Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2
rareAny progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the SLC25A4 gene.
- Identifiers
- MONDO:0012238 OMIM:609283
- Causal genes
- SLC25A4
- Also known as
- PEOA2 · progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in SLC25A4 · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 2 · SLC25A4 progressive external ophthalmoplegia with mitochondrial DNA deletions
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