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MG30.3Z Chronic secondary musculoskeletal pain, unspecified International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 coding note If the pain is related to visceral lesions, it should be considered whether a diagnosis of chronic visceral pain is appropriate;
if it is related to neuropathic mechanisms, it should be coded under chronic neuropathic pain;
and if the pain mechanisms are non-specific, chronic musculoskeletal pain should be coded under chronic primary pain.
postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Associated with - multiple selections are allowed [select] XS7G Psychosocial factors present XS8B No psychosocial factors present Has severity - only one may be selected [select] XS5B No pain XS5D Mild pain XS9Q Moderate pain XS2E Severe pain Has alternative severity1 - only one may be selected [select] XS1J No distress XS3R Mild distress XS7C Moderate distress XS7N Severe distress Has alternative severity2 - only one may be selected [select] XS71 No pain-related interference XS5R Mild pain-related interference XS2L Moderate pain-related interference XS2U Severe pain-related interference Temporal pattern and onset - only one may be selected [select] XT5G Intermittent XT6Z Persistent XT5T Persistent with overlaid attacks Has causing condition - a selection is required - multiple selections are allowed [select] 1A00 Cholera 1A01 Intestinal infection due to other Vibrio 1A02 Intestinal infections due to Shigella 1A03 Intestinal infections due to Escherichia coli – 1A03.0 Enteropathogenic Escherichia coli infection – 1A03.1 Enterotoxigenic Escherichia coli infection – 1A03.2 Enteroinvasive Escherichia coli infection – 1A03.3 Enterohaemorrhagic Escherichia coli infection – 1A03.Y Intestinal infections due to other specified Escherichia coli – 1A03.Z Intestinal infections due to Escherichia coli, unspecified 1A04 Intestinal infections due to Clostridioides difficile 1A05 Intestinal infections due to Yersinia enterocolitica 1A06 Gastroenteritis due to Campylobacter 1A07 Typhoid fever – 1A07.0 Typhoid peritonitis – 1A07.Y Other specified typhoid fever – 1A07.Z Typhoid fever, unspecified 1A08 Paratyphoid fever 1A09 Infections due to other Salmonella – 1A09.0 Salmonella enteritis – 1A09.Y Infections due to other Salmonella in other organs – 1A09.Z Salmonella infection, unspecified 1A0Y Other specified bacterial intestinal infections 1A0Z Bacterial intestinal infections, unspecified 1A10 Foodborne staphylococcal intoxication 1A11 Botulism – 1A11.0 Foodborne intoxication by botulinum toxin – 1A11.1 Other forms of botulism – 1A11.Z Botulism, unspecified 1A12 Foodborne Clostridium perfringens intoxication 1A13 Foodborne Bacillus cereus intoxication 1A1Y Other specified bacterial foodborne intoxications 1A1Z Bacterial foodborne intoxications, unspecified 1A20 Enteritis due to Adenovirus 1A21 Gastroenteritis due to Astrovirus 1A22 Gastroenteritis due to Rotavirus 1A23 Enteritis due to Norovirus 1A24 Intestinal infections due to Cytomegalovirus 1A2Y Other specified viral intestinal infections 1A2Z Viral intestinal infections, unspecified 1A30 Infections due to Balantidium coli 1A31 Giardiasis 1A32 Cryptosporidiosis 1A33 Cystoisosporiasis – 1A33.0 Cystoisosporiasis of small intestine – 1A33.1 Cystoisosporiasis of colon – 1A33.Y Other specified cystoisosporiasis – 1A33.Z Cystoisosporiasis, unspecified 1A34 Sarcocystosis 1A35 Blastocystosis 1A36 Amoebiasis – 1A36.0 Intestinal infections due to Entamoeba – 1A36.1 Extraintestinal infections due to Entamoeba – 1A36.Z Amoebiasis, unspecified –– 1A36.00 Acute amoebiasis –– 1A36.01 Amoeboma of intestine –– 1A36.0Z Intestinal infections due to Entamoeba, unspecified –– 1A36.10 Amoebic liver abscess –– 1A36.11 Amoebic lung abscess –– 1A36.12 Cutaneous amoebiasis –– 1A36.1Y Amoebiasis of other specified sites 1A3Y Other specified protozoal intestinal infections 1A3Z Protozoal intestinal infections, unspecified 1A40 Gastroenteritis or colitis without specification of infectious agent 1A40.0 Gastroenteritis or colitis without specification of origin 1A40.Z Infectious gastroenteritis or colitis without specification of infectious agent 1A60 Congenital syphilis – 1A60.0 Early congenital syphilis, symptomatic – 1A60.1 Early congenital syphilis, latent – 1A60.2 Late congenital syphilitic oculopathy – 1A60.3 Late congenital neurosyphilis – 1A60.4 Other late congenital syphilis, symptomatic – 1A60.5 Late congenital syphilis, latent – 1A60.Z Congenital syphilis, unspecified 1A61 Early syphilis – 1A61.0 Primary genital syphilis – 1A61.1 Primary anal syphilis – 1A61.2 Primary syphilis of other sites – 1A61.3 Secondary syphilis of skin or mucous membranes – 1A61.4 Secondary syphilis of other sites – 1A61.5 Latent early syphilis – 1A61.Y Other specified early syphilis – 1A61.Z Early syphilis, unspecified 1A62 Late syphilis – 1A62.0 Neurosyphilis – 1A62.1 Cardiovascular late syphilis – 1A62.2 Symptomatic late syphilis of other sites – 1A62.Y Other specified late syphilis – 1A62.Z Late syphilis, unspecified –– 1A62.00 Asymptomatic neurosyphilis –– 1A62.01 Symptomatic late neurosyphilis –– 1A62.0Z Neurosyphilis, unspecified –– 1A62.20 Ocular late syphilis –– 1A62.21 Late syphilis involving the musculoskeletal system –– 1A62.22 Late syphilis of skin or mucous membranes –– 1A62.2Y Symptomatic late syphilis of other specified sites –– 1A62.2Z Symptomatic late syphilis of unspecified site 1A63 Latent syphilis, unspecified as early or late 1A6Z Syphilis, unspecified 1A70 Gonococcal genitourinary infection – 1A70.0 Gonococcal infection of lower genitourinary tract without periurethral or accessory gland abscess – 1A70.1 Gonococcal infection of lower genitourinary tract with periurethral or accessory gland abscess – 1A70.Y Gonococcal infection of other specified genitourinary organ – 1A70.Z Gonococcal genitourinary infection, unspecified –– 1A70.00 Gonorrhoea of penis –– 1A70.0Y Other specified gonococcal infection of lower genitourinary tract without periurethral or accessory gland abscess –– 1A70.0Z Gonococcal infection of lower genitourinary tract without periurethral or accessory gland abscess, unspecified 1A71 Gonococcal pelviperitonitis 1A72 Gonococcal infection of other sites – 1A72.0 Gonococcal infection of musculoskeletal system – 1A72.1 Gonococcal infection of rectum – 1A72.2 Gonococcal infection of anus – 1A72.3 Gonococcal pharyngitis – 1A72.4 Gonococcal infection of eye – 1A72.Y Gonococcal infection of other specified sites 1A73 Disseminated gonococcal infection 1A7Z Gonococcal infection, unspecified 1A80 Chlamydial lymphogranuloma 1A81 Non-ulcerative sexually transmitted chlamydial infection – 1A81.0 Chlamydial infection of lower genitourinary tract – 1A81.1 Chlamydial infection of internal reproductive organs – 1A81.Y Non-ulcerative sexually transmitted chlamydial infection of other specified site – 1A81.Z Non-ulcerative sexually transmitted chlamydial infection of unspecified site 1A8Y Other specified sexually transmissible infections due to chlamydia 1A8Z Sexually transmissible infections due to chlamydia, unspecified 1A90 Chancroid 1A91 Granuloma inguinale 1A92 Trichomoniasis 1A93 Sexually transmissible infestations 1A94 Anogenital herpes simplex infection 1A94.0 Herpes simplex infection of genitalia or urogenital tract 1A94.1 Herpes simplex infection of perianal skin or rectum 1A94.Z Anogenital herpes simplex infection without further specification 1A95 Anogenital warts 1A95.0 Anal warts 1A95.1 Genital warts 1A95.2 Extragenital condylomata acuminata 1A95.Z Anogenital warts, unspecified 1A9Y Other specified predominantly sexually transmitted infections 1A9Z Predominantly sexually transmitted infections, unspecified 1B10 Tuberculosis of the respiratory system – 1B10.0 Respiratory tuberculosis, confirmed – 1B10.1 Respiratory tuberculosis, not confirmed – 1B10.Z Respiratory tuberculosis, without mention of bacteriological or histological confirmation 1B11 Tuberculosis of the nervous system – 1B11.0 Tuberculous meningitis – 1B11.1 Tuberculous meningoencephalitis – 1B11.2 Meningeal tuberculoma – 1B11.3 Tuberculous granuloma of brain – 1B11.Y Tuberculosis of other specified part of nervous system – 1B11.Z Tuberculosis of the nervous system, unspecified 1B12 Tuberculosis of other systems and organs – 1B12.0 Tuberculosis of heart – 1B12.1 Tuberculosis of eye – 1B12.2 Tuberculosis of ear – 1B12.3 Tuberculosis of endocrine glands – 1B12.4 Tuberculosis of the musculoskeletal system – 1B12.5 Tuberculosis of the genitourinary system – 1B12.6 Tuberculous peripheral lymphadenopathy – 1B12.7 Tuberculosis of the digestive system – 1B12.8 Cutaneous tuberculosis – 1B12.Y Tuberculosis of other specified organ or site –– 1B12.40 Tuberculosis of bones or joints –– 1B12.41 Tuberculous myositis –– 1B12.4Y Tuberculosis of other specified part of the musculoskeletal system –– 1B12.4Z Tuberculosis of the musculoskeletal system, unspecified 1B13 Miliary tuberculosis – 1B13.0 Acute miliary tuberculosis of a single specified site – 1B13.1 Acute miliary tuberculosis of multiple sites – 1B13.2 Acute miliary tuberculosis, unspecified site – 1B13.Y Other specified miliary tuberculosis – 1B13.Z Miliary tuberculosis, unspecified 1B14 Latent tuberculosis 1B1Y Other specified tuberculosis 1B1Z Tuberculosis, unspecified 1B20 Leprosy 1B20.0 Paucibacillary leprosy 1B20.1 Multibacillary leprosy 1B20.2 Leprosy reactions 1B20.3 Complications of leprosy 1B20.Z Leprosy, unspecified – 1B20.20 Type I leprosy reaction – 1B20.21 Type II leprosy reaction 1B21 Infections due to non-tuberculous mycobacteria 1B21.0 Pulmonary infection due to non-tuberculous mycobacterium 1B21.1 Non-tuberculous mycobacterial lymphadenitis 1B21.2 Cutaneous non-tuberculous mycobacterial infection 1B21.3 Disseminated non-tuberculous mycobacterial infection 1B21.4 Gastrointestinal non-tuberculous mycobacterial infection 1B21.Y Non-tuberculous mycobacterial infection of other specified site 1B21.Z Non-tuberculous mycobacterial infection of unspecified site – 1B21.20 Mycobacterium ulcerans infection – 1B21.2Y Cutaneous infection due to other specified non-tuberculous mycobacteria – 1B21.2Z Cutaneous infection due to unspecified non-tuberculous mycobacteria 1B2Y Other specified mycobacterial diseases 1B2Z Mycobacterial diseases, unspecified 1B40 Acute rheumatic fever without mention of heart involvement – 1B40.0 Rheumatic arthritis, acute or subacute – 1B40.Y Other specified acute rheumatic fever without mention of heart involvement – 1B40.Z Acute rheumatic fever without mention of heart involvement, unspecified 1B41 Acute rheumatic fever with heart involvement – 1B41.0 Acute rheumatic pericarditis – 1B41.1 Acute rheumatic endocarditis – 1B41.2 Acute rheumatic myocarditis – 1B41.Y Other acute rheumatic heart disease – 1B41.Z Acute rheumatic heart disease, unspecified –– 1B41.10 Rheumatic aortitis –– 1B41.1Y Other specified acute rheumatic endocarditis –– 1B41.1Z Acute rheumatic endocarditis, unspecified 1B42 Rheumatic chorea 1B50 Scarlet fever 1B51 Streptococcal pharyngitis 1B53 Meningitis due to Streptococcus 1B54 Meningitis due to Staphylococcus 1B5Y Other specified staphylococcal or streptococcal diseases 1B5Z Staphylococcal or streptococcal diseases, unspecified 1B70 Bacterial cellulitis, erysipelas or lymphangitis 1B70.0 Erysipelas 1B70.1 Streptococcal cellulitis of skin 1B70.2 Staphylococcal cellulitis of skin 1B70.3 Ascending bacterial lymphangitis 1B70.Y Bacterial cellulitis or lymphangitis due to other specified bacterium 1B70.Z Bacterial cellulitis or lymphangitis due to unspecified bacterium – 1B70.00 Erysipelas of face – 1B70.01 Erysipelas of external ear – 1B70.02 Erysipelas of lower limb – 1B70.0Y Erysipelas of other specified site – 1B70.0Z Erysipelas, unspecified 1B71 Necrotising fasciitis 1B71.0 Streptococcal necrotising fasciitis 1B71.1 Polymicrobial necrotising fasciitis 1B71.2 Neonatal necrotising fasciitis 1B71.Y Necrotising fasciitis due to other specified bacterial infection 1B71.Z Necrotising fasciitis, unspecified 1B72 Impetigo 1B72.0 Bullous impetigo 1B72.1 Non-bullous impetigo 1B72.2 Secondary impetiginisation of the skin 1B72.Y Other specified impetigo 1B72.Z Impetigo, unspecified 1B73 Ecthyma 1B73.0 Streptococcal ecthyma 1B73.1 Staphylococcal ecthyma 1B73.2 Ecthyma gangrenosum 1B73.Y Other specified ecthyma 1B73.Z Ecthyma, unspecified 1B74 Superficial bacterial folliculitis 1B74.0 Staphylococcus aureus superficial folliculitis 1B74.Y Superficial bacterial folliculitis due to other specified organism 1B74.Z Superficial bacterial folliculitis due to unspecified organism 1B75 Deep bacterial folliculitis or pyogenic abscess of the skin 1B75.0 Furuncle 1B75.1 Carbuncle 1B75.2 Furunculosis 1B75.3 Pyogenic abscess of the skin 1B75.4 Chronic deep bacterial folliculitis 1B75.Z Deep bacterial folliculitis or pyogenic abscess of the skin, unspecified 1B7Y Other specified pyogenic bacterial infection of skin or subcutaneous tissue 1B7Z Pyogenic bacterial infection of skin or subcutaneous tissue, unspecified 1B90 Rat-bite fevers 1B90.0 Spirillosis 1B90.1 Streptobacillosis 1B91 Leptospirosis 1B92 Glanders 1B93 Plague 1B93.0 Bubonic plague 1B93.1 Cellulocutaneous plague 1B93.2 Pneumonic plague 1B93.3 Plague meningitis 1B93.Y Other specified plague 1B93.Z Plague, unspecified 1B94 Tularaemia 1B94.0 Ulceroglandular tularaemia 1B94.Y Other specified tularaemia 1B94.Z Tularaemia, unspecified 1B95 Brucellosis 1B96 Erysipeloid 1B97 Anthrax 1B98 Cat-scratch disease 1B99 Pasteurellosis 1B9A Extraintestinal yersiniosis 1B9Z Unspecified zoonotic bacterial disease 1C10 Actinomycosis 1C10.0 Pulmonary actinomycosis 1C10.1 Abdominal actinomycosis 1C10.2 Cervicofacial actinomycosis 1C10.3 Primary cutaneous actinomycosis 1C10.Y Other specified forms of actinomycosis 1C10.Z Actinomycosis, unspecified 1C11 Bartonellosis 1C11.0 Carrion disease 1C11.1 Trench fever 1C11.Y Other forms of bartonellosis 1C11.Z Bartonellosis, unspecified – 1C11.00 Oroya fever – 1C11.01 Verruga peruana 1C12 Whooping cough 1C12.0 Whooping cough due to Bordetella pertussis 1C12.1 Whooping cough due to Bordetella parapertussis 1C12.Y Other specified whooping cough 1C12.Z Whooping cough, unspecified 1C13 Tetanus 1C14 Obstetrical tetanus 1C15 Tetanus neonatorum 1C16 Gas gangrene 1C17 Diphtheria 1C17.0 Pharyngeal or tonsillar diphtheria 1C17.1 Nasal diphtheria 1C17.2 Laryngeal diphtheria 1C17.3 Cutaneous diphtheria 1C17.Y Other specified diphtheria 1C17.Z Diphtheria, unspecified – 1C17.00 Postdiphtheritic paralysis of uvula – 1C17.0Y Other specified pharyngeal or tonsillar diphtheria – 1C17.0Z Pharyngeal or tonsillar diphtheria, unspecified 1C18 Brazilian purpuric fever 1C19 Legionellosis 1C19.0 Nonpneumonic Legionnaires' disease 1C19.1 Legionnaires disease 1C19.Z Legionellosis, unspecified 1C1A Listeriosis 1C1A.0 Cutaneous listeriosis 1C1A.1 Listerial meningitis or meningoencephalitis 1C1A.Y Other specified listeriosis 1C1A.Z Listeriosis, unspecified 1C1B Nocardiosis 1C1B.0 Pulmonary nocardiosis 1C1B.1 Cutaneous nocardiosis 1C1B.Y Other specified forms of nocardiosis 1C1B.Z Nocardiosis, unspecified 1C1C Meningococcal disease 1C1C.0 Meningococcal meningitis 1C1C.1 Waterhouse-Friderichsen syndrome 1C1C.2 Meningococcaemia 1C1C.Y Other specified meningococcal disease 1C1C.Z Meningococcal disease, unspecified – 1C1C.20 Acute meningococcaemia – 1C1C.2Y Other specified meningococcaemia – 1C1C.2Z Meningococcaemia, unspecified 1C1D Yaws 1C1D.0 Primary yaws 1C1D.1 Secondary yaws 1C1D.2 Tertiary yaws 1C1D.3 Latent yaws 1C1D.Z Yaws, unspecified 1C1E Pinta 1C1E.0 Primary lesions of pinta 1C1E.1 Intermediate lesions of pinta 1C1E.2 Late lesions of pinta 1C1E.3 Mixed lesions of pinta 1C1E.Z Pinta, unspecified 1C1F Endemic non-venereal syphilis 1C1G Lyme borreliosis 1C1G.0 Early cutaneous Lyme borreliosis 1C1G.1 Disseminated Lyme borreliosis 1C1G.Y Other specified Lyme borreliosis 1C1G.Z Lyme borreliosis, unspecified – 1C1G.10 Lyme neuroborreliosis – 1C1G.11 Lyme carditis – 1C1G.12 Ophthalmic Lyme borreliosis – 1C1G.13 Lyme arthritis – 1C1G.14 Late cutaneous Lyme borreliosis – 1C1G.1Y Other specified disseminated Lyme borreliosis – 1C1G.1Z Disseminated Lyme borreliosis, unspecified 1C1H Necrotising ulcerative gingivitis 1C1H.0 Other Vincent infections 1C1H.Y Other specified necrotising ulcerative gingivitis 1C1H.Z Necrotising ulcerative gingivitis, unspecified 1C1J Relapsing fever 1C1J.0 Tick-borne relapsing fever 1C1J.1 Louse-borne relapsing fever 1C1J.Z Relapsing fever, unspecified 1C20 Chlamydial conjunctivitis 1C21 Chlamydial peritonitis 1C22 Infections due to Chlamydia psittaci 1C23 Trachoma – 1C23.0 Initial stage of trachoma – 1C23.1 Active stage of trachoma – 1C23.Y Other specified trachoma – 1C23.Z Trachoma, unspecified 1C2Y Other specified diseases due to chlamydiae 1C2Z Diseases due to chlamydiae, unspecified 1C30 Typhus fever – 1C30.0 Epidemic louse-borne typhus fever due to Rickettsia prowazekii – 1C30.1 Recrudescent typhus – 1C30.2 Typhus fever due to Rickettsia typhi – 1C30.3 Typhus fever due to Orientia tsutsugamushi – 1C30.Y Other specified typhus fever – 1C30.Z Typhus fever, unspecified 1C31 Spotted fever – 1C31.0 Spotted fever due to Rickettsia rickettsii – 1C31.1 Spotted fever due to Rickettsia conorii – 1C31.2 Spotted fever due to Rickettsia sibirica – 1C31.3 Spotted fever due to Rickettsia australis – 1C31.Y Other specified spotted fever – 1C31.Z Spotted fever, unspecified 1C32 Rickettsialpox 1C33 Q fever 1C3Y Other specified rickettsioses 1C3Z Rickettsioses, unspecified 1C40 Campylobacteriosis 1C41 Bacterial infection of unspecified site 1C42 Melioidosis 1C43 Actinomycetoma 1C44 Non-pyogenic bacterial infections of the skin 1C45 Toxic shock syndrome 1C45.0 Streptococcal toxic shock syndrome 1C45.1 Staphylococcal toxic shock syndrome 1C45.Y Toxic shock syndrome due to other specified infectious agent 1C45.Z Toxic shock syndrome without specified infectious agent 1C4Y Other specified bacterial diseases 1C4Z Unspecified bacterial disease 1C60 Human immunodeficiency virus disease associated with tuberculosis 1C60.0 HIV disease clinical stage 1 associated with tuberculosis 1C60.1 HIV disease clinical stage 2 associated with tuberculosis 1C60.2 HIV disease clinical stage 3 associated with tuberculosis 1C60.3 HIV disease clinical stage 4 associated with tuberculosis 1C60.Z Human immunodeficiency virus disease associated with tuberculosis, clinical stage unspecified – 1C60.30 Kaposi sarcoma associated with human immunodeficiency virus disease associated with tuberculosis – 1C60.3Y Other specified HIV disease clinical stage 4 associated with tuberculosis – 1C60.3Z HIV disease clinical stage 4 associated with tuberculosis, unspecified 1C61 Human immunodeficiency virus disease associated with malaria 1C61.0 HIV disease clinical stage 1 associated with malaria 1C61.1 HIV disease clinical stage 2 associated with malaria 1C61.2 HIV disease clinical stage 3 associated with malaria 1C61.3 HIV disease clinical stage 4 associated with malaria 1C61.Z Human immunodeficiency virus disease associated with malaria, clinical stage unspecified – 1C61.30 Kaposi sarcoma associated with human immunodeficiency virus disease associated with malaria – 1C61.3Y Other specified HIV disease clinical stage 4 associated with malaria – 1C61.3Z HIV disease clinical stage 4 associated with malaria, unspecified 1C62 Human immunodeficiency virus disease without mention of tuberculosis or malaria 1C62.0 HIV disease clinical stage 1 without mention of tuberculosis or malaria 1C62.1 HIV disease clinical stage 2 without mention of tuberculosis or malaria 1C62.2 HIV disease clinical stage 3 without mention of tuberculosis or malaria 1C62.3 HIV disease clinical stage 4 without mention of tuberculosis or malaria 1C62.Z Human immunodeficiency virus disease without mention of associated disease or condition, clinical stage unspecified – 1C62.30 Kaposi sarcoma associated with human immunodeficiency virus disease without mention of tuberculosis or malaria – 1C62.3Y Other specified HIV disease clinical stage 4 without mention of tuberculosis or malaria – 1C62.3Z HIV disease clinical stage 4 without mention of tuberculosis or malaria, unspecified 1C80 Viral encephalitis, not elsewhere classified 1C81 Acute poliomyelitis 1C82 Rabies 1C83 Western equine encephalitis 1C84 Eastern equine encephalitis 1C85 Japanese encephalitis 1C86 St Louis encephalitis 1C87 Rocio viral encephalitis 1C88 Murray Valley encephalitis 1C8B California encephalitis 1C8C Venezuelan equine encephalitis 1C8D La Crosse encephalitis 1C8E Viral meningitis, not elsewhere classified 1C8E.1 Enteroviral meningitis 1C8E.2 Meningitis due to adenovirus 1C8E.Y Other specified viral meningitis, not elsewhere classified 1C8E.Z Viral meningitis, unspecified 1C8F Lymphocytic choriomeningitis 1C8G Tick-borne encephalitis 1C8G.0 Far Eastern tick-borne encephalitis 1C8G.1 Central European tick-borne encephalitis 1C8G.2 Siberian tick-borne encephalitis 1C8G.Z Tick-borne encephalitis, unspecified 1C8Y Other specified viral infections of the central nervous system 1C8Z Viral infections of the central nervous system, unspecified 1D00 Infectious encephalitis, not elsewhere classified 1D00.0 Bacterial encephalitis 1D00.1 Fungal encephalitis 1D00.2 Parasitic or protozoal encephalitis 