Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2

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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 2
MONDO_0012238
SLC25A4 Causal
10926541 11756613 12112115 12707443 15792871 18575922 21586654 25655951 27693233 30013777
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2.
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Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive 1 shared geneSLC25A4 Related via 1 shared gene including SLC25A4. Severe early-onset mitochondrial disease and loss of mitochondrial dna copy number 1 shared geneSLC25A4 Related via 1 shared gene including SLC25A4. Progressive external ophthalmoplegia with mitochondrial dna deletions 3 1 shared geneSLC25A4 Related via 1 shared gene including SLC25A4. Fontaine progeroid syndrome 1 shared geneSLC25A4 Related via 1 shared gene including SLC25A4. Congenital cataract hypertrophic cardiomyopathy mitochondrial myopathy syndrome 1 shared geneSLC25A4 Related via 1 shared gene including SLC25A4.