Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3

MONDO:0012241

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

Also known as: TWNK progressive external ophthalmoplegia with mitochondrial DNA deletions, progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in TWNK, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3, progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 3, PEOA3, progressive external ophthalmoplegia, autosomal dominant 3

19 clinical trials for this condition and its sub-types, 0 tagged with Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3 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 3 (0)

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