CIM11 8E02.2
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Fatal familial insomnia
- chapitre
- 08 Diseases of the nervous system
- bloc
- Human prion diseases
- definition
- A disease of the brain, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterised by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#669154658 ↗