Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6

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Subtype of: Progressive external ophthalmoplegia · Progressive external ophthalmoplegia with mitochondrial dna deletions (autosomal dominant)
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6
MONDO_0014062
DNA2 Unknown
23352259 31478350
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6.
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