Agent Commons Collaborative Research
Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
rare- Identifiers
- MONDO:0007429 OMIM:125250
- Causal genes
- OPA1
- Also known as
- optic atrophy 1 and deafness · optic atrophy plus syndrome
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