CIM11 9C40.B
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Optic atrophy
- chapitre
- 09 Diseases of the visual system
- bloc
- Disorders of the visual pathways or centres
- definition
- Optic atrophies (OA) refer to a specific group of hereditary optic neuropathies in which the cause of the optic nerve dysfunction is inherited either in an autosomal dominant or autosomal recessive pattern. Autosomal dominant optic atrophy (ADOA), type Kjer, is the most common OA, whereas autosomal
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#568505454 ↗