EC23.Y

ICD-11 MMS 2026-01

Other specified genetic disorders of skin pigmentation

Sibling codes

  • EC23.0 – Non-syndromic genetically-determined hypermelanosis or lentiginosis
  • EC23.1 – Syndromic genetically-determined hypermelanosis or lentiginosis
  • EC23.2 – Albinism or other specified genetically-determined hypomelanotic disorders
  • EC23.Z – Genetic disorders of skin pigmentation, unspecified

Foundation entity

Genetic disorders of skin pigmentation – http://id.who.int/icd/entity/1596419171

Part of: EC23: Genetic disorders of skin pigmentation › 14: Diseases of the skin