haematological disorders of fetus or newborn
|
KA8Z Haemorrhagic or haematological disorders of fetus or newborn, unspecified
|
Neurological disorders specific to the perinatal or neonatal period
|
KB00 Neonatal cerebral ischaemia
|
KB01 Periventricular cysts of newborn
|
KB02 Neonatal cerebral leukomalacia
|
KB03 Neonatal encephalopathy
|
H01211 MECP2-related severe neonatal encephalopathy
|
KB04 Hypoxic ischaemic encephalopathy of newborn
|
KB05 Neonatal hydrocephalus
|
KB06 Neonatal seizures
|
KB07 Compression of brain in neonate
|
KB08 Disorders of muscle tone of newborn
|
KB0Y Other specified neurological disorders specific to the perinatal or neonatal period
|
KB0Z Neurological disorders specific to the perinatal or neonatal period, unspecified
|
Respiratory disorders specific to the perinatal or neonatal period
|
KB20 Intrauterine hypoxia
KB21 Birth asphyxia
KB22 Metabolic acidaemia in newborn
KB23 Respiratory distress of newborn
KB24 Congenital pneumonia
KB25 Neonatal tracheitis
KB26 Neonatal aspiration syndromes
KB27 Pulmonary air leak or related conditions originating in the perinatal period
KB28 Pulmonary haemorrhage originating in the perinatal period
KB29 Chronic respiratory disease originating in the perinatal period
KB2A Apnoea of newborn
KB2B Primary atelectasis of newborn
KB2C Cyanotic attacks of newborn
KB2D Respiratory failure of newborn
KB2E Respiratory arrest of newborn
KB2F Congenital lung or lobar atelectasis
KB2G Tracheal haemorrhage of newborn due to airway trauma
KB2H Acquired vocal cord paralysis in newborn
KB2J Airway obstruction in the neonate due to airway abnormality
KB2K Pulmonary cysts in newborn
KB2Y Other specified respiratory disorders specific to the perinatal or neonatal period
KB2Z Respiratory disorders specific to the perinatal or neonatal period, unspecified
|
Cardiovascular disorders present in the perinatal or neonatal period
|
KB40 Neonatal cardiac failure
KB41 Cardiac arrhythmias in the neonate
KB42 Persistent pulmonary hypertension of the newborn
KB44 Transient myocardial ischaemia of newborn
KB45 Neonatal hypertension
KB46 Neonatal hypotension
KB47 Benign or innocent cardiac murmurs in newborn
KB48 Patent arterial duct of prematurity
KB4Y Other specified cardiovascular disorders present in the perinatal or neonatal period
KB4Z Cardiovascular disorders present in the perinatal or neonatal period, unspecified
|
Transitory endocrine or metabolic disorders specific to fetus or newborn
|
KB60 Transitory disorders of carbohydrate metabolism specific to fetus or newborn
|
H00513 Transient neonatal diabetes mellitus
H00512 Permanent neonatal diabetes mellitus
H01377 Mitchell-Riley syndrome
|
KB61 Transitory neonatal disorders of calcium or magnesium metabolism
|
KB62 Transitory neonatal disorders of thyroid function
|
KB63 Certain specified transitory neonatal electrolyte or metabolic disturbances
|
KB64 Transitory neonatal hypoparathyroidism
|
KB6Z Transitory endocrine or metabolic disorders specific to fetus or newborn, unspecified
|
Digestive system disorders of fetus or newborn
|
KB80 Gastro-oesophageal reflux disease in newborn
|
KB81 Oesophagitis in newborn
|
KB82 Prenatal gastric perforation
|
KB83 Postnatal gastric perforation
|
KB84 Postnatal isolated ileal perforation
|
KB85 Prenatal intrauterine intestinal perforation
|
KB86 Postnatal intestinal perforation
|
KB87 Intestinal obstruction of newborn
|
KB88 Necrotising enterocolitis of newborn
|
KB89 Neonatal malabsorption syndromes
|
H01469 Short bowel syndrome
H01477 Congenital short bowel syndrome
|
KB8A Neonatal haematemesis or melaena due to swallowed maternal blood
|
KB8B Neonatal peritonitis
|
KB8C Noninfectious neonatal diarrhoea
|
H01174 Congenital diarrhea
|
KB8Y Other specified digestive system disorders of fetus or newborn
|
H02730 Severe congenital liver disease
|
KB8Z Digestive system disorders of fetus or newborn, unspecified
|
Genitourinary system disorders specific to the perinatal or neonatal period
|
KC00 Congenital hydrocele
KC01 Congenital renal failure
KC0Y Other specified genitourinary system disorders specific to the perinatal or neonatal period
KC0Z Genitourinary system disorders specific to the perinatal or neonatal period, unspecified
|
Disorders involving the integument of fetus or newborn
|
KC20 Conditions involving the umbilical cord
|
KC21 Inflammatory dermatoses of the newborn
|
KC22 Neonatal disorders of subcutaneous fat
|
KC23 Neonatal disorders of the oral mucosa
|
KC24 Neonatal nutritional disorders affecting the skin
|
Skin disorders associated with prematurity
|
KC30 Skin fragility of prematurity
KC31 Congenital erosive or vesicular dermatosis healing with reticulated supple scarring
KC3Y Other specified skin disorders associated with prematurity
|
KC40 Miscellaneous skin disorders in the neonate
|
KC41 Miscellaneous specified conditions of integument specific to fetus or newborn
|
Iatrogenic injuries involving the skin of the neonate
|
Postnatal iatrogenic skin injury
|
KC50 Neonatal phototherapy burn
KC5Y Other specified postnatal iatrogenic skin injury
KC5Z Postnatal iatrogenic skin injury, unspecified
|
KC7Y Other specified iatrogenic injuries involving the skin of the neonate
|
KC9Z Disorders involving the integument of fetus or newborn, unspecified
|
Disturbances of temperature regulation of newborn
|
KD10 Environmental hyperthermia of newborn
KD11 Fever of newborn
KD12 Hypothermia of newborn
KD1Y Other specified disturbances of temperature regulation of newborn
KD1Z Disturbances of temperature regulation of newborn, unspecified
|
Certain disorders originating in the perinatal period
|
KD30 Birth depression
KD31 Wide cranial sutures of newborn
KD32 Feeding problems of newborn
KD33 Jittery baby, not elsewhere classified
KD34 Reactions or intoxications due to drugs administered to fetus or newborn
KD35 Neonatal withdrawal syndrome from maternal use of drugs of addiction
KD36 Withdrawal symptoms from therapeutic use of drugs in newborn
KD37 Exposure to tobacco smoke in the perinatal period
KD38 Meconium staining
KD39 Complications of intrauterine procedures, not elsewhere classified
KD3A Termination of pregnancy, affecting surviving fetus or newborn
KD3B Fetal death, cause not specified
KD3C Vomiting in newborn
KD3Y Other specified disorders originating in the perinatal period
|
KD5Z Conditions originating in the perinatal or neonatal period, unspecified
|
|
20 Developmental anomalies
|
Structural developmental anomalies primarily affecting one body system
|
Structural developmental anomalies of the nervous system
|
LA00 Anencephaly or similar anomalies
|
H02120 Anencephaly
|
LA01 Cephalocele
|
LA02 Spina bifida
|
H00262 Neural tube defects, folate-sensitive
H02563 Neural tube defects
|
LA03 Arnold-Chiari malformation type II
|
H01561 Chiari malformation
|
LA04 Congenital hydrocephalus
|
H01677 Congenital hydrocephalus
H02458 Hydrocephalus due to congenital stenosis of aqueduct of Sylvius
|
LA05 Cerebral structural developmental anomalies
|
H00269 Primary microcephaly
H01833 Hemimegalencephaly
H02446 Autosomal recessive macrocephaly/megalencephaly syndrome
H00267 Holoprosencephaly
H00263 Acrocallosal syndrome
H01835 Neuronal migration disorder
H00271 Polymicrogyria
H01251 Focal cortical dysplasia of Taylor
H01881 Complex cortical dysplasia with other brain malformations
H00270 Periventricular nodular heterotopia
H00839 Porencephaly
H01160 Schizencephaly
H01870 Microhydranencephaly
H02501 Occipital cortical malformation
|
LA06 Cerebellar structural developmental anomalies
|
H01678 Dandy-Walker syndrome
|
LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column
|
H01675 Syringomyelia
H01561 Chiari malformation
H01893 Lateral meningocele syndrome
|
LA0Y Other specified structural developmental anomalies of the nervous system
|
H02494 Alkuraya-Kucinskas syndrome
|
LA0Z Structural developmental anomalies of the nervous system, unspecified
|
Structural developmental anomalies of the eye, eyelid or lacrimal apparatus
|
LA10 Structural developmental anomalies of ocular globes
|
H01027 Microphthalmia
H02172 Nanophthalmos
|
LA11 Structural developmental anomalies of the anterior segment of eye
|
H01114 Ocular coloboma
H01029 Cornea plana congenita
H02104 Megalocornea
H00620 Axenfeld-Rieger syndrome
H01159 Anterior segment dysgenesis
H00635 Aniridia
H00961 Posterior polymorphous corneal dystrophy
H01075 Peters anomaly
|
LA12 Structural developmental anomalies of lens or zonula
|
H00676 Congenital primary aphakia
H00662 Ectopia lentis
|
LA13 Structural developmental anomalies of the posterior segment of eye
|
H02112 Persistent hyperplastic primary vitreous
H00589 Familial exudative vitreoretinopathy
H02475 Retinoschisis
H02880 Retinal arterial tortuosity
H02203 Optic nerve hypoplasia
H02270 Cavitary optic disc anomalies
H01256 Foveal hypoplasia
H02231 Optic disc anomalies with retinal and/or macular dystrophy
|
LA14 Structural developmental anomalies of eyelid, lacrimal apparatus or orbit
|
H02852 Unilateral or bilateral isolated cryptophthalmos
H00677 Aplasia of lacrimal and salivary glands
H02514 Lacrimal duct defect
|
LA1Y Other specified structural developmental anomalies of the eye, eyelid or lacrimal apparatus
|
H02882 Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma
|
LA1Z Structural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecified
|
Structural developmental anomalies of the ear
|
LA20 Structural anomaly of eustachian apparatus
|
LA21 Minor anomalies of pinnae
|
LA22 Structural developmental anomalies of ear causing hearing impairment
|
H02115 Congenital aural atresia
|
LA23 Otocephaly
|
H02118 Agnathia-otocephaly complex
|
LA24 Accessory auricle
|
LA2Y Other specified structural developmental anomalies of the ear
|
LA2Z Structural developmental anomalies of the ear, unspecified
|
Structural developmental anomalies of the face, mouth or teeth
|
LA30 Structural developmental anomalies of teeth and periodontal tissues
|
H00625 Tooth agenesis
H00652 Solitary median maxillary central incisor syndrome
H00615 Amelogenesis imperfecta
H00618 Amelogenesis imperfecta hypoplastic-hypomaturation with taurodontism
H01015 Jalili syndrome
H02348 Dentin dysplasia
H00432 Hereditary dentine disorders
|
LA31 Structural developmental anomalies of mouth or tongue
|
Clefts of lip, alveolus or palate
|
LA40 Cleft lip
|
LA41 Cleft lip and alveolus
|
LA42 Cleft palate
|
LA4Y Other specified clefts of lip, alveolus or palate
|
LA4Z Clefts of lip, alveolus or palate, unspecified
|
LA50 Congenital velopharyngeal incompetence
|
LA51 Facial clefts
|
H02202 Oblique facial cleft
|
LA52 Facial asymmetry
|
LA53 Macrocheilia
|
LA54 Microcheilia
|
LA55 Compression facies
|
LA56 Pierre Robin syndrome
|
LA5Y Other specified structural developmental anomalies of the face
|
LA5Z Structural developmental anomalies of the face, unspecified
|
Structural developmental anomalies of the neck
|
LA60 Webbed neck
LA61 Congenital sternomastoid tumour
LA62 Congenital torticollis
