Leigh syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
LEIGH SYNDROME WITH NEPHROTIC SYNDROME
MONDO:0016816
COQ2 Unknown — GenCC
All107 Causal21 Unknown101
Related Diseases Diseases that share the most curated genes with Leigh syndrome.
5 View disease cluster →
Mitochondrial complex deficiency 48 shared genesNDUFA10, NDUFA12, NDUFA9, NDUFAF2, NDUFAF6, ND2, NDUFS3, NDUFS2, TTC19, LRPPRC, NDUFA2, TIMMDC1 +36 more Related via 48 shared genes including NDUFA10, NDUFA12, NDUFA9. Mitochondrial disease 72 shared genesHIBCH, TRMU, IARS2, MTRFR, NARS2, NDUFA10, NDUFA12, NDUFA9, NDUFAF2, NDUFAF6, ND2, NDUFS3 +60 more Related via 72 shared genes including HIBCH, TRMU, IARS2. Mitochondrial encephalomyopathy 11 shared genesMTRFR, FARS2, NDUFS2, POLG, DNM1L, SCO2, NDUFV2, LONP1, FBXL4, FOXRED1, MFF Related via 11 shared genes including MTRFR, FARS2, NDUFS2. Cytochrome c oxidase deficiency 11 shared genesLRPPRC, SCO2, SCO1, COX15, SURF1, PET100, COX10, TACO1, COX4I1, COX8A, PET117 Related via 11 shared genes including LRPPRC, SCO2, SCO1. Combined oxidative phosphorylation deficiency 14 shared genesMTRFR, NARS2, PNPT1, EARS2, FARS2, AIFM1, TSFM, MTFMT, TARS2, GTPBP3, GFM2, GFM1 +2 more Related via 14 shared genes including MTRFR, NARS2, PNPT1.