×
Entrez Id:
84676
Gene Symbol:
TRIM63
TRIM63
Hypertrophic Cardiomyopathy
0.640
GeneticVariation
CLINVAR
×
Entrez Id:
7134
Gene Symbol:
TNNC1
TNNC1
Hypertrophic Cardiomyopathy
0.500
CausalMutation
CLINVAR
×
Entrez Id:
4634
Gene Symbol:
MYL3
MYL3
Hypertrophic Cardiomyopathy
0.480
CausalMutation
CLINVAR
×
Entrez Id:
3920
Gene Symbol:
LAMP2
LAMP2
Hypertrophic Cardiomyopathy
0.400
GeneticVariation
CLINVAR
×
Entrez Id:
291
Gene Symbol:
SLC25A4
SLC25A4
Hypertrophic Cardiomyopathy
0.400
CausalMutation
CLINVAR
×
Entrez Id:
6016
Gene Symbol:
RIT1
RIT1
Hypertrophic Cardiomyopathy
0.130
CausalMutation
CLINVAR
×
Entrez Id:
1829
Gene Symbol:
DSG2
DSG2
Hypertrophic Cardiomyopathy
0.110
CausalMutation
CLINVAR
×
Entrez Id:
6584
Gene Symbol:
SLC22A5
SLC22A5
Hypertrophic Cardiomyopathy
0.100
CausalMutation
CLINVAR
×
Entrez Id:
846
Gene Symbol:
CASR
CASR
Hypertrophic Cardiomyopathy
0.100
GeneticVariation
CLINVAR
×
Entrez Id:
23203
Gene Symbol:
PMPCA
PMPCA
Hypertrophic Cardiomyopathy
0.100
CausalMutation
CLINVAR
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
1430197
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.
1552912
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation.
1638703
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes.
1944483
1991
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.
1975517
1990
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Central serotonergic S2 binding in Papio anubis measured in vivo with N-omega-[18F]fluoroethylketanserin and PET.
2062450
1991
×
Entrez Id:
4607
Gene Symbol:
MYBPC3
MYBPC3
Hypertrophic Cardiomyopathy
0.700
CausalMutation
CLINVAR
Splicing of messenger RNA precursors.
2943217
1986
×
Entrez Id:
7137
Gene Symbol:
TNNI3
TNNI3
Hypertrophic Cardiomyopathy
0.700
GeneticVariation
CLINVAR
Orthotic services: a need for change.
3144325
1988
×
Entrez Id:
4607
Gene Symbol:
MYBPC3
MYBPC3
Hypertrophic Cardiomyopathy
0.700
CausalMutation
CLINVAR
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.
7493025
1995
×
Entrez Id:
4607
Gene Symbol:
MYBPC3
MYBPC3
Hypertrophic Cardiomyopathy
0.700
GeneticVariation
CLINVAR
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.
7493025
1995
×
Entrez Id:
4607
Gene Symbol:
MYBPC3
MYBPC3
Hypertrophic Cardiomyopathy
0.700
CausalMutation
CLINVAR
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.
7493026
1995
×
Entrez Id:
2717
Gene Symbol:
GLA
GLA
Hypertrophic Cardiomyopathy
0.200
CausalMutation
CLINVAR
Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease.
7504405
1993
RPL36A-HNRNPH2
Hypertrophic Cardiomyopathy
0.100
CausalMutation
CLINVAR
Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease.
7504405
1993
×
Entrez Id:
2717
Gene Symbol:
GLA
GLA
Hypertrophic Cardiomyopathy
0.200
GeneticVariation
CLINVAR
Galactose stabilizes various missense mutants of alpha-galactosidase in Fabry disease.
7575533
1995
RPL36A-HNRNPH2
Hypertrophic Cardiomyopathy
0.100
GeneticVariation
CLINVAR
Galactose stabilizes various missense mutants of alpha-galactosidase in Fabry disease.
7575533
1995