Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4
rareAny progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the POLG2 gene.
- Identifiers
- MONDO:0012415 OMIM:610131
- Causal genes
- POLG2
- Also known as
- PEOA4 · POLG2 progressive external ophthalmoplegia with mitochondrial DNA deletions · progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in POLG2 · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 4
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