CIM11 AB50
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Congenital hearing impairment
- chapitre
- 10 Diseases of the ear or mastoid process
- bloc
- Disorders with hearing impairment
- definition
- Both dominant and recessive genes exist which can cause mild to profound impairment. If a family has a dominant gene for deafness it will persist across generations because it will manifest itself in the offspring even if it is inherited from only one parent. If a family had genetic hearing impairme
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1154032108 ↗