1. Certain infectious and parasitic diseases (A00-B99)
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2. Neoplasms (C00-D48)
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3. Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
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4. Endocrine, nutritional and metabolic diseases (E00-E90)
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5. Mental and behavioural disorders (F00-F99)
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6. Diseases of the nervous system (G00-G99)
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7. Diseases of the eye and adnexa (H00-H59)
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8. Diseases of the ear and mastoid process (H60-H95)
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9. Diseases of the circulatory system (I00-I99)
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10. Diseases of the respiratory system (J00-J99)
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11. Diseases of the digestive system (K00-K93)
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12. Diseases of the skin and subcutaneous tissue (L00-L99)
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13. Diseases of the musculoskeletal system and connective tissue (M00-M99)
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14. Diseases of the genitourinary system (N00-N99)
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15. Pregnancy, childbirth and the puerperium (O00-O99)
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16. Certain conditions originating in the perinatal period (P00-P96)
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17. Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
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Q00-Q07 Congenital malformations of the nervous system
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Q10-Q18 Congenital malformations of eye, ear, face and neck
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Q20-Q28 Congenital malformations of the circulatory system
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Q30-Q34 Congenital malformations of the respiratory system
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Q35-Q37 Cleft lip and cleft palate
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Q38-Q45 Other congenital malformations of the digestive system
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Q50-Q56 Congenital malformations of genital organs
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Q60-Q64 Congenital malformations of the urinary system
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Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
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Q80-Q89 Other congenital malformations
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Q80 Congenital ichthyosis
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Q81 Epidermolysis bullosa
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Q82 Other congenital malformations of skin
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Q84 Other congenital malformations of integument
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Q85 Phakomatoses, not elsewhere classified
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Q87 Other specified congenital malformation syndromes affecting multiple systems
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H00458 Craniosynostosis
H01753 Antley-Bixler syndrome
H01755 Apert syndrome
H01756 Pfeiffer syndrome
H01988 Jackson-Weiss syndrome
H01989 Beare-Stevenson syndrome
H01990 Muenke syndrome
H01991 Saethre-Chotzen syndrome
H01992 Craniofrontonasal syndrome
H00076 Cockayne syndrome
H00478 Prader-Willi syndrome (PWS)
H00403 Disorders of nucleotide excision repair
H00418 Bardet-Biedl syndrome (BBS)
H00454 Oral-facial-digital syndrome 1
H00442 Campomelic dysplasia (CD)
H00443 Osteoglophonic dysplasia (OD)
H00433 Holt-Oram syndrome
H00619 Kenny-Caffey syndrome
H00641 ADULT syndrome
H00847 Al-Awadi/Raas-Rothschild syndrome
H00611 IRF6-related disorders
H00449 Oculodentodigital dysplasia
H00453 Contiguous gene deletion syndrome involving EYA1
H00461 FLNB-related disorders
H00464 Nail-patella syndrome
H00484 Other brachydactylies
H00485 Robinow syndrome
H00492 Langer syndrome
H00493 Dyssegmental dysplasia, Silverman-Handmaker type
H00493 Simpson-Golabi-Behmel syndrome
H00496 Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD)
H00504 Rubinstein-Taybi syndrome
H00205 Peroxisome biogenesis disorder
H01342 Zellweger syndrome (ZS)
H00177 Adrenoleukodystrophy, neonatal (NALD)
H00204 Infantile Refsum disease (IRD)
H00509 3M syndrome
H00510 Feingold syndrome
H00161 Smith-Lemli-Opitz syndrome
H00516 Isolated orofacial clefts
H00519 Type XI collagenopathies
H00520 Stickler syndrome 1
H00522 Parastremmatic dysplasia
H00523 Noonan syndrome and related disorders
H01738 Noonan syndrome
H01745 Cardiofaciocutaneous syndrome
H01747 Costello syndrome
H00529 Cranioectodermal dysplasia
H00530 Joubert syndrome
H00539 PTEN hamartoma tumor syndrome (PHTS)
H00569 Aarskog-Scott syndrome
H00556 CHARGE syndrome
H00561 Smith-Magenis syndrome
H00571 Johanson-Blizzard syndrome
H00573 Townes-Brocks syndrome
H00581 Alport syndrome
H00607 Denys-Drash syndrome and WAGR syndrome
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action)
H00617 Desmosterolosis