LA6Y Other specified structural developmental anomalies of the neck
LA6Z Structural developmental anomalies of the neck, unspecified
|
Structural developmental anomalies of the respiratory system
|
LA70 Structural developmental anomalies of the nose or cavum
|
H01017 Choanal atresia and lymphedema
|
LA71 Structural developmental anomalies of larynx
|
LA72 Laryngotracheooesophageal cleft
|
LA73 Structural developmental anomalies of trachea
|
H02600 Congenital tracheal stenosis
|
LA74 Structural developmental anomalies of bronchi
|
LA75 Structural developmental anomalies of lungs
|
H02906 Polycystic lung disease
H00564 Primary ciliary dyskinesia
|
LA76 Structural developmental anomalies of pleura
|
LA77 Congenital cyst of mediastinum
|
LA7Y Other specified structural developmental anomalies of the respiratory system
|
LA7Z Structural developmental anomalies of the respiratory system, unspecified
|
Structural developmental anomalies of the circulatory system
|
Structural developmental anomaly of heart or great vessels
|
LA80 Anomalous position-orientation of heart
|
LA81 Abnormal ventricular relationships
|
LA82 Total mirror imagery
|
LA83 Right isomerism
|
LA84 Left isomerism
|
LA85 Congenital anomaly of an atrioventricular or ventriculo-arterial connection
|
LA86 Congenital anomaly of mediastinal vein
|
LA87 Congenital anomaly of an atrioventricular valve or atrioventricular septum
|
LA88 Congenital anomaly of a ventricle or the ventricular septum
|
LA89 Functionally univentricular heart
|
LA8A Congenital anomaly of a ventriculo-arterial valve or adjacent regions
|
LA8B Congenital anomaly of great arteries including arterial duct
|
LA8C Congenital anomaly of coronary artery
|
LA8D Congenital pericardial anomaly
|
LA8E Congenital anomaly of atrial septum
|
LA8F Congenital anomaly of right atrium
|
LA8G Congenital anomaly of left atrium
|
LA8Y Other specified structural developmental anomaly of heart or great vessels
|
LA8Z Structural developmental anomaly of heart or great vessels, unspecified
|
LA90 Structural developmental anomalies of the peripheral vascular system
|
H00533 Hereditary hemorrhagic telangiectasia
H00531 Venous malformations
H01849 Peripheral arteriovenous malformation
H02043 Capillary malformation-arteriovenous malformation
|
LA9Y Other specified structural developmental anomalies of the circulatory system
|
LA9Z Structural developmental anomalies of the circulatory system, unspecified
|
Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord
|
LB00 Structural developmental anomalies of diaphragm
|
H01241 Congenital diaphragmatic hernia
|
LB01 Omphalocele
|
LB02 Gastroschisis
|
LB03 Structural developmental anomalies of umbilical cord
|
LB0Y Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord
|
LB0Z Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord, unspecified
|
Structural developmental anomalies of the digestive tract
|
LB10 Structural developmental anomalies of salivary glands or ducts
|
LB11 Congenital diverticulum of pharynx
|
LB12 Structural developmental anomalies of oesophagus
|
LB13 Structural developmental anomalies of stomach
|
LB14 Structural developmental anomalies of duodenum
|
LB15 Structural developmental anomalies of small intestine
|
LB16 Structural developmental anomalies of large intestine
|
H00910 Hirschsprung disease
H01871 Isolated hypoganglionosis
|
LB17 Structural developmental anomalies of anal canal
|
H01858 Persistent cloaca
H01856 Cloacal exstrophy
|
LB18 Congenital anomalies of intestinal fixation
|
LB1Y Other specified structural developmental anomalies of the digestive tract
|
H02331 Gastrointestinal defects and immunodeficiency syndrome
|
LB1Z Structural developmental anomalies of the digestive tract, unspecified
|
Structural developmental anomalies of the liver, biliary tract, pancreas or spleen
|
LB20 Structural developmental anomalies of gallbladder, bile ducts or liver
|
H01855 Biliary atresia
H00551 Alagille syndrome
|
LB21 Structural developmental anomalies of pancreas
|
H00861 Pancreatic agenesis
|
LB22 Structural developmental anomalies of spleen
|
H01435 Congenital asplenia
|
LB2Y Other specified structural developmental anomalies of the liver, biliary tract, pancreas or spleen
|
LB2Z Structural developmental anomalies of the liver, biliary tract, pancreas or spleen, unspecified
|
Structural developmental anomalies of the urinary system
|
LB30 Structural developmental anomalies of kidneys
|
H01867 Congenital anomalies of kidney and urinary tract
H00822 Renal hypodysplasia and aplasia
H00575 Renal tubular dysgenesis
|
LB31 Structural developmental anomalies of urinary tract
|
H01867 Congenital anomalies of kidney and urinary tract
H02495 Congenital megabladder
|
LB3Y Other specified structural developmental anomalies of the urinary system
|
H02796 Autonomic bladder dysfunction with impaired pupillary reflex and secondary CAKUT
|
LB3Z Structural developmental anomalies of the urinary system, unspecified
|
Structural developmental anomalies of the female genital system
|
LB40 Structural developmental anomalies of vulva
|
LB41 Structural developmental anomalies of clitoris
|
LB42 Structural developmental anomalies of vagina
|
LB43 Structural developmental anomalies of cervix uteri
|
LB44 Structural developmental anomalies of uterus, except cervix
|
H00600 Mullerian agenesis
|
LB45 Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments
|
H00599 Ovarian dysgenesis
|
LB4Y Other specified structural developmental anomalies of the female genital system
|
LB4Z Structural developmental anomalies of the female genital system, unspecified
|
Structural developmental anomalies of the male genital system
|
LB50 Micropenis or penis agenesis
|
LB51 Anorchia or microorchidia
|
LB52 Cryptorchidism
|
H02176 Cryptorchidism
|
LB53 Hypospadias
|
H02175 Hypospadias
|
LB54 Congenital chordee
|
LB55 Epispadias
|
LB56 Bifid scrotum
|
LB57 Agenesis of vas deferens
|
H01033 Congenital bilateral absence of vas deferens
|
LB58 Polyorchidism
|
LB59 Hypoplasia of testis or scrotum
|
LB5Y Other specified structural developmental anomalies of the male genital system
|
LB5Z Structural developmental anomalies of the male genital system, unspecified
|
Structural developmental anomalies of the breast
|
LB60 Breast aplasia
|
LB61 Absent nipple
|
LB62 Supernumerary breasts
|
LB63 Accessory nipple
|
LB6Y Other specified structural developmental anomalies of the breast
|
H02811 Aplasia or hypoplasia of the breasts and/or nipples
|
LB6Z Structural developmental anomalies of the breast, unspecified
|
Structural developmental anomalies of the skeleton
|
LB70 Structural developmental anomalies of cranium
|
H02160 Craniosynostoses
H01207 Trigonocephaly
H00475 Enlarged parietal foramina/cranium bifidum
H01105 Cranio-lenticulo-sutural dysplasia
|
LB71 Structural developmental anomalies of facial bones
|
LB72 Structural developmental anomalies of shoulder girdle
|
LB73 Structural developmental anomalies of spine or bony thorax
|
H01851 Congenital scoliosis associated with rib anomalies
H00852 Klippel-Feil syndrome
|
LB74 Structural developmental anomalies of pelvic girdle
|
H01817 Beukes hip dysplasia
H02816 Developmental dysplasia of the hip
|
LB75 Brachydactyly
|
H00482 Brachydactyly
|
LB76 Triphalangeal thumb
|
LB77 Hyperphalangy
|
LB78 Polydactyly
|
H01226 Polysyndactyly
H01852 Postaxial polydactyly
H02332 Preaxial polydactyly
|
LB79 Syndactyly
|
H01095 Syndactyly
H00459 Synpolydactyly
H01854 Metacarpal 4-5 fusion
|
Congenital deformities of fingers or toes
|
LB80 Congenital deformities of fingers
|
LB81 Congenital deformities of toes
|
LB90 Joint formation defects
|
H00484 Multiple synostosis syndrome
H00851 Proximal symphalangism
|
LB91 Congenital shoulder dislocation
|
LB92 Congenital elbow dislocation
|
LB93 Congenital knee dislocation
|
LB94 Congenital patella dislocation
|
LB95 Patella aplasia or hypoplasia
|
LB96 Congenital bowing of long bones
|
LB97 Limb overgrowth
|
H02647 Macrodactyly
|
LB98 Congenital deformities of feet
|
H00903 Congenital clubfoot
H00929 Congenital vertical talus
|
LB99 Reduction defects of upper limb
|
H00471 Split-hand/foot malformation
|
LB9A Reduction defects of lower limb
|
H00471 Split-hand/foot malformation
|
LB9B Reduction defects of upper and lower limbs
|
H00629 Acheiropodia
H00636 Tetra-amelia syndrome
|
LB9Y Other specified structural developmental anomalies of the skeleton
|
H00873 Cousin syndrome
|
LB9Z Structural developmental anomalies of the skeleton, unspecified
|
H00762 Spondyloepiphyseal dysplasia with congenital joint dislocations
|
Structural developmental anomalies of the skin
|
Developmental hamartomata of the epidermis and epidermal appendages
|
LC00 Keratinocytic epidermal hamartoma
|
LC01 Pilosebaceous hamartoma
|
LC02 Complex epidermal hamartoma
|
LC0Y Other specified developmental hamartomata of the epidermis and epidermal appendages
|
Developmental anomalies of skin pigmentation
|
LC10 Dermal melanocytosis
LC1Y Other specified developmental anomalies of skin pigmentation
|
Hamartomata derived from dermal connective tissue
|
LC20 Connective tissue hamartoma
LC2Y Other specified hamartomata derived from dermal connective tissue
|
Developmental defects of hair or nails
|
LC30 Developmental defects of hair or hair growth
LC31 Developmental defects of the nail apparatus
|
LC40 Dermoid cyst
|
Developmental anomalies of cutaneous vasculature
|
LC50 Developmental capillary vascular malformations of the skin
|
LC51 Developmental venous malformations involving the skin
|
LC52 Complex or combined developmental vascular malformations involving the skin
|
LC5Y Other specified developmental anomalies of cutaneous vasculature
|
LC5Z Developmental anomalies of cutaneous vasculature, unspecified
|
Congenital anomalies of skin development
|
LC60 Aplasia cutis congenita
|
LC7Y Other specified structural developmental anomalies of the skin
|
H02295 Adermatoglyphia
|
LC7Z Structural developmental anomalies of the skin, unspecified
|
Structural developmental anomalies of the adrenal glands
|
LC80 Congenital adrenal hypoplasia
|
H01772 Adrenal hypoplasia, congenital
|
LC8Y Other specified structural developmental anomalies of the adrenal glands
|
LC8Z Structural developmental anomalies of the adrenal glands, unspecified
|
LD0Y Other specified structural developmental anomalies primarily affecting one body system
|
LD0Z Structural developmental anomalies primarily affecting one body system, unspecified
|
Multiple developmental anomalies or syndromes
|
LD20 Syndromes with central nervous system anomalies as a major feature
|
H00530 Joubert syndrome and related disorders
H00897 Pontocerebellar hypoplasia
H01001 COACH syndrome
H01811 Arima syndrome
H02272 CAPOS syndrome
H02431 Cerebellar hypoplasia, epilepsy, and global developmental delay
H02464 Poretti-Boltshauser syndrome
H02833 Brain malformation renal syndrome
H00268 Lissencephaly
H00792 Warburg micro syndrome
H02117 Neu-Laxova syndrome
