Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Polymorphic catecholergic ventricular tachycardia RYR2 disease C1631597 Biomarker 1 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia RYR2 disease C1631597 CausalMutation 1 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia RYR2 disease C1631597 AlteredExpression 1 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia RYR2 disease C1631597 GeneticVariation 1 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CALM1 disease C1631597 Biomarker 0.74 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CALM1 disease C1631597 GermlineCausalMutation 0.74 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia TRDN disease C1631597 CausalMutation 0.74 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia TRDN disease C1631597 Biomarker 0.74 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CALM1 disease C1631597 GeneticVariation 0.74 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia TRDN disease C1631597 GeneticVariation 0.74 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia TRDN disease C1631597 GermlineCausalMutation 0.74 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CASQ2 disease C1631597 GeneticVariation 0.7 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CASQ2 disease C1631597 Biomarker 0.7 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CASQ2 disease C1631597 CausalMutation 0.7 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia TECRL disease C1631597 GeneticVariation 0.52 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia TECRL disease C1631597 Biomarker 0.52 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia TECRL disease C1631597 GermlineCausalMutation 0.52 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia KCNJ2 disease C1631597 GeneticVariation 0.36 disgenet
Polymorphic catecholergic ventricular tachycardia KCNJ2 disease C1631597 Biomarker 0.36 disgenet
Polymorphic catecholergic ventricular tachycardia CALM3 disease C1631597 Biomarker 0.34 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CALM3 disease C1631597 GeneticVariation 0.34 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CALM2 disease C1631597 GeneticVariation 0.34 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia CALM2 disease C1631597 Biomarker 0.34 orphanet , disgenet
Polymorphic catecholergic ventricular tachycardia ANK2 disease C1631597 GeneticVariation 0.32 disgenet
Polymorphic catecholergic ventricular tachycardia ANK2 disease C1631597 Biomarker 0.32 disgenet
Polymorphic catecholergic ventricular tachycardia KCNE1 disease C1631597 Biomarker 0.31 disgenet
Polymorphic catecholergic ventricular tachycardia FKBP1B disease C1631597 GeneticVariation 0.21 disgenet
Polymorphic catecholergic ventricular tachycardia FKBP1B disease C1631597 Biomarker 0.21 disgenet
Polymorphic catecholergic ventricular tachycardia TRDN-AS1 disease C1631597 CausalMutation 0.1 disgenet
Polymorphic catecholergic ventricular tachycardia TRDN-AS1 disease C1631597 GeneticVariation 0.1 disgenet
Polymorphic catecholergic ventricular tachycardia SCN5A disease C1631597 GeneticVariation 0.04 disgenet
Polymorphic catecholergic ventricular tachycardia KCNH2 disease C1631597 GeneticVariation 0.04 disgenet
Polymorphic catecholergic ventricular tachycardia KCNH2 disease C1631597 Biomarker 0.04 disgenet
Polymorphic catecholergic ventricular tachycardia KCNQ1 disease C1631597 Biomarker 0.04 disgenet
Polymorphic catecholergic ventricular tachycardia KCNQ1 disease C1631597 GeneticVariation 0.04 disgenet
Polymorphic catecholergic ventricular tachycardia SCN5A disease C1631597 Biomarker 0.04 disgenet
Polymorphic catecholergic ventricular tachycardia ARVD3 disease C1631597 Biomarker 0.02 disgenet
Polymorphic catecholergic ventricular tachycardia ARVD3 disease C1631597 GeneticVariation 0.02 disgenet
Polymorphic catecholergic ventricular tachycardia RYR1 disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia CNTN3 disease C1631597 Biomarker 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia CACNA1S disease C1631597 Biomarker 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia CTRL disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia ASPH disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia CAVIN1 disease C1631597 Biomarker 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia KRIT1 disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia FXN disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia AIP disease C1631597 Biomarker 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia SNAP91 disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia SCN10A disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia THEM5 disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia CAMKMT disease C1631597 GeneticVariation 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia KCNE2 disease C1631597 Biomarker 0.01 disgenet
Polymorphic catecholergic ventricular tachycardia PICALM disease C1631597 GeneticVariation 0.01 disgenet
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