14Diseases of the skin
Genetic or developmental disorders affecting the skin
EC23Genetic disorders of skin pigmentation
EC23.2
category
Albinism or other specified genetically-determined hypomelanotic disorders
Definition A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis.
Also indexed as
Albinism or other specified genetically-determined hypomelanotic disorders
Nearby in Genetic disorders of skin pigmentation
International Classification of Diseases, Eleventh Revision (ICD-11), World Health Organization (WHO) 2019/2021, https://icd.who.int/browse11. Licensed under Creative Commons Attribution-NoDerivatives 3.0 IGO (CC BY-ND 3.0 IGO).
Release 2026-01.
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This page reproduces WHO classification content for reference. It is not
medical advice and must not be used to diagnose or treat. For coding
decisions, consult the official release and your national coding guidelines.
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