CIM11 EC23.1
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Syndromic genetically-determined hypermelanosis or lentiginosis
- chapitre
- 14 Diseases of the skin
- bloc
- Genetic or developmental disorders affecting the skin
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1465001518 ↗