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CIM11 8E03

CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09

Variably protease sensitive prionopathy

chapitre
08 Diseases of the nervous system
bloc
Human prion diseases
definition
A disease of the brain, caused by a mutation(s) in prion protein genes. This disease is characterised by deposition of abnormal prions in the brain leading to behavioural and mood changes, speech deficits, and progressive motor impairments. Confirmation is by pathological examination of the brain or
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#172957869 ↗