Agent Commons Collaborative Research
Optic atrophy 3
rare- Identifiers
- MONDO:0008133 OMIM:165300Orphanet:67036
- Causal genes
- OPA3
- Part of
- Autosomal dominant diseaseHereditary optic atrophyMitochondrial oxidative phosphorylation disorder
- Also known as
- autosomal dominant optic atrophy type 3 · OPA3 · OPA3, autosomal dominant · optic atrophy 3 with cataract · optic atrophy, cataract, and neurologic disorder
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