Progressive external ophthalmoplegia with mitochondrial dna deletions 3

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Subtype of: Progressive external ophthalmoplegia
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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 3
MONDO_0012238
SLC25A4 Unknown
27604308
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Progressive external ophthalmoplegia with mitochondrial dna deletions 3.
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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, autosomal dominant, 2 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.