Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFS8 disease C1838951 Biomarker 0.5 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFA9 disease C1838951 Biomarker 0.5 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFS3 disease C1838951 Biomarker 0.5 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFA12 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFS7 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFV2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency IARS2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency SUCLG1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NARS2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFV1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency TTC19 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency GFM1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency PET117 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency FARS2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency LRPPRC disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFA10 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency SUCLA2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency BCS1L disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFA1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency GFM2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency COX15 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency FOXRED1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency SLC19A3 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency COX10 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency UQCRQ disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency SURF1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFS1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency TACO1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency SCO2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFS4 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency PDHA1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency PTCD3 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency ETHE1 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFAF6 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency SDHA disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency PET100 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency NDUFA2 disease C1838951 Biomarker 0.3 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency ND6 disease C1838951 CausalMutation 0.1 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency ND2 disease C1838951 CausalMutation 0.1 disgenet
Leigh Syndrome Due To Mitochondrial Complex I Deficiency ND5 disease C1838951 CausalMutation 0.1 disgenet
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