autosomal dominant optic atrophy
MeSH: D029241ORPHA: 98672
Overview
autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
D029241Orphanet Code
ORPHA:98672autosomal dominant optic atrophy
| MeSH | D029241 |
| Orphanet | ORPHA:98672 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO