PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5

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Summary

Literature (0)

MIM:613077 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5

Xenbase Genes: rrm2b

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008003 - autosomal dominant progressive external ophthalmoplegia
MONDO:0013117 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5

MONDO:0008003 - autosomal dominant progressive external ophthalmoplegia

MONDO:0013117 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5

Disease Ontology (DO):

DOID:0111518 - autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5

DOID:0111518 - autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5