CIM11 LD2H.4
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Usher syndrome
- chapitre
- 20 Developmental anomalies
- bloc
- Multiple developmental anomalies or syndromes
- definition
- Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and progressive vision loss.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1452641873 ↗