EC21.3 Genetic syndromes with alopecia or hypotrichosis

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Hereditary syndromes in which sparse or absent hair is a component

code elsewhere

• Argininosuccinic aciduria  (5C50.A0)
• Hidrotic ectodermal dysplasia, Clouston type  (LD27.03)
• Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy  (4A01.1Y)
• Ichthyosis – hypotrichosis syndrome  (LD27.2)
• Neonatal sclerosing cholangitis – ichthyosis – hypotrichosis syndrome  (DB96.2Y)
• Odonto-onycho-dermal dysplasia  (LD27.0Y)
• Woolly hair – hypotrichosis – everted lower lip – outstanding ears  (LD27.0Y)
• Autosomal dominant palmoplantar keratoderma and congenital alopecia  (LD27.0Y)
• Autosomal recessive palmoplantar keratoderma and congenital alopecia  (LD27.0Y)
• Alopecia - contractures - dwarfism - intellectual deficit  (LD27.0Y)
• Alopecia – psychomotor epilepsy – periodontal pyorrhoea – intellectual disability syndrome  (LD90.Y)
• Cataract - alopecia - sclerodactyly  (LD27.0Y)
• Odonto-onycho dysplasia - alopecia  (LD27.0Y)
• Schöpf-Schulz-Passarge syndrome  (LD27.0Y)
• Macrocephaly – alopecia – cutis laxa – scoliosis syndrome  (LD28.2)

synonyms

• Genetic syndromes with alopecia or hypotrichosis

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