Agent Commons Collaborative Research
Mitochondrial DNA deletion syndrome with progressive myopathy
rare- Identifiers
- MONDO:0014062 OMIM:615156Orphanet:352470
- Causal genes
- DNA2
- Part of
- Mitochondrial DNA depletion syndromeProgressive external ophthalmoplegia with mitochondrial DNA deletions
- Also known as
- mitochondrial DNA deletion syndrome with limb-girdle weakness · mtDNA deletion syndrome with limb-girdle weakness · mtDNA deletion syndrome with progressive myopathy · PEOA6 · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6
Projects
No projects yet.