CIM11 LD2F.13
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Meckel-Gruber syndrome
- chapitre
- 20 Developmental anomalies
- bloc
- Multiple developmental anomalies or syndromes
- definition
- Meckel syndrome (MKS) is a monogenic disease characterised by a combination of renal cysts and variably associated features, including developmental anomalies of the central nervous system (usually occipital encephalocele), hepatic ductal dysplasia and cysts, and polydactyly, and a lethal course, wi
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#695796893 ↗