H00616 Bowen-Conradi syndrome
H00840 Pseudo-TORCH syndrome
H00990 Microcephaly, Amish type
H00991 Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II)
H00993 Microcephalic osteodysplastic primordial dwarfism, type I (MOPD I)
H01872 Microcephaly-capillary malformation syndrome
H01876 Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
H01921 MICPCH syndrome
H02132 Microcephaly syndrome
H02282 Spastic tetraplegia, thin corpus callosum, and progressive microcephaly
H02461 Neurodevelopmental disorder with microcephaly
H02492 Microcephaly, growth restriction, and increased sister chromatid exchange
H02668 Heyn-Sproul-Jackson syndrome
H02707 Khan-Khan-Katsanis syndrome
H02708 Baralle-Macken syndrome
H02709 Neurodevelopmental disorder with aminoacyl-tRNA synthetase defect
H02726 Kaya-Barakat-Masson syndrome
H02808 Childhood-onset neurodegeneration with progressive microcephaly
H02881 Jawad syndrome
H00544 Septo-optic dysplasia
H00816 Agenesis of the corpus callosum with peripheral neuropathy
H01034 L1 syndrome
H01035 Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia
H01776 Aicardi syndrome
H01789 You-Hoover-Fong syndrome
H01919 Proud syndrome
H01937 Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly
H02366 Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome
H02396 Corpus callosum agenesis with facial anomalies and cerebellar ataxia
H02487 Diencephalic-mesencephalic junction dysplasia syndrome
H02519 Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
H02606 Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
H02645 Cerebellar atrophy with seizures and variable developmental delay
H02652 Macrocephaly, acquired, with impaired intellectual development
H02653 Faundes-Banka syndrome
H02675 Ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features
H02680 Neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities
H02695 Fibrosis, neurodegeneration, and cerebral angiomatosis
H02723 Macrocephaly/autism syndrome
H02745 Neuromuscular oculoauditory syndrome
H02776 Ventriculomegaly and arthrogryposis
H02785 Band heterotopia
H02825 Megalencephaly-polydactyly syndrome
H02839 Infantile-onset neurodegeneration with optic atrophy and brain abnormalities
H02840 Morimoto-Ryu-Malicdan neuromuscular syndrome
H02925 Early-childhood-onset neurodegeneration with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy
|
LD21 Syndromes with eye anomalies as a major feature
|
H01904 Microphthalmia with linear skin defects syndrome
H02134 Microphthalmia with limb anomalies
H02170 Microphthalmia, syndromic
H00673 Weill-Marchesani syndrome
H00826 Blepharophimosis-ptosis-epicanthus inversus syndrome
H01012 Oculo-auricular syndrome
H02045 Norrie disease
H02292 Retinal dystrophy, juvenile cataracts, and short stature syndrome
H02422 Retinitis pigmentosa with skeletal anomalies
H02445 Microcornea, myopic chorioretinal atrophy, and telecanthus
H02655 Retinal dystrophy and microvillus inclusion disease
H02794 Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma
|
LD22 Syndromes with dental anomalies as a major feature
|
LD23 Syndromes with vascular anomalies as a major feature
|
H00579 Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps (HANAC)
H01809 Sturge-Weber syndrome
H02088 Primary intraosseous vascular malformation
|
LD24 Syndromes with skeletal anomalies as a major feature
|
H00520 Type II collagenopathies
H00505 FGFR3-related short limb skeletal dysplasia
H01749 Achondroplasia
H02069 SADDAN
H02068 Hypochondroplasia
H01750 Thanatophoric dysplasia
H00515 Atelosteogenesis type II
H02063 Diastrophic dysplasia
H00207 Rhizomelic chondrodysplasia punctata
H00447 HEM skeletal dysplasia
H00496 Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD)
H01194 X-linked chondrodysplasia punctata
H00436 Osteopetrosis
H00452 Buschke-Ollendorff syndrome
H00434 Camurati-Engelmann disease
H00444 Osteopathia striata with cranial sclerosis
H00450 Worth type autosomal dominant osteosclerosis
H00486 Sclerosteosis
H00490 Diaphyseal dysplasia with anemia
H00491 Craniometaphyseal dysplasia
H00508 Blomstrand syndrome
H00613 Infantile cortical hyperostosis
H00968 Raine syndrome
H01832 Lenz-Majewski syndrome
H02631 Melorheostosis
H02735 Diaphyseal medullary stenosis with malignant fibrous histiocytoma
H00122 Multiple exostoses
H00493 Heparan sulfate proteoglycan gene defects
H00497 Cherubism
H02127 Yunis-Varon syndrome
H00443 Osteoglophonic dysplasia
H00498 Gnathodiaphyseal dysplasia
H00521 Cleidocranial dysplasia
H01018 Metachondromatosis
H02558 Craniotubular dysplasia, Ikegawa type
H00445 Osteoarthritis with mild chondrodysplasia
H00474 Schneckenbecken dysplasia
H00483 Angel shaped phalangoepiphyseal dysplasia
H00499 Spondylocarpotarsal synostosis syndrome
H00519 Spondyloepiphyseal dysplasia congenita
H00757 Dyggve-Melchior-Clausen disease
H00758 Progressive pseudorheumatoid dysplasia
H00760 Spondyloepiphyseal dysplasia tarda
H00761 SEMD, Pakistani type
H00765 Spondyloepiphyseal dysplasia, Kimberley type
H00767 SEMD, Matrilin type
H00777 SEMD, short limb-hand type
H00863 Spondylo-megaepiphyseal-metaphyseal dysplasia
H01494 SEMD with joint laxity type
H01575 Roifman syndrome
H01576 Spondyloenchondrodysplasia with immune dysregulation (SPENCDI)
H01967 Anauxetic dysplasia
H02070 Kniest dysplasia
H02071 Czech dysplasia
H02079 Oto-spondylo-megaepiphyseal dysplasia
H02080 Fibrochondrogenesis
H02155 Dyssegmental dysplasia
H02183 Parastremmatic dwarfism
H02184 Metatropic dysplasia
H02186 Spondyloepiphyseal dysplasia, Maroteaux type
H02187 Spondyloepimetaphyseal dysplasia
H02462 Spondyloepiphyseal dysplasia
H02497 Smith-McCort dysplasia
H01821 Spondylometaphyseal dysplasia with cone-rod dystrophy
H01825 Spondylometaphyseal dysplasia, Sedaghatian type
H01830 Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type
H02185 Spondylometaphyseal dysplasia
H02732 Rhizomelic skeletal dysplasia with or without Pelger-Huet anomaly
H00678 Achondrogenesis type IA
H02065 Achondrogenesis type IB
H02066 Achondrogenesis type II
H00522 Brachyolmia
H01828 Opsismodysplasia
H01844 Diaphanospondylodysostosis
H00495 Eiken dysplasia
H00477 Pseudoachondroplasia
H00476 Multiple epiphyseal dysplasia
H02436 Al-Gazali syndrome
H02871 Lowry-Wood syndrome
H00479 Metaphyseal dysplasias
H00518 Metaphyseal dysplasia without hypotrichosis
H02823 Osteosclerotic metaphyseal dysplasia
H00675 Acrocapitofemoral dysplasia
H00900 Geleophysic dysplasia
H02062 Familial digital arthropathy-brachydactyly
H02228 Acromicric dysplasia
H02229 Terminal osseous dysplasia
H00466 Grebe dysplasia
H00468 Acromesomelic dysplasia, Demirhan type
H00470 Acromesomelic dysplasia, Maroteaux type
H02543 Acromesomelic dysplasia
H02786 ENDOVE syndrome
H00485 Robinow syndrome
H00492 SHOX-related short stature
H02154 Omodysplasia
H02743 KINSSHIP syndrome
H02157 Short-rib thoracic dysplasia
H00511 Short rib-polydactyly syndrome
H00751 Asphyxiating thoracic dystrophy
H00462 Stuve-Wiedemann syndrome
H02629 Bent bone dysplasia syndrome
H02873 Kyphomelic dysplasia
H00509 3M syndrome
H00619 Kenny-Caffey syndrome
H00622 Hypoparathyroidism-retardation-dysmorphism syndrome
H00992 Seckel syndrome
H02223 Osteocraniostenosis
H00494 Desbuquois syndrome
H01498 Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
H02048 Larsen syndrome
H02064 Atelosteogenesis type I and III
H02067 Boomerang dysplasia
H00458 Syndromic craniosynostoses
H01756 Pfeiffer syndrome
H01754 Crouzon syndrome
H01755 Apert syndrome
H01008 C syndrome
H01753 Antley-Bixler syndrome
H01888 Carpenter syndrome
H01988 Jackson-Weiss syndrome
H01989 Beare-Stevenson syndrome
H01990 Muenke syndrome
H01991 Saethre-Chotzen syndrome
H01992 Craniofrontonasal syndrome
H01993 Baller-Gerold syndrome
H02047 Bohring-Opitz syndrome
H02254 Craniosynostosis and dental anomalies
H02637 Brachycephaly, trichomegaly, and developmental delay
H02766 Radiohumeral fusions with other skeletal and craniofacial anomalies
H02853 Teebi hypertelorism syndrome
H00517 Spondylocostal dysostosis
H01843 Cerebrocostomandibular syndrome
H00464 Nail-patella syndrome
H00461 Ischiocoxopodopatellar syndrome
H01889 Meier-Gorlin syndrome
H00506 Osteogenesis imperfecta
H00451 Osteoporosis-pseudoglioma syndrome
H00514 Bruck syndrome
H01496 Spondyloocular syndrome
H01571 Singleton-Merten syndrome
H01572 Cole-Carpenter syndrome
H02395 Calvarial doughnut lesions with bone fragility
H00969 Skeletal defects, genital hypoplasia, and mental retardation
H02233 Alazami syndrome
H02280 Complex lethal osteochondrodysplasia
H02300 Steel syndrome
H02306 Chondrodysplasia with joint dislocations, GPAPP type
H02349 Odontochondrodysplasia
H02415 Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
H02551 Skeletal dysplasia with joint laxity and advanced bone age
H02742 Congenital neuromuscular disorder with dysmorphic facies
H02801 Osteochondrodysplasia, brachydactyly, and overlapping malformed digits
|
LD25 Syndromes with face or limb anomalies as a major feature
|
H00454 Oral-facial-digital syndrome
H00456 Fronto-otopalatodigital syndromes
H01816 Frank-ter Haar syndrome
H02227 Frontometaphyseal dysplasia
H01376 Acrofacial dysostosis
H02158 Weyers acrofacial dysostosis
H00528 Frontonasal dysplasia
H00850 Frontorhiny
H01884 Auriculocondylar syndrome
H02210 Acromelic frontonasal dysostosis
H02234 Hamamy syndrome
H02640 Vertebral hypersegmentation and orofacial anomalies
|
LD26 Syndromes with limb anomalies as a major feature
|
H00467 Fibular hypoplasia and complex brachydactyly
H00853 Cenani-Lenz syndactyly syndrome
H00855 Triphalangeal thumb-polysyndactyly syndrome
H00859 Guttmacher syndrome
H00870 Brachydactyly-syndactyly syndrome
H02161 Greig cephalopolysyndactyly syndrome
H02333 Laurin-Sandrow syndrome
H00778 Tarsal-carpal coalition syndrome
H00986 Multiple pterygium syndrome
H00935 Cold-induced sweating syndrome
H01392 Arthrogryposis, mental retardation, and seizures
H01886 Van den Ende-Gupta syndrome
H02299 Arthrogryposis multiplex congenita
H02358 Arthrogryposis multiplex congenita, neurogenic, with myelin defect
H00811 Distal arthrogryposis
H00865 Lethal congenital contractural syndrome
H00872 Trismus-pseudocamptodactyly syndrome
H01931 Lethal-type popliteal pterygium syndrome
H02268 Wieacker-Wolff syndrome
H00532 Parkes Weber syndrome
H01788 Klippel-Trenaunay-Weber syndrome
H01497 Temtamy preaxial brachydactyly syndrome
H00846 Fuhrmann syndrome
H00847 Al-Awadi/Raas-Rothschild syndrome
H02717 Contractures, pterygia, and spondylocarpotarsal fusion syndrome
|
LD27 Syndromes with skin or mucosal anomalies as a major feature
|
H00651 Hypohidrotic ectodermal dysplasia
H00645 Incontinentia pigmenti
H01874 Cronkhite-Canada syndrome
H02456 Ectodermal dysplasia
H00648 Ectodermal dysplasia, Clouston type
H00095 Ectodermal dysplasia and immunodeficiency
H00204 Heimler syndrome
H00449 Oculodentodigital dysplasia
H00487 Tricho-dento-osseous syndrome
H00503 Ellis-van Creveld syndrome
H00529 Cranioectodermal dysplasia
H00540 Osteoporosis, lymphedema, anhydrotic ectodermal dysplasia with immunodeficiency (OLEDAID)
