CIM11 EC23.20
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Oculocutaneous albinism
- chapitre
- 14 Diseases of the skin
- bloc
- Genetic or developmental disorders affecting the skin
- definition
- Oculocutaneous albinism is a genetically heterogeneous congenital disorder characterised by decreased or absent pigmentation in the hair, skin, and eyes.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1189424097 ↗