Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Cardiomyopathy, Familial Restrictive, 1 TNNI3 disease C1861861 CausalMutation 0.8 disgenet
Cardiomyopathy, Familial Restrictive, 1 TNNI3 disease C1861861 AlteredExpression 0.8 disgenet
Cardiomyopathy, Familial Restrictive, 1 TNNI3 disease C1861861 GeneticVariation 0.8 disgenet
Cardiomyopathy, Familial Restrictive, 1 TNNI3 disease C1861861 Biomarker 0.8 disgenet
Cardiomyopathy, Familial Restrictive, 1 CRYAB disease C1861861 CausalMutation 0.11 disgenet
Cardiomyopathy, Familial Restrictive, 1 CRYAB disease C1861861 GeneticVariation 0.11 disgenet
Cardiomyopathy, Familial Restrictive, 1 DES disease C1861861 Biomarker 0.04 disgenet
Cardiomyopathy, Familial Restrictive, 1 DES disease C1861861 GeneticVariation 0.04 disgenet
Cardiomyopathy, Familial Restrictive, 1 FLNC disease C1861861 Biomarker 0.03 disgenet
Cardiomyopathy, Familial Restrictive, 1 FLNC disease C1861861 GeneticVariation 0.03 disgenet
Cardiomyopathy, Familial Restrictive, 1 MYBPC3 disease C1861861 GeneticVariation 0.02 disgenet
Cardiomyopathy, Familial Restrictive, 1 MYBPC3 disease C1861861 Biomarker 0.02 disgenet
Cardiomyopathy, Familial Restrictive, 1 ACTB disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 PRKCB disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 ACE disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 BAG3 disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 ACTC1 disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 REN disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 AGT disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 FOXM1 disease C1861861 Biomarker 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 MYL2 disease C1861861 Biomarker 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 RBM20 disease C1861861 Biomarker 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 MYL3 disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 MYH7 disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 PRKCA disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 MYPN disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 PRRT2 disease C1861861 GeneticVariation 0.01 disgenet
Cardiomyopathy, Familial Restrictive, 1 TNNT2 disease C1861861 Biomarker 0.01 disgenet
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