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EC23 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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