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MIM:615156 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 6; PEOA6
Xenbase Genes: dna2
Human Disease Resource: MIM
MONDO:0014062 - mitochondrial DNA deletion syndrome with progressive myopathy |
DOID:0111519 - autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 |