progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2

Rare Disease

MONDO:0012238

Also known as:

SLC25A4 progressive external ophthalmoplegia with mitochondrial DNA deletionsprogressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in SLC25A4progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2

Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the SLC25A4 gene.

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progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2

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