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
       H00520  Type II collagenopathies
       H00505  FGFR3-related short limb skeletal dysplasia
       H01749  Achondroplasia
       H02069  SADDAN
       H02068  Hypochondroplasia
       H01750  Thanatophoric dysplasia
       H00515  Atelosteogenesis type II
       H02063  Diastrophic dysplasia
       H00207  Rhizomelic chondrodysplasia punctata
       H00447  HEM skeletal dysplasia
       H00496  Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD)
       H01194  X-linked chondrodysplasia punctata
       H00436  Osteopetrosis
       H00452  Buschke-Ollendorff syndrome
       H00434  Camurati-Engelmann disease
       H00444  Osteopathia striata with cranial sclerosis
       H00450  Worth type autosomal dominant osteosclerosis
       H00486  Sclerosteosis
       H00490  Diaphyseal dysplasia with anemia
       H00491  Craniometaphyseal dysplasia
       H00508  Blomstrand syndrome
       H00613  Infantile cortical hyperostosis
       H00968  Raine syndrome
       H01832  Lenz-Majewski syndrome
       H00122  Multiple exostoses
       H00493  Heparan sulfate proteoglycan gene defects
       H00497  Cherubism
       H02127  Yunis-Varon syndrome
       H00443  Osteoglophonic dysplasia
       H00498  Gnathodiaphyseal dysplasia
       H00521  Cleidocranial dysplasia
       H01018  Metachondromatosis
       H00445  Osteoarthritis with mild chondrodysplasia
       H00474  Schneckenbecken dysplasia
       H00483  Angel shaped phalangoepiphyseal dysplasia
       H00499  Spondylocarpotarsal synostosis syndrome
       H00519  Spondyloepiphyseal dysplasia congenita
       H00757  Dyggve-Melchior-Clausen disease and Smith-McCort dysplasia
       H00758  Progressive pseudorheumatoid dysplasia
       H00760  Spondyloepiphyseal dysplasia tarda
       H00761  SEMD, Pakistani type
       H00765  Spondyloepiphyseal dysplasia, Kimberley type
       H00767  SEMD, Matrilin type
       H00777  SEMD, short limb-hand type
       H00863  Spondylo-megaepiphyseal-metaphyseal dysplasia
       H01494  SEMD with joint laxity type
       H01575  Roifman syndrome
       H01576  Spondyloenchondrodysplasia with immune dysregulation (SPENCDI)
       H01967  Anauxetic dysplasia
       H02070  Kniest dysplasia
       H02071  Czech dysplasia
       H02079  Oto-spondylo-megaepiphyseal dysplasia
       H02080  Fibrochondrogenesis
       H02155  Dyssegmental dysplasia
       H02183  Parastremmatic dwarfism
       H02184  Metatropic dysplasia
       H02186  Spondyloepiphyseal dysplasia, Maroteaux type
       H02187  Spondyloepimetaphyseal dysplasia
       H01821  Spondylometaphyseal dysplasia with cone-rod dystrophy
       H01825  Spondylometaphyseal dysplasia, Sedaghatian type
       H01830  Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type
       H02185  Spondylometaphyseal dysplasia
       H00678  Achondrogenesis type IA
       H02065  Achondrogenesis type IB
       H02066  Achondrogenesis type II
       H00522  Brachyolmia
       H01828  Opsismodysplasia
       H01844  Diaphanospondylodysostosis
       H00495  Eiken dysplasia
       H00477  Pseudoachondroplasia
       H00476  Multiple epiphyseal dysplasia
       H00479  Metaphyseal dysplasias
       H00518  Metaphyseal dysplasia without hypotrichosis
       H00675  Acrocapitofemoral dysplasia
       H00900  Geleophysic dysplasia
       H02062  Familial digital arthropathy-brachydactyly
       H02228  Acromicric dysplasia
       H02229  Terminal osseous dysplasia
       H00466  Grebe dysplasia
       H00468  Acromesomelic dysplasia, Demirhan type
       H00470  Acromesomelic dysplasia, Maroteaux type
       H00485  Robinow syndrome
       H00492  SHOX-related short stature
       H02154  Omodysplasia
       H00511  Short rib-polydactyly syndrome
       H00751  Asphyxiating thoracic dystrophy
       H02157  Short-rib thoracic dysplasia
       H00462  Stuve-Wiedemann syndrome
       H00509  3M syndrome
       H00619  Kenny-Caffey syndrome
       H00622  Hypoparathyroidism-retardation-dysmorphism syndrome
       H00992  Seckel syndrome
       H02223  Osteocraniostenosis
       H00494  Desbuquois syndrome
       H01498  Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
       H02048  Larsen syndrome
       H02064  Atelosteogenesis type I and III
       H02067  Boomerang dysplasia
       H00458  Syndromic craniosynostoses
       H01756  Pfeiffer syndrome
       H01754  Crouzon syndrome
       H01755  Apert syndrome
       H01008  C syndrome
       H01753  Antley-Bixler syndrome
       H01888  Carpenter syndrome
       H01988  Jackson-Weiss syndrome
       H01989  Beare-Stevenson syndrome
       H01990  Muenke syndrome
       H01991  Saethre-Chotzen syndrome
       H01992  Craniofrontonasal syndrome
       H01993  Baller-Gerold syndrome
       H02047  Bohring-Opitz syndrome
       H02254  Craniosynostosis and dental anomalies
       H00517  Spondylocostal dysostosis
       H01843  Cerebrocostomandibular syndrome
       H00464  Nail-patella syndrome
       H00461  Ischiocoxopodopatellar syndrome
       H01889  Meier-Gorlin syndrome
       H00506  Osteogenesis imperfecta
       H00451  Osteoporosis-pseudoglioma syndrome
       H00514  Bruck syndrome
       H01496  Spondyloocular syndrome
       H01571  Singleton-Merten syndrome
       H01572  Cole-Carpenter syndrome
       H02395  Calvarial doughnut lesions with bone fragility
       H00969  Skeletal defects, genital hypoplasia, and mental retardation
       H02233  Alazami syndrome
       H02280  Complex lethal osteochondrodysplasia
       H02300  Steel syndrome
       H02306  Chondrodysplasia with joint dislocations, GPAPP type
       H02349  Odontochondrodysplasia
       H02415  Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
     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
     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

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Last updated: May 20, 2020
ICD-11 by World Health Organization

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