1D00.Y Other specified infectious encephalitis, not elsewhere classified 1D00.Z Infectious encephalitis, unspecified 1D01 Infectious meningitis, not elsewhere classified 1D01.0 Bacterial meningitis 1D01.1 Fungal meningitis 1D01.2 Parasitic or protozoal meningitis 1D01.3 Benign recurrent meningitis 1D01.Y Other specified infectious meningitis, not elsewhere classified 1D01.Z Infectious meningitis, unspecified – 1D01.00 Meningitis due to Haemophilus influenzae – 1D01.0Y Other specified bacterial meningitis – 1D01.0Z Bacterial meningitis, unspecified 1D02 Infectious myelitis, not elsewhere classified 1D02.0 Bacterial myelitis 1D02.1 Viral myelitis 1D02.2 Fungal myelitis 1D02.3 Parasitic myelitis 1D02.Y Other specified infectious myelitis, not elsewhere classified 1D02.Z Infectious myelitis, unspecified 1D03 Infectious abscess of the central nervous system 1D03.0 Intraspinal intramedullary abscess 1D03.1 Intraspinal subdural abscess 1D03.2 Intraspinal extradural abscess 1D03.3 Intracranial abscess 1D03.4 Intraspinal epidural abscess 1D03.5 Spinal cord abscess 1D03.Y Other specified site of infectious abscess of the central nervous system 1D03.Z Infectious abscess of the central nervous system, site unspecified – 1D03.30 Deep cerebral hemispheric abscess – 1D03.31 Abscess of the corpus callosum – 1D03.32 Pituitary abscess – 1D03.33 Multiple or widespread intracranial abscess – 1D03.3Y Other specified intracranial abscess – 1D03.3Z Intracranial abscess, unspecified 1D04 Infectious granulomas of the central nervous system 1D04.0 Parasitic intracerebral granuloma 1D04.1 Intracranial granuloma 1D04.2 Intraspinal intramedullary granuloma 1D04.3 Intraspinal subdural granuloma 1D04.4 Intraspinal extradural granuloma 1D04.5 Intraspinal epidural granuloma 1D04.Y Other specified site of infectious granulomas of the central nervous system 1D04.Z Infectious granulomas of the central nervous system, site unspecified – 1D04.10 Fungal intracranial granuloma – 1D04.1Y Other specified intracranial granuloma – 1D04.1Z Intracranial granuloma, unspecified 1D05 Infectious cysts of the central nervous system 1D05.0 Epidural infectious cyst 1D05.1 Subdural infectious cyst 1D05.Y Other specified infectious cysts of the central nervous system 1D05.Z Infectious cysts of the central nervous system, unspecified 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 1D20 Dengue without warning signs 1D21 Dengue with warning signs 1D22 Severe dengue 1D2Z Dengue fever, unspecified 1D40 Chikungunya virus disease 1D41 Colorado tick fever 1D42 O'nyong-nyong fever 1D43 Oropouche virus disease 1D44 Rift Valley fever 1D45 Sandfly fever 1D46 West Nile virus infection 1D47 Yellow fever 1D48 Zika virus disease 1D49 Crimean-Congo haemorrhagic fever 1D4A Omsk haemorrhagic fever 1D4B Kyasanur Forest disease 1D4C Alkhurma haemorrhagic fever 1D4D Ross River disease 1D4E Severe fever with thrombocytopenia syndrome 1D4Y Other specified arthropod-borne viral fevers 1D4Z Arthropod-borne viral fever, virus unspecified 1D60 Filovirus disease 1D60.0 Ebola disease 1D60.1 Marburg disease 1D60.Y Other specified filovirus disease 1D60.Z Filovirus disease, virus unspecified – 1D60.00 Bundibugyo virus disease – 1D60.01 Ebola virus disease – 1D60.02 Sudan virus disease – 1D60.03 Atypical Ebola disease – 1D60.0Y Other specified Ebola disease – 1D60.0Z Ebola disease, virus unspecified – 1D60.10 Marburg virus disease – 1D60.11 Atypical Marburg disease – 1D60.1Y Other specified Marburg disease – 1D60.1Z Marburg disease, virus unspecified 1D61 Arenavirus disease 1D61.0 Argentinian haemorrhagic fever 1D61.1 Bolivian haemorrhagic fever 1D61.2 Lassa fever 1D61.3 Venezuelan haemorrhagic fever 1D61.Y Other specified arenavirus disease 1D61.Z Arenavirus disease, unspecified 1D62 Hantavirus disease 1D62.0 Haemorrhagic fever with renal syndrome 1D62.1 Hantavirus pulmonary syndrome 1D62.2 Atypical hantavirus disease 1D62.Y Other specified hantavirus disease 1D62.Z Hantavirus disease, unspecified 1D63 Henipavirus encephalitis 1D64 Middle East respiratory syndrome 1D65 Severe acute respiratory syndrome 1D6Y Other specified zoonotic viral diseases 1D6Z Zoonotic viral disease, virus unspecified 1D80 Mumps 1D80.0 Mumps without complication 1D80.1 Orchitis due to mumps virus 1D80.2 Meningitis due to mumps virus 1D80.3 Encephalitis due to mumps virus 1D80.4 Pancreatitis due to mumps virus 1D80.Y Other specified mumps 1D81 Infectious mononucleosis 1D81.0 Mononucleosis due to Epstein-Barr virus 1D81.1 Mononucleosis due to cytomegalovirus 1D81.Y Other specified infectious mononucleosis 1D81.Z Infectious mononucleosis, unspecified 1D82 Cytomegaloviral disease 1D82.0 Cytomegaloviral hepatitis 1D82.1 Cytomegaloviral pancreatitis 1D82.Y Other specified cytomegaloviral disease 1D82.Z Cytomegaloviral disease, unspecified 1D83 Epidemic myalgia 1D84 Viral conjunctivitis 1D84.0 Conjunctivitis due to adenovirus 1D84.1 Acute epidemic haemorrhagic conjunctivitis 1D84.Y Other specified viral conjunctivitis 1D84.Z Viral conjunctivitis, unspecified 1D85 Viral carditis 1D85.0 Dilated cardiomyopathy secondary to viral myocarditis 1D85.1 Acute viral carditis 1D85.2 Chronic viral carditis 1D85.3 Aseptic myocarditis of newborn 1D85.4 Coxsackie carditis 1D85.Y Other specified viral carditis 1D85.Z Viral carditis, unspecified 1D86 Viral haemorrhagic fever, not elsewhere classified 1D90 Adenovirus infection of unspecified site 1D91 Enterovirus infection of unspecified site 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 1E30 Influenza due to identified seasonal influenza virus 1E31 Influenza due to identified zoonotic or pandemic influenza virus 1E32 Influenza, virus not identified 1E50 Acute viral hepatitis 1E50.0 Acute hepatitis A 1E50.1 Acute hepatitis B 1E50.2 Acute hepatitis C 1E50.3 Acute hepatitis D 1E50.4 Acute hepatitis E 1E50.Y Other specified acute viral hepatitis 1E50.Z Acute viral hepatitis, unspecified 1E51 Chronic viral hepatitis 1E51.0 Chronic hepatitis B 1E51.1 Chronic hepatitis C 1E51.2 Chronic hepatitis D 1E51.3 Chronic hepatitis E 1E51.Y Other specified chronic viral hepatitis 1E51.Z Chronic viral hepatitis, unspecified – 1E51.00 Chronic hepatitis B with human immunodeficiency virus co-infection – 1E51.0Y Other specified chronic hepatitis B – 1E51.0Z Chronic hepatitis B, unspecified 1E5Z Viral hepatitis, unspecified 1E70 Smallpox 1E71 Mpox 1E72 Cowpox 1E73 Vaccinia 1E74 Buffalopox 1E75 Orf 1E76 Molluscum contagiosum 1E7Y Other specified infections due to poxvirus 1E7Z Infections due to poxvirus, unspecified 1E80 Common warts – 1E80.0 Digital or periungual warts – 1E80.1 Plantar warts – 1E80.Y Other specified common warts – 1E80.Z Common warts, unspecified 1E81 Plane warts 1E82 Warts of lips or oral cavity – 1E82.0 Focal epithelial hyperplasia of oral mucous membranes 1E83 Wart virus proliferation in immune-deficient states 1E8Z Viral warts, not elsewhere classified 1E90 Varicella – 1E90.0 Varicella without complication – 1E90.1 Varicella meningitis – 1E90.2 Varicella encephalitis – 1E90.Y Varicella with other specified complication – 1E90.Z Varicella, unspecified 1E91 Zoster – 1E91.0 Zoster without complications – 1E91.1 Ophthalmic zoster – 1E91.2 Disseminated zoster – 1E91.3 Zoster with central nervous system involvement – 1E91.4 Acute neuropathy of cranial nerve due to zoster – 1E91.5 Postherpetic polyneuropathy – 1E91.Y Zoster with other specified complications – 1E91.Z Zoster, unspecified –– 1E91.40 Acute trigeminal zoster neuropathy –– 1E91.41 Acute herpetic geniculate ganglionitis –– 1E91.4Y Other specified acute neuropathy of cranial nerve due to zoster –– 1E91.4Z Acute neuropathy of cranial nerve due to zoster, unspecified 1F00 Herpes simplex infections 1F00.0 Herpes simplex infection of skin or mucous membrane 1F00.1 Herpes simplex infection of the eye 1F00.2 Herpes simplex infection of central nervous system 1F00.3 Disseminated herpes simplex infection 1F00.Y Other specified herpes simplex infections 1F00.Z Herpes simplex infections, unspecified – 1F00.00 Herpes simplex infection of skin – 1F00.01 Herpes simplex labialis – 1F00.02 Herpes simplex gingivostomatitis – 1F00.03 Disseminated cutaneous herpes simplex infection complicating other skin diseases – 1F00.0Y Other specified herpes simplex infection of skin or mucous membrane – 1F00.10 Herpes simplex keratitis – 1F00.11 Herpes simplex infection of eyelid – 1F00.1Y Other specified herpes simplex infection of the eye – 1F00.1Z Herpes simplex infection of the eye, unspecified – 1F00.20 Herpes simplex meningitis – 1F00.21 Encephalitis due to herpes simplex virus – 1F00.2Y Other specified herpes simplex infection of central nervous system 1F01 Roseola infantum 1F02 Rubella 1F02.0 Rubella with neurological complications 1F02.1 Rubella arthritis 1F02.2 Rubella without complication 1F02.Y Rubella with other specified complication 1F03 Measles 1F03.0 Measles without complication 1F03.1 Measles complicated by encephalitis 1F03.2 Measles complicated by meningitis 1F03.Y Measles with other complications 1F04 Erythema infectiosum 1F05 Picornavirus infections presenting in the skin or mucous membranes 1F05.0 Enteroviral vesicular stomatitis 1F05.1 Enteroviral vesicular pharyngitis 1F05.2 Enteroviral exanthematous fever 1F05.3 Foot and mouth disease 1F05.Y Other specified picornavirus infections presenting in the skin or mucous membranes 1F0Y Other specified viral infections characterised by skin or mucous membrane lesions 1F0Z Viral infections characterised by skin or mucous membrane lesions, unspecified 1F20 Aspergillosis 1F20.0 Invasive aspergillosis 1F20.1 Non-invasive aspergillosis 1F20.Z Aspergillosis, unspecified – 1F20.00 Invasive aspergillosis of the digestive tract – 1F20.01 Invasive cerebral aspergillosis – 1F20.02 Disseminated aspergillosis – 1F20.0Y Invasive aspergillosis of other specified site – 1F20.0Z Invasive aspergillosis, unspecified – 1F20.10 Aspergillus otomycosis – 1F20.11 Chronic aspergillosis of the paranasal sinuses – 1F20.12 Chronic pulmonary aspergillosis – 1F20.13 Tonsillar aspergillosis – 1F20.14 Aspergillus bronchitis – 1F20.15 Obstructing aspergillus tracheobronchitis – 1F20.1Y Other specified non-invasive aspergillosis – 1F20.1Z Non-invasive aspergillosis, unspecified 1F21 Basidiobolomycosis 1F22 Blastomycosis 1F23 Candidosis 1F23.0 Candidosis of lips or oral mucous membranes 1F23.1 Candidosis of skin or mucous membranes 1F23.2 Candidosis of gastrointestinal tract 1F23.3 Systemic or invasive candidosis 1F23.Y Other specified candidosis 1F23.Z Candidosis, unspecified – 1F23.10 Vulvovaginal candidosis – 1F23.11 Candida balanoposthitis – 1F23.12 Flexural or intertriginous candidosis – 1F23.13 Candidosis of nail or paronychium – 1F23.14 Chronic mucocutaneous candidosis – 1F23.15 Disseminated cutaneous candidosis – 1F23.16 Candida otomycosis – 1F23.1Y Candidosis of skin or mucous membrane of other specified site – 1F23.1Z Candidosis of skin or mucous membranes, unspecified – 1F23.30 Candida meningitis – 1F23.31 Pulmonary candidosis – 1F23.3Y Other specified systemic or invasive candidosis – 1F23.3Z Systemic or invasive candidosis, unspecified 1F24 Chromoblastomycosis 1F25 Coccidioidomycosis 1F25.0 Pulmonary coccidioidomycosis 1F25.1 Extrathoracic coccidioidomycosis 1F25.Z Coccidioidomycosis, unspecified – 1F25.00 Acute pulmonary coccidioidomycosis – 1F25.01 Chronic pulmonary coccidioidomycosis – 1F25.10 Disseminated coccidioidomycosis – 1F25.11 Primary cutaneous coccidioidomycosis – 1F25.12 Coccidioides meningitis – 1F25.1Y Other specified extrathoracic coccidioidomycosis – 1F25.1Z Extrathoracic coccidioidomycosis, unspecified 1F26 Conidiobolomycosis 1F27 Cryptococcosis 1F27.0 Pulmonary cryptococcosis 1F27.1 Cerebral cryptococcosis 1F27.2 Disseminated cryptococcosis 1F27.Y Other specified cryptococcosis 1F27.Z Cryptococcosis, unspecified – 1F27.10 Meningitis due to Cryptococcus neoformans 1F28 Dermatophytosis 1F28.0 Dermatophytosis of scalp 1F28.1 Dermatophytosis of nail 1F28.2 Dermatophytosis of foot 1F28.3 Genitocrural dermatophytosis 1F28.4 Kerion 1F28.5 Disseminated dermatophytosis 1F28.Y Other specified dermatophytosis 1F28.Z Dermatophytosis, unspecified 1F29 Eumycetoma 1F2A Histoplasmosis 1F2A.0 Pulmonary histoplasmosis capsulati 1F2A.1 Histoplasmosis due to Histoplasma duboisii 1F2A.Y Other specified histoplasmosis 1F2A.Z Histoplasmosis, unspecified 1F2B Lobomycosis 1F2C Mucormycosis 1F2D Non-dermatophyte superficial dermatomycoses 1F2D.0 Pityriasis versicolor 1F2D.1 Malassezia folliculitis 1F2D.2 White piedra 1F2D.3 Black piedra 1F2D.4 Tinea nigra 1F2D.5 Onychomycosis due to non-dermatophyte mould 1F2D.Y Other specified non-dermatophyte superficial dermatomycoses 1F2D.Z Non-dermatophyte superficial dermatomycoses, unspecified 1F2E Paracoccidioidomycosis 1F2E.0 Pulmonary paracoccidioidomycosis 1F2E.1 Disseminated paracoccidioidomycosis 1F2E.Y Other specified paracoccidioidomycosis 1F2E.Z Paracoccidioidomycosis, unspecified 1F2F Phaeohyphomycosis 1F2G Pneumocystosis 1F2G.0 Pulmonary pneumocystosis 1F2G.Z Pneumocystosis, unspecified 1F2H Scedosporiosis 1F2J Sporotrichosis 1F2J.0 Lymphocutaneous sporotrichosis 1F2J.1 Fixed cutaneous sporotrichosis 1F2J.2 Pulmonary sporotrichosis 1F2J.3 Disseminated sporotrichosis 1F2J.Y Other specified sporotrichosis 1F2J.Z Sporotrichosis, unspecified 1F2K Talaromycosis 1F2L Emmonsiosis 1F2L.0 Disseminated adiaspiromycosis 1F2L.1 Pulmonary adiaspiromycosis 1F2L.Y Other specified emmonsiosis 1F2L.Z Emmonsiosis, unspecified 1F2Y Other specified mycoses 1F2Z Mycoses, unspecified 1F40 Malaria due to Plasmodium falciparum – 1F40.0 Plasmodium falciparum malaria with cerebral complications – 1F40.Y Other severe and complicated Plasmodium falciparum malaria – 1F40.Z Malaria due to Plasmodium falciparum, unspecified 1F41 Malaria due to Plasmodium vivax – 1F41.0 Plasmodium vivax malaria with rupture of spleen – 1F41.Y Malaria due to Plasmodium vivax with other complications – 1F41.Z Plasmodium vivax malaria without complication 1F42 Malaria due to Plasmodium malariae – 1F42.0 Plasmodium malariae malaria with nephropathy – 1F42.Y Malaria due to Plasmodium malariae with other complications – 1F42.Z Plasmodium malariae malaria without complication 1F43 Malaria due to Plasmodium ovale 1F44 Other parasitologically confirmed malaria 1F45 Malaria without parasitological confirmation 1F4Z Malaria, unspecified 1F50 Acanthamoebiasis 1F51 African trypanosomiasis – 1F51.0 Gambiense trypanosomiasis – 1F51.1 Rhodesiense trypanosomiasis – 1F51.Y Other specified african trypanosomiasis – 1F51.Z African trypanosomiasis, unspecified –– 1F51.00 Meningitis in Gambiense trypanosomiasis –– 1F51.0Y Other specified gambiense trypanosomiasis –– 1F51.0Z Gambiense trypanosomiasis, unspecified –– 1F51.10 Meningitis in Rhodesiense trypanosomiasis –– 1F51.1Y Other specified rhodesiense trypanosomiasis –– 1F51.1Z Rhodesiense trypanosomiasis, unspecified 1F52 Babesiosis 1F53 Chagas disease – 1F53.1 Acute Chagas disease without heart involvement – 1F53.2 Chronic Chagas disease with heart involvement – 1F53.3 Chagas disease with digestive system involvement – 1F53.4 Meningitis in Chagas disease – 1F53.Y Other specified Chagas disease – 1F53.Z Chagas disease, unspecified 1F54 Leishmaniasis – 1F54.0 Visceral leishmaniasis – 1F54.1 Cutaneous leishmaniasis – 1F54.2 Mucocutaneous leishmaniasis – 1F54.Z Leishmaniasis, unspecified 1F55 Naegleriasis 1F56 Rhinosporidiosis 1F57 Toxoplasmosis – 1F57.0 Hepatitis due to Toxoplasma gondii – 1F57.1 Meningoencephalitis due to Toxoplasma gondii – 1F57.2 Pulmonary toxoplasmosis due to Toxoplasma gondii – 1F57.3 Eye disease due to Toxoplasma gondii – 1F57.Y Other specified toxoplasmosis – 1F57.Z Toxoplasmosis, unspecified 1F58 Microsporidiosis 1F5Z Unspecified protozoal disease – 1F60 Angiostrongyliasis –– 1F60.0 Eosinophilic meningitis due to Angiostrongylus cantonensis –– 1F60.1 Intestinal angiostrongyliasis –– 1F60.Y Other specified angiostrongyliasis –– 1F60.Z Angiostrongyliasis, unspecified – 1F61 Anisakiasis – 1F62 Ascariasis – 1F63 Capillariasis –– 1F63.0 Capillariasis of the intestine –– 1F63.Y Other specified capillariasis –– 1F63.Z Capillariasis, unspecified – 1F64 Dracunculiasis – 1F65 Enterobiasis – 1F66 Filariasis –– 1F66.0 Loiasis –– 1F66.1 Mansonelliasis –– 1F66.2 Filariasis due to Brugia species –– 1F66.3 Lymphatic filariasis –– 1F66.4 Subcutaneous dirofilariasis –– 1F66.Y Other specified filariasis –– 1F66.Z Filariasis, unspecified ––– 1F66.30 Filariasis due to Wuchereria bancrofti ––– 1F66.31 Filariasis due to Brugia malayi ––– 1F66.32 Filariasis due to Brugia timori ––– 1F66.3Z Lymphatic filariasis, unspecified – 1F67 Gnathostomiasis – 1F68 Hookworm diseases –– 1F68.0 Ancylostomiasis –– 1F68.1 Necatoriasis –– 1F68.2 Cutaneous larva migrans – 1F69 Oesophagostomiasis – 1F6A Onchocerciasis –– 1F6A.0 Onchocerciasis of the eye –– 1F6A.1 Onchocerciasis of the skin –– 1F6A.Y Other specified onchocerciasis –– 1F6A.Z Onchocerciasis, unspecified – 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 – 1F70 Cysticercosis –– 1F70.0 Cysticercosis of central nervous system –– 1F70.1 Cysticercosis of eye –– 1F70.Y Other specified cysticercosis –– 1F70.Z Cysticercosis, unspecified ––– 1F70.00 Meningitis due to Cysticercosis ––– 1F70.0Y Other specified cysticercosis of central nervous system – 1F71 Diphyllobothriasis – 1F72 Dipylidiasis – 1F73 Echinococcosis –– 1F73.0 Echinococcus infection of liver –– 1F73.1 Echinococcus infection of lung –– 1F73.2 Echinococcus infection of bone –– 1F73.3 Echinococcus infection of central nervous system –– 1F73.Y Other specified echinococcosis –– 1F73.Z Echinococcosis, unspecified – 1F74 Hymenolepiasis – 1F75 Sparganosis – 1F76 Taeniasis –– 1F76.0 Taeniasis due to Taenia solium –– 1F76.1 Taeniasis due to Taenia saginata –– 1F76.Y Other specified taeniasis –– 1F76.Z Taeniasis, unspecified – 1F7Y Other specified diseases due to cestodes – 1F7Z Diseases due to cestodes, unspecified – 1F80 Clonorchiasis – 1F81 Dicrocoeliasis – 1F82 Fascioliasis – 1F83 Fasciolopsiasis – 1F84 Opisthorchiasis – 1F85 Paragonimiasis – 1F86 Schistosomiasis –– 1F86.0 Schistosomiasis due to Schistosoma haematobium –– 1F86.1 Schistosomiasis due to Schistosoma mansoni –– 1F86.2 Schistosomiasis due to Schistosoma japonicum –– 1F86.3 Other schistosomiases –– 1F86.4 Cercarial dermatitis –– 1F86.5 Schistosomal pneumonitis –– 1F86.Z Schistosomiasis due to unspecified or unknown Schistosoma species – 1F8Y Other specified diseases due to trematodes – 1F8Z Diseases due to trematodes, unspecified 1F90 Other and unspecified infestation by parasitic worms – 1F90.0 Mixed intestinal helminthiases – 1F90.1 Intestinal parasitic infestation not otherwise specified – 1F90.2 Intestinal helminthiasis, unspecified – 1F90.Y Other specified other and unspecified infestation by parasitic worms – 1F90.Z Other and unspecified infestation by parasitic worms, unspecified 1F91 Diphyllobothriasis and sparganosis 1F9Z Helminthiases, unspecified 1G00 Pediculosis – 1G00.0 Pediculosis capitis – 1G00.1 Pediculosis corporis – 1G00.Z Pediculosis of unspecified site or type 1G01 Myiasis – 1G01.0 Ocular myiasis – 1G01.1 Nasopharyngeal myiasis – 1G01.2 Laryngeal myiasis – 1G01.3 Cutaneous myiasis – 1G01.Y Other specified myiasis – 1G01.Z Myiasis, unspecified 1G02 External hirudiniasis 1G03 Pthiriasis 1G04 Scabies – 1G04.0 Classical scabies – 1G04.1 Crusted scabies – 1G04.Y Other and unspecified scabies 1G05 Tungiasis 1G06 Cimicosis 1G07 Infestation by mites – 1G07.0 Infestation by Demodex – 1G07.Y Infestation of the skin by other specified parasitic mites 1G0Y Infestation by other specified ectoparasite 1G0Z Infestation by unknown or unspecified ectoparasite 1G2Y Other specified parasitic diseases 1G2Z Unspecified parasitic diseases 1G40 Sepsis without septic shock 1G41 Sepsis with septic shock 1G60 Certain other disorders of infectious origin 1G60.0 Mycetoma of unknown or unspecified type 1G60.1 Pythiosis 1G60.2 Protothecosis 1G60.Y Other specified disorders of infectious origin not elsewhere classified 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 4A00 Primary immunodeficiencies due to disorders of innate immunity 4A00.0 Functional neutrophil defects 4A00.1 Defects in the complement system 4A00.2 Genetic susceptibility to particular pathogens 4A00.3 Immunodeficiency with natural-killer cell deficiency 4A00.Y Other specified primary immunodeficiencies due to disorders of innate immunity 4A00.Z Primary immunodeficiencies due to disorders of innate immunity, unspecified – 4A00.00 Neutrophil immunodeficiency syndrome – 4A00.0Y Other specified functional neutrophil defects – 4A00.0Z Functional neutrophil defects, unspecified – 4A00.10 Immunodeficiency with an early component of complement deficiency – 4A00.11 Immunodeficiency with a late component of complement deficiency – 4A00.12 Immunodeficiency with factor B deficiency – 4A00.13 Immunodeficiency with factor D anomaly – 4A00.14 Hereditary angioedema – 4A00.15 Acquired angioedema – 4A00.1Y Other specified defects in the complement system – 4A00.1Z Defects in the complement system, unspecified 4A01 Primary immunodeficiencies due to disorders of adaptive immunity 4A01.0 Immunodeficiencies with predominantly antibody defects 4A01.1 Combined immunodeficiencies 4A01.2 Diseases of immune dysregulation 4A01.3 Other well-defined