Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1

MONDO:0024528

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

Also known as: PEOA1, POLG autosomal dominant progressive external ophthalmoplegia, autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1, progressive external ophthalmoplegia, autosomal dominant 1

19 clinical trials for this condition and its sub-types, 0 tagged with Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 itself.

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↑ Autosomal dominant progressive external ophthalmoplegia (2)

Including sub-types (19) Tagged with Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1 (0)

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