Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Cardiomyopathy, Familial Hypertrophic, 2 TNNT2 disease C1861864 CausalMutation 0.9 disgenet
Cardiomyopathy, Familial Hypertrophic, 2 TNNT2 disease C1861864 GeneticVariation 0.9 disgenet
Cardiomyopathy, Familial Hypertrophic, 2 TNNT2 disease C1861864 Biomarker 0.9 disgenet
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