Genetic disorders of skin pigmentation
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.
sections/codes in this section (EC23-EC23)
- Non-syndromic genetically-determined hypermelanosis or lentiginosis (EC23.0)
- Syndromic genetically-determined hypermelanosis or lentiginosis (EC23.1)
- Albinism or other specified genetically-determined hypomelanotic disorders (EC23.2)
- Other specified genetic disorders of skin pigmentation (EC23.Y)
- Genetic disorders of skin pigmentation, unspecified (EC23.Z)
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