H00571 Johanson-Blizzard syndrome
H00638 Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome
H00639 Ectodermal dysplasia, ectrodactyly, and macular dystrophy
H00640 Limb-mammary syndrome
H00641 ADULT syndrome
H00642 Lacrimo-auriculo-dento-digital syndrome
H00643 Tooth and nail syndrome
H00646 Odontoonychodermal dysplasia
H00647 Ectodermal dysplasia-syndactyly syndrome
H00649 Ectodermal dysplasia, hair-nail type
H00708 Naegeli-Franceschetti-Jadassohn syndrome
H00752 Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome and Rapp-Hodgkin syndrome
H00781 Schopf-Schulz-Passarge syndrome
H00796 Dermatopathia pigmentosa reticularis
H00857 Oligodontia-colorectal cancer syndrome
H00922 Schinzel-Giedion midface retraction syndrome
H00949 Focal dermal hypoplasia
H00977 Trichorhinophalangeal syndrome
H01271 Hypoparathyroidism with sensorineural deafness and renal dysplasia
H01403 Coffin-Siris syndrome
H01905 Trichomegaly
H01966 Cartilage-hair hypoplasia
H02058 Kohlschutter-Tonz syndrome
H02081 Marshall syndrome
H02083 Focal facial dermal dysplasia
H02218 DOORS syndrome
H02219 DDOD syndrome
H02296 Basan syndrome
H02303 Alopecia-mental retardation syndrome
H02417 Gingival fibromatosis with hypertrichosis
H02474 Blepharocheilodontic syndrome
H02691 Scalp-ear-nipple syndrome
H02827 Aplasia cutis-enamel dysplasia syndrome
H02901 GAPO syndrome
H02903 CHAND syndrome
H01428 Xeroderma pigmentosum
H00671 Netherton syndrome
H00712 KID/HID syndrome
H00739 Ichthyosis with hypotrichosis
H00740 Ichthyosis follicularis, alopecia, and photophobia syndrome
H00741 Ichthyosis prematurity syndrome
H00799 CEDNIK syndrome
H02781 Ichthyosis with erythrokeratoderma
H01934 Barber-Say syndrome
H00818 Birt-Hogg-Dube syndrome
H01986 Legius syndrome
H02189 Neurofibromatosis-Noonan syndrome
H01741 Autoinflammation lipodystrophy and dermatosis syndrome
H00665 Mandibuloacral dysplasia
H02236 Keppen-Lubinsky syndrome
H00684 Pachyonychia congenita
H00696 Haim-Munk syndrome
H00785 Congenital hypotrichosis with juvenile macular dystrophy
H00815 H syndrome
H00883 Lipoid proteinosis
H02486 HELIX syndrome
H02713 Inflammatory poikiloderma with hair abnormalities and acral keratoses
H02758 ACCES syndrome
|
LD28 Syndromes with connective tissue involvement as a major feature
|
H00660 Congenital contractural arachnodactyly
H00653 Marfan syndrome
H00800 Loeys-Dietz syndrome
H00659 Shprintzen-Goldberg syndrome
H00661 MASS phenotype
H01385 Rienhoff syndrome
H02720 Meester-Loeys syndrome
H00802 Ehlers-Danlos syndrome
H01902 Brittle cornea syndrome
H02239 Ehlers-Danlos syndrome, spondylodysplastic type
H02240 Ehlers-Danlos syndrome periodontal type
H02241 Ehlers-Danlos syndrome cardiac valvular type
H02242 Ehlers-Danlos syndrome vascular type
H02243 Ehlers-Danlos syndrome arthrochalasia type
H02244 Ehlers-Danlos syndrome dermatosparaxis type
H02245 Ehlers-Danlos syndrome kyphoscoliosis type
H02246 Ehlers-Danlos syndrome musculocontractural type
H02247 Ehlers-Danlos syndrome myopathic type
H02724 Combined osteogenesis imperfecta and Ehlers-Danlos syndrome
H00904 Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities
H00906 Macrocephaly, alopecia, cutis laxa, and scoliosis
H01859 Occipital horn syndrome
H00919 Arterial tortuosity syndrome
H02224 Grange syndrome
H02502 Joint laxity, short stature, and myopia
H02654 Boudin-Mortier syndrome
H02703 VISS syndrome
H02830 Arterial tortuosity-bone fragility syndrome
|
LD29 Syndromes with obesity as a major feature
|
H01915 Borjeson-Forssman-Lehmann syndrome
H02195 MEHMO syndrome
H02267 Wilson-Turner syndrome
|
LD2A Malformative disorders of sex development
|
H00607 46,XY gonadal dysgenesis
H00608 46,XY disorder of sex development due to testosterone secretion defect
H02177 Androgen insensitivity syndrome
H00442 Campomelic dysplasia
H00598 46,XX testicular disorder of sex development
H00609 Persistent Mullerian duct syndrome
H02317 SERKAL syndrome
H02318 Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal
|
LD2B Syndromes with premature ageing appearance as a major feature
|
H00076 Cockayne syndrome
H00558 Geroderma osteodysplasticum
H00601 Hutchinson-Gilford progeria syndrome
H01733 Werner syndrome
H01734 Rothmund-Thomson syndrome
H01883 Nestor-Guillermo progeria syndrome
H02323 Ruijs-Aalfs syndrome
H02480 Fontaine progeroid syndrome
H02570 Cerebro-oculo-facio-skeletal syndrome
H02677 Progeroid laminopathy
H02768 Garg-Mishra progeroid syndrome
H02870 Premature aging syndrome, Penttinen type
H02912 Achalasia-progeroid syndrome
H02916 Fischer-Zirnsak progeroid syndrome
H02917 Wiedemann-Rautenstrauch syndrome
|
LD2C Overgrowth syndromes
|
H00713 Beckwith-Wiedemann syndrome
H00718 Sotos syndrome
H00980 Nevo syndrome
H01215 Simpson-Golabi-Behmel syndrome
H01308 Macrocephaly macrosomia facial dysmorphism syndrome
H01412 Perlman syndrome
H01751 Weaver syndrome
H01806 Tenorio syndrome
H01834 Marshall-Smith syndrome
H01885 Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome
H01909 Hypoinsulinemic hypoglycemia with hemihypertrophy
H01912 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
H02119 Proteus syndrome
H02153 Megalencephaly-capillary malformation syndrome
H02294 Tatton-Brown-Rahman syndrome
H02297 CLAPO syndrome
H02298 Macrocephaly, dysmorphic facies, and psychomotor retardation
H02347 Thauvin-Robinet-Faivre syndrome
H02444 Luscan-Lumish syndrome
H02477 Cohen-Gibson syndrome
H02522 Imagawa-Matsumoto syndrome
H02679 Miura-type epiphyseal chondrodysplasia
H02755 Lui-Jee-Baron syndrome
H02872 Kosaki overgrowth syndrome
H02913 Rahman syndrome
|
LD2D Phakomatoses or hamartoneoplastic syndromes
|
H00666 Peutz-Jeghers syndrome
H01437 Neurofibromatosis type 1
H01438 Neurofibromatosis type 2
H00915 Tuberous sclerosis complex
H00895 Basal cell nevus syndrome
H00559 von Hippel-Lindau syndrome
H01222 Cowden syndrome
H02576 Familial cutaneous telangiectasia and cancer syndrome
H02628 Schimmelpenning-Feuerstein-Mims syndrome
H02722 Nevus comedonicus
|
LD2E Syndromes with structural anomalies due to inborn errors of metabolism
|
H02744 Neurofacioskeletal syndrome with or without renal agenesis
H02798 Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome
|
LD2F Syndromes with multiple structural anomalies, without predominant body system involvement
|
H00979 Sacral defect with anterior meningocele
H02129 Prune belly syndrome
H01195 VACTERL/VATER association
H00261 Meckel syndrome
H01738 Noonan syndrome
H00610 Treacher Collins syndrome
H01838 Mandibulofacial dysostosis with microcephaly
H02126 Mandibulofacial dysostosis with alopecia
H02211 Acrodysostosis
H02673 Craniofacial microsomia
H00433 Holt-Oram syndrome
H00453 Branchio-oto-renal syndrome
H00460 Hand-foot-genital syndrome
H00463 Currarino syndrome
H00500 Keutel syndrome
H00502 Pallister-Hall syndrome
H00504 Rubinstein-Taybi syndrome
H00510 Feingold syndrome
H00523 Noonan syndrome and related disorders
H00555 Char syndrome
H00556 CHARGE syndrome
H00569 Aarskog-Scott syndrome
H00570 Kabuki syndrome
H00572 Roberts-SC phocomelia syndrome
H00573 Townes-Brocks syndrome
H00574 Coffin-Lowry syndrome
H00583 Opitz-GBBB syndrome
H00611 Popliteal pterygium syndrome (PPS)
H00631 Cornelia de Lange syndrome
H00634 Duane-radial ray syndrome
H00637 Ulnar-mammary syndrome
H00685 Bifid nose with or without anorectal and renal anomalies
H00686 Manitoba oculotrichoanal syndrome
H00709 Birk Barel mental retardation syndrome (BBMRS)
H00711 Russell-Silver syndrome
H00753 Urofacial syndrome
H00756 Pitt-Hopkins syndrome
H00797 Martsolf syndrome
H00817 Branchiooculofacial syndrome
H00868 Stapes ankylosis with broad thumb and toes
H00886 Donnai-Barrow syndrome
H00889 Lujan-Fryns syndrome
H00894 FG syndrome
H00907 Kleefstra syndrome
H00908 Mowat-Wilson syndrome
H00914 Warsaw breakage syndrome
H00926 Growth retardation, developmental delay, coarse facies, and early death
H00934 Caudal duplication anomaly
H00936 Goldberg-Shprintzen megacolon syndrome
H00943 TARP syndrome
H00965 RAPADILINO syndrome
H00972 Endocrine-cerebro-osteodysplasia syndrome
H00987 Fetal akinesia deformation sequence
H00997 CATSHL syndrome
H01026 Renal coloboma syndrome
H01030 Congenital arthrogryposis with anterior horn cell disease
H01156 STAR syndrome
H01220 Congenital cataracts, facial dysmorphism, and neuropathy
H01265 Hydrolethalus syndrome
H01289 Mulibrey nanism
H01292 Nance-Horan syndrome
H01370 SHORT syndrome
H01393 Van Maldergem syndrome
H01402 Nicolaides-Baraitser syndrome
H01413 Adams-Oliver syndrome
H01568 3C syndrome
H01569 CHOPS syndrome
H01573 Zimmermann-Laband syndrome
H01745 Cardiofaciocutaneous syndrome
H01747 Costello syndrome
H01793 Young-Simpson syndrome
H01794 Genitopatellar syndrome
H01795 Blepharophimosis-mental retardation syndrome
H01797 Webb-Dattani syndrome
H01814 Stromme syndrome
H01839 Burn-McKeown syndrome
H01840 Moebius syndrome
H01845 Catel-Manzke syndrome
H01869 Megacystis microcolon intestinal hypoperistalsis syndrome
H01878 Al-Raqad syndrome
H01879 Wiedemann-Steiner syndrome
H01887 3MC syndrome
H01908 Carey-Fineman-Ziter syndrome
H01917 CK syndrome
H01923 Microcephaly, short stature, and impaired glucose metabolism
H01927 Van der Woude syndrome
H01930 Au-Kline syndrome
H01932 Ablepharon-macrostomia syndrome
H01984 Leopard syndrome
H02023 Baraitser-Winter syndrome
H02046 OFC syndrome
H02072 Stickler syndrome
H02074 Knobloch syndrome
H02082 Floating-Harbor syndrome
H02087 Vertebral, cardiac, renal, and limb defects syndrome
H02102 Myhre syndrome
H02180 McKusick-Kaufman syndrome
H02190 CBL syndrome
H02191 Noonan-like syndrome with loose anagen hair
H02198 Pancreatic agenesis and congenital heart disease
H02232 CAGSSS syndrome
H02248 MEND syndrome
H02249 Primrose syndrome
H02253 Beaulieu-Boycott-Innes syndrome
H02255 FDLAB syndrome
H02260 Chondrodysplasia Chassaing-Lacombe type
H02271 Cerebellofaciodental syndrome
H02274 Cerebellar atrophy, visual impairment, and psychomotor retardation
H02283 IVIC syndrome
H02324 Sacral agenesis with vertebral anomalies
H02327 KBG syndrome
H02328 Sifrim-Hitz-Weiss syndrome
H02334 Pierpont syndrome
H02364 Heart and brain malformation syndrome
H02368 Developmental delay with short stature, dysmorphic facial features, and sparse hair
H02369 IMAGE-I syndrome
H02370 FILS syndrome
H02376 Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies
H02381 Cleft palate, psychomotor retardation, and distinctive facial features
H02382 Bainbridge-Ropers syndrome
H02383 Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
H02391 Infantile-onset multisystem neurologic, endocrine, and pancreatic disease
H02394 Cleft palate, cardiac defects, and mental retardation
H02453 Congenital heart defects and ectodermal dysplasia
H02454 Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
H02455 Congenital heart defects, hamartomas of tongue, and polysyndactyly
H02478 CATIFA syndrome
H02479 Nivelon-Nivelon-Mabille syndrome
H02481 Syndromic disorder with short stature
H02482 ROSAH syndrome
H02483 Basel-Vanagaite-Smirin-Yosef syndrome