immunodeficiency syndromes due to defects in adaptive immunity 4A01.Z Primary immunodeficiencies due to disorders of adaptive immunity, unspecified – 4A01.00 Hereditary agammaglobulinaemia with profoundly reduced or absent B cells – 4A01.01 Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells – 4A01.02 Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells – 4A01.03 Transient hypogammaglobulinaemia of infancy – 4A01.04 Immunodeficiencies with isotype or light chain deficiencies with normal number of B cells – 4A01.05 Immunodeficiencies with severe reduction in serum IgG or IgA with normal or elevated IgM and normal numbers of B-cells – 4A01.0Y Other specified immunodeficiencies with predominantly antibody defects – 4A01.0Z Immunodeficiencies with predominantly antibody defects, unspecified – 4A01.10 Severe combined immunodeficiencies – 4A01.11 Major histocompatibility complex class I deficiency – 4A01.12 Major histocompatibility complex class II deficiency – 4A01.1Y Other specified combined immunodeficiencies – 4A01.1Z Combined immunodeficiencies, unspecified – 4A01.20 Immune dysregulation syndromes with hypopigmentation – 4A01.21 Immune dysregulation syndromes presenting primarily with autoimmunity – 4A01.22 Immune dysregulation syndromes presenting primarily with lymphoproliferation – 4A01.23 Primary haemophagocytic lymphohistiocytosis – 4A01.2Y Other specified diseases of immune dysregulation – 4A01.2Z Diseases of immune dysregulation, unspecified – 4A01.30 Immunodeficiency due to defects of the thymus – 4A01.31 DNA repair defects other than combined T-cell or B-cell immunodeficiencies – 4A01.32 Immuno-osseous dysplasia – 4A01.33 Hepatic veno-occlusive disease - immunodeficiency syndrome – 4A01.34 Hyperimmunoglobulin E syndromes 4A0Y Other specified primary immunodeficiencies 4A0Z Primary immunodeficiencies, unspecified 4A20 Acquired immunodeficiencies 4A20.0 Adult-onset immunodeficiency 4A20.1 Acquired immunodeficiency due to loss of immunoglobulin 4A20.Y Other specified acquired immunodeficiencies 4A20.Z Acquired immunodeficiencies, unspecified 4A40 Lupus erythematosus 4A40.0 Systemic lupus erythematosus 4A40.1 Drug-induced lupus erythematosus 4A40.Y Other specified lupus erythematosus 4A40.Z Lupus erythematosus, unspecified – 4A40.00 Systemic lupus erythematosus with skin involvement – 4A40.0Y Other specified systemic lupus erythematosus – 4A40.0Z Systemic lupus erythematosus, unspecified 4A41 Idiopathic inflammatory myopathy 4A41.0 Dermatomyositis 4A41.1 Polymyositis 4A41.2 Inclusion body myopathy 4A41.Y Other specified idiopathic inflammatory myopathy 4A41.Z Idiopathic inflammatory myopathy, unspecified – 4A41.00 Adult dermatomyositis – 4A41.01 Juvenile dermatomyositis – 4A41.0Z Dermatomyositis, unspecified – 4A41.10 Juvenile polymyositis – 4A41.11 Paraneoplastic polymyositis – 4A41.1Y Other specified polymyositis – 4A41.1Z Polymyositis, unspecified – 4A41.20 Inflammatory inclusion body myositis – 4A41.21 Noninflammatory inclusion body myopathy – 4A41.2Z Inclusion body myopathy, unspecified 4A42 Systemic sclerosis 4A42.0 Paediatric onset systemic sclerosis 4A42.1 Diffuse systemic sclerosis 4A42.2 Limited systemic sclerosis 4A42.Z Systemic sclerosis, unspecified 4A43 Overlap or undifferentiated nonorgan specific systemic autoimmune disease 4A43.0 IgG4 related disease 4A43.1 Mikulicz disease 4A43.2 Sjögren syndrome 4A43.3 Mixed connective tissue disease 4A43.4 Diffuse eosinophilic fasciitis 4A43.Y Other specified overlap non-organ specific systemic autoimmune disease 4A43.Z Undifferentiated non-organ specific systemic autoimmune disease – 4A43.20 Primary Sjögren syndrome – 4A43.21 Secondary Sjögren syndrome – 4A43.22 Paediatric onset Sjögren syndrome – 4A43.2Y Other specified sjögren syndrome – 4A43.2Z Sjögren syndrome, unspecified 4A44 Vasculitis 4A44.0 Rhizomelic pseudopolyarthritis 4A44.1 Aortic arch syndrome 4A44.2 Giant cell arteritis 4A44.3 Single organ vasculitis 4A44.4 Polyarteritis nodosa 4A44.5 Mucocutaneous lymph node syndrome 4A44.6 Sneddon syndrome 4A44.7 Primary angiitis of the central nervous system 4A44.8 Thromboangiitis obliterans 4A44.9 Immune complex small vessel vasculitis 4A44.A Antineutrophil cytoplasmic antibody-associated vasculitis 4A44.B Leukocytoclastic vasculitis 4A44.Y Other specified vasculitis 4A44.Z Vasculitis, unspecified – 4A44.90 Cryoglobulinaemic vasculitis – 4A44.91 Hypocomplementaemic urticarial vasculitis – 4A44.92 IgA vasculitis – 4A44.9Y Other specified immune complex small vessel vasculitis – 4A44.9Z Immune complex small vessel vasculitis, unspecified – 4A44.A0 Microscopic polyangiitis – 4A44.A1 Granulomatosis with polyangiitis – 4A44.A2 Eosinophilic granulomatosis with polyangiitis – 4A44.AY Other specified antineutrophil cytoplasmic antibody-associated vasculitis – 4A44.AZ Antineutrophil cytoplasmic antibody-associated vasculitis, unspecified – 4A44.B0 Cutaneous leukocytoclastic vasculitis – 4A44.BY Other specified leukocytoclastic vasculitis – 4A44.BZ Leukocytoclastic vasculitis, unspecified 4A45 Antiphospholipid syndrome 4A45.0 Primary antiphospholipid syndrome 4A45.1 Secondary antiphospholipid syndrome 4A45.2 Antiphospholipid syndrome in pregnancy 4A45.3 Lupus anticoagulant-hypoprothrombinaemia syndrome 4A45.Z Antiphospholipid syndrome, unspecified 4A4Y Other specified nonorgan specific systemic autoimmune disorders 4A4Z Nonorgan specific systemic autoimmune disorders, unspecified 4A60 Monogenic autoinflammatory syndromes 4A60.0 Familial Mediterranean fever 4A60.1 Cryopyrin-associated periodic syndromes 4A60.2 Tumour necrosis factor receptor 1 associated periodic syndrome 4A60.Y Other specified monogenic autoinflammatory syndromes 4A60.Z Autoimflammatory syndrome, unspecified 4A61 SAPHO syndrome 4A62 Behçet disease 4A6Y Other specified autoinflammatory disorders 4A6Z Autoinflammatory disorders, unspecified 4A80 Allergic or hypersensitivity disorders involving the respiratory tract 4A80.0 Drug-induced bronchospasm 4A80.1 Bronchospasm provoked by allergy to food substance 4A80.Y Other specified allergic or hypersensitivity disorders involving the respiratory tract 4A80.Z Allergic or hypersensitivity disorders involving the respiratory tract, unspecified 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 4A83.0 Food-induced eosinophilic gastroenteritis 4A83.1 Food-induced eosinophilic oesophagitis 4A83.Y Other specified allergic or hypersensitivity disorders involving the gastrointestinal tract 4A83.Z Allergic or hypersensitivity disorders involving the gastrointestinal tract, unspecified 4A84 Anaphylaxis 4A84.0 Anaphylaxis due to allergic reaction to food 4A84.1 Drug-induced anaphylaxis 4A84.2 Anaphylaxis due to insect venom 4A84.3 Anaphylaxis provoked by physical factors 4A84.4 Anaphylaxis due to inhaled allergens 4A84.5 Anaphylaxis due to contact with allergens 4A84.6 Anaphylaxis secondary to mast cell disorder 4A84.Y Other specified anaphylaxis 4A84.Z Anaphylaxis, unspecified – 4A84.30 Exercise-induced anaphylaxis – 4A84.31 Cold-induced anaphylaxis – 4A84.3Y Anaphylaxis provoked by other specified physical factors – 4A84.3Z Anaphylaxis provoked by unspecified physical factors 4A85 Complex allergic or hypersensitivity conditions 4A85.0 Drug or pharmacological agents hypersensitivity 4A85.1 Hypersensitivity to herbal and alternative medical therapies 4A85.2 Food hypersensitivity 4A85.3 Allergic or hypersensitivity reactions to arthropods 4A85.Y Other specified complex allergic or hypersensitivity conditions 4A85.Z Complex allergic or hypersensitivity conditions, unspecified – 4A85.00 Drug-induced liver hypersensitivity disease – 4A85.01 Drug-induced kidney hypersensitivity – 4A85.02 Drug-induced cytopenia – 4A85.03 Drug-induced vasculitis – 4A85.04 Multiple drug hypersensitivity syndrome – 4A85.0Y Drug hypersensitivity of other specified type – 4A85.0Z Drug hypersensitivity of unspecified type – 4A85.20 Food-induced gastrointestinal hypersensitivity – 4A85.21 Food-induced urticaria or angioedema – 4A85.22 Allergic contact dermatitis due to food allergen – 4A85.2Y Other specified food hypersensitivity – 4A85.2Z Food hypersensitivity, unspecified – 4A85.30 Systemic allergic reaction due to Hymenoptera venom – 4A85.31 Cutaneous allergic or hypersensitivity reactions to Hymenoptera venom – 4A85.32 Cutaneous allergic or hypersensitivity reactions to arthropods 4A8Y Allergic or hypersensitivity conditions of other specified type 4A8Z Allergic or hypersensitivity conditions of unspecified type 4B00 Disorders of neutrophil number 4B00.0 Neutropaenia 4B00.1 Neutrophilia 4B00.Y Other specified disorders of neutrophil number – 4B00.00 Constitutional neutropaenia – 4B00.01 Acquired neutropaenia – 4B00.0Z Neutropaenia, unspecified – 4B00.10 Constitutional neutrophilia – 4B00.11 Acquired neutrophilia – 4B00.1Z Neutrophilia, unspecified 4B01 Disorders of neutrophil function 4B01.0 Constitutional disorders of neutrophil function 4B01.1 Acquired disorders of neutrophil function 4B01.Z Disorders of neutrophil function, unspecified – 4B01.00 Disorders of neutrophil adhesion – 4B01.01 Disorders of neutrophil chemotaxis – 4B01.02 Disorders of neutrophil granule formation or release – 4B01.03 Disorders of neutrophil oxidative metabolism – 4B01.0Y Other specified constitutional disorders of neutrophil function – 4B01.0Z Constitutional disorders of neutrophil function, unspecified 4B02 Eosinopenia 4B02.0 Constitutional decrease in eosinophil number 4B02.1 Acquired decrease in eosinophil number 4B02.Z Eosinopenia, unspecified 4B03 Eosinophilia 4B03.0 Constitutional eosinophilia 4B03.1 Acquired eosinophilia 4B03.Z Eosinophilia, unspecified 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 4B0Z Immune system disorders involving white cell lineages, unspecified 4B20 Sarcoidosis 4B20.0 Sarcoidosis of lung 4B20.1 Sarcoidosis of lymph nodes 4B20.2 Sarcoidosis of the digestive system 4B20.3 Neurosarcoidosis 4B20.4 Ocular sarcoidosis 4B20.5 Cutaneous sarcoidosis 4B20.Y Other specified sarcoidosis 4B20.Z Sarcoidosis, unspecified 4B21 Polyclonal hypergammaglobulinaemia 4B22 Cryoglobulinaemia 4B23 Immune reconstitution inflammatory syndrome 4B24 Graft-versus-host disease 4B24.0 Acute graft-versus-host disease 4B24.1 Chronic graft-versus-host disease 4B24.Y Other specified graft-versus-host disease 4B24.Z Graft-versus-host disease, unspecified 4B2Y Other specified disorders involving the immune system 4B40 Diseases of thymus 4B40.0 Persistent hyperplasia of thymus 4B40.1 Abscess of thymus 4B40.2 Good syndrome 4B40.Y Other specified diseases of thymus 4B40.Z Diseases of thymus, unspecified 4B4Y Other specified diseases of the immune system 4B4Z Diseases of the immune system, unspecified 8A00 Parkinsonism 8A00.0 Parkinson disease 8A00.1 Atypical parkinsonism 8A00.2 Secondary parkinsonism 8A00.3 Functional parkinsonism 8A00.Y Other specified parkinsonism 8A00.Z Parkinsonism, unspecified – 8A00.00 Sporadic Parkinson disease – 8A00.01 Familial Parkinson disease – 8A00.0Y Other specified Parkinson disease – 8A00.0Z Parkinson disease, unspecified – 8A00.10 Progressive supranuclear palsy – 8A00.1Y Other specified atypical parkinsonism – 8A00.1Z Atypical parkinsonism, unspecified – 8A00.20 Parkinsonism due to heredodegenerative disorders – 8A00.21 Hemiparkinsonism hemiatrophy syndrome – 8A00.22 Infectious or postinfectious parkinsonism – 8A00.23 Vascular parkinsonism – 8A00.24 Drug-induced parkinsonism – 8A00.25 Post traumatic Parkinsonism – 8A00.26 Parkinsonism due to structural lesions – 8A00.2Y Other specified secondary parkinsonism – 8A00.2Z Secondary parkinsonism, unspecified 8A01 Choreiform disorders 8A01.0 Benign hereditary chorea 8A01.1 Secondary Chorea 8A01.2 Hemichorea or hemiballismus 8A01.Y Other specified choreiform disorders 8A01.Z Choreiform disorders, unspecified – 8A01.10 Huntington disease – 8A01.11 Chorea due to Huntington disease-like conditions – 8A01.12 Chorea due to Dentatorubral pallidoluysian atrophy – 8A01.13 Chorea due to Wilson disease – 8A01.14 Chorea due to infectious or para-infectious causes – 8A01.15 Chorea due to systemic lupus erythematosus – 8A01.16 Drug-induced chorea – 8A01.1Y Other specified secondary chorea – 8A01.1Z Secondary chorea, unspecified – 8A01.20 Hemichorea – 8A01.21 Ballism – 8A01.22 Hemiballism – 8A01.2Y Other specified hemichorea or hemiballismus – 8A01.2Z Hemichorea or hemiballismus, unspecified 8A02 Dystonic disorders 8A02.0 Primary dystonia 8A02.1 Secondary dystonia 8A02.2 Paroxysmal dystonia 8A02.3 Functional dystonia or spasms 8A02.Y Other specified dystonic disorders 8A02.Z Dystonic disorders, unspecified – 8A02.00 Benign essential blepharospasm – 8A02.0Y Other specified primary dystonia – 8A02.0Z Primary dystonia, unspecified – 8A02.10 Drug-induced dystonia – 8A02.11 Dystonia-plus – 8A02.12 Dystonia associated with heredodegenerative disorders – 8A02.1Y Other specified secondary dystonia – 8A02.1Z Secondary dystonia, unspecified 8A03 Ataxic disorders 8A03.0 Congenital ataxia 8A03.1 Hereditary ataxia 8A03.2 Non-hereditary degenerative ataxia 8A03.3 Acquired ataxia 8A03.Y Other specified ataxic disorders 8A03.Z Ataxic disorders, unspecified – 8A03.10 Friedreich ataxia – 8A03.11 Ataxia due to Cerebrotendinous xanthomatosis – 8A03.12 Ataxia due to Refsum disease – 8A03.13 Ataxia due to abetalipoproteinemia – 8A03.14 Hereditary episodic ataxia – 8A03.15 Ataxia due to mitochondrial mutations – 8A03.16 Spinocerebellar ataxia – 8A03.1Y Other specified hereditary ataxia – 8A03.1Z Hereditary ataxia, unspecified – 8A03.20 Late onset cerebellar cortical atrophy – 8A03.2Y Other specified non-hereditary degenerative ataxia – 8A03.2Z Non-hereditary degenerative ataxia, unspecified – 8A03.30 Ataxia due to alcoholic cerebellar degeneration – 8A03.3Y Other specified acquired ataxia – 8A03.3Z Acquired ataxia, unspecified 8A04 Disorders associated with tremor 8A04.0 Enhanced physiological tremor 8A04.1 Essential tremor or related tremors 8A04.2 Rest tremor 8A04.3 Secondary tremor 8A04.4 Functional tremor 8A04.Y Other specified disorders associated with tremor 8A04.Z Disorders associated with tremor, unspecified – 8A04.30 Tremor due to metabolic disorders – 8A04.31 Tremor due to chronic or acute substance use – 8A04.32 Tremor due to drug withdrawal – 8A04.33 Tremor due to certain specified central nervous system diseases – 8A04.3Y Other specified secondary tremor – 8A04.3Z Secondary tremor, unspecified 8A05 Tic disorders 8A05.0 Primary tics or tic disorders 8A05.1 Secondary tics 8A05.Y Other specified tic disorders 8A05.Z Tic disorders, unspecified – 8A05.00 Tourette syndrome – 8A05.01 Chronic motor tic disorder – 8A05.02 Chronic phonic tic disorder – 8A05.03 Transient motor tics – 8A05.0Y Other specified primary tics or tic disorders – 8A05.0Z Primary tics or tic disorders, unspecified – 8A05.10 Infectious or postinfectious tics – 8A05.11 Tics associated with developmental disorders – 8A05.1Y Other specified secondary tics – 8A05.1Z Secondary tics, unspecified 8A06 Myoclonic disorders 8A06.0 Essential myoclonus 8A06.1 Segmental myoclonus 8A06.2 Focal myoclonus 8A06.Y Other specified myoclonic disorders 8A06.Z Myoclonic disorders, unspecified – 8A06.20 Palatal myoclonus – 8A06.21 Chronic hiccups – 8A06.2Y Other specified focal myoclonus – 8A06.2Z Focal myoclonus, unspecified 8A07 Certain specified movement disorder 8A07.0 Stereotypies 8A07.1 Akathisia 8A07.2 Excessive startle reflex – 8A07.00 Primary stereotypy – 8A07.01 Secondary stereotypy – 8A07.0Y Other specified stereotypies – 8A07.0Z Stereotypies, unspecified 8A0Y Other specified movement disorders 8A0Z Movement disorders, unspecified 8A20 Alzheimer disease 8A21 Progressive focal atrophies 8A21.0 Posterior cortical atrophy 8A21.Y Other specified progressive focal atrophies 8A21.Z Progressive focal atrophies, unspecified 8A22 Lewy body disease 8A23 Frontotemporal lobar degeneration 8A2Y Other specified disorders with neurocognitive impairment as a major feature 8A2Z Disorders with neurocognitive impairment as a major feature, unspecified 8A40 Multiple sclerosis 8A40.0 Relapsing-remitting multiple sclerosis 8A40.1 Primary progressive multiple sclerosis 8A40.2 Secondary progressive multiple sclerosis 8A40.Y Other specified multiple sclerosis 8A40.Z Multiple sclerosis, unspecified 8A41 Isolated demyelinating syndromes of the central nervous system 8A41.0 Transverse myelitis 8A41.1 Neuromyelitis optica myelin oligodendrocyte glycoprotein antibody-positive 8A41.Y Other specified isolated demyelinating syndromes of the central nervous system 8A41.Z Isolated demyelinating syndromes of the central nervous system, unspecified 8A42 Acute disseminated encephalomyelitis 8A42.0 Acute haemorrhagic leukoencephalitis 8A42.Y Other specified acute disseminated encephalomyelitis 8A42.Z Acute disseminated encephalomyelitis, unspecified 8A43 Neuromyelitis optica 8A43.0 Neuromyelitis optica aquaporin-4 antibody positive 8A43.1 Neuromyelitis optica aquaporin-4 antibody negative 8A43.2 Single transverse myelitis aquaporin-4 antibody positive 8A43.3 Recurrent transverse myelitis aquaporin-4 antibody positive 8A43.4 Single optic neuritis aquaporin-4 antibody positive 8A43.5 Recurrent optic neuritis aquaporin-4 antibody positive 8A43.Y Other specified neuromyelitis optica 8A43.Z Neuromyelitis optica, unspecified 8A44 Leukodystrophies 8A44.0 Pelizaeus-Merzbacher disease 8A44.1 Adrenoleukodystrophy 8A44.2 Alexander disease 8A44.3 Certain specified leukodystrophies 8A44.4 Krabbe disease 8A44.Z Leukodystrophies, unspecified 8A45 Secondary white matter disorders 8A45.0 White matter disorders due to infections 8A45.1 White matter disorders due to toxicity 8A45.2 White matter disorders due to vascular abnormality or ischemia 8A45.3 White matter disorders due to nutritional deficiency 8A45.4 White matter disorders due to certain specified systemic disease 8A45.Y Other specified secondary white matter disorders 8A45.Z Secondary white matter disorders, unspecified – 8A45.00 Human T-cell lymphotropic virus-associated myelopathy – 8A45.01 Subacute sclerosing panencephalitis – 8A45.02 Progressive multifocal leukoencephalopathy – 8A45.0Y Other specified white matter disorders due to infections – 8A45.0Z White matter disorders due to infections, unspecified – 8A45.20 White matter disorder due to CADASIL – 8A45.21 Subacute necrotising myelitis – 8A45.2Y Other specified white matter disorders due to vascular abnormality or ischemia – 8A45.2Z White matter disorders due to vascular abnormality or ischemia, unspecified – 8A45.30 White matter disorder due to vitamin B12 deficiency – 8A45.31 Central pontine myelinolysis – 8A45.3Y Other specified white matter disorders due to nutritional deficiency – 8A45.3Z White matter disorders due to nutritional deficiency, unspecified – 8A45.40 Demyelination due to sarcoidosis – 8A45.41 Demyelination due to systemic lupus erythematosus – 8A45.42 Demyelination due to Sjögren disease – 8A45.43 Demyelination due to Behcet disease – 8A45.44 Demyelination due to systemic vasculitis – 8A45.45 Demyelination due to mitochondrial disease – 8A45.4Z White matter disorders due to certain specified systemic disease, unspecified 8A46 Central demyelination of corpus callosum 8A4Y Other specified multiple sclerosis or other white matter disorders 8A4Z Multiple sclerosis or other white matter disorders, unspecified 8A60 Epilepsy due to structural or metabolic conditions or diseases 8A60.0 Epilepsy due to prenatal or perinatal brain insults 8A60.1 Epilepsy due to cerebrovascular disorders 8A60.2 Epilepsy due to degenerative brain disorders 8A60.3 Epilepsy due to dementias 8A60.4 Epilepsy due to central nervous system infections or infestations 8A60.5 Epilepsy due to injuries to the head 8A60.6 Epilepsy due to tumours of the nervous system 8A60.7 Epilepsy with mesial temporal sclerosis 8A60.8 Epilepsy due to immune disorders 8A60.9 Epilepsy due to abnormalities of brain development 8A60.A Epilepsy due to genetic syndromes with widespread or progressive effects 8A60.B Epilepsy due to multiple sclerosis or other demyelinating disorders 8A60.Y Epilepsy due to other structural or metabolic condition or disease 8A60.Z Epilepsy due to unspecified structural or metabolic condition or disease – 8A60.00 Epilepsy due to prenatal or perinatal vascular insults – 8A60.01 Epilepsy due to neonatal hypoxic ischemic encephalopathy – 8A60.0Y Epilepsy due to other prenatal or perinatal brain insults – 8A60.0Z Epilepsy due to unspecified prenatal or perinatal brain insults 8A61 Genetic or presumed genetic syndromes primarily expressed as epilepsy 8A61.0 Genetic epileptic syndromes with neonatal onset 8A61.1 Genetic epileptic syndromes with onset in infancy 8A61.2 Genetic epileptic syndromes with childhood onset 8A61.3 Genetic epileptic syndrome with adolescent or adult onset 8A61.4 Genetic epileptic syndromes with variable age of onset 8A61.Y Other specified genetic or presumed genetic syndromes primarily expressed as epilepsy 8A61.Z Genetic or presumed genetic syndromes primarily expressed as epilepsy, unspecified – 8A61.00 Pyridoxal dependent epilepsy – 8A61.0Y Other specified genetic epileptic syndromes with neonatal onset – 8A61.0Z Genetic epileptic syndromes with neonatal onset, unspecified – 8A61.10 Benign familial infantile epilepsy – 8A61.11 Dravet syndrome – 8A61.12 Epilepsy of infancy with migrating