Other specified genetically-determined hypomelanotic disorders

Sibling codes

EC23.20 – Oculocutaneous albinism

Foundation entity

Albinism or other specified genetically-determined hypomelanotic disorders – http://id.who.int/icd/entity/143807416

Part of: EC23.2: Albinism or other specified genetically-determined hypomelanotic disorders › EC23: Genetic disorders of skin pigmentation › 14: Diseases of the skin