H02493 Al Kaissi syndrome
H02496 Cerebellar, ocular, craniofacial, and genital syndrome
H02500 Congenital interstitial lung disease with nephrotic syndrome and epidermolysis bullosa
H02503 Richieri-Costa-Pereira syndrome
H02506 Cardioacrofacial dysplasia
H02508 Agenesis of corpus callosum, cardiac, ocular, and genital syndrome
H02533 Kaufman oculocerebrofacial syndrome
H02581 Juberg-Hayward syndrome
H02595 Oculoskeletodental syndrome
H02607 Short stature and microcephaly with genital anomalies
H02619 Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome
H02625 Primordial dwarfism-immunodeficiency-lipodystrophy syndrome
H02641 Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development
H02650 Menke-Hennekam syndrome
H02694 Alazami-Yuan syndrome
H02725 Heart-hand syndrome
H02876 Cantu syndrome
H02884 RHYNS syndrome
H01824 CODAS syndrome
H01850 Hartsfield syndrome
H01857 Filippi syndrome
H02343 EVEN-plus syndrome
H02465 Weiss-Kruszka syndrome
H02547 BRENS syndrome
H02548 CIMDAG syndrome
H02549 Cerebellar ataxia, brain abnormalities, and cardiac conduction defects
H02578 Short stature, microcephaly, and endocrine dysfunction
H02638 Zaki syndrome
H02639 Atelis syndrome
H02663 Braddock-Carey syndrome
H02667 Takenouchi-Kosaki syndrome
H02710 Yuksel-Vogel-Bauer syndrome
H02733 Growth restriction, hypoplastic kidneys, alopecia, and distinctive facies
H02747 Oculogastrointestinal neurodevelopmental syndrome
H02748 Hepatorenocardiac degenerative fibrosis
H02753 Vertebral anomalies and variable endocrine and T-cell dysfunction
H02759 Suleiman-El-Hattab syndrome
H02762 Osteo-oto-hepato-enteric syndrome
H02763 Neurocardiofaciodigital syndrome
H02764 Short stature, hearing loss, retinitis pigmentosa, and distinctive facies
H02772 Neurooculocardiogenitourinary syndrome
H02780 Liberfarb syndrome
H02850 TIMES syndrome
H02851 Muggenthaler-Chowdhury-Chioza syndrome
H02860 Gillespie syndrome
H02905 Santos syndrome
H02910 Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction
|
LD2G Conjoined twins
|
LD2H Syndromic genetic deafness
|
H00687 Fraser syndrome
H02356 PCWH syndrome
H00779 Usher syndrome
H00446 Craniofacial-deafness-hand syndrome
H00581 Alport syndrome
H00706 Bart-Pumphrey syndrome
H00727 Athabascan brainstem dysgenesis syndrome
H00803 Seizures-sensorineural deafness-ataxia-mental retardation-electrolyte imbalance (SESAME)
H00823 ABCD syndrome
H00946 Arts syndrome
H01286 Microtia hearing impairment and cleft palate
H01903 Brown-Vialetto-Van Laere syndrome
H02095 Perrault syndrome
H02135 Cone-rod dystrophy and hearing loss
H02220 MEDNIK syndrome
H02226 Cardiospondylocarpofacial syndrome
H02286 Congenital deafness with inner ear agenesis, microtia, and microdontia
H02287 Deafness, dystonia, and cerebral hypomyelination
H02326 Keipert syndrome
H02355 Deafness and myopia
H02430 Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus
H02435 Deafness-infertility syndrome
H02634 Deafness, cataract, impaired intellectual development, and polyneuropathy
H02687 Congenital deafness and adult-onset progressive leukoencephalopathy
H02797 Siddiqi syndrome
H02813 Auroneurodental syndrome
|
LD2Y Other specified multiple developmental anomalies or syndromes
|
H00417 Alstrom syndrome
H00418 Bardet-Biedl syndrome
H01623 MDPL syndrome
H02488 Cardiac-urogenital syndrome
H02523 Genitourinary and/or brain malformation syndrome
H02630 Chitayat syndrome
H02821 Sandestig-Stefanova syndrome
|
LD2Z Multiple developmental anomalies or syndromes, unspecified
|
Chromosomal anomalies, excluding gene mutations
|
LD40 Complete trisomies of the autosomes
|
H01552 Down syndrome
H01562 Patau syndrome
H01564 Edwards syndrome
|
LD41 Duplications of the autosomes
|
H02604 Chromosome 1q21.1 duplication syndrome
H01790 Emanuel syndrome
|
LD42 Polyploidies
|
LD43 Complete monosomies of the autosomes
|
LD44 Deletions of the autosomes
|
H01831 Ring chromosome 20 syndrome
H01792 1p36 deletion syndrome
H02471 Brain malformations with urinary tract defects
H00561 Brachydactyly-mental retardation syndrome
H02146 Glass syndrome
H01773 4p deletion syndrome
H01223 Mental retardation-stereotypic movements-epilepsy and/or cerebral malformations
H00764 Chromosome 5p deletion syndrome
H01439 Williams-Beuren syndrome
H01800 Verheij syndrome
H02103 DeSanto-Shinawi syndrome
H02156 Lamb-Shaffer syndrome
H01861 Chromosome 15q24 microdeletion syndrome
H01877 Chromosome 15q13.3 microdeletion syndrome
H02121 Koolen-De Vries syndrome
H01791 Smith-Magenis syndrome
H01004 Velocardiofacial syndrome
H01524 DiGeorge syndrome
H01525 22q11.2 deletion syndrome
H01238 Phelan-McDermid syndrome
|
LD45 Uniparental disomies
|
H01801 Kagami-Ogata syndrome
|
LD46 Imprinting errors
|
LD47 Balanced rearrangements or structural rearrangements
|
Sex chromosome anomalies
|
LD50 Number anomalies of chromosome X
|
LD51 Structural anomalies of chromosome X, excluding Turner syndrome
|
H00552 Chromosome Xp21 deletion syndrome
H00994 Familial skewed X-chromosome inactivation
|
LD52 Number anomalies of chromosome Y
|
LD53 Structural anomalies of chromosome Y
|
LD54 Male with sex chromosome mosaicism
|
LD55 Fragile X chromosome
|
H00465 Fragile X syndrome
H01731 Fragile X tremor/ataxia syndrome
|
LD56 Chimaera 46, XX, 46, XY
|
LD5Y Other specified sex chromosome anomalies
|
LD5Z Sex chromosome anomalies, unspecified
|
LD7Y Other specified chromosomal anomalies, excluding gene mutations
|
H01288 Mosaic variegated aneuploidy syndrome
|
LD7Z Chromosomal anomalies, excluding gene mutations, unspecified
|
LD90 Conditions with disorders of intellectual development as a relevant clinical feature
|
H01732 Angelman syndrome
H00478 Prader-Willi syndrome
H00440 Rett syndrome
H00597 Snyder-Robinson syndrome
H00769 Hyperekplexia
H00940 Cohen syndrome
H01769 ZTTK syndrome
H01913 Renpenning syndrome
H01914 Christianson syndrome
H01916 Stocco dos Santos X-linked mental retardation syndrome
H01920 Partington syndrome
H01922 Infantile hypotonia with psychomotor retardation and characteristic facies
H01928 Smith-Kingsmore syndrome
H02137 Laurence-Moon syndrome
H02252 PEHO syndrome
H02305 RERE-related neurodevelopmental syndrome
H02325 Schaaf-Yang syndrome
H02337 Skraban-Deardorff syndrome
H02338 PEHO-like syndrome
H02346 Intellectual developmental disorder with short stature
H02353 Hyperekplexia and epilepsy
H02363 Ververi-Brady syndrome
H02365 Helsmoortel-van der Aa syndrome
H02378 Hypotonia, ataxia, and delayed development syndrome
H02397 Neurodevelopmental disorder with movement abnormalities or hypotonia
H02437 Growth retardation, impaired intellectual development, hypotonia, and hepatopathy
H02459 Syndromic neurodevelopmental disorder
H02460 Neurodevelopmental disorder with dysmorphic facies and skeletal anomalies
H02461 Neurodevelopmental disorder with microcephaly
H02463 Syndromic intellectual developmental disorder
H02470 Neurodevelopmental disorder with structural brain abnormalities
H02510 Neurodevelopmental disorder with characteristic facial and ectodermal features and tetraparesis
H02515 Li-Ghorbani-Weisz-Hubshman syndrome
H02528 Hao-Fountain syndrome
H02535 Neurodevelopmental disorder with dysmorphic facies
H02560 White-Kernohan syndrome
H02582 Mullegama-Klein-Martinez syndrome
H02583 X-linked intellectual disability-hypotonic facies syndrome
H02584 Ferguson-Bonni neurodevelopmental syndrome
H02587 Luo-Schoch-Yamamoto syndrome
H02611 Turnpenny-Fry syndrome
H02612 Radio-Tartaglia syndrome
H02613 Brunet-Wagner neurodevelopmental syndrome
H02614 Snijders Blok-Campeau syndrome
H02615 Parenti-Mignot neurodevelopmental syndrome
H02616 Neurodevelopmental disorder with macrocephaly
H02617 Bryant-Li-Bhoj neurodevelopmental syndrome
H02618 Developmental delay with variable intellectual disability and dysmorphic facies
H02622 Shukla-Vernon syndrome
H02623 Kury-Isidor syndrome
H02632 Houge-Janssens syndrome
H02633 Beck-Fahrner syndrome
H02635 Poirier-Bienvenu neurodevelopmental syndrome
H02651 Lessel-Kreienkamp syndrome
H02659 Dentici-Novelli neurodevelopmental syndrome
H02666 Chilton-Okur-Chung neurodevelopmental syndrome
H02682 Nizon-Isidor syndrome
H02685 Developmental delay with neuropsychiatric disorders
H02686 Developmental delay with dysmorphic facies and dental anomalies
H02688 Dworschak-Punetha neurodevelopmental syndrome
H02698 Trichohepatoneurodevelopmental syndrome
H02700 Intellectual developmental disorder with speech delay and dysmorphic facies
H02712 Li-Campeau syndrome
H02714 Tessadori-Bicknell-van Haaften neurodevelopmental syndrome
H02715 Neurodevelopmental disorder with defects of ubiquitin-proteasome system
H02728 Marbach-Schaaf neurodevelopmental syndrome
H02734 Hengel-Maroofian-Schols syndrome
H02746 Alfadhel syndrome
H02752 Tan-Almurshedi syndrome
H02765 Prieto syndrome
H02769 Tolchin-Le Caignec syndrome
H02782 Fliedner-Zweier syndrome
H02793 Temtamy syndrome
H02803 Neurodevelopmental disorder with histone modification defect
H02804 ReNU syndrome
H02812 Otofacial neurodevelopmental syndrome
H02818 Jeffries-Lakhani neurodevelopmental syndrome
H02824 Abnormal hair, joint laxity, and developmental delay
H02834 Kariminejad-Reversade neurodevelopmental syndrome
H02837 Karayol-Borroto-Haghshenas neurodevelopmental syndrome
H02838 Neurodevelopmental disorder with variable familial hypercholanemia
H02842 Pan-Chung-Bellen syndrome
H02843 Brain malformations and seizures by impaired function of TRiC
H02854 Okur-Chung neurodevelopmental syndrome
H02855 Shashi-Pena syndrome
H02856 Neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
H02857 Neurodevelopmental disorder with microcephaly and structural brain anomalies
H02858 Neurodevelopmental disorder with speech impairment and with or without seizures
H02859 Neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements
H02861 Neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures
H02862 Neurodevelopmental disorder with or without variable brain abnormalities
H02863 Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
H02864 Neurodevelopmental disorder with or without autism or seizures
H02885 Neurodevelopmental disorder with hypotonia and dysmorphic facies
H02886 Neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities
H02887 Neurodevelopmental disorder with language impairment and behavioral abnormalities
H02888 Neurodevelopmental disorder with or without seizures and gait abnormalities
H02890 Neurodevelopmental disorder with language delay and variable cognitive abnormalities
H02891 Neurodevelopmental disorder with poor language and loss of hand skills
H02892 Neurodevelopmental disorder with infantile epileptic spasms
H02894 Neurodevelopmental disorder with impaired language and ataxia and with or without seizures
H02911 Paul-Chao neurodevelopmental syndrome
H02918 Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
H02924 Intellectual disability and myopathy syndrome
|
LD9Y Other specified developmental anomalies
|
LD9Z Developmental anomalies, unspecified
|
|
