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Summary Literature (0)
MIM:615156 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 6; PEOA6


Xenbase Genes: dna2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014062 - mitochondrial DNA deletion syndrome with progressive myopathy

Disease Ontology (DO):
DOID:0111519 - autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6