Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4

MONDO:0012415

Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the POLG2 gene.

Also known as: POLG2 progressive external ophthalmoplegia with mitochondrial DNA deletions, progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in POLG2, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 4, PEOA4, progressive external ophthalmoplegia, autosomal dominant 4

19 clinical trials for this condition and its sub-types, 0 tagged with Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4 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 4 (0)

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