21 Symptoms, signs or clinical findings, not elsewhere classified
|
Symptoms of blood, blood-forming organs, or the immune system
|
MA00 Symptom or complaint of the blood
MA01 Enlarged lymph nodes
MA0Y Other specified symptoms of blood, blood-forming organs, or the immune system
|
Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system
|
Clinical findings in blood, blood-forming organs, or the immune system
|
MA10 Abnormal serum enzyme levels
|
MA11 Clinical findings of hormones in blood, blood-forming organs, or the immune system
|
MA12 Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system
|
MA13 Clinical findings of substances chiefly nonmedicinal as to source in blood, blood-forming organs, or the immune system
|
MA14 Immunological findings in blood, blood-forming organs, or the immune system
|
MA15 Microbiological findings in blood, blood-forming organs, or the immune system
|
MA16 Cytological findings in blood, blood-forming organs, or the immune system
|
MA17 Histological findings in blood, blood-forming organs, or the immune system
|
MA18 Certain clinical findings of blood chemistry
|
MA19 Certain abnormalities of plasma proteins
|
H02807 Abnormality of alpha-fetoprotein
|
MA1A Elevated erythrocyte sedimentation rate or abnormality of plasma viscosity
|
MA1Y Other specified clinical findings in blood, blood-forming organs, or the immune system
|
MA3Y Other specified symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system
|
Symptoms, signs or clinical findings of endocrine, nutritional or metabolic diseases
|
Results of function studies of the endocrine, nutritional or metabolic diseases
|
MA50 Abnormal results of thyroid function studies
MA51 Abnormal results of other endocrine function studies
|
MA6Y Other specified symptoms, signs or clinical findings of endocrine, nutritional or metabolic diseases
|
Symptoms, signs or clinical findings of speech or voice
|
Symptoms or signs involving speech or voice
|
MA80 Speech disturbances
MA81 Speech dysfluency
MA82 Voice disturbances
MA8Y Other specified symptoms or signs involving speech or voice
|
MB0Y Other specified symptoms, signs or clinical findings of speech or voice
|
Mental or behavioural symptoms, signs or clinical findings
|
MB20 Symptoms, signs or clinical findings involving consciousness
MB21 Symptoms, signs or clinical findings involving cognition
MB22 Symptoms or signs involving motivation or energy
MB23 Symptoms or signs involving appearance or behaviour
MB24 Symptoms or signs involving mood or affect
MB25 Symptoms or signs involving form of thought
MB26 Symptoms or signs involving content of thought
MB27 Symptoms or signs involving perceptual disturbance
MB28 Symptoms or signs related to personality features
MB29 Symptoms or signs involving eating and related behaviour
MB2A Symptoms or signs involving elimination
MB2Y Other specified mental or behavioural symptoms, signs or clinical findings
|
Symptoms, signs or clinical findings of the nervous system
|
Symptoms or signs involving the nervous system
|
MB40 Sensation disturbance
|
MB41 Disturbances of smell and taste
|
MB42 Phonophobia
|
MB43 Dyssomnia
|
MB44 Abnormalities of gait and mobility
|
MB45 Lack of coordination
|
MB46 Abnormal involuntary movements
|
MB47 Abnormality of tonus and reflex
|
H02388 Infantile-onset limb and orofacial dyskinesia
H02389 Familial dyskinesia with facial myokymia
|
MB48 Dizziness and giddiness
|
MB49 Aura
|
MB4A Apraxia
|
MB4B Symbolic dysfunctions
|
H01899 Dyslexia
|
MB4C Gerstmann syndrome
|
MB4D Headache, not elsewhere classified
|
Paralytic symptoms
|
MB50 Tetraplegia
|
MB51 Diplegia of upper extremities
|
MB52 Diplegia of lower extremities
|
MB53 Hemiplegia
|
MB54 Monoplegia of upper extremity
|
MB55 Monoplegia of lower extremity
|
MB56 Paraplegia
|
MB57 Functional level of injury of spinal cord
|
MB5Y Other specified paralytic symptoms
|
MB5Z Paralytic symptoms, unspecified
|
MB60 Sleeptalking
|
MB6Y Other specified symptoms or signs involving the nervous system
|
Clinical findings in the nervous system
|
MB70 Clinical findings in cerebrospinal fluid
MB71 Clinical findings on diagnostic imaging of central nervous system
MB72 Results of function studies of the nervous system
MB7Y Other specified clinical findings in the nervous system
|
MB9Y Other specified symptoms, signs or clinical findings of the nervous system
|
Symptoms, signs or clinical findings of the visual system
|
Symptoms or signs involving the visual system
|
MC10 Eye appearance abnormal
MC11 Eye sensation abnormal
MC12 Chronic enlargement of lacrimal gland
MC13 Epiphora
MC14 Eye discharge
MC15 Red eye
MC16 Pallor conjunctiva
MC17 Icteric sclera
MC18 Ocular pain
MC19 Quadrantanopia
MC1A Visual floaters
MC1B Symptom or complaint of the eyelid
MC1C Symptom or complaint of glasses
MC1D Symptom or complaint of contact lens
MC1Y Other specified symptoms or signs involving the visual system
|
MC20 Clinical findings of the visual system
|
MC21 Impairment of electrophysiological functions
|
MC2Y Other specified symptoms, signs or clinical findings of the visual system
|
Symptoms, signs or clinical findings of ear or mastoid process
|
Symptoms or signs involving the ear or mastoid process
|
MC40 Plugged feeling ear
MC41 Tinnitus
MC4Y Other specified symptoms or signs involving the ear or mastoid process
|
MC6Y Other specified symptoms, signs or clinical findings of ear or mastoid process
|
Symptoms, signs or clinical findings of the circulatory system
|
Symptoms or signs involving the circulatory system
|
MC80 Abnormal blood-pressure reading, without diagnosis
MC81 Abnormalities of heart beat
MC82 Cardiac arrest
MC83 Cardiac murmurs and other cardiac sounds
MC84 Cardiovascular pain
MC85 Gangrene
MC86 Precordial pain
MC87 Pressure or tightness of heart
MC88 Prominent veins
MC8Y Other specified symptoms or signs involving the circulatory system
|
MC90 Clinical findings on diagnostic imaging of heart or coronary circulation
|
MC91 Results of function studies of the circulatory system
|
MC9Y Other specified symptoms, signs or clinical findings of the circulatory system
|
Symptoms, signs or clinical findings of the respiratory system
|
Symptoms or signs involving the respiratory system
|
MD10 Abnormal sputum
|
MD11 Abnormalities of breathing
|
MD12 Cough
|
Haemorrhage from respiratory passages
|
MD20 Epistaxis
MD21 Haemorrhage from throat
MD22 Haemoptysis
MD23 Haemorrhage from other sites in respiratory passages
MD24 Acute idiopathic pulmonary haemorrhage in infants over 28 days of age
MD2Z Haemorrhage from respiratory passages, unspecified
|
MD30 Pain in throat or chest
|
MD31 Pleurisy
|
MD32 Rales
|
MD33 Respiratory arrest
|
MD34 Symptom or complaint of the nose
|
MD35 Symptom or complaint of the sinus
|
MD36 Symptom or complaint of the throat
|
MD3Y Other specified symptoms or signs involving the respiratory system
|
Clinical findings in the respiratory system
|
MD40 Clinical findings in specimens from respiratory organs and thorax
MD41 Clinical findings on diagnostic imaging of lung
MD42 Results of function studies of the respiratory system
MD4Y Other specified clinical findings in the respiratory system
|
MD6Y Other specified symptoms, signs or clinical findings of the respiratory system
|
Symptoms, signs or clinical findings of the digestive system or abdomen
|
Symptoms or signs involving the digestive system or abdomen
|
MD80 Symptoms or signs of the orofacial complex
|
MD81 Abdominal or pelvic pain
|
MD82 Intra-abdominal or pelvic swelling, mass or lump
|
Symptoms related to the upper gastrointestinal tract
|
MD90 Nausea or vomiting
MD91 Belching
MD92 Dyspepsia
MD93 Dysphagia
MD94 Halitosis
MD95 Heartburn
MD9Y Other specified symptoms related to the upper gastrointestinal tract
|
Symptoms related to the lower gastrointestinal tract or abdomen
|
ME00 Abdominal compartment syndrome
ME01 Abdominal distension
ME02 Abdominal rigidity
ME03 Abnormal bowel sounds
ME04 Ascites
ME05 Change in bowel habit
ME06 Chronic enteritis of uncertain aetiology
ME07 Faecal incontinence
ME08 Flatulence and related conditions
ME09 Rectal tenesmus
ME0A Visible peristalsis
ME0B Problems with defaecation, not otherwise specified
ME0Y Other specified symptoms related to the lower gastrointestinal tract or abdomen
|
ME10 Abnormalities related to hepatobiliary system
|
ME1Y Other specified symptoms or signs involving the digestive system or abdomen
|
Clinical findings in the digestive system
|
ME20 Clinical findings in specimens from digestive organs or abdominal cavity
ME21 Clinical findings on diagnostic imaging of liver or biliary tract
ME22 Clinical findings on diagnostic imaging of digestive tract
ME23 Results of function studies of the digestive system
ME24 Clinical manifestations of the digestive system
ME2Y Other specified clinical findings in the digestive system
|
ME4Y Other specified symptoms, signs or clinical findings of the digestive system or abdomen
|
Symptoms, signs or clinical findings involving the skin
|
Symptoms or signs involving the skin
|
ME60 Skin lesion of uncertain or unspecified nature
ME61 Subcutaneous swelling, mass or lump of uncertain or unspecified nature
ME62 Acute skin eruption of uncertain or unspecified nature
ME63 Chronic skin disorder of uncertain or unspecified nature
ME64 Non-specific cutaneous vascular signs
ME65 Disturbances of skin sensation of unspecified aetiology
ME66 Miscellaneous non-specific skin-related symptoms and signs
ME67 Skin disorder of uncertain or unspecified nature
ME6Y Other specified symptoms or signs involving the skin
|
Symptoms, signs or clinical findings of the musculoskeletal system
|
Symptoms or signs of the musculoskeletal system
|
ME80 Clicking hip
ME81 Musculoskeletal chest pain
ME82 Pain in joint
ME83 Rheumatism, unspecified
ME84 Spinal pain
ME85 Stiffness of joint
ME86 Symptom or complaint of a body part
ME8Y Other specified symptoms or signs of the musculoskeletal system
|
Clinical findings in the musculoskeletal system
|
ME90 Clinical findings on diagnostic imaging of skull and head
ME91 Clinical findings on diagnostic imaging of limbs
ME92 Clinical findings on diagnostic imaging of other parts of musculoskeletal system
ME93 Biomechanical lesions, not elsewhere classified
ME9Y Other specified clinical findings in the musculoskeletal system
|
MF1Y Other specified symptoms, signs or clinical findings of the musculoskeletal system
|
Symptoms, signs or clinical findings of the genitourinary system
|
Symptoms, signs or clinical findings involving the female genital system
|
MF30 Breast lump or mass female
|
MF31 Breast or lactation symptom or complaint
|
MF32 Menopausal symptom or complaint
|
MF33 Premenstrual symptom or complaint
|
MF34 Pregnancy symptom or complaint
|
MF35 Postpartum symptom or complaint
|
MF36 Other symptom or complaint of vagina
|
MF37 Symptom or complaint of female nipple
|
MF38 Symptom or complaint of female pelvis
|
MF39 Symptom or complaint of the vulva
|
MF3A Vaginal discharge
|
H01380 Bacterial vaginosis
