Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
rareAny autosomal recessive progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene.
- Identifiers
- MONDO:0009783 OMIM:258450
- Causal genes
- POLG
- Part of
- Autosomal recessive progressive external ophthalmoplegiaProgressive external ophthalmoplegia with mitochondrial DNA deletions
- Also known as
- arPEO · autosomal recessive progressive external ophthalmoplegia · autosomal recessive progressive external ophthalmoplegia caused by mutation in POLG · cerebellar ataxia infantile with progressive external ophthalmoplegia · PEOB1
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