H00622 Hypoparathyroidism-retardation-dysmorphism syndrome
H00631 Cornelia de Lange syndrome (CdLS)
H00639 Ectodermal dysplasia, ectrodactyly, and macular dystrophy (EEM syndrome)
H00640 Limb-mammary syndrome
H00643 Tooth and nail syndrome
H00673 Weill-Marchesani syndrome
H00665 Mandibuloacral dysplasia
H00669 Naxos disease
H00711 Russell-Silver syndrome
H00713 Beckwith-Wiedemann syndrome
H00718 Sotos syndrome
H01751 Weaver syndrome
H00653 Marfan syndrome
H00660 Congenital contractural arachnodactyly
H00687 Fraser syndrome
H00752 Ankyloblepharon-ctodermal defects-cleft lip/palate (AEC) syndrome and Rapp-Hodgkin syndrome
H00811 Distal arthrogryposis (DA)
H00757 Dyggve-Melchior-Clausen disease and Smith-McCort dysplasia
H00797 Martsolf syndrome
H00785 Hypotrichosis, congenital, with juvenile macular dystrophy
H00889 MED12-related disorders
H00894 FG syndrome (FGS)
H00868 Stapes ankylosis with broad thumb and toes
H00886 Donnai-Barrow syndrome
H00922 Schinzel-Giedion midface retraction syndrome
H00935 Cold-induced sweating syndrome (CISS) and Crisponi syndrome (CRISPS)
H00940 Cohen syndrome
H00943 TARP syndrome
H00946 Arts syndrome
H00965 RAPADILINO syndrome
H00997 CATSHL syndrome
H00986 Multiple pterygium syndrome
H00987 Fetal akinesia deformation sequence (FADS)
H00993 Microcephalic osteodysplastic primordial dwarfism, type I (MOPD I)
H00991 Microcephalic osteodysplastic primordial dwarfism, type II (MOPD II)
H00992 Seckel syndrome
H01008 C syndrome
H01195 VACTERL/VATER association
H01265 Hydrolethalus syndrome
H01271 Hypoparathyroidism with sensorineural deafness and renal dysplasia
H01281 Lathosterolosis
H01370 SHORT syndrome
H00727 Bosley-Salih-Alorainy syndrome and Athabascan brainstem dysgenesis syndrome
H00934 Caudal duplication anomaly
H00972 Endocrine-cerebro-osteodysplasia syndrome
H01035 Corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia
H01289 Mulibrey nanism
H01403 Coffin-Siris syndrome
H01428 Xeroderma pigmentosum (XP)
H01412 Perlman syndrome
H01413 Adams-Oliver syndrome (AOS)
H01486 Multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS)
H01487 CHIME syndrome
H01496 Spondyloocular syndrome (SOS)
H01497 Temtamy preaxial brachydactyly syndrome (TPBS)
H01568 3C syndrome
H01569 CHOPS syndrome
H01571 Singleton-Merten syndrome (SMS)
H01572 Cole-Carpenter syndrome
H01573 Zimmermann-Laband syndrome (ZLS)
H01752 ATR-X syndrome
H01776 Aicardi syndrome
H01788 Klippel-Trenaunay-Weber syndrome
H01793 Young-Simpson syndrome
H01794 Genitopatellar syndrome (GPS)
H01795 Blepharophimosis-mental retardation syndrome (BMRS)
H01796 Uncombable hair syndrome
H01797 Webb-Dattani syndrome
H01800 Verheij syndrome
H01814 Stromme syndrome
H01816 Frank-ter Haar syndrome (FTHS)
H01824 CODAS syndrome
H01832 Lenz-Majewski syndrome
H01834 Marshall-Smith syndrome
H00908 Mowat-Wilson syndrome
H01838 Mandibulofacial dysostosis with microcephaly
H01839 Burn-McKeown syndrome
H01840 Moebius syndrome
H01843 Cerebrocostomandibular syndrome
H01845 Catel-Manzke syndrome
H01847 Thrombocytopenia-absent radius syndrome
H01850 Hartsfield syndrome
H01857 Filippi syndrome
H02132 Microcephaly syndrome
H01872 Microcephaly-capillary malformation syndrome
H01876 Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)
H01923 Microcephaly, short stature, and impaired glucose metabolism
H01880 Autosomal recessive microcephaly and chorioretinopathy
H01878 Al-Raqad syndrome
H01879 Wiedemann-Steiner syndrome
H01885 Megalencephaly-capillary malformation syndrome (MCAP) and megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH)
H01886 Van den Ende-Gupta syndrome
H01887 3MC syndrome
H01888 Carpenter syndrome
H01889 Meier-Gorlin syndrome
H01893 Lateral meningocele syndrome
H01908 Carey-Fineman-Ziter syndrome
H01912 Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
H01913 Renpenning syndrome
H01914 Christianson syndrome
H01915 Borjeson-Forssman-Lehmann syndrome
H01916 Stocco dos Santos X-linked mental retardation syndrome
H01917 CK syndrome
H01919 Proud syndrome
H01927 Van der Woude syndrome
H01930 Au-Kline syndrome
H01931 Lethal-type popliteal pterygium syndrome
H01932 Ablepharon-macrostomia syndrome
H01933 Porokeratosis
H01934 Barber-Say syndrome
H01984 Leopard syndrome
H02023 Baraitser-Winter syndrome
H02046 OFC syndrome
H02047 Bohring-Opitz syndrome
H02067 Boomerang dysplasia
H02072 Stickler syndrome
H02081 Marshall syndrome
H02082 Floating-Harbor syndrome
H02095 Perrault syndrome
H02102 Myhre syndrome
H02151 Hereditary congenital facial paresis
H02153 Megalencephaly-capillary malformation syndrome
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Q89 Other congenital malformations, not elsewhere classified
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Q90-Q99 Chromosomal abnormalities, not elsewhere classified
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18. Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R99)
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19. Injury, poisoning and certain other consequences of external causes (S00-T98)
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20. External causes of morbidity and mortality (V01-Y98)
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21. Factors influencing health status and contact with health services (Z00-Z99)
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22. Codes for special purposes (U00-U85)
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