focal seizures – 8A61.1Y Other specified genetic epileptic syndromes with onset in infancy – 8A61.1Z Genetic epileptic syndromes with onset in infancy, unspecified – 8A61.20 Benign childhood epilepsy with centro-temporal spikes – 8A61.21 Childhood absence epilepsy – 8A61.22 Epilepsy with myoclonic-astatic seizures – 8A61.23 Myoclonic absences or absences with myoclonias – 8A61.2Y Other specified genetic epileptic syndromes with childhood onset – 8A61.2Z Genetic epileptic syndromes with childhood onset, unspecified – 8A61.30 Juvenile myoclonic epilepsy – 8A61.31 Juvenile absence epilepsy – 8A61.32 Benign adult familial myoclonus epilepsy – 8A61.3Y Other specified genetic epileptic syndrome with adolescent or adult onset – 8A61.3Z Genetic epileptic syndrome with adolescent or adult onset, unspecified – 8A61.40 Reflex epilepsies – 8A61.41 Progressive myoclonic epilepsy – 8A61.4Y Other specified genetic epileptic syndromes with variable age of onset – 8A61.4Z Genetic epileptic syndromes with variable age of onset, unspecified 8A62 Epileptic encephalopathies 8A62.0 Infantile spasms 8A62.1 Lennox-Gastaut syndrome 8A62.2 Acquired epileptic aphasia 8A62.Y Other specified epileptic encephalopathies 8A62.Z Epileptic encephalopathies, unspecified 8A63 Seizure due to acute causes 8A63.0 Febrile seizures 8A63.Y Seizure due to other acute cause 8A63.Z Seizure due to unspecified acute cause – 8A63.00 Simple febrile seizures – 8A63.01 Complex febrile seizures – 8A63.0Y Other specified febrile seizures – 8A63.0Z Febrile seizures, unspecified 8A64 Single seizure due to remote causes 8A65 Single unprovoked seizure 8A66 Status epilepticus 8A66.0 Convulsive status epilepticus 8A66.1 Non-convulsive status epilepticus 8A66.Y Other specified status epilepticus 8A66.Z Status epilepticus, unspecified – 8A66.10 Absence status epilepticus – 8A66.1Y Other specified non-convulsive status epilepticus – 8A66.1Z Non-convulsive status epilepticus, unspecified 8A67 Acute repetitive seizures 8A68 Types of seizures 8A68.0 Focal unaware seizure 8A68.1 Absence seizures, atypical 8A68.2 Absence seizures, typical 8A68.3 Focal aware seizure 8A68.4 Generalised tonic-clonic seizure 8A68.5 Generalised myoclonic seizure 8A68.6 Generalised tonic seizure 8A68.7 Generalised atonic seizure 8A68.Y Other specified type of seizure 8A68.Z Type of seizure, unspecified 8A6Y Other specified epilepsy or seizures 8A6Z Epilepsy or seizures, unspecified 8A80 Migraine 8A80.0 Migraine without aura 8A80.1 Migraine with aura 8A80.2 Chronic migraine 8A80.3 Complications related to migraine 8A80.4 Cyclic vomiting syndrome 8A80.Y Other specified migraine 8A80.Z Migraine, unspecified – 8A80.10 Hemiplegic migraine – 8A80.1Y Other specified migraine with aura – 8A80.1Z Migraine with aura, unspecified – 8A80.30 Status migrainosus – 8A80.3Y Other specified complications related to migraine 8A81 Tension-type headache 8A81.0 Infrequent episodic tension-type headache 8A81.1 Frequent episodic tension-type headache 8A81.2 Chronic tension-type headache 8A81.Y Other specified tension-type headache 8A81.Z Tension-type headache, unspecified 8A82 Trigeminal autonomic cephalalgias 8A83 Other primary headache disorder 8A84 Secondary headache 8A84.0 Acute headache associated with traumatic injury to the head 8A84.1 Persistent headache associated with traumatic injury to the head 8A84.Y Other specified secondary headache 8A84.Z Secondary headache, unspecified 8A85 Painful cranial neuropathies or other facial pains 8A8Y Other specified headache disorders 8A8Z Headache disorders, unspecified 8B00 Intracerebral haemorrhage – 8B00.0 Deep hemispheric haemorrhage – 8B00.1 Lobar haemorrhage – 8B00.2 Brainstem haemorrhage – 8B00.3 Cerebellar haemorrhage – 8B00.4 Intraventricular haemorrhage without parenchymal haemorrhage – 8B00.5 Haemorrhage of multiple sites – 8B00.Z Intracerebral haemorrhage, site unspecified 8B01 Subarachnoid haemorrhage – 8B01.0 Aneurysmal subarachnoid haemorrhage – 8B01.1 Non-aneurysmal subarachnoid haemorrhage – 8B01.2 Subarachnoid haemorrhage not known if aneurysmal or non-aneurysmal 8B02 Nontraumatic subdural haemorrhage 8B03 Nontraumatic epidural haemorrhage 8B0Z Intracranial haemorrhage, unspecified 8B10 Transient ischaemic attack – 8B10.0 Amaurosis fugax – 8B10.Y Other specified transient ischaemic attack – 8B10.Z Transient ischaemic attack, unspecified 8B11 Cerebral ischaemic stroke – 8B11.0 Cerebral ischaemic stroke due to extracranial large artery atherosclerosis – 8B11.1 Cerebral ischaemic stroke due to intracranial large artery atherosclerosis – 8B11.2 Cerebral ischaemic stroke due to embolic occlusion – 8B11.3 Cerebral ischaemic stroke due to small artery occlusion – 8B11.4 Cerebral ischaemic stroke due to other known cause – 8B11.5 Cerebral ischaemic stroke of unknown cause –– 8B11.20 Cerebral ischaemic stroke due to cardiac embolism –– 8B11.21 Cerebral ischaemic stroke due to aortic arch embolism –– 8B11.22 Cerebral ischaemic stroke due to paradoxical embolism –– 8B11.2Y Cerebral ischaemic stroke due to other specified embolic occlusion –– 8B11.2Z Cerebral ischaemic stroke due to embolic occlusion, unspecified –– 8B11.40 Cerebral ischaemic stroke due to global hypoperfusion with watershed infarct –– 8B11.41 Cerebral ischaemic stroke due to other non-atherosclerotic arteriopathy –– 8B11.42 Cerebral ischaemic stroke due to hypercoagulable state –– 8B11.43 Cerebral ischaemic stroke in association with subarachnoid haemorrhage –– 8B11.44 Cerebral ischemic stroke from dissection –– 8B11.50 Cerebral ischaemic stroke due to unspecified occlusion or stenosis of extracranial large artery –– 8B11.51 Cerebral ischaemic stroke due to unspecified occlusion or stenosis of intracranial large artery –– 8B11.5Z Cerebral ischaemic stroke, unspecified 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 8B21.0 Silent cerebral infarct 8B21.1 Silent cerebral microbleed 8B21.Y Other specified cerebrovascular disease with no acute cerebral symptom 8B21.Z Cerebrovascular disease with no acute cerebral symptom, unspecified 8B22 Certain specified cerebrovascular diseases 8B22.0 Dissection of cerebral arteries 8B22.1 Cerebral venous thrombosis 8B22.2 Cerebral vasoconstriction syndromes 8B22.3 Isolated cerebral amyloid angiopathy 8B22.4 Intracranial vascular malformation 8B22.5 Cerebral aneurysm, nonruptured 8B22.6 Familial cerebral saccular aneurysm 8B22.7 Cerebral arteritis, not elsewhere classified 8B22.8 Hypertensive encephalopathy 8B22.9 Migraine-induced stroke 8B22.A Subclavian steal syndrome 8B22.B Moyamoya syndrome 8B22.C Hereditary cerebrovascular diseases 8B22.Y Other specified cerebrovascular disease – 8B22.40 Arteriovenous malformation of cerebral vessels – 8B22.41 Cerebral cavernous malformation – 8B22.42 Dural arteriovenous fistula – 8B22.43 Carotid cavernous fistula – 8B22.4Y Other specified intracranial vascular malformation – 8B22.4Z Intracranial vascular malformation, unspecified – 8B22.70 Primary cerebral arteritis – 8B22.7Y Other specified cerebral arteritis, not elsewhere classified – 8B22.7Z Cerebral arteritis, not elsewhere classified, unspecified – 8B22.C0 CADASIL - [cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome – 8B22.C1 CARASIL - [cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy] syndrome – 8B22.CY Other specified hereditary cerebrovascular diseases – 8B22.CZ Hereditary cerebrovascular diseases, unspecified 8B23 Cerebrovascular abnormalities 8B24 Hypoxic-ischaemic encephalopathy 8B24.0 Anoxic-ischaemic encephalopathy 8B24.Y Other specified hypoxic-ischaemic encephalopathy 8B24.Z Hypoxic-ischaemic encephalopathy, unspecified 8B25 Late effects of cerebrovascular disease 8B25.0 Late effects of cerebral ischemic stroke 8B25.1 Late effects of intracerebral haemorrhage 8B25.2 Late effects of subarachnoid haemorrhage 8B25.3 Late effects of other nontraumatic intracranial haemorrhage 8B25.4 Late effects of stroke not known if ischaemic or haemorrhagic 8B25.Y Late effects of other specified cerebrovascular disease 8B25.Z Late effects of cerebrovascular disease, unspecified 8B26 Vascular syndromes of brain in cerebrovascular diseases 8B26.0 Brainstem stroke syndrome 8B26.1 Cerebellar stroke syndrome 8B26.2 Middle cerebral artery syndrome 8B26.3 Anterior cerebral artery syndrome 8B26.4 Posterior cerebral artery syndrome 8B26.5 Lacunar syndromes 8B26.Y Other specified vascular syndromes of brain in cerebrovascular diseases 8B26.Z Vascular syndromes of brain in cerebrovascular diseases, unspecified – 8B26.50 Pure motor lacunar syndrome – 8B26.51 Pure sensory lacunar syndrome – 8B26.5Y Other specified lacunar syndromes – 8B26.5Z Lacunar syndromes, unspecified 8B2Z Cerebrovascular diseases, unspecified 8B40 Cauda equina syndrome 8B41 Myelitis 8B42 Myelopathy 8B43 Non-compressive vascular myelopathies 8B43.0 Acute arterial infarction of the spinal cord 8B43.1 Acute venous infarction of the spinal cord 8B43.2 Chronic venous infarction of the spinal cord 8B43.Y Other specified non-compressive vascular myelopathies 8B43.Z Non-compressive vascular myelopathies, unspecified 8B44 Degenerative myelopathic disorders 8B44.0 Hereditary spastic paraplegia 8B44.Y Other specified degenerative myelopathic disorders 8B44.Z Degenerative myelopathic disorders, unspecified – 8B44.00 Autosomal dominant hereditary spastic paraplegia – 8B44.01 Autosomal recessive hereditary spastic paraplegia – 8B44.02 X-linked hereditary spastic paraplegia – 8B44.0Y Other specified hereditary spastic paraplegia – 8B44.0Z Hereditary spastic paraplegia, unspecified 8B4Y Other specified spinal cord disorders excluding trauma 8B4Z Spinal cord disorders excluding trauma, unspecified 8B60 Motor neuron disease 8B60.0 Amyotrophic lateral sclerosis 8B60.1 Progressive bulbar palsy 8B60.2 Progressive pseudobulbar palsy 8B60.3 Progressive muscular atrophy 8B60.4 Primary lateral sclerosis 8B60.5 Amyotrophic lateral sclerosis-Plus 8B60.6 Monomelic amyotrophy 8B60.7 Madras type motor neuron disease 8B60.Y Other specified motor neuron disease 8B60.Z Motor neuron disease, unspecified 8B61 Spinal muscular atrophy 8B61.0 Infantile spinal muscular atrophy, Type I 8B61.1 Late infantile spinal muscular atrophy, Type II 8B61.2 Juvenile form spinal muscular dystrophy, Type III 8B61.3 Adult onset spinal muscular atrophy, Type IV 8B61.4 Localised spinal muscular atrophy 8B61.Y Other specified spinal muscular atrophy 8B61.Z Spinal muscular atrophy, unspecified 8B62 Post polio progressive muscular atrophy 8B6Y Other specified motor neuron diseases or related disorders 8B6Z Motor neuron diseases or related disorders, unspecified 8B80 Disorders of olfactory nerve 8B81 Disorders of vestibulocochlear nerve – 8B81.0 Brainstem lesion – 8B81.Y Other specified disorders of vestibulocochlear nerve – 8B81.Z Disorders of vestibulocochlear nerve, unspecified 8B82 Disorders of trigeminal nerve – 8B82.0 Trigeminal neuralgia – 8B82.Z Disorders of trigeminal nerve, unspecified 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 – 8B88.0 Bell palsy – 8B88.1 Facial myokymia – 8B88.2 Hemifacial spasm – 8B88.3 Facial neuritis – 8B88.Y Other specified disorders of facial nerve – 8B88.Z Disorders of facial nerve, unspecified 8B8Y Other specified disorders of cranial nerves 8B8Z Disorders of cranial nerves, unspecified 8B90 Nerve root and plexus compressions 8B91 Brachial plexus disorders – 8B91.0 Neuralgic shoulder amyotrophy – 8B91.1 Thoracic outlet syndrome due to cervical rib – 8B91.Y Other specified brachial plexus disorders – 8B91.Z Brachial plexus disorders, unspecified 8B92 Lumbosacral plexus disorders – 8B92.0 Post radiation lumbosacral plexopathy – 8B92.1 Vasculitic lumbosacral plexopathy – 8B92.2 Diabetic lumbosacral plexopathy – 8B92.3 Lumbosacral radiculoplexopathy – 8B92.Y Other specified lumbosacral plexus disorders – 8B92.Z Lumbosacral plexus disorders, unspecified 8B93 Radiculopathy – 8B93.0 Radiculopathy due to compression – 8B93.1 Radiculopathy due to metabolic disorders – 8B93.2 Radiculopathy due to electric shock or lightning – 8B93.3 Radiculopathy due to radiation injury – 8B93.4 Radiculopathy due to nutritional deficiencies – 8B93.5 Radiculopathy due to toxicity – 8B93.6 Radiculopathy due to intervertebral disc disorders – 8B93.7 Radiculopathy due to neoplastic disease – 8B93.8 Radiculopathy due to spondylosis – 8B93.Y Other specified radiculopathy – 8B93.Z Radiculopathy, unspecified 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 8C00 Idiopathic progressive neuropathy 8C01 Inflammatory polyneuropathy – 8C01.0 Acute inflammatory demyelinating polyneuropathy – 8C01.1 Post vaccinal neuropathy – 8C01.2 Subacute inflammatory demyelinating polyneuropathy – 8C01.3 Chronic inflammatory demyelinating polyneuropathy – 8C01.Y Other specified inflammatory polyneuropathy – 8C01.Z Inflammatory polyneuropathy, unspecified 8C03 Other secondary polyneuropathy – 8C03.0 Diabetic polyneuropathy – 8C03.1 Polyneuropathy due to infectious diseases – 8C03.2 Polyneuropathy in neoplastic disease – 8C03.3 Polyneuropathy in nutritional deficiency – 8C03.4 Polyneuropathy in systemic connective tissue disorders – 8C03.Y Other specified secondary polyneuropathy – 8C03.Z Other secondary polyneuropathy, unspecified 8C0Y Other specified polyneuropathy 8C0Z Polyneuropathy, unspecified 8C10 Mononeuropathies of upper limb – 8C10.0 Carpal tunnel syndrome – 8C10.1 Lesion of ulnar nerve – 8C10.2 Lesion of radial nerve – 8C10.Y Other specified mononeuropathies of upper limb – 8C10.Z Mononeuropathies of upper limb, unspecified 8C11 Mononeuropathies of lower limb – 8C11.0 Lesion of sciatic nerve – 8C11.1 Meralgia paraesthetica – 8C11.2 Lesion of femoral nerve – 8C11.3 Lesion of common peroneal nerve – 8C11.4 Lesion of tibial nerve – 8C11.5 Tarsal tunnel syndrome – 8C11.6 Lesion of plantar nerve – 8C11.Y Other specified mononeuropathies of lower limb – 8C11.Z Mononeuropathies of lower limb, unspecified –– 8C11.00 Sciatic nerve piriformis syndrome –– 8C11.0Y Other specified lesion of sciatic nerve –– 8C11.0Z Lesion of sciatic nerve, unspecified 8C12 Certain specified mononeuropathies – 8C12.0 Intercostal neuropathy – 8C12.1 Mononeuritis multiplex – 8C12.2 Lesion of suprascapular nerve – 8C12.3 Lesion of axillary nerve – 8C12.4 Lesion of long thoracic nerve – 8C12.5 Traumatic neuroma, not otherwise specified – 8C12.Y Mononeuropathy of other specified nerve 8C1Y Mononeuropathy of other specified site 8C1Z Mononeuropathy of unspecified site 8C20 Hereditary motor and sensory neuropathy – 8C20.0 Charcot-Marie-Tooth disease 1 demyelinating – 8C20.1 Charcot-Marie-Tooth disease 2 axonal – 8C20.2 Intermediate Charcot-Marie-Tooth disease – 8C20.Y Other specified hereditary motor and sensory neuropathy – 8C20.Z Hereditary motor and sensory neuropathy, unspecified 8C21 Hereditary sensory or autonomic neuropathy – 8C21.0 Hereditary sensory and autonomic neuropathy type I – 8C21.1 Hereditary sensory and autonomic neuropathy type III – 8C21.2 Hereditary sensory and autonomic neuropathy type IV – 8C21.3 Hereditary sensory and autonomic neuropathy type V – 8C21.Y Other specified hereditary sensory or autonomic neuropathy – 8C21.Z Hereditary sensory or autonomic neuropathy, unspecified 8C2Y Other specified hereditary neuropathy 8C2Z Hereditary neuropathy, unspecified 8C4Y Other specified disorders of nerve root, plexus or peripheral nerves 8C4Z Disorders of nerve root, plexus or peripheral nerves, unspecified 8C60 Myasthenia gravis – 8C60.0 Drug-induced myasthenia gravis – 8C60.Y Other specified myasthenia gravis – 8C60.Z Myasthenia gravis, unspecified 8C61 Congenital myasthenic syndromes 8C62 Lambert-Eaton syndrome 8C6Y Other specified myasthenia gravis and neuromuscular junction disorders 8C6Z Unspecified myasthenia gravis or neuromuscular junction disorders 8C70 Muscular dystrophy – 8C70.0 Becker muscular dystrophy – 8C70.1 Duchenne muscular dystrophy – 8C70.2 Emery-Dreifuss muscular dystrophy – 8C70.3 Facioscapulohumeral muscular dystrophy – 8C70.4 Limb-girdle muscular dystrophy – 8C70.5 Scapuloperoneal muscular dystrophy – 8C70.6 Congenital muscular dystrophy – 8C70.Y Other specified muscular dystrophy – 8C70.Z Muscular dystrophy, unspecified –– 8C70.40 Dominant limb-girdle muscular dystrophy –– 8C70.41 Recessive limb-girdle muscular dystrophy –– 8C70.4Y Other specified limb-girdle muscular dystrophy –– 8C70.4Z Limb-girdle muscular dystrophy, unspecified 8C71 Myotonic disorders – 8C71.0 Myotonic dystrophy – 8C71.1 Chondrodystrophic myotonia – 8C71.2 Myotonia congenita – 8C71.3 Drug-induced myotonia – 8C71.4 Neuromyotonia – 8C71.5 Pseudomyotonia – 8C71.Y Other specified myotonic disorders – 8C71.Z Myotonic disorders, unspecified 8C72 Congenital myopathies – 8C72.0 Congenital myopathy with structural abnormalities – 8C72.1 Congenital myopathy with no structural abnormalities – 8C72.Y Other specified congenital myopathies – 8C72.Z Congenital myopathies, unspecified –– 8C72.00 Nemaline myopathy –– 8C72.01 Centronuclear myopathy –– 8C72.02 Central core disease –– 8C72.0Y Other specified congenital myopathy with structural abnormalities –– 8C72.0Z Congenital myopathy with structural abnormalities, unspecified 8C73 Mitochondrial myopathies – 8C73.0 Autosomal recessive cardiomyopathy or ophthalmoplegia – 8C73.1 Neuropathy, ataxia, and retinitis pigmentosa – 8C73.Y Other specified mitochondrial myopathies – 8C73.Z Mitochondrial myopathies, unspecified 8C74 Periodic paralyses or disorders of muscle membrane excitability – 8C74.0 Paramyotonia congenita – 8C74.1 Periodic paralysis – 8C74.Y Other specified periodic paralyses or disorders of muscle membrane excitability – 8C74.Z Periodic paralyses or disorders of muscle membrane excitability, unspecified –– 8C74.10 Hypokalaemic periodic paralysis –– 8C74.11 Hyperkalaemic periodic paralysis –– 8C74.1Y Other specified periodic paralysis –– 8C74.1Z Periodic paralysis, unspecified 8C75 Distal myopathies 8C76 Myofibrillar myopathy 8C77 Ocular myopathy 8C78 Malignant hyperthermia or hyperpyrexia 8C7Y Other specified primary disorders of muscles 8C7Z Primary disorders of muscles, unspecified 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 8D20 Spastic cerebral palsy 8D20.0 Spastic unilateral cerebral palsy 8D20.1 Spastic bilateral cerebral palsy 8D20.Y Other specified spastic cerebral palsy 8D20.Z Spastic cerebral palsy, unspecified – 8D20.10 Spastic quadriplegic cerebral palsy – 8D20.11 Spastic diplegic cerebral palsy – 8D20.1Z Spastic bilateral cerebral palsy, unspecified 8D21 Dyskinetic cerebral palsy 8D22 Ataxic cerebral palsy 8D23 Worster-Drought syndrome 8D2Y Other specified cerebral palsy 8D2Z Cerebral palsy, unspecified 8D40 Neurological disorders due to nutrient deficiency 8D40.0 Encephalopathy due to nutritional deficiency 8D40.1 Neuropathy due to nutritional deficiency 8D40.2 Myopathy due to nutritional deficiency 8D40.3 Intellectual developmental disorder due to nutritional deficiency 8D40.Y Other specified neurological disorders due to nutrient deficiency 8D40.Z Neurological disorders due to nutrient deficiency, unspecified 8D41 Neurological disorders due to an excess of micro or macro nutrients 8D41.0 Peripheral neuropathy due to vitamin B6 hyperalimentation 8D41.1 Myopathy due to hypercalcaemia 8D41.2 Pseudotumour Cerebri related to Hypervitaminosis A 8D41.Y Other specified neurological disorders due to an excess of micro or macro nutrients 8D41.Z Neurological disorders due to an excess of micro or macro nutrients, unspecified 8D42 Neurological disorders due to overweight or obesity in adults or children 8D43 Neurological disorders due to toxicity 8D43.0 Encephalopathy due to toxicity 8D43.1 Cognitive impairment due to toxicity 8D43.2 Neuropathy due to toxicity 8D43.3 Myopathy due to toxicity 8D43.4 Movement disorders due to toxicity 8D43.5 Cassava poisoning 8D43.Y Other specified neurological disorders due to toxicity 8D43.Z Neurological disorders due to toxicity, unspecified – 8D43.00 Encephalopathy due to ammonia – 8D43.0Y Other specified encephalopathy due to toxicity – 8D43.0Z Encephalopathy due to toxicity, unspecified – 8D43.20 Drug-induced polyneuropathy – 8D43.21 Post radiation polyneuropathy – 8D43.2Y Other specified neuropathy due to toxicity – 8D43.2Z Neuropathy due to toxicity, unspecified 8D44 Alcohol-related neurological disorders 8D44.0 Alcoholic polyneuropathy 8D44.1 Alcoholic myopathy 8D44.Y Other specified alcohol-related neurological disorders 8D44.Z Alcohol-related neurological disorders, unspecified 8D4Y Other specified nutritional or toxic disorders of the nervous system 8D4Z Nutritional or toxic disorders of the nervous system, unspecified 8D60 Increased intracranial pressure 8D60.0 Brain herniation syndromes 8D60.1 Cerebral oedema 8D60.Y Other specified increased intracranial pressure 8D60.Z Increased intracranial pressure, unspecified 8D61 Intracranial hypotension 8D61.0 Spontaneous intracranial hypotension 8D61.1 Secondary intracranial hypotension 8D61.Y Other specified intracranial hypotension 8D61.Z Intracranial hypotension, unspecified 8D62 Cerebrospinal fluid rhinorrhoea 8D63 Cerebrospinal fluid otorrhoea 8D64 Hydrocephalus 8D64.0 Communicating hydrocephalus 8D64.1 Non-communicating hydrocephalus 8D64.2 Ex-vacuo hydrocephalus 8D64.Z Hydrocephalus, unspecified – 8D64.00 Increased cerebrospinal fluid production – 8D64.01 Congenital agenesis of arachnoid