Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
rareAny progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RRM2B gene.
- Identifiers
- MONDO:0013117 OMIM:613077
- Causal genes
- RRM2B
- Also known as
- PEOA5 · progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5 · RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions
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