Melas syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
MELAS SYNDROME
C0162671
NDUFS1 Causal — Disgenet
POLG Causal — Disgenet
All18 Causal2 Unknown16
Related Diseases Diseases that share the most curated genes with Melas syndrome.
5 View disease cluster →
Leber hereditary optic neuropathy 15 shared genesIL1A, IL1B, ND1, ND2, SOD2, ATP6, ND6, COX3, ATP8, COX1, ND5, COX2 +3 more Related via 15 shared genes including IL1A, IL1B, ND1. Neuropathy, ataxia, and retinitis pigmentosa 10 shared genesND1, ND2, ATP6, COX3, ATP8, COX1, ND5, COX2, ND3, ND4 Related via 10 shared genes including ND1, ND2, ATP6. Cleft palate and bilateral cleft lip 10 shared genesND1, ND2, ATP6, COX3, ATP8, COX1, ND5, COX2, ND3, ND4 Related via 10 shared genes including ND1, ND2, ATP6. Postaxial polydactyly 10 shared genesND1, ND2, ATP6, COX3, ATP8, COX1, ND5, COX2, ND3, ND4 Related via 10 shared genes including ND1, ND2, ATP6. Rod-cone dystrophy 10 shared genesND1, ND2, ATP6, COX3, ATP8, COX1, ND5, COX2, ND3, ND4 Related via 10 shared genes including ND1, ND2, ATP6.