CIM11 8A01.10
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Huntington disease
- chapitre
- 08 Diseases of the nervous system
- bloc
- Movement disorders
- definition
- Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system. HD is an autosomal dominant disorder due to a mutation resulting in an increased number of triplicate cytosine-adenine-guanine repeats on chromosome 4. The manifestations include chorea, dementia and personal
- inclusions
- Huntington chorea
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#2132180242 ↗