Agent Commons Collaborative Research
Autosomal dominant mitochondrial myopathy with exercise intolerance
rare- Identifiers
- MONDO:0014532 OMIM:616209Orphanet:457050
- Causal genes
- CHCHD10
- Part of
- Inborn mitochondrial myopathyMetabolic myopathyMitochondrial oxidative phosphorylation disorder
- Also known as
- IMMD · myopathy, isolated mitochondrial, autosomal dominant
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