villi – 8D64.02 Post haemorrhagic hydrocephalus – 8D64.03 Post traumatic hydrocephalus – 8D64.04 Normal-pressure hydrocephalus – 8D64.0Y Other specified communicating hydrocephalus – 8D64.0Z Communicating hydrocephalus, unspecified – 8D64.10 Hydrocephalus due to structural malformations – 8D64.1Y Other specified non-communicating hydrocephalus – 8D64.1Z Non-communicating hydrocephalus, unspecified 8D65 Cerebrospinal fluid fistula 8D66 Syringomyelia or syringobulbia 8D66.0 Idiopathic syringomyelia 8D66.1 Syringomyelia due to certain specified cause 8D66.2 Syringobulbia 8D66.Y Other specified syringomyelia or syringobulbia 8D66.Z Syringomyelia or syringobulbia, unspecified 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 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 8D87.0 Multiple system atrophy 8D87.Y Other specified autonomic nervous system disorder due to specified neurodegenerative disorder – 8D87.00 Multiple system atrophy, Cerebellar type – 8D87.01 Multiple system atrophy, Parkinsonism – 8D87.0Y Other specified multiple system atrophy – 8D87.0Z Multiple system atrophy, unspecified 8D88 Autonomic neuropathies 8D88.0 Autonomic neuropathy due to sodium channelopathies 8D88.1 Autonomic neuropathy due to diabetes mellitus 8D88.2 Immune mediated autonomic neuropathy 8D88.3 Autonomic disorder due to toxins 8D88.4 Autonomic neuropathy in endocrine and metabolic diseases 8D88.Y Other specified autonomic neuropathies 8D88.Z Autonomic neuropathies, unspecified 8D89 Disorders of orthostatic tolerance 8D89.0 Reflex syncope 8D89.1 Syncope due to autonomic failure 8D89.2 Postural orthostatic tachycardia syndrome 8D89.3 Baroreflex failure 8D89.Y Other specified disorders of orthostatic tolerance 8D89.Z Disorders of orthostatic tolerance, unspecified 8D8A Focal or segmental autonomic disorders 8D8A.1 Horner syndrome 8D8A.2 Episodic anisocoria 8D8A.Y Other specified focal or segmental autonomic disorders 8D8A.Z Focal or segmental autonomic disorders, unspecified 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 8E00 Sporadic Creutzfeldt-Jakob Disease 8E01 Acquired prion disease 8E01.0 Iatrogenically acquired Creutzfeldt-Jakob Disease 8E01.1 Kuru 8E01.2 Variant Creutzfeldt-Jakob Disease 8E01.3 Other acquired Creutzfeldt-Jakob Disease 8E01.Z Acquired prion disease, unspecified 8E02 Genetic prion diseases 8E02.0 Genetic Creutzfeldt-Jakob disease 8E02.1 Gerstmann-Straussler-Scheinker syndrome 8E02.2 Fatal familial insomnia 8E02.3 Other genetic prion diseases 8E02.Y Other specified Creutzfeldt-Jakob disease 8E02.Z Creutzfeldt-Jakob disease, unspecified 8E03 Variably protease sensitive prionopathy 8E0Y Other specified human prion diseases 8E0Z Human prion diseases, unspecified 8E20 Persistent vegetative state 8E21 Permanent vegetative state 8E22 Minimally conscious state 8E22.0 Minimally conscious state plus 8E22.1 Minimally conscious state minus 8E22.Y Other specified minimally conscious state 8E22.Z Minimally conscious state, unspecified 8E2Y Other specified disorders of consciousness 8E2Z Disorders of consciousness, unspecified 8E40 Disorders of the meninges excluding infection 8E40.0 Neoplastic meningitis 8E40.1 Chemical meningitis 8E40.2 Inflammatory meningitis 8E40.3 Arachnoiditis 8E40.Y Other specified disorders of the meninges excluding infection 8E40.Z Disorders of the meninges excluding infection, unspecified 8E41 Pachymeningitis 8E41.0 Pachymeningitis due to infection 8E41.1 Idiopathic hypertrophic pachymeningitis 8E41.Y Other specified pachymeningitis 8E41.Z Pachymeningitis, unspecified 8E42 Superficial siderosis of the nervous system 8E43 Pain disorders 8E43.0 Neuropathic pain 8E43.Y Other specified pain disorders 8E43.Z Pain disorders, unspecified – 8E43.00 Phantom limb syndrome – 8E43.0Y Other specified neuropathic pain – 8E43.0Z Neuropathic pain, unspecified 8E44 Post anoxic brain damage 8E45 Locked-in syndrome 8E46 Reye syndrome 8E47 Encephalopathy, not elsewhere classified 8E48 Encephalitis, not elsewhere classified 8E49 Postviral fatigue syndrome 8E4A Paraneoplastic or autoimmune disorders of the nervous system 8E4A.0 Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord 8E4A.1 Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system 8E4A.2 Paraneoplastic or autoimmune neuromuscular transmission disorders 8E4A.3 Paraneoplastic or autoimmune disorders of the muscle 8E4A.Y Other specified paraneoplastic or autoimmune disorders of the nervous system 8E4A.Z Paraneoplastic or autoimmune disorders of the nervous system, unspecified 8E4Y Other specified disorders of the nervous system 8E60 Post ventricular shunting leak 8E61 Post radiation injury of the nervous system 8E61.0 Radiation-induced brain injury 8E61.1 Spinal cord irradiation 8E61.Z Post radiation injury of the nervous system, unspecified 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 FA00 Osteoarthritis of hip – FA00.0 Primary osteoarthritis of hip – FA00.1 Post traumatic osteoarthritis of hip – FA00.2 Other secondary osteoarthritis of hip – FA00.Z Osteoarthritis of hip, unspecified FA01 Osteoarthritis of knee – FA01.0 Primary osteoarthritis of knee – FA01.1 Post traumatic osteoarthritis of knee – FA01.2 Other secondary osteoarthritis of knee – FA01.Z Osteoarthritis of knee, unspecified FA02 Osteoarthritis of wrist or hand – FA02.0 Primary osteoarthritis of wrist or hand – FA02.1 Post traumatic osteoarthritis of wrist or hand – FA02.2 Other secondary osteoarthritis of wrist or hand – FA02.Z Osteoarthritis of wrist or hand, unspecified FA03 Osteoarthritis of other specified joint – FA03.0 Primary osteoarthritis of other specified joint – FA03.1 Post traumatic osteoarthritis of other specified joint – FA03.2 Other secondary osteoarthritis of other specified joint – FA03.Z Osteoarthritis of other specified joint, unspecified FA04 Oligoosteoarthritis FA05 Polyosteoarthritis FA0Z Osteoarthritis, unspecified FA10 Direct infections of joint – FA10.0 Bacterial infection of joint – FA10.1 Viral infection of joint – FA10.2 Fungal infection of joint – FA10.Z Direct infections of joint, unspecified FA11 Reactive arthropathies – FA11.0 Arthropathy following intestinal bypass – FA11.1 Arthropathy following vaccination – FA11.2 Arthropathy following genitourinary infection – FA11.Y Other specified reactive arthropathies – FA11.Z Reactive arthropathies, unspecified FA12 Postinfectious arthropathies – FA12.0 Bacterial postinfectious arthropathy – FA12.1 Viral postinfectious arthropathies – FA12.2 Fungal postinfectious arthropathies – FA12.3 Parasitic postinfectious arthropathies – FA12.Y Other specified postinfectious arthropathies – FA12.Z Postinfectious arthropathies, unspecified FA13 Infectious spondyloarthritis FA1Y Other specified infection related arthropathies FA1Z Infection related arthropathies, unspecified FA20 Rheumatoid arthritis – FA20.0 Seropositive rheumatoid arthritis – FA20.1 Seronegative rheumatoid arthritis – FA20.Z Rheumatoid arthritis, serology unspecified FA21 Psoriatic arthritis – FA21.0 Psoriatic spondyloarthritis – FA21.Y Other specified psoriatic arthritis – FA21.Z Psoriatic arthritis, unspecified FA22 Polymyalgia rheumatica FA23 Adult-onset Still disease FA24 Juvenile idiopathic arthritis – FA24.0 Juvenile idiopathic oligoarthritis – FA24.1 Juvenile idiopathic polyarthritis – FA24.2 Juvenile psoriatic arthritis – FA24.3 Juvenile enthesitis related arthritis – FA24.4 Juvenile systemic arthritis – FA24.Y Other specified juvenile idiopathic arthritis – FA24.Z Juvenile idiopathic arthritis, unspecified –– FA24.00 Juvenile idiopathic oligoarthritis, onset persistent –– FA24.01 Juvenile idiopathic oligoarthritis, onset extended –– FA24.0Z Juvenile idiopathic oligoarthritis, onset unspecified FA25 Gout – FA25.0 Primary gout – FA25.1 Secondary gout – FA25.2 Gout without specification whether primary or secondary –– FA25.10 Lead-induced gout –– FA25.11 Drug-induced gout –– FA25.12 Gouty arthropathy due to enzyme defects or other inherited disorders –– FA25.1Y Other specified secondary gout –– FA25.1Z Secondary gout, unspecified –– FA25.20 Tophaceous gout –– FA25.2Y Other specified gout without specification whether primary or secondary –– FA25.2Z Gout, unspecified FA26 Certain specified crystal arthropathies – FA26.0 Calcium pyrophosphate dehydrate deposition disease – FA26.1 Hydroxyapatite deposition disease – FA26.2 Chondrocalcinosis – FA26.Y Other specified crystal arthropathies – FA26.Z Crystal arthropathies, unspecified FA27 Certain specified inflammatory arthropathies – FA27.0 Kashin-Beck disease – FA27.1 Pigmented villonodular synovitis – FA27.2 Palindromic rheumatism – FA27.3 Transient synovitis – FA27.4 Intermittent hydrarthrosis – FA27.Y Other specified inflammatory arthropathies FA2Z Inflammatory arthropathies, unspecified FA30 Acquired deformities of fingers or toes – FA30.0 Acquired hallux valgus – FA30.1 Hallux rigidus – FA30.2 Acquired hammer toe – FA30.Y Other specified acquired deformities of fingers or toes – FA30.Z Acquired deformities of fingers or toes, unspecified FA31 Other acquired deformities of limbs – FA31.0 Valgus deformity, not elsewhere classified – FA31.1 Varus deformity, not elsewhere classified – FA31.2 Flexion deformity – FA31.3 Acquired wrist drop – FA31.4 Acquired foot drop – FA31.5 Acquired pes planus – FA31.6 Acquired clawhand or clubhand – FA31.7 Acquired clawfoot or clubfoot – FA31.8 Acquired unequal limb length – FA31.Y Other specified acquired deformities of limbs – FA31.Z Acquired deformities of limbs, unspecified FA32 Disorders of patella – FA32.0 Recurrent instability of patella – FA32.1 Patellofemoral disorders – FA32.Y Other specified disorders of patella – FA32.Z Disorders of patella, unspecified FA33 Internal derangement of knee – FA33.0 Cystic meniscus – FA33.1 Discoid meniscus – FA33.2 Derangement of meniscus due to old tear or injury – FA33.3 Loose body in knee – FA33.4 Chronic instability of knee – FA33.Y Other specified internal derangement of knee – FA33.Z Internal derangement of knee, unspecified –– FA33.40 Chronic instability of knee, medial collateral ligament or other or unspecified part of medial meniscus –– FA33.4Y Other specified chronic instability of knee –– FA33.4Z Chronic instability of knee, unspecified FA34 Certain specified joint derangements – FA34.0 Loose body in joint – FA34.1 Disorder of ligament – FA34.2 Recurrent instability of joint – FA34.3 Contracture of joint – FA34.4 Ankylosis of joint – FA34.5 Impingement syndrome of hip – FA34.Y Other joint derangements FA35 Wear of articular bearing surface of joint prosthesis – FA35.0 Wear of articular bearing surface of joint prosthesis of hip – FA35.1 Wear of articular bearing surface of joint prosthesis of knee – FA35.2 Wear of articular bearing surface of joint prosthesis of other joint – FA35.Z Wear of articular bearing surface of joint prosthesis of unspecified joint FA36 Effusion of joint – FA36.0 Effusion of joint containing blood – FA36.Y Other specified effusion of joint – FA36.Z Effusion of joint, unspecified FA37 Certain joint disorders, not elsewhere classified – FA37.0 Osteophyte – FA37.Y Other specified certain joint disorders, not elsewhere classified – FA37.Z Certain joint disorders, not elsewhere classified, unspecified FA38 Arthropathy in diseases classified elsewhere – FA38.0 Diabetic arthropathy – FA38.1 Neuropathic arthropathy – FA38.2 Arthropathy in hypersensitivity reactions classified elsewhere – FA38.3 Haemophilic arthropathy – FA38.Y Other specified arthropathy in diseases classified elsewhere – FA38.Z Unspecified arthropathy in diseases classified elsewhere –– FA38.10 Diabetic Charcot arthropathy –– FA38.1Y Other specified neuropathic arthropathy –– FA38.1Z Neuropathic arthropathy, unspecified FA3Z Unspecified joint disorders and deformities of limbs FA5Y Other specified arthropathies FA5Z Arthropathies, unspecified FA70 Spinal deformities – FA70.0 Kyphosis – FA70.1 Scoliosis – FA70.2 Lordosis – FA70.Z Spinal deformities, unspecified FA71 Torticollis FA72 Disorders of vertebra – FA72.0 Ankylosing hyperostosis – FA72.1 Kissing spine – FA72.2 Traumatic spondylopathy – FA72.3 Fatigue fracture of vertebra – FA72.4 Collapsed vertebra, not elsewhere classified – FA72.Y Other specified disorders of vertebra – FA72.Z Disorders of vertebra, unspecified FA7Y Other specified structural disorders of spine FA7Z Structural disorders of spine, unspecified FA80 Intervertebral disc degeneration – FA80.0 Intervertebral disc degeneration of cervical spine without prolapsed disc – FA80.1 Intervertebral disc degeneration of cervical spine with prolapsed disc – FA80.2 Intervertebral disc degeneration of cervical spine with bony spur at the vertebra – FA80.3 Intervertebral disc degeneration of cervical spine with nervous system involvement – FA80.4 Intervertebral disc degeneration of thoracic spine without prolapsed disc – FA80.5 Intervertebral disc degeneration of thoracic spine with prolapsed disc – FA80.6 Intervertebral disc degeneration of thoracic spine with bony spur at the vertebra – FA80.7 Intervertebral disc degeneration of thoracic spine with nervous system involvement – FA80.8 Intervertebral disc degeneration of lumbar spine without prolapsed disc – FA80.9 Intervertebral disc degeneration of lumbar spine with prolapsed disc – FA80.A Intervertebral disc degeneration of lumbar spine with bony spur at the vertebra – FA80.B Intervertebral disc degeneration of lumbar spine with nervous system involvement – FA80.Y Other specified intervertebral disc degeneration – FA80.Z Intervertebral disc degeneration, unspecified FA81 Spondylolysis – FA81.0 Spondylolysis with slippage – FA81.1 Spondylolysis without slippage – FA81.Z Spondylolysis, unspecified FA82 Spinal stenosis FA83 Ossification of spinal ligaments FA84 Spondylolisthesis – FA84.0 Spondylolisthesis with pars defect – FA84.1 Spondylolisthesis without pars defect – FA84.Z Spondylolisthesis, unspecified FA85 Spinal endplate defects – FA85.0 Spinal epiphysiopathy with no determinant – FA85.1 Spinal epiphysiopathy with determinants – FA85.Y Other specified spinal endplate defects – FA85.Z Spinal endplate defects, unspecified –– FA85.10 Localised central endplate defect –– FA85.11 Multiple anterior endplate defect –– FA85.12 Separation of ring apophysis –– FA85.1Y Other specified spinal epiphysiopathy with determinants –– FA85.1Z Spinal epiphysiopathy with determinants, unspecified FA8Y Other specified degenerative condition of spine FA8Z Degenerative condition of spine, unspecified FA90 Infection of vertebra – FA90.0 Infection of vertebra with no determinant – FA90.1 Infection of vertebra with determinants – FA90.Y Other specified infection of vertebra – FA90.Z Infection of vertebra, unspecified FA91 Infection of intervertebral disc FA92 Inflammatory spondyloarthritis – FA92.0 Axial spondyloarthritis – FA92.1 Peripheral spondyloarthritis – FA92.Y Other specified inflammatory spondyloarthritis – FA92.Z Inflammatory spondyloarthritis, unspecified –– FA92.00 Spinal enthesitis –– FA92.01 Sacroiliitis, not elsewhere classified –– FA92.0Y Other specified axial spondyloarthritis –– FA92.0Z Axial spondyloarthritis, unspecified FA9Y Other specified inflammation of spine FA9Z Inflammation of spine, unspecified 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 FB30 Infectious myositis FB31 Calcification or ossification of muscle – FB31.0 Progressive osseous heteroplasia – FB31.1 Fibrodysplasia ossificans progressiva – FB31.Y Other specified calcification or ossification of muscle – FB31.Z Calcification or ossification of muscle, unspecified FB32 Certain specified disorders of muscle – FB32.0 Diastasis of muscle – FB32.1 Spontaneous rupture of muscle – FB32.2 Ischaemic infarction of muscle – FB32.3 Immobility syndrome – FB32.4 Contracture of muscle – FB32.5 Muscle strain or sprain – FB32.Y Other specified disorders of muscles –– FB32.20 Idiopathic rhabdomyolysis –– FB32.2Y Other specified ischaemic infarction of muscle –– FB32.2Z Ischaemic infarction of muscle, unspecified FB33 Secondary disorders of muscle FB3Z Disorders of muscles, unspecified FB40 Tenosynovitis – FB40.0 Infectious tenosynovitis – FB40.1 Plantar fasciitis – FB40.2 Posterior tibial tendonitis – FB40.3 Calcific tendinitis – FB40.4 Trigger finger – FB40.5 Radial styloid tenosynovitis – FB40.Y Other specified tenosynovitis – FB40.Z Tenosynovitis, unspecified FB41 Spontaneous rupture of synovium or tendon – FB41.0 Spontaneous rupture of popliteal cyst – FB41.1 Spontaneous rupture of synovium – FB41.2 Spontaneous rupture of tendon – FB41.Y Other specified spontaneous rupture of synovium or tendon – FB41.Z Spontaneous rupture of synovium or tendon, unspecified FB42 Certain specified disorders of synovium or tendon – FB42.0 Acquired short Achilles tendon – FB42.1 Contracture of tendon sheath – FB42.2 Ganglion – FB42.3 Synovial hypertrophy, not elsewhere classified FB43 Secondary disorders of synovium or tendon FB4Y Other specified disorders of synovium or tendon FB4Z Disorders of synovium or tendon, unspecified FB50 Bursitis – FB50.0 Infectious bursitis – FB50.1 Bursitis related to use, overuse or pressure – FB50.2 Synovial cyst of popliteal space – FB50.3 Calcium deposit in bursa – FB50.Y Other specified bursitis – FB50.Z Bursitis, unspecified FB51 Fibroblastic disorders – FB51.0 Palmar fascial fibromatosis – FB51.1 Knuckle pads – FB51.2 Fasciitis and fibromatosis – FB51.3 Fibroblastic rheumatism – FB51.4 Retroperitoneal fibrosis – FB51.Y Other specified fibroblastic disorders – FB51.Z Fibroblastic disorders, unspecified –– FB51.40 Primary retroperitoneal fibrosis –– FB51.4Y Other specified retroperitoneal fibrosis –– FB51.4Z Retroperitoneal fibrosis, unspecified FB52 Soft tissue disorders in diseases classified elsewhere FB53 Shoulder lesions – FB53.0 Adhesive capsulitis of shoulder – FB53.1 Rotator cuff syndrome – FB53.2 Impingement syndrome of shoulder – FB53.Y Other specified shoulder lesions – FB53.Z Shoulder lesions, unspecified FB54 Enthesopathies of lower limb – FB54.0 Iliac crest spur – FB54.1 Iliotibial band syndrome – FB54.2 Tibial collateral bursitis – FB54.3 Calcaneal spur – FB54.4 Metatarsalgia – FB54.Y Other specified enthesopathies of lower limb – FB54.Z Enthesopathies of lower limb, unspecified FB55 Certain specified enthesopathies – FB55.0 Medial epicondylitis of elbow – FB55.1 Lateral epicondylitis of elbow – FB55.2 Periarthritis of wrist – FB55.Z Enthesopathies, unspecified FB56 Specified soft tissue disorders, not elsewhere classified – FB56.0 Foreign body granuloma of soft tissue, not elsewhere classified – FB56.1 Residual foreign body in soft tissue – FB56.2 Myalgia – FB56.3 Hypertrophy of infrapatellar fat pad – FB56.4 Pain in limb – FB56.6 Other specified soft tissue disorders FB6Z Soft tissue disorders, unspecified FB80 Certain specified disorders of bone density or structure FB80.0 Fibrous dysplasia of bone FB80.1 Skeletal fluorosis FB80.2 Osteitis condensans FB80.3 Hyperostosis of skull FB80.4 Osteosclerosis FB80.5 Solitary bone cyst FB80.6 Aneurysmal bone cyst FB80.7 Malunion of fracture FB80.8 Nonunion of fracture FB80.9 Delayed union of fracture FB80.A Stress fracture, not elsewhere classified FB80.B Pathological fracture FB80.Y Other specified disorders of bone density and structure FB80.Z Disorder of bone density and structure, unspecified FB81 Osteonecrosis FB81.0 Idiopathic aseptic osteonecrosis FB81.1 Osteonecrosis due to dialysis FB81.2 Drug-induced osteonecrosis FB81.3 Osteonecrosis due to trauma FB81.4 Osteonecrosis due to haemoglobinopathy FB81.5 Osteonecrosis due to ionizing radiation FB81.6 Alcohol induced osteonecrosis FB81.Y Other specified osteonecrosis FB81.Z Osteonecrosis, unspecified FB82 Chondropathies FB82.0 Chondromalacia FB82.1 Osteochondrosis or osteochondritis dissecans FB82.2 Slipped upper femoral epiphysis FB82.3 Relapsing polychondritis FB82.Y Other specified chondropathies FB82.Z Chondropathies, unspecified – FB82.00 Chondromalacia patellae – FB82.0Y Other specified chondromalacia – FB82.0Z Chondromalacia, unspecified FB83 Low bone mass disorders FB83.0 Osteopenia FB83.1 Osteoporosis FB83.2 Adult osteomalacia – FB83.00 Premenopausal idiopathic osteopenia – FB83.01 Postmenopausal osteopenia – FB83.02 Senile osteopenia – FB83.03 Osteopenia of disuse – FB83.04 Drug-induced osteopenia – FB83.0Y Other specified osteopenia – FB83.0Z Osteopenia, unspecified – FB83.10 Premenopausal idiopathic osteoporosis – FB83.11 Postmenopausal osteoporosis – FB83.12 Osteoporosis of disuse – FB83.13 Drug-induced osteoporosis – FB83.14 Osteoporosis due to malabsorption – FB83.1Y Other specified osteoporosis – FB83.1Z Osteoporosis, unspecified – FB83.20 Aluminium bone disease – FB83.21 Adult osteomalacia due to malnutrition – FB83.22 Drug-induced adult osteomalacia – FB83.2Y Other specified adult osteomalacia – FB83.2Z Adult osteomalacia, unspecified FB84 Osteomyelitis or osteitis FB84.0 Acute haematogenous osteomyelitis FB84.1 Other acute osteomyelitis FB84.2 Subacute osteomyelitis FB84.3 Chronic multifocal osteomyelitis FB84.4 Chronic osteomyelitis with draining sinus FB84.5 Other chronic haematogenous osteomyelitis FB84.Y Other specified osteomyelitis or osteitis FB84.Z Osteomyelitis or osteitis, unspecified FB85 Paget disease of bone FB85.0 Juvenile Paget disease FB85.1 Paget disease of bone in neoplastic disease FB85.Y