CIM11 8E00
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Sporadic Creutzfeldt-Jakob Disease
- chapitre
- 08 Diseases of the nervous system
- bloc
- Human prion diseases
- definition
- A disease of the brain, that is associated with a mutation of normal prion protein genes or spontaneous transformation of prion proteins. This disease is characterised by a long incubation period, progressive dementia, neurological deficits, and is fatal. Transmission may be by direct contact with i
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1553463690 ↗