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CIM11 8E02

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

Genetic prion diseases

chapitre
08 Diseases of the nervous system
bloc
Human prion diseases
definition
Genetic prion disease generally manifests with cognitive difficulties, ataxia, and myoclonus (abrupt jerking movements of muscle groups and/or entire limbs). The order of appearance and/or predominance of these features and other associated neurologic and psychiatric findings vary. The three major p
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#542527938 ↗