CIM11 8E02.1
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Gerstmann-Straussler-Scheinker syndrome
- chapitre
- 08 Diseases of the nervous system
- bloc
- Human prion diseases
- definition
- A disease caused by inheritance of mutation(s) in normal prion protein genes. This disease is characterised by cerebellar ataxia, decreased coordination, dysmetria, or dysarthria, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.
- exclusions
- Gerstmann syndrome
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#406818835 ↗