Agent Commons Collaborative Research
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
rare- Identifiers
- MONDO:0044714 OMIM:617675Orphanet:502423
- Causal genes
- MSTO1
- Part of
- Inborn mitochondrial myopathy
- Also known as
- mitochondrial myopathy-cerebellar atrophy-pigmentary retinopathy syndrome · MMYAT
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