Disease Information |
Disease Name |
Gene Name |
Type |
UMLS |
Association Type |
Score |
Source |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYH7 |
disease |
C3495498 |
Biomarker |
0.7 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYH7 |
disease |
C3495498 |
GeneticVariation |
0.7 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYH7 |
disease |
C3495498 |
CausalMutation |
0.7 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
CAV3 |
disease |
C3495498 |
Biomarker |
0.6 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYLK2 |
disease |
C3495498 |
Biomarker |
0.6 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYLK2 |
disease |
C3495498 |
GeneticVariation |
0.6 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
CAV3 |
disease |
C3495498 |
GeneticVariation |
0.6 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYH6 |
disease |
C3495498 |
CausalMutation |
0.4 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYH6 |
disease |
C3495498 |
Biomarker |
0.4 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYL3 |
disease |
C3495498 |
GeneticVariation |
0.1 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
MYBPC3 |
disease |
C3495498 |
CausalMutation |
0.1 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
TNNT2 |
disease |
C3495498 |
GeneticVariation |
0.1 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
CACNA1C |
disease |
C3495498 |
GeneticVariation |
0.1 |
disgenet |
Cardiomyopathy, Familial Hypertrophic, 1 |
CALR3 |
disease |
C3495498 |
CausalMutation |
0.1 |
disgenet |
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