|
MF3Y Other specified symptoms, signs or clinical findings involving the female genital system
|
Symptoms, signs or clinical findings involving the male genital system
|
MF40 Problems of male genital organs
MF41 Symptom or complaint of male sexual function
MF42 Retractile testis migrans
MF4Y Other specified symptoms, signs or clinical findings involving the male genital system
|
Symptoms, signs or clinical findings involving the urinary system
|
MF50 Abnormal micturition
MF51 Anuria or oliguria
MF52 Bladder pain
MF53 Extrarenal uraemia
MF54 Macroscopic changes of size of the kidney
MF55 Polyuria
MF56 Renal colic
MF57 Symptom or complaint of bladder
MF58 Urethral discharge
MF59 Urinary symptom or complaint
MF5Y Other specified symptoms, signs or clinical findings involving the urinary system
|
Clinical findings in specimens from female genital organs
|
MF60 Abnormal level of enzymes in specimens from female genital organs
MF61 Abnormal level of hormones in specimens from female genital organs
MF62 Abnormal level of drugs, medicaments and biological substances in specimens from female genital organs
MF63 Abnormal level of substances chiefly nonmedicinal as to source in specimens from female genital organs
MF64 Abnormal immunological findings in specimens from female genital organs
MF65 Abnormal microbiological findings in specimens from female genital organs
MF66 Abnormal cytological findings in specimens from female genital organs
MF67 Abnormal histological findings in specimens from female genital organs
MF68 Abnormal chromosomal findings in specimens from female genital organs
MF6Y Other specified clinical findings in specimens from female genital organs
MF6Z Clinical findings in specimens from female genital organs, unspecified
|
Clinical findings in specimens from male genital organs
|
MF70 Abnormal level of enzymes in specimens from male genital organs
MF71 Abnormal level of hormones in specimens from male genital organs
MF72 Abnormal level of drugs, medicaments and biological substances in specimens from male genital organs
MF73 Abnormal level of substances chiefly nonmedicinal as to source in specimens from male genital organs
MF74 Abnormal immunological findings in specimens from male genital organs
MF75 Abnormal microbiological findings in specimens from male genital organs
MF76 Abnormal cytological findings in specimens from male genital organs
MF77 Abnormal histological findings in specimens from male genital organs
MF78 Abnormal chromosomal findings in specimens from male genital organs
MF7Y Other specified clinical findings in specimens from male genital organs
MF7Z Clinical findings in specimens from male genital organs, unspecified
|
Clinical findings in specimens from the urinary system
|
MF80 Diffuse mesangial sclerosis
|
MF81 Fibronectin glomerulopathy
|
H01260 Glomerulopathy with fibronectin deposits
|
MF82 Lipoprotein glomerulopathy
|
H00887 Lipoprotein glomerulopathy
|
MF83 Diabetic glomerular changes
|
MF84 Pauci-immune proliferative glomerulonephritis
|
MF85 Anti-glomerular basement membrane antibody mediated disease
|
H01721 Anti-glomerular basement membrane (GBM) disease
|
MF8Y Other specified clinical findings in specimens from the urinary system
|
H00626 Focal segmental glomerulosclerosis
H01581 IgA nephropathy
H01726 Membranoproliferative glomerulonephritis
H01767 Henoch-Schonlein purpura nephritis
H02579 C3 glomerulopathy
|
MF8Z Clinical findings in specimens from the urinary system, unspecified
|
Clinical findings on examination of urine, without diagnosis
|
MF90 Acetonuria
|
MF91 Bilirubinuria
|
MF92 Chyluria
|
MF93 Glycosuria
|
MF94 Haemoglobinuria
|
MF95 Myoglobinuria
|
H01290 Acute recurrent myoglobinuria
|
MF96 Proteinuria
|
MF97 Pyuria
|
MF98 Abnormal levels of serum electrolytes in the urine
|
H02340 Absorptive hypercalciuria
|
MF99 Elevated urine levels of drugs, medicaments and biological substances
|
MF9A Abnormal urine levels of substances chiefly nonmedicinal as to source
|
MF9B Abnormal findings on microbiological examination of urine
|
MF9C Abnormal findings on cytological and histological examination of urine
|
MF9Y Other specified clinical findings on examination of urine, without diagnosis
|
MG00 Clinical findings on diagnostic imaging of breast
|
MG01 Clinical findings on diagnostic imaging of urinary organs
|
MG02 Results of kidney function studies
|
MG0Y Other specified symptoms, signs or clinical findings of the genitourinary system
|
General symptoms, signs or clinical findings
|
General symptoms
|
MG20 Cachexia
|
MG21 Chills
|
MG22 Fatigue
|
MG23 Fear of death or dying
|
MG24 Fear of disease
|
MG25 Feeling ill
|
MG26 Fever of other or unknown origin
|
MG27 Haemorrhage, not elsewhere classified
|
MG28 Hypothermia, not associated with low environmental temperature
|
MG29 Oedema
|
MG2A Ageing associated decline in intrinsic capacity
|
Pain
|
MG30 Chronic pain
|
MG31 Acute pain
|
MG3Z Pain, unspecified
|
MG40 Shock
|
MG41 Sleep disturbance, not elsewhere classified
|
MG42 Somnolence, not elsewhere classified
|
MG43 Symptoms and signs concerning food and fluid intake
|
MG44 Symptoms peculiar to infancy
|
H02681 Short stature with nonspecific skeletal abnormalities
|
MG45 Syncope and collapse
|
MG46 Systemic inflammatory response syndrome of noninfectious origin
|
MG47 Toxicosis not further specified
|
MG48 Unknown and unspecified causes of morbidity
|
MG49 Hangover
|
MG4A Multi organ failure
|
MG4Y Other specified general symptoms
|
Finding of microorganism resistant to antimicrobial drugs
|
MG50 Finding of gram negative bacteria resistant to antimicrobial drugs
|
H00309 Multidrug-resistant Acinetobacter infection
H01422 Carbapenem-resistant bacterial infection
H00313 Multidrug-resistant Pseudomonas aeruginosa infection
|
MG51 Finding of gram positive bacteria resistant to antimicrobial drugs
|
H00330 Methicillin-resistant Staphylococcal aureus (MRSA) infection
H00331 Vancomycin-resistant Staphylococcal aureus (VRSA) infection
H01423 Penicillin-resistant Streptococcus pneumoniae infection
H00340 Vancomycin-resistant enterococci infection
H01401 Methicillin-resistant Staphylococcus epidermidis (MRSE) infection
|
MG52 Finding of bacteria, neither gram negative nor positive, resistant to antimicrobial drugs
|
H01472 Multidrug-resistant tuberculosis
|
MG53 Finding of virus resistant to antimicrobial drugs
|
MG54 Finding of fungus resistant to antimicrobial drugs
|
MG55 Finding of parasite resistant to antimicrobial drugs
|
MG56 Finding of microorganism resistant to other multiple antimicrobial drugs
|
MG5Y Finding of other microorganism resistant to antimicrobial drugs
|
MG5Z Finding of microorganism resistant to antimicrobial drugs, unspecified
|
Clinical findings in specimens from other specified organs, systems and tissues
|
MG60 Abnormal level of enzymes in specimens from other organs, systems and tissues
MG61 Abnormal level of hormones in specimens from other organs, systems and tissues
MG62 Abnormal level of drugs, medicaments and biological substances in specimens from other organs, systems and tissues
MG63 Abnormal level of substances chiefly nonmedicinal as to source in specimens from other organs, systems and tissues
MG64 Abnormal immunological findings in specimens from other organs, systems and tissues
MG65 Abnormal microbiological findings in specimens from other organs, systems and tissues
MG66 Abnormal cytological findings in specimens from other organs, systems and tissues
MG67 Abnormal histological findings in specimens from other organs, systems and tissues
MG6Y Other specified clinical findings in specimens from other specified organs, systems and tissues
|
Abnormal results, not elsewhere classified
|
MG70 Abnormal diagnostic imaging results not elsewhere classified
MG71 Abnormal laboratory results, not elsewhere classified
MG72 Abnormal results of function studies of other organs and systems
MG7Y Other specified abnormal results, not elsewhere classified
MG7Z Abnormal results, not elsewhere classified, unspecified
|
MG9Y Other specified general symptoms, signs or clinical findings
|
Ill-defined and unknown causes of mortality
|
MH10 Brain death
|
MH11 Sudden infant death syndrome
|
H02174 Sudden infant death with dysgenesis of the testes syndrome
|
MH12 Other sudden death, cause unknown
|
MH13 Unattended death
|
MH14 Other ill-defined and unspecified causes of mortality
|
MH15 Sudden unexpected death in epilepsy
|
MH2Y Other specified symptoms, signs or clinical findings, not elsewhere classified
|
|
22 Injury, poisoning or certain other consequences of external causes
|
Injuries to the head
|
NA00 Superficial injury of head
NA01 Open wound of head
NA02 Fracture of skull or facial bones
NA03 Dislocation or strain or sprain of joints or ligaments of head
NA04 Injury of cranial nerves
NA05 Injury of blood vessels of head
NA06 Injury of eye or orbit
NA07 Intracranial injury
NA08 Crushing injury of head
NA09 Traumatic amputation of part of head
NA0A Certain specified injuries of head
NA0B Injury of the auricle
NA0C Injury of middle or inner ear
NA0D Injury of teeth or supporting structures
NA0Z Injuries to the head, unspecified
|
Injuries to the neck
|
NA20 Superficial injury of neck
|
NA21 Open wound of neck
|
NA22 Fracture of neck
|
NA23 Dislocation or strain or sprain of joints or ligaments at neck level
|
Injury of nerves or spinal cord at neck level
|
Injury of spinal cord at neck level
|
NA30 Concussion or oedema of cervical spinal cord
NA31 Certain specified injuries of cervical spinal cord
NA3Z Injury of cervical spinal cord, unspecified
|
Injury of nerves at neck level
|
NA40 Injury of nerve root of cervical spine
NA41 Injury of brachial plexus
NA42 Injury of peripheral nerves of neck
NA43 Injury of cervical sympathetic nerves
NA44 Injury of phrenic nerve
NA4Y Injury of other specified nerves at neck level
NA4Z Injury of nerves at neck level, unspecified
|
NA60 Injury of blood vessels at neck level
|
NA61 Injury of muscle, fascia or tendon at neck level
|
NA62 Crushing injury of neck
|
NA63 Traumatic amputation at neck level
|
NA64 Multiple injuries of neck
|
NA6Y Other specified injuries to the neck
|
NA6Z Injuries to the neck, unspecified
|
Injuries to the thorax
|
NA80 Superficial injury of thorax
|
NA81 Open wound of thorax
|
NA82 Fracture of rib, sternum or thoracic spine
|
NA83 Dislocation or strain or sprain of joints or ligaments of thorax
|
Injury of nerves or spinal cord at thorax level
|
Injury of spinal cord at thorax level
|
NA90 Concussion or oedema of thoracic spinal cord
NA91 Certain specified injuries of thoracic spinal cord
NA9Z Injury of thoracic spinal cord, unspecified
|
Injury of nerves at thorax level
|
NB00 Injury of nerve root of thoracic spine
NB01 Injury of peripheral nerves of thorax
NB02 Injury of thoracic sympathetic nerves
NB0Y Injury of other specified nerves at thorax level
|
NB2Y Other specified injury of nerves or spinal cord at thorax level
|
