Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2
rareAny progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RNASEH1 gene.
- Identifiers
- MONDO:0014656 OMIM:616479
- Causal genes
- RNASEH1
- Part of
- Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathyProgressive external ophthalmoplegia with mitochondrial DNA deletions
- Also known as
- PEOB2 · progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1 · progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2 · RNASEH1 progressive external ophthalmoplegia with mitochondrial DNA deletions
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