Other specified Paget disease of bone FB85.Z Paget disease of bone, unspecified FB86 Disorders associated with bone growth FB86.0 Epiphyseal arrest FB86.1 Bone hyperplasias FB86.2 Osteolysis FB86.Y Other specified disorders associated with bone growth FB86.Z Disorders associated with bone growth, unspecified – FB86.10 Hypertrophic osteoarthropathy – FB86.11 Hypertrophy of bone – FB86.1Y Other specified bone hyperplasias – FB86.1Z Bone hyperplasias, unspecified 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 FC00.0 Acquired deformity of nose FC00.1 Acquired deformity of neck FC00.2 Acquired deformity of chest or rib FC00.3 Acquired deformity of pelvis FC00.4 Acquired deformity of trunk FC00.Y Acquired deformities of musculoskeletal system and connective tissue, not classified elsewhere, other specified sites FC01 Postprocedural disorders of the musculoskeletal system FC01.0 Pseudarthrosis after fusion or arthrodesis FC01.1 Postlaminectomy syndrome, not elsewhere classified FC01.2 Post radiation kyphosis FC01.3 Postlaminectomy kyphosis FC01.4 Postsurgical lordosis FC01.5 Post radiation scoliosis FC01.6 Fracture of bone following insertion of orthopaedic implant, joint prosthesis, or bone plate FC01.7 Nonunion after arthrodesis FC01.8 Postsurgical osteolysis FC01.9 Postoophorectomy osteoporosis FC01.A Postsurgical malabsorption osteoporosis FC01.70 Nonunion after spinal arthrodesis FC01.7Y Nonunion after arthrodesis of other sites FC0Y Other specified diseases of the musculoskeletal system or connective tissue FC0Z Diseases of the musculoskeletal system or connective tissue, unspecified LA00 Anencephaly or similar anomalies – LA00.0 Anencephaly – LA00.1 Iniencephaly – LA00.2 Acephaly – LA00.3 Amyelencephaly – LA00.Y Other specified anencephaly or similar anomalies – LA00.Z Anencephaly or similar anomalies, unspecified –– LA00.00 Craniorachischisis –– LA00.0Y Other specified anencephaly –– LA00.0Z Anencephaly, unspecified LA01 Cephalocele LA02 Spina bifida – LA02.0 Spina bifida cystica – LA02.1 Spina bifida aperta – LA02.Y Other specified spina bifida – LA02.Z Spina bifida, unspecified –– LA02.00 Myelomeningocele with hydrocephalus –– LA02.01 Myelomeningocele without hydrocephalus –– LA02.02 Myelocystocele –– LA02.0Y Other specified spina bifida cystica –– LA02.0Z Spina bifida cystica, unspecified LA03 Arnold-Chiari malformation type II LA04 Congenital hydrocephalus – LA04.0 Hydrocephalus with stenosis of the aqueduct of Sylvius – LA04.Y Other specified congenital hydrocephalus – LA04.Z Congenital hydrocephalus, unspecified LA05 Cerebral structural developmental anomalies – LA05.0 Microcephaly – LA05.1 Megalencephaly – LA05.2 Holoprosencephaly – LA05.3 Corpus callosum agenesis – LA05.4 Arrhinencephaly – LA05.5 Abnormal neuronal migration – LA05.6 Encephaloclastic disorders – LA05.7 Brain cystic malformations – LA05.8 Colpocephaly – LA05.Y Other specified cerebral structural developmental anomalies – LA05.Z Cerebral structural developmental anomalies, unspecified –– LA05.50 Polymicrogyria –– LA05.51 Cortical dysplasia –– LA05.5Y Other specified abnormal neuronal migration –– LA05.5Z Abnormal neuronal migration, unspecified –– LA05.60 Porencephaly –– LA05.61 Schizencephaly –– LA05.62 Hydranencephaly –– LA05.6Y Other specified encephaloclastic disorders –– LA05.6Z Encephaloclastic disorders, unspecified LA06 Cerebellar structural developmental anomalies – LA06.0 Dandy-Walker malformation – LA06.1 Hypoplasia or agenesis of cerebellar hemispheres – LA06.2 Focal cerebellar dysplasia – LA06.Y Other specified cerebellar structural developmental anomalies – LA06.Z Cerebellar structural developmental anomalies, unspecified LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column – LA07.0 Primary tethered cord syndrome – LA07.1 Diastematomyelia – LA07.2 Amyelia – LA07.3 Primary syringomyelia or hydromyelia – LA07.4 Arnold-Chiari malformation type I – LA07.Y Other specified structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column – LA07.Z Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column, unspecified LA0Y Other specified structural developmental anomalies of the nervous system LA0Z Structural developmental anomalies of the nervous system, unspecified LA10 Structural developmental anomalies of ocular globes – LA10.0 Microphthalmos – LA10.1 Clinical anophthalmos – LA10.2 Buphthalmos – LA10.3 Congenital macrophthalmos – LA10.Y Other specified structural developmental anomalies of ocular globes – LA10.Z Structural developmental anomalies of ocular globes, unspecified LA11 Structural developmental anomalies of the anterior segment of eye – LA11.0 Blue sclera – LA11.1 Structural developmental anomalies of cornea – LA11.2 Anterior segment dysgenesis – LA11.3 Aniridia – LA11.4 Coloboma of iris – LA11.5 Congenital corneal opacity – LA11.6 Structural disorders of the pupil – LA11.Y Other specified structural developmental anomalies of the anterior segment of eye – LA11.Z Structural developmental anomalies of the anterior segment of eye, unspecified –– LA11.60 Irregular pupil of the eye –– LA11.61 Iridoschisis –– LA11.62 Anomalies of pupillary function –– LA11.6Y Other specified structural disorders of the pupil –– LA11.6Z Structural disorders of the pupil, unspecified LA12 Structural developmental anomalies of lens or zonula – LA12.0 Coloboma of lens – LA12.1 Congenital cataract – LA12.2 Congenital aphakia – LA12.3 Spherophakia – LA12.Y Other specified structural developmental anomalies of lens or zonula – LA12.Z Structural developmental anomalies of lens or zonula, unspecified LA13 Structural developmental anomalies of the posterior segment of eye – LA13.0 Congenital anomalies of the vitreous – LA13.1 Coloboma of choroid or retina – LA13.2 Coloboma of macula – LA13.3 Congenital vitreoretinal dysplasia – LA13.5 Congenital retinal aneurysm – LA13.6 Congenital malformations of choroid – LA13.7 Congenital malformation of optic disc – LA13.8 Certain congenital malformations of posterior segment of eye – LA13.Y Other specified structural developmental anomalies of the posterior segment of eye – LA13.Z Structural developmental anomalies of the posterior segment of eye, unspecified –– LA13.70 Isolated optic nerve hypoplasia –– LA13.71 Optic nerve aplasia –– LA13.72 Congenitally elevated optic disc –– LA13.73 Optic disc dysplasia –– LA13.74 Megalopapilla –– LA13.76 Coloboma of optic disc –– LA13.7Y Other specified congenital malformation of optic disc –– LA13.7Z Congenital malformation of optic disc, unspecified –– LA13.80 Anastomosis of retinal or choroidal vessels LA14 Structural developmental anomalies of eyelid, lacrimal apparatus or orbit – LA14.0 Structural developmental anomalies of eyelids – LA14.1 Structural developmental anomalies of lacrimal apparatus – LA14.2 Structural developmental anomalies of orbit – LA14.Y Other specified structural developmental anomalies of eyelid, lacrimal apparatus or orbit – LA14.Z Structural developmental anomalies of eyelid, lacrimal apparatus or orbit, unspecified –– LA14.00 Palpebral cleft or coloboma –– LA14.01 Cryptophthalmia –– LA14.02 Congenital entropion –– LA14.03 Congenital ectropion –– LA14.04 Congenital ptosis –– LA14.05 Congenital eyelid retraction –– LA14.06 Epibulbar choristoma –– LA14.07 Ankyloblepharon filiforme adnatum –– LA14.0Y Other specified structural developmental anomalies of eyelids –– LA14.10 Aplasia of lacrimal or salivary glands –– LA14.11 Agenesis of lacrimal ducts –– LA14.12 Congenital dacryocele –– LA14.13 Congenital agenesis of lacrimal punctum –– LA14.14 Congenital stenosis or stricture of lacrimal duct –– LA14.1Y Other specified structural developmental anomalies of lacrimal apparatus –– LA14.1Z Structural developmental anomalies of lacrimal apparatus, unspecified LA1Y Other specified structural developmental anomalies of the eye, eyelid or lacrimal apparatus LA1Z Structural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecified LA20 Structural anomaly of eustachian apparatus LA21 Minor anomalies of pinnae – LA21.0 Macrotia – LA21.1 Protruding ear – LA21.2 Low-set ear – LA21.3 Misshapen ear – LA21.Y Other specified minor anomalies of pinnae – LA21.Z Minor anomalies of pinnae, unspecified LA22 Structural developmental anomalies of ear causing hearing impairment – LA22.0 Microtia – LA22.1 Anotia – LA22.2 Aplasia or hypoplasia of external auditory canal – LA22.3 Structural developmental anomalies of ear ossicles – LA22.4 Structural developmental anomalies of inner ear – LA22.Y Other specified structural developmental anomalies of ear causing hearing impairment – LA22.Z Structural developmental anomalies of ear causing hearing impairment, unspecified LA23 Otocephaly LA24 Accessory auricle LA2Y Other specified structural developmental anomalies of the ear LA2Z Structural developmental anomalies of the ear, unspecified LA30 Structural developmental anomalies of teeth and periodontal tissues – LA30.0 Anodontia – LA30.1 Hypodontia – LA30.2 Oligodontia – LA30.3 Hyperdontia – LA30.4 Abnormalities of size or form of teeth – LA30.5 Anomalies in tooth resorption or loss – LA30.6 Amelogenesis imperfecta – LA30.7 Dentine dysplasia – LA30.8 Dentinogenesis imperfecta – LA30.9 Odontogenesis imperfecta – LA30.Y Other specified structural developmental anomalies of teeth and periodontal tissues – LA30.Z Structural developmental anomalies of teeth and periodontal tissues, unspecified –– LA30.50 Early exfoliation of teeth –– LA30.51 Late exfoliation of teeth –– LA30.5Y Other specified anomalies in tooth resorption or loss –– LA30.5Z Anomalies in tooth resorption or loss, unspecified LA31 Structural developmental anomalies of mouth or tongue – LA31.0 Congenital macroglossia – LA31.1 Hypoglossia or aglossia – LA31.2 Ankyloglossia – LA31.3 Macrostomia – LA31.4 Microstomia – LA31.Y Other specified structural developmental anomalies of mouth or tongue – LA31.Z Structural developmental anomalies of mouth or tongue, unspecified – LA40 Cleft lip –– LA40.0 Cleft lip, unilateral –– LA40.1 Cleft lip, bilateral –– LA40.2 Cleft lip, median –– LA40.Z Cleft lip, unspecified – LA41 Cleft lip and alveolus –– LA41.0 Cleft lip and alveolus, unilateral –– LA41.1 Cleft lip and alveolus, bilateral –– LA41.Z Cleft lip and alveolus, unspecified – LA42 Cleft palate –– LA42.0 Cleft hard palate –– LA42.1 Cleft soft palate –– LA42.2 Cleft uvula –– LA42.Z Cleft palate, unspecified – LA4Y Other specified clefts of lip, alveolus or palate – LA4Z Clefts of lip, alveolus or palate, unspecified LA50 Congenital velopharyngeal incompetence LA51 Facial clefts 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 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 LA70 Structural developmental anomalies of the nose or cavum – LA70.0 Arrhinia – LA70.1 Bifid nose – LA70.2 Choanal atresia – LA70.3 Congenital perforated nasal septum – LA70.Y Other specified structural developmental anomalies of the nose or cavum – LA70.Z Structural developmental anomalies of the nose or cavum, unspecified LA71 Structural developmental anomalies of larynx – LA71.0 Congenital laryngomalacia – LA71.1 Laryngocele – LA71.2 Laryngeal hypoplasia – LA71.3 Congenital subglottic stenosis – LA71.Y Other specified structural developmental anomalies of larynx – LA71.Z Structural developmental anomalies of larynx, unspecified LA72 Laryngotracheooesophageal cleft LA73 Structural developmental anomalies of trachea – LA73.0 Congenital stenosis of trachea – LA73.1 Congenital tracheomalacia – LA73.Y Other specified structural developmental anomalies of trachea – LA73.Z Structural developmental anomalies of trachea, unspecified LA74 Structural developmental anomalies of bronchi – LA74.0 Congenital stenosis or atresia of bronchus – LA74.1 Congenital bronchomalacia – LA74.Y Other specified structural developmental anomalies of bronchi – LA74.Z Structural developmental anomalies of bronchi, unspecified LA75 Structural developmental anomalies of lungs – LA75.0 Accessory lobe of lung – LA75.1 Agenesis of lung – LA75.2 Congenital hypoplasia of lung – LA75.3 Congenital hyperplasia of lung – LA75.4 Congenital pulmonary airway malformations – LA75.5 Congenital lobar emphysema – LA75.6 Congenital sequestration of lung – LA75.Y Other specified structural developmental anomalies of lungs – LA75.Z Structural developmental anomalies of lungs, unspecified 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 – LA80 Anomalous position-orientation of heart –– LA80.0 Laevocardia –– LA80.1 Dextrocardia –– LA80.2 Mesocardia –– LA80.3 Extrathoracic heart –– LA80.Y Other specified anomalous position-orientation of heart –– LA80.Z Anomalous position-orientation of heart, unspecified – LA81 Abnormal ventricular relationships – LA82 Total mirror imagery – LA83 Right isomerism – LA84 Left isomerism – LA85 Congenital anomaly of an atrioventricular or ventriculo-arterial connection –– LA85.0 Discordant atrioventricular connections –– LA85.1 Transposition of the great arteries –– LA85.2 Double outlet right ventricle –– LA85.3 Double outlet left ventricle –– LA85.4 Common arterial trunk –– LA85.Y Other specified congenital anomaly of an atrioventricular or ventriculo-arterial connection –– LA85.Z Congenital anomaly of an atrioventricular or ventriculo-arterial connection, unspecified ––– LA85.00 Congenitally corrected transposition of great arteries ––– LA85.0Y Other specified discordant atrioventricular connections ––– LA85.0Z Discordant atrioventricular connections, unspecified ––– LA85.20 Double outlet right ventricle with subpulmonary ventricular septal defect, transposition type ––– LA85.21 Double outlet right ventricle with non-committed ventricular septal defect ––– LA85.22 Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis, ventricular septal defect type ––– LA85.23 Double outlet right ventricle with subaortic or doubly committed ventricular septal defect and pulmonary stenosis, Fallot type ––– LA85.2Y Other specified double outlet right ventricle ––– LA85.2Z Double outlet right ventricle, unspecified ––– LA85.40 Common arterial trunk with aortic dominance ––– LA85.41 Common arterial trunk with pulmonary dominance and interrupted aortic arch ––– LA85.4Y Other specified common arterial trunk ––– LA85.4Z Common arterial trunk, unspecified – LA86 Congenital anomaly of mediastinal vein –– LA86.0 Left superior caval vein –– LA86.1 Unroofed coronary sinus –– LA86.2 Anomalous pulmonary venous connection –– LA86.3 Congenital pulmonary venous stenosis or hypoplasia –– LA86.Y Other specified congenital anomaly of mediastinal vein –– LA86.Z Congenital anomaly of mediastinal vein, unspecified ––– LA86.20 Total anomalous pulmonary venous connection ––– LA86.21 Partial anomalous pulmonary venous connection ––– LA86.22 Scimitar syndrome ––– LA86.2Y Other specified anomalous pulmonary venous connection ––– LA86.2Z Anomalous pulmonary venous connection, unspecified – LA87 Congenital anomaly of an atrioventricular valve or atrioventricular septum –– LA87.0 Congenital anomaly of tricuspid valve –– LA87.1 Congenital anomaly of mitral valve –– LA87.3 Common atrioventricular junction without an atrioventricular septal defect –– LA87.4 Common atrioventricular junction with atrioventricular septal defect –– LA87.Y Other specified congenital anomaly of an atrioventricular valve or atrioventricular septum –– LA87.Z Congenital anomaly of an atrioventricular valve or atrioventricular septum, unspecified ––– LA87.00 Congenital tricuspid regurgitation ––– LA87.01 Congenital tricuspid valvar stenosis ––– LA87.02 Dysplasia of tricuspid valve ––– LA87.03 Ebstein malformation of tricuspid valve ––– LA87.0Y Other specified congenital anomaly of tricuspid valve ––– LA87.0Z Congenital anomaly of tricuspid valve, unspecified ––– LA87.10 Congenital mitral regurgitation ––– LA87.11 Congenital mitral valvar stenosis ––– LA87.12 Dysplasia of mitral valve ––– LA87.13 Congenital anomaly of mitral subvalvar apparatus ––– LA87.1Y Other specified congenital anomaly of mitral valve ––– LA87.1Z Congenital anomaly of mitral valve, unspecified ––– LA87.40 Atrioventricular septal defect with communication at the atrial level only ––– LA87.41 Atrioventricular septal defect with communication at the ventricular level only ––– LA87.42 Atrioventricular septal defect with communication at atrial level and restrictive communication at ventricular level ––– LA87.43 Atrioventricular septal defect with communication at atrial level and unrestrictive communication at ventricular level ––– LA87.44 Atrioventricular septal defect with ventricular imbalance ––– LA87.45 Atrioventricular septal defect and tetralogy of Fallot ––– LA87.4Y Other specified common atrioventricular junction with atrioventricular septal defect ––– LA87.4Z Common atrioventricular junction with atrioventricular septal defect, unspecified – LA88 Congenital anomaly of a ventricle or the ventricular septum –– LA88.0 Congenital right ventricular outflow tract obstruction –– LA88.1 Double chambered right ventricle –– LA88.2 Tetralogy of Fallot –– LA88.3 Congenital left ventricular outflow tract obstruction –– LA88.4 Ventricular septal defect –– LA88.Y Other specified congenital anomaly of a ventricle or the ventricular septum –– LA88.Z Congenital anomaly of a ventricle or the ventricular septum, unspecified ––– LA88.20 Tetralogy of Fallot with absent pulmonary valve syndrome ––– LA88.21 Tetralogy of Fallot with pulmonary atresia ––– LA88.22 Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery ––– LA88.2Y Other specified tetralogy of Fallot ––– LA88.2Z Tetralogy of Fallot, unspecified ––– LA88.40 Trabecular muscular ventricular septal defect ––– LA88.41 Perimembranous central ventricular septal defect ––– LA88.42 Ventricular septal defect haemodynamically insignificant ––– LA88.4Y Other specified ventricular septal defect ––– LA88.4Z Ventricular septal defect, unspecified – LA89 Functionally univentricular heart –– LA89.0 Double inlet atrioventricular connection –– LA89.1 Tricuspid atresia –– LA89.2 Mitral atresia –– LA89.3 Hypoplastic left heart syndrome –– LA89.Y Other specified functionally univentricular heart –– LA89.Z Functionally univentricular heart, unspecified – LA8A Congenital anomaly of a ventriculo-arterial valve or adjacent regions –– LA8A.0 Congenital anomaly of pulmonary valve –– LA8A.1 Congenital pulmonary atresia –– LA8A.2 Congenital anomaly of aortic valve –– LA8A.3 Congenital supravalvar aortic stenosis –– LA8A.4 Aneurysm of aortic sinus of Valsalva –– LA8A.5 Congenital subaortic stenosis –– LA8A.6 Congenital subpulmonary stenosis –– LA8A.Y Other specified congenital anomaly of a ventriculo-arterial valve or adjacent regions –– LA8A.Z Congenital anomaly of a ventriculo-arterial valve or adjacent regions, unspecified ––– LA8A.00 Congenital pulmonary valvar stenosis ––– LA8A.01 Congenital pulmonary regurgitation ––– LA8A.0Y Other specified congenital anomaly of pulmonary valve ––– LA8A.0Z Congenital anomaly of pulmonary valve, unspecified ––– LA8A.10 Pulmonary atresia with intact ventricular septum ––– LA8A.1Y Other specified congenital pulmonary atresia ––– LA8A.1Z Congenital pulmonary atresia, unspecified ––– LA8A.20 Congenital aortic valvar stenosis ––– LA8A.21 Congenital aortic regurgitation ––– LA8A.22 Bicuspid aortic valve ––– LA8A.23 Aortic valvar atresia ––– LA8A.24 Unicuspid aortic valve ––– LA8A.2Y Other specified congenital anomaly of aortic valve ––– LA8A.2Z Congenital anomaly of aortic valve, unspecified – LA8B Congenital anomaly of great arteries including arterial duct –– LA8B.0 Congenital aortopulmonary window –– LA8B.1 Congenital anomaly of pulmonary arterial tree –– LA8B.2 Congenital anomaly of aorta or its branches –– LA8B.3 Tracheo-oesophageal compressive syndrome –– LA8B.4 Patent arterial duct –– LA8B.Y Other specified congenital anomaly of great arteries including arterial duct –– LA8B.Z Congenital anomaly of great arteries including arterial duct, unspecified ––– LA8B.21 Coarctation of aorta ––– LA8B.22 Interrupted aortic arch ––– LA8B.23 Congenital anomaly of descending thoracic or abdominal aorta ––– LA8B.24 Congenital anomaly of aortic arch branch ––– LA8B.2Y Other specified congenital anomaly of aorta or its branches ––– LA8B.2Z Congenital anomaly of aorta or its branches, unspecified – LA8C Congenital anomaly of coronary artery –– LA8C.0 Anomalous origin of coronary artery from pulmonary arterial tree –– LA8C.1 Anomalous aortic origin or course of coronary artery –– LA8C.2 Congenital coronary arterial fistula –– LA8C.Y Other specified congenital anomaly of coronary artery –– LA8C.Z Congenital anomaly of coronary artery, unspecified – LA8D Congenital pericardial anomaly – LA8E Congenital anomaly of atrial septum –– LA8E.0 Patent oval foramen –– LA8E.1 Atrial septal defect within oval fossa –– LA8E.2 Sinus venosus defect –– LA8E.3 Interatrial communication through coronary sinus orifice –– LA8E.Y Other specified congenital anomaly of atrial septum –– LA8E.Z Congenital anomaly of atrial septum, unspecified – LA8F Congenital anomaly of right atrium – LA8G Congenital anomaly of left atrium –– LA8G.0 Divided left atrium –– LA8G.Y Other specified congenital anomaly of left atrium –– LA8G.Z Congenital anomaly of left atrium, unspecified – 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 – LA90.0 Capillary malformations – LA90.1 Lymphatic malformations – LA90.2 