Autosomal dominant optic atrophy
Autosomal dominant optic atrophy
Definition
An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss.
Also known as ADOA, DOA, optic atrophy, autosomal dominant — per MONDO
Also identified as
- MESH D029241 per MONDO
- NCIT C84577 per MONDO
- Orphanet 98672 per MONDO
- SCTID 2065009 per MONDO
- UMLS C4551508 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Camera-type eye | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Camera-type eye | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |