Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5

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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 5
MONDO_0008003
RRM2B Causal
19138848 19664747 21646632 25929793 27604308
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5.
5 View disease cluster →
Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Progressive external ophthalmoplegia with mitochondrial dna deletions (autosomal dominant) 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Chronic progressive external ophthalmoplegia 1 shared geneRRM2B Related via 1 shared gene including RRM2B. Camptocormia 1 shared geneRRM2B Related via 1 shared gene including RRM2B.