Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 4

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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 4
MONDO_0008003
POLG2 Causal
16685652 21555342 25655951 25929793 27592148 27604308 30157269 31286721 31778857
Open Targets
All1 Causal1 Unknown0
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Progressive external ophthalmoplegia 1 shared genePOLG2 Related via 1 shared gene including POLG2. Mitochondrial dna depletion syndrome 1 shared genePOLG2 Related via 1 shared gene including POLG2. Liver failure 1 shared genePOLG2 Related via 1 shared gene including POLG2. Hereditary spastic paraplegia 1 shared genePOLG2 Related via 1 shared gene including POLG2. Respiratory system disease 1 shared genePOLG2 Related via 1 shared gene including POLG2.