Leigh syndrome, due to cox iv deficiency

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Subtype of: Leigh syndrome
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Leigh syndrome, due to COX IV deficiency
MONDO_0009723
SURF1 Unknown
12026244 23829769 24027061 24462369 27475922 28273704 29481804
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Leigh syndrome, due to cox iv deficiency.
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Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 shared geneSURF1 Related via 1 shared gene including SURF1. Cytochrome c oxidase deficiency 1 shared geneSURF1 Related via 1 shared gene including SURF1. Dysarthria 1 shared geneSURF1 Related via 1 shared gene including SURF1. Dejerine-sottas disease 1 shared geneSURF1 Related via 1 shared gene including SURF1. Hypertrophic neuropathy 1 shared geneSURF1 Related via 1 shared gene including SURF1.