Peripheral venous malformations – LA90.3 Peripheral arteriovenous malformations – LA90.4 Peripheral arterial malformations – LA90.5 Pulmonary arteriovenous fistula – LA90.Y Other specified structural developmental anomalies of the peripheral vascular system – LA90.Z Structural developmental anomalies of the peripheral vascular system, unspecified –– LA90.00 Hereditary haemorrhagic telangiectasia –– LA90.0Y Other specified capillary malformations –– LA90.0Z Capillary malformations, unspecified –– LA90.10 Macrocystic lymphatic malformation –– LA90.11 Microcystic lymphatic malformation –– LA90.12 Lymphatic malformations of certain specified sites –– LA90.13 Cystic hygroma in fetus –– LA90.1Y Other specified lymphatic malformations –– LA90.1Z Lymphatic malformations, unspecified –– LA90.20 Vein of Galen aneurysm –– LA90.21 Congenital portosystemic shunt –– LA90.2Y Other specified peripheral venous malformations –– LA90.2Z Peripheral venous malformations, unspecified –– LA90.30 Portal vein-hepatic artery fistula –– LA90.31 Arteriovenous malformation of precerebral vessels –– LA90.32 Uterine arteriovenous malformations –– LA90.3Y Other specified peripheral arteriovenous malformations –– LA90.3Z Peripheral arteriovenous malformations, unspecified –– LA90.40 Congenital renal artery stenosis –– LA90.41 Congenital precerebral nonruptured aneurysm –– LA90.42 Congenital cerebral nonruptured aneurysm –– LA90.4Y Other specified peripheral arterial malformations –– LA90.4Z Peripheral arterial malformations, unspecified LA9Y Other specified structural developmental anomalies of the circulatory system LA9Z Structural developmental anomalies of the circulatory system, unspecified LB00 Structural developmental anomalies of diaphragm – LB00.0 Congenital diaphragmatic hernia – LB00.1 Absence of diaphragm – LB00.Y Other specified structural developmental anomalies of diaphragm – LB00.Z Structural developmental anomalies of diaphragm, unspecified LB01 Omphalocele LB02 Gastroschisis LB03 Structural developmental anomalies of umbilical cord – LB03.0 Allantoic duct remnants or cysts – LB03.1 Single umbilical cord artery – LB03.Y Other specified structural developmental anomalies of umbilical cord – LB03.Z Structural developmental anomalies of umbilical cord, unspecified 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 LB10 Structural developmental anomalies of salivary glands or ducts LB11 Congenital diverticulum of pharynx LB12 Structural developmental anomalies of oesophagus – LB12.0 Congenital oesophageal web or ring – LB12.1 Atresia of oesophagus – LB12.2 Oesophageal fistula without atresia – LB12.3 Congenital stenosis or stricture of oesophagus – LB12.4 Congenital diverticulum of oesophagus – LB12.5 Congenital dilatation of oesophagus – LB12.Y Other specified structural developmental anomalies of oesophagus – LB12.Z Structural developmental anomalies of oesophagus, unspecified –– LB12.10 Atresia of oesophagus with oesophagobronchial fistula –– LB12.1Y Other specified atresia of oesophagus –– LB12.1Z Atresia of oesophagus, unspecified LB13 Structural developmental anomalies of stomach – LB13.0 Congenital hypertrophic pyloric stenosis – LB13.1 Congenital hiatus hernia – LB13.2 Congenital antral web – LB13.Y Other specified structural developmental anomalies of stomach – LB13.Z Structural developmental anomalies of stomach, unspecified LB14 Structural developmental anomalies of duodenum LB15 Structural developmental anomalies of small intestine – LB15.0 Meckel diverticulum – LB15.1 Atresia of small intestine – LB15.2 Congenital short bowel – LB15.3 Congenital diverticulitis of small intestine – LB15.4 Congenital diverticulosis of small intestine – LB15.5 Congenital diverticulum of small intestine – LB15.Y Other specified structural developmental anomalies of small intestine – LB15.Z Structural developmental anomalies of small intestine, unspecified LB16 Structural developmental anomalies of large intestine – LB16.0 Congenital absence, atresia or stenosis of large intestine – LB16.1 Hirschsprung disease – LB16.2 Immature ganglionosis of large intestine – LB16.3 Congenital hypoganglionosis of large intestine – LB16.Y Other specified structural developmental anomalies of large intestine – LB16.Z Structural developmental anomalies of large intestine, unspecified LB17 Structural developmental anomalies of anal canal – LB17.0 Anorectal malformations – LB17.1 Ectopic anus – LB17.2 Persistent cloaca – LB17.3 Cloacal exstrophy – LB17.4 Perineal groove – LB17.Y Other specified structural developmental anomalies of anal canal – LB17.Z Structural developmental anomalies of anal canal, unspecified LB18 Congenital anomalies of intestinal fixation LB1Y Other specified structural developmental anomalies of the digestive tract LB1Z Structural developmental anomalies of the digestive tract, unspecified LB20 Structural developmental anomalies of gallbladder, bile ducts or liver – LB20.0 Structural developmental anomalies of liver – LB20.1 Structural developmental anomalies of gallbladder – LB20.2 Structural developmental anomalies of bile ducts – LB20.Y Other specified structural developmental anomalies of gallbladder, bile ducts or liver – LB20.Z Structural developmental anomalies of gallbladder, bile ducts or liver, unspecified –– LB20.00 Fibropolycystic liver disease –– LB20.0Y Other specified structural developmental anomalies of liver –– LB20.0Z Structural developmental anomalies of liver, unspecified –– LB20.10 Agenesis, aplasia or hypoplasia of gallbladder –– LB20.1Y Other specified structural developmental anomalies of gallbladder –– LB20.1Z Structural developmental anomalies of gallbladder, unspecified –– LB20.20 Choledochal cyst –– LB20.21 Biliary atresia –– LB20.22 Congenital stenosis or stricture of bile ducts –– LB20.23 Structural developmental anomalies of cystic duct –– LB20.24 Accessory bile duct –– LB20.2Y Other specified structural developmental anomalies of bile ducts –– LB20.2Z Structural developmental anomalies of bile ducts, unspecified LB21 Structural developmental anomalies of pancreas – LB21.0 Annular pancreas – LB21.1 Pancreas divisum – LB21.2 Accessory pancreas – LB21.3 Agenesis-aplasia of pancreas – LB21.4 Partial agenesis of pancreas – LB21.5 Hypoplasia of pancreas – LB21.Y Other specified structural developmental anomalies of pancreas – LB21.Z Structural developmental anomalies of pancreas, unspecified LB22 Structural developmental anomalies of spleen – LB22.0 Congenital asplenia – LB22.1 Polysplenia – LB22.2 Ectopic spleen – LB22.Y Other specified structural developmental anomalies of spleen – LB22.Z Structural developmental anomalies of spleen, unspecified 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 LB30 Structural developmental anomalies of kidneys – LB30.0 Renal agenesis or other reduction defects of kidney – LB30.1 Renal dysplasia – LB30.2 Congenital single renal cyst – LB30.3 Renal tubular dysgenesis – LB30.4 Oligomeganephronia – LB30.5 Accessory kidney – LB30.6 Fusion anomaly of kidneys – LB30.7 Ectopic or pelvic kidney – LB30.8 Medullary sponge kidney – LB30.9 Multicystic renal dysplasia – LB30.Y Other specified structural developmental anomalies of kidneys – LB30.Z Structural developmental anomalies of kidneys, unspecified –– LB30.00 Renal agenesis –– LB30.0Y Other specified renal agenesis or other reduction defects of kidney –– LB30.0Z Renal agenesis or other reduction defects of kidney, unspecified –– LB30.60 Lobulated kidney –– LB30.61 Fused pelvic kidney –– LB30.62 Horseshoe kidney –– LB30.6Y Other specified fusion anomaly of kidneys –– LB30.6Z Fusion anomaly of kidneys, unspecified LB31 Structural developmental anomalies of urinary tract – LB31.0 Congenital hydronephrosis – LB31.1 Congenital primary megaureter – LB31.2 Fetal lower urinary tract obstruction – LB31.3 Exstrophy of urinary bladder – LB31.4 Congenital diverticulum of urinary bladder – LB31.5 Duplication of urethra – LB31.6 Congenital megalourethra – LB31.7 Megacystis-megaureter – LB31.8 Atresia or stenosis of ureter – LB31.9 Agenesis of ureter – LB31.A Duplication of ureter – LB31.B Malposition of ureter – LB31.C Congenital absence of bladder or urethra – LB31.D Congenital vesico-uretero-renal reflux – LB31.Y Other specified structural developmental anomalies of urinary tract – LB31.Z Structural developmental anomalies of urinary tract, unspecified LB3Y Other specified structural developmental anomalies of the urinary system LB3Z Structural developmental anomalies of the urinary system, unspecified LB40 Structural developmental anomalies of vulva – LB40.0 Absence of vulva – LB40.1 Embryonic cyst of vulva – LB40.2 Fusion of labia – LB40.Y Other specified structural developmental anomalies of vulva – LB40.Z Structural developmental anomalies of vulva, unspecified LB41 Structural developmental anomalies of clitoris – LB41.0 Agenesis of clitoris – LB41.1 Duplication of clitoris – LB41.2 Clitoromegaly – LB41.Y Other specified structural developmental anomalies of clitoris – LB41.Z Structural developmental anomalies of clitoris, unspecified LB42 Structural developmental anomalies of vagina – LB42.0 Absence of vagina – LB42.1 Septate vagina – LB42.2 Congenital rectovaginal fistula – LB42.3 Tight hymenal ring – LB42.4 Imperforate hymen – LB42.5 Stricture or atresia of vagina – LB42.Y Other specified structural developmental anomalies of vagina – LB42.Z Structural developmental anomalies of vagina, unspecified LB43 Structural developmental anomalies of cervix uteri – LB43.0 Embryonic cyst of cervix – LB43.1 Agenesis or aplasia of cervix – LB43.Y Other specified structural developmental anomalies of cervix uteri – LB43.Z Structural developmental anomalies of cervix uteri, unspecified LB44 Structural developmental anomalies of uterus, except cervix – LB44.0 Agenesis or aplasia of uterine body – LB44.1 Hypoplasia of uterus – LB44.2 Unicornuate uterus – LB44.3 Bicornuate uterus – LB44.4 Septate uterus – LB44.5 Congenital fistulae between uterus and digestive and urinary tracts – LB44.6 Uterovaginal malformation due to diethylstilbestrol syndrome – LB44.Y Other specified structural developmental anomalies of uterus, except cervix – LB44.Z Structural developmental anomalies of uterus, except cervix, unspecified LB45 Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments – LB45.0 Congenital absence of ovary – LB45.1 46,XX gonadal dysgenesis – LB45.2 Developmental ovarian cyst – LB45.3 Congenital torsion of ovary – LB45.4 Accessory ovary – LB45.5 Congenital absence of fallopian tube – LB45.6 Atresia of fallopian tube – LB45.7 Accessory fallopian tube – LB45.8 Embryonic cyst of fallopian tube – LB45.9 Embryonic cyst of broad ligament – LB45.Y Other specified structural developmental anomalies of ovaries, fallopian tubes or broad ligaments – LB45.Z Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments, unspecified LB4Y Other specified structural developmental anomalies of the female genital system LB4Z Structural developmental anomalies of the female genital system, unspecified LB50 Micropenis or penis agenesis LB51 Anorchia or microorchidia LB52 Cryptorchidism – LB52.0 Ectopic testis – LB52.1 Undescended testicle, unilateral – LB52.2 Undescended testicle, bilateral – LB52.Y Other specified cryptorchidism – LB52.Z Cryptorchidism, unspecified LB53 Hypospadias – LB53.0 Hypospadias, balanic – LB53.1 Hypospadias, penile – LB53.2 Hypospadias, penoscrotal – LB53.3 Hypospadias, scrotal – LB53.4 Hypospadias, perineal – LB53.Y Other specified hypospadias – LB53.Z Hypospadias, unspecified –– LB53.00 Hypospadias, coronal –– LB53.01 Hypospadias, glandular –– LB53.0Y Other specified hypospadias, balanic –– LB53.0Z Hypospadias, balanic, unspecified LB54 Congenital chordee LB55 Epispadias LB56 Bifid scrotum LB57 Agenesis 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 LB60 Breast aplasia LB61 Absent nipple LB62 Supernumerary breasts LB63 Accessory nipple LB6Y Other specified structural developmental anomalies of the breast LB6Z Structural developmental anomalies of the breast, unspecified LB70 Structural developmental anomalies of cranium – LB70.0 Craniosynostosis – LB70.1 Wormian bones – LB70.2 J-shaped sella turcica – LB70.3 Macrocephaly – LB70.Y Other specified structural developmental anomalies of cranium – LB70.Z Structural developmental anomalies of cranium, unspecified –– LB70.00 Plagiocephaly –– LB70.0Y Other specified craniosynostosis –– LB70.0Z Craniosynostosis, unspecified LB71 Structural developmental anomalies of facial bones – LB71.0 Hypotelorism – LB71.1 Hypertelorism – LB71.Y Other specified structural developmental anomalies of facial bones – LB71.Z Structural developmental anomalies of facial bones, unspecified LB72 Structural developmental anomalies of shoulder girdle – LB72.0 Cervical rib – LB72.1 Sprengel deformity – LB72.2 Deformation of scapula – LB72.Y Other specified structural developmental anomalies of shoulder girdle – LB72.Z Structural developmental anomalies of shoulder girdle, unspecified LB73 Structural developmental anomalies of spine or bony thorax – LB73.0 Occult spinal dysraphism – LB73.1 Structural developmental anomalies of chest wall – LB73.2 Structural developmental anomalies of spine – LB73.Y Other specified structural developmental anomalies of spine or bony thorax – LB73.Z Structural developmental anomalies of spine or bony thorax, unspecified –– LB73.10 Poland syndrome –– LB73.11 Bifid rib –– LB73.12 Accessory rib –– LB73.13 Structural developmental anomalies of sternum –– LB73.1Y Other specified structural developmental anomalies of chest wall –– LB73.1Z Structural developmental anomalies of chest wall, unspecified –– LB73.20 Klippel-Feil anomaly –– LB73.21 Occipitalisation of atlas –– LB73.22 Atlanto-axial instability or subluxation –– LB73.23 Aplasia or hypoplasia of the odontoid process of axis –– LB73.24 Segmentation anomalies of vertebrae –– LB73.25 Congenital scoliosis due to congenital bony malformation –– LB73.26 Sacralisation of the last lumbar vertebra –– LB73.27 Lumbarisation of the first sacral vertebra –– LB73.28 Sacrum agenesis or hypoplasia –– LB73.29 Caudal appendage –– LB73.2A Congenital spondylolisthesis –– LB73.2Y Other specified structural developmental anomalies of spine –– LB73.2Z Structural developmental anomalies of spine, unspecified LB74 Structural developmental anomalies of pelvic girdle – LB74.0 Developmental dysplasia of hip – LB74.1 Congenital subluxation of hip – LB74.2 Unstable hip – LB74.3 Congenital coxa vara – LB74.4 Congenital coxa valga – LB74.5 Wide symphysis pubis – LB74.Y Other specified structural developmental anomalies of pelvic girdle – LB74.Z Structural developmental anomalies of pelvic girdle, unspecified LB75 Brachydactyly – LB75.0 Brachydactyly of fingers – LB75.1 Brachydactyly of toes – LB75.2 Symbrachydactyly of hands or feet – LB75.Y Other specified brachydactyly – LB75.Z Brachydactyly, unspecified LB76 Triphalangeal thumb LB77 Hyperphalangy LB78 Polydactyly – LB78.0 Polydactyly of the thumb – LB78.1 Polysyndactyly – LB78.2 Postaxial polydactyly of fingers – LB78.3 Polydactyly of toes – LB78.Y Other specified polydactyly – LB78.Z Polydactyly, unspecified LB79 Syndactyly – LB79.0 Fused fingers – LB79.1 Webbed fingers – LB79.2 Fused toes – LB79.3 Webbed toes – LB79.Y Other specified syndactyly – LB79.Z Syndactyly, unspecified – LB80 Congenital deformities of fingers –– LB80.0 Clinodactyly of fingers –– LB80.2 Radial deviation of fingers –– LB80.Y Other specified congenital deformities of fingers –– LB80.Z Congenital deformities of fingers, unspecified – LB81 Congenital deformities of toes –– LB81.0 Clinodactyly of toes –– LB81.Y Other specified congenital deformities of toes –– LB81.Z Congenital deformities of toes, unspecified LB90 Joint formation defects – LB90.0 Humero-radio-ulnar synostosis – LB90.1 Humero-radial synostosis – LB90.2 Humero-ulnar synostosis – LB90.3 Radio-ulnar synostosis – LB90.4 Madelung deformity – LB90.5 Congenital digital clubbing – LB90.6 Tibio-fibular synostosis – LB90.7 Cubitus valgus – LB90.8 Cubitus varus – LB90.Y Other specified joint formation defects – LB90.Z Joint formation defects, unspecified LB91 Congenital shoulder dislocation LB92 Congenital elbow dislocation LB93 Congenital knee dislocation – LB93.0 Congenital genu recurvatum – LB93.1 Congenital genu flexum – LB93.Y Other specified congenital knee dislocation – LB93.Z Congenital knee dislocation, unspecified LB94 Congenital patella dislocation LB95 Patella aplasia or hypoplasia LB96 Congenital bowing of long bones – LB96.0 Congenital bowing of femur – LB96.1 Congenital bowing of tibia – LB96.Y Other specified congenital bowing of long bones – LB96.Z Congenital bowing of long bones, unspecified LB97 Limb overgrowth – LB97.0 Macrodactyly of fingers – LB97.1 Macrodactyly of toes – LB97.2 Upper limb hypertrophy – LB97.3 Lower limb hypertrophy – LB97.Y Other specified limb overgrowth – LB97.Z Limb overgrowth, unspecified LB98 Congenital deformities of feet – LB98.0 Congenital varus deformities of feet – LB98.1 Congenital pes planus – LB98.2 Congenital valgus deformities of feet – LB98.3 Congenital pes cavus – LB98.4 Congenital vertical talus – LB98.5 Congenital hammer toe – LB98.Y Other specified congenital deformities of feet – LB98.Z Congenital deformities of feet, unspecified –– LB98.00 Talipes equinovarus –– LB98.01 Talipes calcaneovarus –– LB98.02 Metatarsus varus –– LB98.0Y Other specified congenital varus deformities of feet –– LB98.0Z Congenital varus deformities of feet, unspecified –– LB98.20 Congenital hallux valgus –– LB98.21 Metatarsus valgus –– LB98.22 Talipes calcaneovalgus –– LB98.2Y Other specified congenital valgus deformities of feet –– LB98.2Z Congenital valgus deformities of feet, unspecified LB99 Reduction defects of upper limb – LB99.0 Amelia of upper limb – LB99.1 Humeral agenesis or hypoplasia – LB99.2 Radial hemimelia – LB99.3 Ulnar hemimelia – LB99.4 Congenital absence of upper arm or forearm with hand present – LB99.5 Congenital absence of both forearm and hand – LB99.6 Acheiria – LB99.7 Adactyly of hands – LB99.8 Split hand – LB99.Y Other specified reduction defects of upper limb – LB99.Z Reduction defects of upper limb, unspecified LB9A Reduction defects of lower limb – LB9A.0 Amelia of lower limb – LB9A.1 Tibial hemimelia – LB9A.2 Fibular hemimelia – LB9A.3 Congenital absence of thigh or lower leg with foot present – LB9A.4 Apodia – LB9A.5 Adactyly of feet – LB9A.6 Split foot – LB9A.7 Congenital absence of both lower leg and foot – LB9A.8 Femoral agenesis or hypoplasia – LB9A.Y Other specified reduction defects of lower limb – LB9A.Z Reduction defects of lower limb, unspecified LB9B Reduction defects of upper and lower limbs LB9Y Other specified structural developmental anomalies of the skeleton LB9Z Structural developmental anomalies of the skeleton, unspecified – LC00 Keratinocytic epidermal hamartoma –– LC00.0 Epidermal naevus –– LC00.Y Other specified keratinocytic epidermal hamartoma –– LC00.Z Keratinocytic epidermal hamartoma, unspecified – LC01 Pilosebaceous hamartoma – LC02 Complex epidermal hamartoma – LC0Y Other specified developmental hamartomata of the epidermis and epidermal appendages – LC10 Dermal melanocytosis – LC1Y Other specified developmental anomalies of skin pigmentation – LC20 Connective tissue hamartoma – LC2Y Other specified hamartomata derived from dermal connective tissue – LC30 Developmental defects of hair or hair growth – LC31 Developmental defects of the nail apparatus LC40 Dermoid cyst – LC50 Developmental capillary vascular malformations of the skin –– LC50.0 Salmon patch –– LC50.1 Port-wine stain –– LC50.Y Other specified cutaneous capillary vascular malformation – 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 – LC60 Aplasia cutis congenita LC7Y Other specified structural developmental anomalies of the skin LC7Z Structural developmental anomalies of the skin, unspecified LC80 Congenital adrenal hypoplasia 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 LD20 Syndromes with central nervous system anomalies as a major feature LD20.0 Syndromes with cerebellar anomalies as a major feature LD20.1 Syndromes with lissencephaly as a major feature LD20.2 Syndromes with microcephaly as a major feature LD20.3 Syndromes with holoprosencephaly as a major feature LD20.4 Syndromes with brain calcifications as a major feature LD20.Y Other specified syndromes with central nervous system anomalies as a major feature LD20.Z Syndromes with central nervous system anomalies as a major feature, unspecified – LD20.00 Joubert syndrome – LD20.01 Pontocerebellar hypoplasia – LD20.0Y Other specified syndromes with cerebellar anomalies as a major feature – LD20.0Z Syndromes with cerebellar anomalies as a major feature, unspecified LD21 Syndromes with eye anomalies as a major feature LD21.0 Syndromes with microphthalmia as a major feature LD21.Y Other specified syndromes with eye anomalies as a major feature LD21.Z Syndromes with eye anomalies as a major feature, unspecified LD22 Syndromes with dental anomalies as a major feature LD23 Syndromes with vascular anomalies as a major feature LD24 Syndromes with skeletal anomalies as a major feature LD24.0 Syndromes with micromelia LD24.1 Bone diseases with increased bone density LD24.2 Bone diseases with disorganised development of skeletal