Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Mitochondrial Complex II Deficiency SDHD disease C1855008 Biomarker 0.72 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHD disease C1855008 GeneticVariation 0.72 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHD disease C1855008 CausalMutation 0.72 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHD disease C1855008 GermlineCausalMutation 0.72 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHAF1 disease C1855008 GermlineCausalMutation 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHAF1 disease C1855008 GeneticVariation 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHA disease C1855008 CausalMutation 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHAF1 disease C1855008 CausalMutation 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHAF1 disease C1855008 Biomarker 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHA disease C1855008 GermlineCausalMutation 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHA disease C1855008 Biomarker 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHA disease C1855008 GeneticVariation 0.7 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHB disease C1855008 GeneticVariation 0.33 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHB disease C1855008 GermlineCausalMutation 0.33 orphanet , disgenet
Mitochondrial Complex II Deficiency SDHB disease C1855008 Biomarker 0.33 orphanet , disgenet
Mitochondrial Complex II Deficiency SORD disease C1855008 Biomarker 0.02 disgenet
Mitochondrial Complex II Deficiency SDS disease C1855008 GeneticVariation 0.02 disgenet
Mitochondrial Complex II Deficiency SORD disease C1855008 GeneticVariation 0.02 disgenet
Mitochondrial Complex II Deficiency SDS disease C1855008 Biomarker 0.02 disgenet
Mitochondrial Complex II Deficiency SARDH disease C1855008 GeneticVariation 0.02 disgenet
Mitochondrial Complex II Deficiency SARDH disease C1855008 Biomarker 0.02 disgenet
Mitochondrial Complex II Deficiency HTT disease C1855008 Biomarker 0.01 disgenet
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