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MIM:609286 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3
Xenbase Genes: twnk
Human Disease Resource: OMIM
MONDO:0008003 - autosomal dominant progressive external ophthalmoplegia |
MONDO:0012241 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3 |
DOID:0111520 - autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 |