 01 Certain infectious or parasitic diseases
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02 Neoplasms
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03 Diseases of the blood or blood-forming organs
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04 Diseases of the immune system
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05 Endocrine, nutritional or metabolic diseases
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06 Mental, behavioural or neurodevelopmental disorders
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07 Sleep-wake disorders
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08 Diseases of the nervous system
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09 Diseases of the visual system
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10 Diseases of the ear or mastoid process
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11 Diseases of the circulatory system
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12 Diseases of the respiratory system
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13 Diseases of the digestive system
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14 Diseases of the skin
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15 Diseases of the musculoskeletal system or connective tissue
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16 Diseases of the genitourinary system
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17 Conditions related to sexual health
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18 Pregnancy, childbirth or the puerperium
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19 Certain conditions originating in the perinatal period
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 20 Developmental anomalies
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Structural developmental anomalies primarily affecting one body system
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Multiple developmental anomalies or syndromes
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LD20 Syndromes with central nervous system anomalies as a major feature
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LD21 Syndromes with eye anomalies as a major feature
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 LD22 Syndromes with dental anomalies as a major feature
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LD23 Syndromes with vascular anomalies as a major feature
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LD24 Syndromes with skeletal anomalies as a major feature
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LD25 Syndromes with face or limb anomalies as a major feature
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LD26 Syndromes with limb anomalies as a major feature
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H00467 Fibular hypoplasia and complex brachydactyly
H00853 Cenani-Lenz syndactyly syndrome
H00855 Triphalangeal thumb-polysyndactyly syndrome
H00859 Guttmacher syndrome
H00870 Brachydactyly-syndactyly syndrome
H02161 Greig cephalopolysyndactyly syndrome
H02333 Laurin-Sandrow syndrome
H00778 Tarsal-carpal coalition syndrome
H00986 Multiple pterygium syndrome
H00935 Cold-induced sweating syndrome
H01392 Arthrogryposis, mental retardation, and seizures
H01886 Van den Ende-Gupta syndrome
H02299 Arthrogryposis multiplex congenita
H02358 Arthrogryposis multiplex congenita, neurogenic, with myelin defect
H00811 Distal arthrogryposis
H00865 Lethal congenital contractural syndrome
H00872 Trismus-pseudocamptodactyly syndrome
H01931 Lethal-type popliteal pterygium syndrome
H02268 Wieacker-Wolff syndrome
H00532 Parkes Weber syndrome
H01788 Klippel-Trenaunay-Weber syndrome
H01497 Temtamy preaxial brachydactyly syndrome
H00846 Fuhrmann syndrome
H00847 Al-Awadi/Raas-Rothschild syndrome
H02717 Contractures, pterygia, and spondylocarpostarsal fusion syndrome
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LD27 Syndromes with skin or mucosal anomalies as a major feature
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LD28 Syndromes with connective tissue involvement as a major feature
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LD29 Syndromes with obesity as a major feature
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LD2A Malformative disorders of sex development
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LD2B Syndromes with premature ageing appearance as a major feature
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LD2C Overgrowth syndromes
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LD2D Phakomatoses or hamartoneoplastic syndromes
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LD2E Syndromes with structural anomalies due to inborn errors of metabolism
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LD2F Syndromes with multiple structural anomalies, without predominant body system involvement
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LD2G Conjoined twins
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LD2H Syndromic genetic deafness
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LD2Y Other specified multiple developmental anomalies or syndromes
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LD2Z Multiple developmental anomalies or syndromes, unspecified
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Chromosomal anomalies, excluding gene mutations
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LD90 Conditions with disorders of intellectual development as a relevant clinical feature
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LD9Y Other specified developmental anomalies
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LD9Z Developmental anomalies, unspecified
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21 Symptoms, signs or clinical findings, not elsewhere classified
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22 Injury, poisoning or certain other consequences of external causes
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25 Codes for special purposes
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Human Diseases in ICD-11 Classification