×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
Biomarker
CTD_human
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Hereditary cardiovascular dysplasia. A form of familial cardiomyopathy.
13732753
1961
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Child abuse and neglect: a study of cases reported to Douglas County Child Protective Service from 1967-1973.
1186938
1975
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product.
2249844
1990
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
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
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.
1975599
1990
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
UNIPROT
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
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes.
1944483
1991
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
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
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.
1430197
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
UNIPROT
Novel missense mutation in cardiac beta myosin heavy chain gene found in a Japanese patient with hypertrophic cardiomyopathy.
1417858
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
UNIPROT
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
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Expression of a missense mutation in the messenger RNA for beta-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy.
1634614
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Accumulation and assembly of myosin in hypertrophic cardiomyopathy with the 403 Arg to Gln beta-myosin heavy chain mutation.
1423936
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.
1552912
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.
1739523
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
UNIPROT
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy.
1552912
1992
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.
8254035
1993
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy.
8514894
1993
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy.
8268932
1993
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.
8483915
1993
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
GeneticVariation
CLINVAR
Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.
8483915
1993
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.
8435239
1993
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.
8250038
1993
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
0.700
CausalMutation
CLINVAR
Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene.
8335820
1993