Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Ataxia with vitamin E deficiency TTPA disease C1848533 GermlineCausalMutation 1 orphanet , disgenet
Ataxia with vitamin E deficiency TTPA disease C1848533 Biomarker 1 orphanet , disgenet
Ataxia with vitamin E deficiency TTPA disease C1848533 CausalMutation 1 orphanet , disgenet
Ataxia with vitamin E deficiency TTPA disease C1848533 GeneticVariation 1 orphanet , disgenet
Ataxia with vitamin E deficiency APOA1 disease C1848533 Biomarker 0.3 disgenet
Ataxia with vitamin E deficiency APOB disease C1848533 Biomarker 0.3 disgenet
Ataxia with vitamin E deficiency FXN disease C1848533 Biomarker 0.05 disgenet
Ataxia with vitamin E deficiency FXN disease C1848533 GeneticVariation 0.05 disgenet
Ataxia with vitamin E deficiency ZFP36 disease C1848533 GeneticVariation 0.03 disgenet
Ataxia with vitamin E deficiency SH3BP4 disease C1848533 GeneticVariation 0.03 disgenet
Ataxia with vitamin E deficiency APTX disease C1848533 GeneticVariation 0.02 disgenet
Ataxia with vitamin E deficiency SETX disease C1848533 Biomarker 0.02 disgenet
Ataxia with vitamin E deficiency SETX disease C1848533 GeneticVariation 0.02 disgenet
Ataxia with vitamin E deficiency APTX disease C1848533 Biomarker 0.02 disgenet
Ataxia with vitamin E deficiency MTHFR disease C1848533 GeneticVariation 0.01 disgenet
Ataxia with vitamin E deficiency COPRS disease C1848533 GeneticVariation 0.01 disgenet
Ataxia with vitamin E deficiency COQ8A disease C1848533 GeneticVariation 0.01 disgenet
Ataxia with vitamin E deficiency NOS3 disease C1848533 GeneticVariation 0.01 disgenet
Ataxia with vitamin E deficiency SRR disease C1848533 Biomarker 0.01 disgenet
Ataxia with vitamin E deficiency AFP disease C1848533 Biomarker 0.01 disgenet
Ataxia with vitamin E deficiency GNB3 disease C1848533 GeneticVariation 0.01 disgenet
Ataxia with vitamin E deficiency TNF disease C1848533 AlteredExpression 0.01 disgenet
Ataxia with vitamin E deficiency RRS1 disease C1848533 Biomarker 0.01 disgenet
Ataxia with vitamin E deficiency IL6 disease C1848533 AlteredExpression 0.01 disgenet
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