Human Diseases in ICD-11 Classification

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 01 Certain infectious or parasitic diseases
 02 Neoplasms
 03 Diseases of the blood or blood-forming organs
 04 Diseases of the immune system
 05 Endocrine, nutritional or metabolic diseases
 06 Mental, behavioural or neurodevelopmental disorders
 07 Sleep-wake disorders
 08 Diseases of the nervous system
 09 Diseases of the visual system
 10 Diseases of the ear or mastoid process
 11 Diseases of the circulatory system
 12 Diseases of the respiratory system
 13 Diseases of the digestive system
 14 Diseases of the skin
 15 Diseases of the musculoskeletal system or connective tissue
 16 Diseases of the genitourinary system
 17 Conditions related to sexual health
 18 Pregnancy, childbirth or the puerperium
 19 Certain conditions originating in the perinatal period
 20 Developmental anomalies
   Structural developmental anomalies primarily affecting one body system
   Multiple developmental anomalies or syndromes
     LD20  Syndromes with central nervous system anomalies as a major feature
     LD21  Syndromes with eye anomalies as a major feature
     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
     LD25  Syndromes with face or limb anomalies as a major feature
     LD26  Syndromes with limb anomalies as a major feature
     LD27  Syndromes with skin or mucosal anomalies as a major feature
     LD28  Syndromes with connective tissue involvement as a major feature
     LD29  Syndromes with obesity as a major feature
     LD2A  Malformative disorders of sex development
     LD2B  Syndromes with premature ageing appearance as a major feature
     LD2C  Overgrowth syndromes
     LD2D  Phakomatoses or hamartoneoplastic syndromes
     LD2E  Syndromes with structural anomalies due to inborn errors of metabolism
     LD2F  Syndromes with multiple structural anomalies, without predominant body system involvement
       H00979  Caudal regression syndrome and Sirenomelia
       H02129  Prune belly syndrome
       H01195  VACTERL/VATER association
       H00261  Meckel syndrome
       H01738  Noonan syndrome
       H00610  Treacher Collins syndrome
       H01838  Mandibulofacial dysostosis with microcephaly
       H02126  Mandibulofacial dysostosis with alopecia
       H02211  Acrodysostosis
       H00433  Holt-Oram syndrome
       H00453  Branchio-oto-renal syndrome
       H00460  Hand-foot-genital syndrome
       H00463  Currarino syndrome
       H00500  Keutel syndrome
       H00502  Pallister-Hall syndrome
       H00504  Rubinstein-Taybi syndrome
       H00510  Feingold syndrome
       H00523  Noonan syndrome and related disorders
       H00555  Char syndrome
       H00556  CHARGE syndrome
       H00569  Aarskog-Scott syndrome
       H00570  Kabuki syndrome
       H00572  ESCO2-related disorders
       H00573  Townes-Brocks syndrome
       H00574  Coffin-Lowry syndrome
       H00583  Opitz-GBBB syndrome
       H00611  Popliteal pterygium syndrome (PPS)
       H00631  Cornelia de Lange syndrome
       H00634  Duane-radial ray syndrome
       H00637  Ulnar-mammary syndrome
       H00685  Bifid nose with or without anorectal and renal anomalies
       H00686  Manitoba oculotrichoanal syndrome
       H00709  Birk Barel mental retardation syndrome (BBMRS)
       H00711  Russell-Silver syndrome
       H00753  Urofacial syndrome
       H00756  Pitt-Hopkins syndrome
       H00797  Martsolf syndrome
       H00817  Branchiooculofacial syndrome
       H00868  Stapes ankylosis with broad thumb and toes
       H00886  Donnai-Barrow syndrome
       H00889  Lujan-Fryns syndrome
       H00894  FG syndrome
       H00907  Kleefstra syndrome
       H00908  Mowat-Wilson syndrome
       H00914  Warsaw breakage syndrome
       H00926  Growth retardation, developmental delay, coarse facies, and early death
       H00934  Caudal duplication anomaly
       H00936  Goldberg-Shprintzen megacolon syndrome
       H00943  TARP syndrome
       H00965  RAPADILINO syndrome
       H00972  Endocrine-cerebro-osteodysplasia syndrome
       H00987  Fetal akinesia deformation sequence
