progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1

Rare Disease

MONDO:0024528

Also known as:

PEOA1POLG autosomal dominant progressive external ophthalmoplegiaautosomal dominant progressive external ophthalmoplegia caused by mutation in POLG

Any autosomal dominant progressive external ophthalmoplegia in which the cause of the disease is a mutation in the POLG gene.

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