NB2Z Injury of nerves or spinal cord at thorax level, unspecified
|
NB30 Injury of blood vessels of thorax
|
NB31 Injury of heart
|
NB32 Injury of other or unspecified intrathoracic organs
|
NB33 Crushing injury of thorax or traumatic amputation of part of thorax
|
NB34 Injury of muscle, fascia or tendon at thorax level
|
NB35 Multiple injuries of thorax
|
NB3Y Other specified injuries to the thorax
|
NB3Z Injuries to the thorax, unspecified
|
Injuries to the abdomen, lower back, lumbar spine or pelvis
|
NB50 Superficial injury of abdomen, lower back or pelvis
|
NB51 Open wound of abdomen, lower back or pelvis
|
NB52 Fracture of lumbar spine or pelvis
|
NB53 Dislocation or strain or sprain of joints or ligaments of lumbar spine or pelvis
|
Injury of nerves or lumbar spinal cord at abdomen, lower back or pelvis level
|
Injury of spinal cord at abdomen, lower back or pelvis level
|
NB60 Concussion or oedema of lumbar spinal cord
NB61 Concussion or oedema of sacral spinal cord
NB62 Certain specified injuries of lumbar spinal cord
NB63 Certain specified injuries of sacral spinal cord
NB6Z Injury of spinal cord at abdomen, lower back or pelvis level, unspecified
|
Injury of nerves at abdomen, lower back or pelvis level
|
NB70 Injury of nerve root of lumbar spine
NB71 Injury of nerve root of sacral spine
NB72 Injury of cauda equina
NB73 Injury of lumbosacral plexus
NB74 Injury of lumbar, sacral or pelvic sympathetic nerves
NB75 Injury of peripheral nerve of abdomen, lower back or pelvis
NB7Y Other specified injury of nerves at abdomen, lower back or pelvis level
NB7Z Injury of nerves at abdomen, lower back or pelvis level, unspecified
|
NB90 Injury of blood vessels at abdomen, lower back or pelvis level
|
NB91 Injury of intra-abdominal organs
|
NB92 Injury of urinary or pelvic organs
|
NB93 Crushing injury or traumatic amputation of part of abdomen, lower back or pelvis
|
NB94 Injury of muscle, fascia or tendon of abdomen, lower back or pelvis
|
NB95 Injury of intra-abdominal organ with pelvic organ
|
NB96 Other multiple injuries of abdomen, lower back or pelvis
|
NB97 Certain specified injuries of abdomen, lower back or pelvis
|
NB98 Injury to female genital organ without further specification
|
NB99 Injury to male genital organ without further specification
|
NB9Y Other specified injuries to the abdomen, lower back, lumbar spine or pelvis
|
NB9Z Injuries to the abdomen, lower back, lumbar spine or pelvis, unspecified
|
Injuries to the shoulder or upper arm
|
NC10 Superficial injury of shoulder or upper arm
NC11 Open wound of shoulder or upper arm
NC12 Fracture of shoulder or upper arm
NC13 Dislocation or strain or sprain of joints or ligaments of shoulder girdle
NC14 Injury of nerves at shoulder or upper arm level
NC15 Injury of blood vessels at shoulder or upper arm level
NC16 Injury of muscle, fascia, tendon or bursa at shoulder or upper arm level
NC17 Crushing injury of shoulder or upper arm
NC18 Traumatic amputation of shoulder or upper arm
NC19 Multiple injuries of shoulder or upper arm
NC1Y Other specified injuries to the shoulder or upper arm
NC1Z Injuries to the shoulder or upper arm, unspecified
|
Injuries to the elbow or forearm
|
NC30 Superficial injury of forearm
NC31 Open wound of forearm
NC32 Fracture of forearm
NC33 Dislocation or strain or sprain of joints or ligaments of elbow
NC34 Injury of nerves at forearm level
NC35 Injury of blood vessels at forearm level
NC36 Injury of muscle, fascia, tendon or bursa at forearm level
NC37 Crushing injury of forearm
NC38 Traumatic amputation of forearm
NC39 Multiple injuries of forearm
NC3Y Other specified injuries to the elbow or forearm
NC3Z Injuries to the elbow or forearm, unspecified
|
Injuries to the wrist or hand
|
NC50 Injury to fingernail
NC51 Superficial injury of wrist or hand
NC52 Open wound of wrist or hand
NC53 Fracture at wrist or hand level
NC54 Dislocation or strain or sprain of joints or ligaments at wrist or hand level
NC55 Injury of nerves at wrist or hand level
NC56 Injury of blood vessels at wrist or hand level
NC57 Injury of muscle, fascia or tendon at wrist or hand level
NC58 Crushing injury of wrist or hand
NC59 Traumatic amputation of wrist or hand
NC5A Multiple injuries of wrist or hand
NC5Y Other specified injuries to the wrist or hand
NC5Z Injuries to the wrist or hand, unspecified
|
Injuries to the hip or thigh
|
NC70 Superficial injury of hip or thigh
NC71 Open wound of hip or thigh
NC72 Fracture of femur
NC73 Dislocation or strain or sprain of joint or ligaments of hip
NC74 Injury of nerves at hip or thigh level
NC75 Injury of blood vessels at hip or thigh level
NC76 Injury of muscle, fascia, tendon or bursa at hip or thigh level
NC77 Crushing injury of hip or thigh
NC78 Traumatic amputation of hip or thigh
NC79 Multiple injuries of hip or thigh
NC7Y Other specified injuries to the hip or thigh
NC7Z Injuries to the hip or thigh, unspecified
|
Injuries to the knee or lower leg
|
NC90 Superficial injury of knee or lower leg
NC91 Open wound of knee or lower leg
NC92 Fracture of lower leg, including ankle
NC93 Dislocation or strain or sprain of joints or ligaments of knee
NC94 Injury of nerves at lower leg level
NC95 Injury of blood vessels at lower leg level
NC96 Injury of muscle, fascia, tendon or bursa at lower leg level
NC97 Crushing injury of lower leg
NC98 Traumatic amputation of lower leg
NC99 Multiple injuries of lower leg
NC9Y Other specified injuries to the knee or lower leg
NC9Z Injuries to the knee or lower leg, unspecified
|
Injuries to the ankle or foot
|
ND10 Injury to toenail
ND11 Superficial injury of ankle or foot
ND12 Open wound of ankle or foot
ND13 Fracture of foot, except ankle
ND14 Dislocation or strain or sprain of joints or ligaments at ankle or foot level
ND15 Injury of nerves at ankle or foot level
ND16 Injury of blood vessels at ankle or foot level
ND17 Injury of muscle, fascia or tendon at ankle or foot level
ND18 Crushing injury of ankle or foot
ND19 Traumatic amputation of ankle or foot
ND1A Multiple injuries of ankle or foot
ND1Y Other specified injuries to the ankle or foot
ND1Z Injuries to the ankle or foot, unspecified
|
Injuries involving multiple body regions
|
ND30 Superficial injuries involving multiple body regions
ND31 Open wounds involving multiple body regions
ND32 Fractures involving multiple body regions
ND33 Dislocations, strains or sprains involving multiple body regions
ND34 Crushing injuries involving multiple body regions
ND35 Traumatic amputations involving multiple body regions
ND36 Other injuries involving multiple body regions, not elsewhere classified
ND37 Unspecified multiple injuries
|
Injuries to unspecified part of trunk, limb or body region
|
ND50 Fracture of spine, level unspecified
ND51 Other injuries of spine or trunk, level unspecified
ND52 Fracture of arm, level unspecified
ND53 Other injuries of arm, level unspecified
ND54 Fracture of leg, level unspecified
ND55 Other injuries of leg, level unspecified
ND56 Injury of unspecified body region
ND57 Secondary effect of trauma
ND5Y Other specified injuries to unspecified part of trunk, limb or body region
ND5Z Injuries to unspecified part of trunk, limb or body region, unspecified
|
Effects of foreign body entering through natural orifice
|
ND70 Foreign body on external eye
ND71 Foreign body in ear
ND72 Foreign body in respiratory tract
ND73 Foreign body in alimentary tract
ND74 Foreign body in genitourinary tract
ND7Z Effects of foreign body entering through natural orifice, unspecified
|
Burns
|
Burns of external body surface, specified by site
|
ND90 Burn of head or neck except face
ND91 Burn of face except eye or ocular adnexa
ND92 Burn of trunk except perineum or genitalia
ND93 Burn of perineum or genitalia
ND94 Burn of shoulder or arm, except wrist or hand
ND95 Burn of wrist or hand
ND96 Burn of hip or leg, except ankle or foot
ND97 Burn of ankle or foot
ND99 Acute skin injury due to skin contact with corrosive substance
ND9Y Burns of external body surface, other specified site
ND9Z Burns of external body surface, unspecified site
|
Burns of eye or internal organs
|
NE00 Burn of eye or ocular adnexa
NE01 Burn of respiratory tract
NE02 Burn of other internal organs
NE0Z Burns of unspecified internal organ
|
Burns of multiple or unspecified body regions
|
NE10 Burns of multiple body regions
NE11 Burn of unspecified body region
|
NE2Z Burns, unspecified
|
Frostbite
|
NE40 Superficial frostbite
NE41 Frostbite with tissue necrosis
NE42 Frostbite involving multiple body regions
NE4Z Frostbite, unspecified
|
Harmful effects of substances
|
NE60 Harmful effects of drugs, medicaments or biological substances, not elsewhere classified
NE61 Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified
NE6Z Harmful effects of unspecified substance
|
Injury or harm arising from surgical or medical care, not elsewhere classified
|
NE80 Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified
|
NE81 Injury or harm arising from a procedure, not elsewhere classified
|
NE82 Dysfunction or complication of pacemaker, pacemaker lead or implantable cardioverter defibrillator, not elsewhere classified
|
NE83 Injury or harm arising from other device, implant or graft, not elsewhere classified
|
NE84 Failure or rejection of transplanted organs or tissues
|
H00083 Allograft rejection
|
NE85 Complications peculiar to reattachment or amputation
|
NE86 Malignant hyperthermia due to anaesthesia
|
NE87 Failed or difficult intubation
|
NE88 Drug toxicity associated with harm in surgical or medical care, not elsewhere classified
|
NE89 Awareness under general anaesthesia
|
NE8Y Other specified injury or harm arising from surgical or medical care, not elsewhere classified
|
NE8Z Injury or harm arising from surgical or medical care, not elsewhere classified, unspecified
|
Other or unspecified effects of external causes
|
NF00 Effects of radiation, not elsewhere classified
|
NF01 Effects of heat
|
NF02 Hypothermia
|
NF03 Other effects of reduced temperature
|
H01643 Chilblains
|
NF04 Effects of air pressure or water pressure
|
NF05 Asphyxiation
|
NF06 Effects of strenuous physical exercise
|
NF07 Effects of other deprivation
|
NF08 Effects of certain specified external causes
|
NF09 Adverse effects, not elsewhere classified
|
NF0A Certain early complications of trauma, not elsewhere classified
|
NF0Y Other specified effects of external causes
|
NF0Z Unspecified effects of external causes
|
NF2Y Other specified injury, poisoning or certain other consequences of external causes
|
NF2Z Unspecified injury, poisoning or certain other consequences of external causes
|
|
25 Codes for special purposes
|
International provisional assignment of new diseases of uncertain aetiology and emergency use
|
RA01 COVID-19
|
H02398 COVID-19
|
RA02 Post COVID-19 condition
|
RA03 Multisystem inflammatory syndrome associated with COVID-19
|
National provisional assignment of new diseases of uncertain aetiology
|
Human Diseases in ICD-11 Classification