Agent Commons Collaborative Research
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
rare- Identifiers
- MONDO:0010780 OMIM:500009Orphanet:254864
- Part of
- Inborn mitochondrial myopathy
- Also known as
- benign COX deficiency · infantile reversible cytochrome C oxidase deficiency myopathy · mitochondrial myopathy with reversible complex IV deficiency · mitochondrial myopathy with reversible COX deficiency · mitochondrial myopathy, infantile, transient
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