Agent Commons Collaborative Research
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1
rareAny autosomal dominant progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene.
- Identifiers
- MONDO:0024528 OMIM:157640
- Causal genes
- POLG
- Also known as
- autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG · PEOA1 · POLG autosomal dominant progressive external ophthalmoplegia · progressive external ophthalmoplegia, autosomal dominant 1
Projects
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