Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Familial neurocardiogenic syncope AVP disease C1836438 Biomarker 0.02 disgenet
Familial neurocardiogenic syncope NOS3 disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope MBL2 disease C1836438 GeneticVariation 0.01 disgenet
Familial neurocardiogenic syncope EDN1 disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope GPR174 disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope TNF disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope PRKCE disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope CD59 disease C1836438 GeneticVariation 0.01 disgenet
Familial neurocardiogenic syncope GNAS disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope ADM disease C1836438 AlteredExpression 0.01 disgenet
Familial neurocardiogenic syncope ACE disease C1836438 GeneticVariation 0.01 disgenet
Familial neurocardiogenic syncope NPY disease C1836438 AlteredExpression 0.01 disgenet
Familial neurocardiogenic syncope NLRP3 disease C1836438 GeneticVariation 0.01 disgenet
Familial neurocardiogenic syncope SLC6A2 disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope ARIH1 disease C1836438 Biomarker 0.01 disgenet
Familial neurocardiogenic syncope GNG2 disease C1836438 Biomarker 0.01 disgenet
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