       H00997  CATSHL syndrome
       H01026  Renal coloboma syndrome
       H01030  Congenital arthrogryposis with anterior horn cell disease
       H01156  STAR syndrome
       H01220  Congenital cataracts, facial dysmorphism, and neuropathy
       H01265  Hydrolethalus syndrome
       H01289  Mulibrey nanism
       H01292  Nance-Horan syndrome
       H01370  SHORT syndrome
       H01413  Adams-Oliver syndrome
       H01568  3C syndrome
       H01569  CHOPS syndrome
       H01573  Zimmermann-Laband syndrome
       H01745  Cardiofaciocutaneous syndrome
       H01747  Costello syndrome
       H01793  Young-Simpson syndrome
       H01794  Genitopatellar syndrome
       H01795  Blepharophimosis-mental retardation syndrome
       H01797  Webb-Dattani syndrome
       H01814  Stromme syndrome
       H01839  Burn-McKeown syndrome
       H01840  Moebius syndrome
       H01845  Catel-Manzke syndrome
       H01869  Megacystis microcolon intestinal hypoperistalsis syndrome
       H01878  Al-Raqad syndrome
       H01879  Wiedemann-Steiner syndrome
       H01887  3MC syndrome
       H01908  Carey-Fineman-Ziter syndrome
       H01917  CK syndrome
       H01923  Microcephaly, short stature, and impaired glucose metabolism
       H01927  Van der Woude syndrome
       H01930  Au-Kline syndrome
       H01932  Ablepharon-macrostomia syndrome
       H01984  Leopard syndrome
       H02023  Baraitser-Winter syndrome
       H02046  OFC syndrome
       H02072  Stickler syndrome
       H02074  Knobloch syndrome
       H02082  Floating-Harbor syndrome
       H02087  Vertebral, cardiac, renal, and limb defects syndrome
       H02102  Myhre syndrome
       H02180  McKusick-Kaufman syndrome
       H02190  CBL syndrome
       H02191  Noonan-like syndrome with loose anagen hair
       H02198  Pancreatic agenesis and congenital heart disease
       H02232  CAGSSS syndrome
       H02248  MEND syndrome
       H02249  Primrose syndrome
       H02253  Beaulieu-Boycott-Innes syndrome
       H02255  FDLAB syndrome
       H02260  Chondrodysplasia Chassaing-Lacombe type
       H02271  Cerebellofaciodental syndrome
       H02274  Cerebellar atrophy, visual impairment, and psychomotor retardation
       H02283  IVIC syndrome
       H02324  Sacral agenesis with vertebral anomalies
       H02327  KBG syndrome
       H02328  Sifrim-Hitz-Weiss syndrome
       H02334  Pierpont syndrome
       H02364  Heart and brain malformation syndrome
       H02368  Developmental delay with short stature, dysmorphic facial features, and sparse hair
       H02369  IMAGE-I syndrome
       H02370  FILS syndrome
       H02376  Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies
       H02381  Cleft palate, psychomotor retardation, and distinctive facial features
       H02382  Bainbridge-Ropers syndrome
       H02383  Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
       H02391  Infantile-onset multisystem neurologic, endocrine, and pancreatic disease
       H02394  Cleft palate, cardiac defects, and mental retardation
       H02453  Congenital heart defects and ectodermal dysplasia
       H02454  Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
       H02455  Congenital heart defects, hamartomas of tongue, and polysyndactyly
       H01824  CODAS syndrome
       H01850  Hartsfield syndrome
       H01857  Filippi syndrome
       H02343  EVEN-plus syndrome
     LD2G  Conjoined twins
     LD2H  Syndromic genetic deafness
     LD2Y  Other specified multiple developmental anomalies or syndromes
     LD2Z  Multiple developmental anomalies or syndromes, unspecified
   Chromosomal anomalies, excluding gene mutations
   LD90  Conditions with disorders of intellectual development as a relevant clinical feature
   LD9Y  Other specified developmental anomalies
   LD9Z  Developmental anomalies, unspecified
 21 Symptoms, signs or clinical findings, not elsewhere classified
 22 Injury, poisoning or certain other consequences of external causes

Last updated: November 21, 2020
ICD-11 by World Health Organization

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