components LD24.3 Spondyloepiphyseal or spondyloepimetaphyseal dysplasias LD24.4 Spondylometaphyseal dysplasias LD24.5 Spondylodysplastic dysplasias LD24.6 Multiple epiphyseal dysplasia or pseudoachondroplasia LD24.7 Multiple metaphyseal dysplasias LD24.8 Acromelic dysplasias LD24.9 Acromesomelic dysplasias LD24.A Mesomelic or rhizomesomelic dysplasias LD24.B Short rib syndromes LD24.C Bent bone dysplasias LD24.D Slender bone dysplasias LD24.E Bone dysplasias with multiple joint dislocations LD24.F Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments LD24.G Syndromic craniosynostoses LD24.H Dysostoses with predominant vertebral and costal involvement LD24.J Patellar dysostoses LD24.K Genetic bone diseases with decreased bone density LD24.Y Other specified syndromes with skeletal anomalies as a major feature LD24.Z Syndromes with skeletal anomalies as a major feature, unspecified – LD24.00 Achondroplasia – LD24.01 Hypochondroplasia – LD24.02 Thanatophoric dysplasia – LD24.03 Diastrophic dysplasia – LD24.04 Chondrodysplasia punctata – LD24.0Y Other specified syndromes with micromelia – LD24.0Z Syndromes with micromelia, unspecified – LD24.10 Osteopetrosis – LD24.11 Osteopoikilosis – LD24.1Y Other specified bone diseases with increased bone density – LD24.1Z Bone diseases with increased bone density, unspecified – LD24.20 Multiple osteochondromas – LD24.21 Exostoses with anetodermia and brachydactyly type E – LD24.22 Cherubism – LD24.23 Yunis-Varon disease – LD24.2Y Other specified bone diseases with disorganised development of skeletal components – LD24.2Z Bone diseases with disorganised development of skeletal components, unspecified – LD24.50 Achondrogenesis – LD24.51 Hypochondrogenesis – LD24.5Y Other specified spondylodysplastic dysplasias – LD24.5Z Spondylodysplastic dysplasias, unspecified – LD24.60 Pseudoachondroplasia – LD24.61 Multiple epiphyseal dysplasias – LD24.6Y Other specified multiple epiphyseal dysplasia or pseudoachondroplasia – LD24.6Z Multiple epiphyseal dysplasia or pseudoachondroplasia, unspecified – LD24.80 Langer-Giedion syndrome – LD24.8Y Other specified acromelic dysplasias – LD24.8Z Acromelic dysplasias, unspecified – LD24.B0 Short rib-polydactyly syndrome – LD24.B1 Asphyxiating thoracic dystrophy – LD24.BY Other specified short rib syndromes – LD24.BZ Short rib syndromes, unspecified – LD24.G0 Pfeiffer syndrome – LD24.G1 Crouzon disease – LD24.G2 Apert syndrome – LD24.GY Other specified syndromic craniosynostoses – LD24.GZ Syndromic craniosynostoses, unspecified – LD24.J0 Nail-patella syndrome – LD24.JY Other specified patellar dysostoses – LD24.JZ Patellar dysostoses, unspecified – LD24.K0 Osteogenesis imperfecta – LD24.KY Other specified genetic bone diseases with decreased bone density – LD24.KZ Genetic bone diseases with decreased bone density, unspecified LD25 Syndromes with face or limb anomalies as a major feature LD25.0 Oromandibular-limb anomaly syndrome LD25.1 Fronto-otopalatodigital syndromes LD25.2 Acrofacial dysostoses LD25.3 Craniofacial dysostoses LD25.Y Other specified syndromes with face or limb anomalies as a major feature LD25.Z Syndromes with face or limb anomalies as a major feature, unspecified – LD25.00 Oral-facial-digital syndrome – LD25.0Y Other specified oromandibular-limb anomaly syndrome – LD25.0Z Oromandibular-limb anomaly syndrome, unspecified LD26 Syndromes with limb anomalies as a major feature LD26.0 Combined reduction defects of upper and lower limbs LD26.1 Complex brachydactylies LD26.2 Syndromes with limb duplication, polydactyly, syndactyly or triphalangism LD26.3 Syndromes with synostoses of limbs LD26.4 Arthrogryposis syndromes LD26.5 Constriction rings LD26.6 Congenital vascular bone syndromes LD26.Y Other specified syndromes with limb anomalies as a major feature LD26.Z Syndromes with limb anomalies as a major feature, unspecified – LD26.40 Multiple pterygium syndrome – LD26.41 Arthrogryposis multiplex congenita – LD26.4Y Other specified arthrogryposis syndromes – LD26.4Z Arthrogryposis syndromes, unspecified – LD26.60 Angio-osteohypertrophic syndrome – LD26.6Y Other specified congenital vascular bone syndromes – LD26.6Z Congenital vascular bone syndromes, unspecified LD27 Syndromes with skin or mucosal anomalies as a major feature LD27.0 Ectodermal dysplasia syndromes LD27.1 Xeroderma pigmentosum LD27.2 Syndromic ichthyosis LD27.3 Genetic syndromes with hypertrichosis LD27.4 Genetic syndromes affecting nails LD27.5 Genetic hamartoneoplastic syndromes affecting the skin LD27.6 Genetic lipodystrophy LD27.Y Other specified syndromes with skin or mucosal anomalies as a major feature LD27.Z Syndromes with skin or mucosal anomalies as a major feature, unspecified – LD27.00 Incontinentia pigmenti – LD27.01 Cronkhite-Canada syndrome – LD27.02 Hypohidrotic ectodermal dysplasia – LD27.03 Hidrotic ectodermal dysplasia, Clouston type – LD27.0Y Other specified ectodermal dysplasia syndromes – LD27.60 Congenital generalised lipodystrophy – LD27.6Z Genetic lipodystrophy, unspecified LD28 Syndromes with connective tissue involvement as a major feature LD28.0 Marfan syndrome or Marfan-related disorders LD28.1 Ehlers-Danlos syndrome LD28.2 Genetically-determined cutis laxa LD28.Y Other specified syndromes with connective tissue involvement as a major feature LD28.Z Syndromes with connective tissue involvement as a major feature, unspecified – LD28.00 Congenital contractural arachnodactyly – LD28.01 Marfan syndrome – LD28.0Y Other specified Marfan syndrome or Marfan-related disorders – LD28.0Z Marfan syndrome or Marfan-related disorders, unspecified – LD28.10 Ehlers-Danlos syndrome, classical type – LD28.1Y Other specified types of Ehlers-Danlos syndrome LD29 Syndromes with obesity as a major feature LD2A Malformative disorders of sex development LD2A.0 Ovotesticular disorder of sex development LD2A.1 46,XY gonadal dysgenesis LD2A.2 Testicular agenesis LD2A.3 46,XY disorder of sex development due to a defect in testosterone metabolism LD2A.4 46,XY disorder of sex development due to androgen resistance LD2A.Y Other specified malformative disorders of sex development LD2A.Z Malformative disorders of sex development, unspecified LD2B Syndromes with premature ageing appearance as a major feature LD2C Overgrowth syndromes LD2D Phakomatoses or hamartoneoplastic syndromes LD2D.0 Peutz-Jeghers syndrome LD2D.1 Neurofibromatoses LD2D.2 Tuberous sclerosis LD2D.3 Gardner syndrome LD2D.4 Gorlin syndrome LD2D.Y Other specified phakomatoses or hamartoneoplastic syndromes LD2D.Z Phakomatoses or hamartoneoplastic syndromes, unspecified – LD2D.10 Neurofibromatosis type 1 – LD2D.11 Neurofibromatosis type 2 – LD2D.12 Neurofibromatosis type 3 – LD2D.1Y Other specified neurofibromatoses – LD2D.1Z Neurofibromatosis, unspecified LD2E Syndromes with structural anomalies due to inborn errors of metabolism LD2F Syndromes with multiple structural anomalies, without predominant body system involvement LD2F.0 Toxic or drug-related embryofetopathies LD2F.1 Syndromes with multiple structural anomalies, not of environmental origin LD2F.Y Other specified syndromes with multiple structural anomalies, without predominant body system involvement LD2F.Z Syndromes with multiple structural anomalies, without predominant body system involvement, unspecified – LD2F.00 Fetal alcohol syndrome – LD2F.01 Fetal hydantoin syndrome – LD2F.02 Embryofetopathy due to oral anticoagulant therapy – LD2F.03 Fetal Valproate Spectrum Disorder – LD2F.0Y Other specified toxic or drug-related embryofetopathies – LD2F.0Z Toxic or drug-related embryofetopathies, unspecified – LD2F.10 Prune belly syndrome – LD2F.11 VATER association – LD2F.12 Sirenomelia – LD2F.13 Meckel-Gruber syndrome – LD2F.14 MURCS association – LD2F.15 Noonan syndrome – LD2F.16 Otomandibular dysplasia – LD2F.1Y Other specified syndromes with multiple structural anomalies, not of environmental origin – LD2F.1Z Syndromes with multiple structural anomalies, not of environmental origin, unspecified LD2G Conjoined twins LD2H Syndromic genetic deafness LD2H.0 Fraser syndrome LD2H.1 Neuropathy with hearing impairment LD2H.2 Progressive deafness with stapes fixation LD2H.3 Waardenburg-Shah syndrome LD2H.4 Usher syndrome LD2H.Y Other specified syndromic genetic deafness LD2H.Z Syndromic genetic deafness, unspecified LD2Y Other specified multiple developmental anomalies or syndromes LD2Z Multiple developmental anomalies or syndromes, unspecified LD40 Complete trisomies of the autosomes LD40.0 Complete trisomy 21 LD40.1 Complete trisomy 13 LD40.2 Complete trisomy 18 LD40.Y Other specified complete trisomies of the autosomes LD40.Z Complete trisomies of the autosomes, unspecified LD41 Duplications of the autosomes LD41.0 Duplications of chromosome 1 LD41.1 Duplications of chromosome 2 LD41.2 Duplications of chromosome 3 LD41.3 Duplications of chromosome 4 LD41.4 Duplications of chromosome 5 LD41.5 Duplications of chromosome 6 LD41.6 Duplications of chromosome 7 LD41.7 Duplications of chromosome 8 LD41.8 Duplications of chromosome 9 LD41.9 Duplications of chromosome 10 LD41.A Duplications of chromosome 11 LD41.B Duplications of chromosome 12 LD41.C Duplications of chromosome 13 LD41.D Duplications of chromosome 14 LD41.E Duplications of chromosome 15 LD41.F Duplications of chromosome 16 LD41.G Duplications of chromosome 17 LD41.H Duplications of chromosome 18 LD41.J Duplications of chromosome 19 LD41.K Duplications of chromosome 20 LD41.L Duplications of chromosome 21 LD41.M Duplications of chromosome 22 LD41.N Extra ring or dicentric chromosomes LD41.P Duplications with other complex rearrangements LD41.Q Extra marker chromosomes LD41.Y Other specified duplications of the autosomes LD41.Z Duplications of the autosomes, unspecified – LD41.00 Duplications of the long arm of chromosome 1 – LD41.01 Duplications of the short arm of chromosome 1 – LD41.0Y Other specified duplications of chromosome 1 – LD41.0Z Duplications of chromosome 1, unspecified – LD41.10 Duplications of the long arm of chromosome 2 – LD41.11 Duplications of the short arm of chromosome 2 – LD41.1Y Other specified duplications of chromosome 2 – LD41.1Z Duplications of chromosome 2, unspecified – LD41.20 Duplications of the long arm of chromosome 3 – LD41.21 Duplications of the short arm of chromosome 3 – LD41.2Y Other specified duplications of chromosome 3 – LD41.2Z Duplications of chromosome 3, unspecified – LD41.30 Duplications of the long arm of chromosome 4 – LD41.31 Duplications of the short arm of chromosome 4 – LD41.3Y Other specified duplications of chromosome 4 – LD41.3Z Duplications of chromosome 4, unspecified – LD41.40 Duplications of the long arm of chromosome 5 – LD41.41 Duplications of the short arm of chromosome 5 – LD41.4Y Other specified duplications of chromosome 5 – LD41.4Z Duplications of chromosome 5, unspecified – LD41.50 Duplications of the long arm of chromosome 6 – LD41.51 Duplications of the short arm of chromosome 6 – LD41.5Y Other specified duplications of chromosome 6 – LD41.5Z Duplications of chromosome 6, unspecified – LD41.60 Duplications of the long arm of chromosome 7 – LD41.61 Duplications of the short arm of chromosome 7 – LD41.6Y Other specified duplications of chromosome 7 – LD41.6Z Duplications of chromosome 7, unspecified – LD41.70 Duplications of the long arm of chromosome 8 – LD41.71 Duplications of the short arm of chromosome 8 – LD41.7Y Other specified duplications of chromosome 8 – LD41.7Z Duplications of chromosome 8, unspecified – LD41.80 Duplications of the long arm of chromosome 9 – LD41.81 Duplications of the short arm of chromosome 9 – LD41.8Y Other specified duplications of chromosome 9 – LD41.8Z Duplications of chromosome 9, unspecified – LD41.90 Duplications of the long arm of chromosome 10 – LD41.91 Duplications of the short arm of chromosome 10 – LD41.9Y Other specified duplications of chromosome 10 – LD41.9Z Duplications of chromosome 10, unspecified – LD41.B0 Duplications of the long arm of chromosome 12 – LD41.B1 Duplications of the short arm of chromosome 12 – LD41.BY Other specified duplications of chromosome 12 – LD41.BZ Duplications of chromosome 12, unspecified – LD41.F0 Duplications of the long arm of chromosome 16 – LD41.F1 Duplications of the short arm of chromosome 16 – LD41.FY Other specified duplications of chromosome 16 – LD41.FZ Duplications of chromosome 16, unspecified – LD41.G0 Duplications of the long arm of chromosome 17 – LD41.G1 Duplications of the short arm of chromosome 17 – LD41.GY Other specified duplications of chromosome 17 – LD41.GZ Duplications of chromosome 17, unspecified – LD41.H0 Duplications of the long arm of chromosome 18 – LD41.H1 Duplications of the short arm of chromosome 18 – LD41.HY Other specified duplications of chromosome 18 – LD41.HZ Duplications of chromosome 18, unspecified – LD41.J0 Duplications of the long arm of chromosome 19 – LD41.J1 Duplications of the short arm of chromosome 19 – LD41.JY Other specified duplications of chromosome 19 – LD41.JZ Duplications of chromosome 19, unspecified – LD41.K0 Duplications of the long arm of chromosome 20 – LD41.K1 Duplications of the short arm of chromosome 20 – LD41.KY Other specified duplications of chromosome 20 – LD41.KZ Duplications of chromosome 20, unspecified LD42 Polyploidies LD42.0 Triploidy LD42.1 Tetraploidy LD42.Y Other specified polyploidies LD42.Z Polyploidies, unspecified LD43 Complete monosomies of the autosomes LD43.0 Complete monosomy of autosome LD43.1 Mosaic monosomy of autosome LD43.Y Other specified complete monosomies of the autosomes LD43.Z Complete monosomies of the autosomes, unspecified LD44 Deletions of the autosomes LD44.1 Deletions of chromosome 1 LD44.2 Deletions of chromosome 2 LD44.3 Deletions of chromosome 3 LD44.4 Deletions of chromosome 4 LD44.5 Deletions of chromosome 5 LD44.6 Deletions of chromosome 6 LD44.7 Deletions of chromosome 7 LD44.8 Deletions of chromosome 8 LD44.9 Deletions of chromosome 9 LD44.A Deletions of chromosome 10 LD44.B Deletions of chromosome 11 LD44.C Deletions of chromosome 12 LD44.D Deletions of chromosome 13 LD44.E Deletions of chromosome 14 LD44.F Deletions of chromosome 15 LD44.G Deletions of chromosome 16 LD44.H Deletions of chromosome 17 LD44.J Deletions of chromosome 18 LD44.K Deletions of chromosome 19 LD44.L Deletions of chromosome 20 LD44.M Deletions of chromosome 21 LD44.N Deletions of chromosome 22 LD44.P Deletions with other complex rearrangements LD44.Y Other specified deletions of the autosomes LD44.Z Deletions of the autosomes, unspecified – LD44.10 Deletions of the long arm of chromosome 1 – LD44.11 Deletions of the short arm of chromosome 1 – LD44.1Y Other specified deletions of chromosome 1 – LD44.1Z Deletions of chromosome 1, unspecified – LD44.20 Deletions of the long arm of chromosome 2 – LD44.21 Deletions of the short arm of chromosome 2 – LD44.2Y Other specified deletions of chromosome 2 – LD44.2Z Deletions of chromosome 2, unspecified – LD44.30 Deletions of the long arm of chromosome 3 – LD44.31 Deletions of the short arm of chromosome 3 – LD44.3Y Other specified deletions of chromosome 3 – LD44.3Z Deletions of chromosome 3, unspecified – LD44.40 Deletions of the long arm of chromosome 4 – LD44.41 Deletions of the short arm of chromosome 4 – LD44.4Y Other specified deletions of chromosome 4 – LD44.4Z Deletions of chromosome 4, unspecified – LD44.50 Deletions of the long arm of chromosome 5 – LD44.51 Deletions of the short arm of chromosome 5 – LD44.5Y Other specified deletions of chromosome 5 – LD44.5Z Deletions of chromosome 5, unspecified – LD44.60 Deletions of the long arm of chromosome 6 – LD44.61 Deletions of the short arm of chromosome 6 – LD44.6Y Other specified deletions of chromosome 6 – LD44.6Z Deletions of chromosome 6, unspecified – LD44.70 Deletions of the long arm of chromosome 7 – LD44.71 Deletions of the short arm of chromosome 7 – LD44.7Y Other specified deletions of chromosome 7 – LD44.7Z Deletions of chromosome 7, unspecified – LD44.80 Deletions of the long arm of chromosome 8 – LD44.81 Deletions of the short arm of chromosome 8 – LD44.8Y Other specified deletions of chromosome 8 – LD44.8Z Deletions of chromosome 8, unspecified – LD44.90 Deletions of the long arm of chromosome 9 – LD44.91 Deletions of the short arm of chromosome 9 – LD44.9Y Other specified deletions of chromosome 9 – LD44.9Z Deletions of chromosome 9, unspecified – LD44.A0 Deletions of the long arm of chromosome 10 – LD44.A1 Deletions of the short arm of chromosome 10 – LD44.AY Other specified deletions of chromosome 10 – LD44.AZ Deletions of chromosome 10, unspecified – LD44.B0 Deletions of the long arm of chromosome 11 – LD44.B1 Deletions of the short arm of chromosome 11 – LD44.BY Other specified deletions of chromosome 11 – LD44.BZ Deletions of chromosome 11, unspecified – LD44.C0 Deletions of the long arm of chromosome 12 – LD44.C1 Deletions of the short arm of chromosome 12 – LD44.CY Other specified deletions of chromosome 12 – LD44.CZ Deletions of chromosome 12, unspecified – LD44.G0 Deletions of the long arm of chromosome 16 – LD44.G1 Deletions of the short arm of chromosome 16 – LD44.GY Other specified deletions of chromosome 16 – LD44.GZ Deletions of chromosome 16, unspecified – LD44.H0 Deletions of the long arm of chromosome 17 – LD44.H1 Deletions of the short arm of chromosome 17 – LD44.HY Other specified deletions of chromosome 17 – LD44.HZ Deletions of chromosome 17, unspecified – LD44.J0 Deletions of the long arm of chromosome 18 – LD44.J1 Deletions of the short arm of chromosome 18 – LD44.JY Other specified deletions of chromosome 18 – LD44.JZ Deletions of chromosome 18, unspecified – LD44.K0 Deletions of the long arm of chromosome 19 – LD44.K1 Deletions of the short arm of chromosome 19 – LD44.KY Other specified deletions of chromosome 19 – LD44.KZ Deletions of chromosome 19, unspecified – LD44.L0 Deletions of the long arm of chromosome 20 – LD44.L1 Deletions of the short arm of chromosome 20 – LD44.LY Other specified deletions of chromosome 20 – LD44.LZ Deletions of chromosome 20, unspecified – LD44.N0 CATCH 22 phenotype – LD44.NY Other specified deletions of chromosome 22 – LD44.NZ Deletions of chromosome 22, unspecified LD45 Uniparental disomies LD45.0 Uniparental disomies of maternal origin LD45.1 Uniparental disomies of paternal origin LD45.Y Other specified uniparental disomies LD45.Z Uniparental disomies, unspecified LD46 Imprinting errors LD46.0 Maternal imprinting error LD46.1 Paternal imprinting error LD46.Y Other specified imprinting errors LD46.Z Imprinting errors, unspecified LD47 Balanced rearrangements or structural rearrangements LD47.0 Balanced translocation and insertion in normal individual LD47.1 Chromosome inversion in normal individual LD47.2 Balanced autosomal rearrangement in abnormal individual LD47.3 Balanced sex or autosomal rearrangement in abnormal individual LD47.4 Autosomal fragile site LD47.Y Other specified balanced rearrangements or structural rearrangements LD47.Z Balanced rearrangements or structural rearrangements, unspecified LD50 Number anomalies of chromosome X – LD50.0 Turner syndrome – LD50.1 Karyotype 47,XXX – LD50.2 Mosaicism, lines with various numbers of X chromosomes – LD50.3 Klinefelter syndrome – LD50.Y Other specified number anomalies of chromosome X – LD50.Z Number anomalies of chromosome X, unspecified –– LD50.00 Karyotype 45, X –– LD50.01 Karyotype 46, X iso Xq –– LD50.02 Karyotype 46, X with abnormal sex chromosome, except iso Xq –– LD50.03 Mosaicism, 45, X, 46, XX or XY –– LD50.04 Mosaicism, 45, X or other cell line with abnormal sex chromosome –– LD50.30 Klinefelter syndrome with karyotype 47,XXY, regular –– LD50.31 Klinefelter syndrome, male with more than two X chromosomes –– LD50.3Y Other specified Klinefelter syndrome –– LD50.3Z Klinefelter syndrome, unspecified LD51 Structural anomalies of chromosome X, excluding Turner syndrome LD52 Number anomalies of chromosome Y – LD52.0 Male with 46,XX karyotype – LD52.1 Male with double or multiple Y – LD52.Y Other specified number anomalies of chromosome Y – LD52.Z Number anomalies of chromosome Y, unspecified LD53 Structural anomalies of chromosome Y LD54 Male with sex chromosome mosaicism LD55 Fragile X chromosome LD56 Chimaera 46, XX, 46, XY – LD56.0 Androgenetic chimaera – LD56.1 Gynogenetic chimaera – LD56.Y Other specified chimaera 46, XX, 46, XY – LD56.Z Chimaera 46, XX, 46, XY, unspecified LD5Y Other specified sex chromosome anomalies LD5Z Sex chromosome anomalies, unspecified LD7Y Other specified chromosomal anomalies, excluding gene mutations LD7Z Chromosomal anomalies, excluding gene mutations, unspecified LD90 Conditions with disorders of intellectual development as a relevant clinical feature LD90.0 Angelman syndrome LD90.1 Early-onset parkinsonism - intellectual deficit LD90.2 Pelizaeus-Merzbacher-like disease LD90.3 Prader-Willi syndrome LD90.4 Rett syndrome LD90.Y Other specified conditions with disorders of intellectual development as a relevant clinical feature LD90.Z Conditions with disorders of intellectual development as a relevant clinical feature, unspecified LD9Y Other specified developmental anomalies LD9Z Developmental anomalies, unspecified
synonyms Chronic secondary musculoskeletal pain, unspecified Chronic secondary musculoskeletal pain
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