×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy.
29907873
2018
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience.
29497013
2018
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Hypertrophic cardiomyopathy disease results from disparate impairments of cardiac myosin function and auto-inhibition.
30275503
2018
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel.
29300372
2018
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel.
29300372
2018
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.
27841901
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Biophysical properties of human β-cardiac myosin with converter mutations that cause hypertrophic cardiomyopathy.
28246639
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Effects of myosin variants on interacting-heads motif explain distinct hypertrophic and dilated cardiomyopathy phenotypes.
28606303
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Molecular mechanisms and structural features of cardiomyopathy-causing troponin T mutants in the tropomyosin overlap region.
28973951
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.
29255176
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Hypertrophic Cardiomyopathy Without Ventricular Hypertrophy: Usefulness of Genetic and Pathological Study in Preventing Sudden Death.
28073646
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Life-long tailoring of management for patients with hypertrophic cardiomyopathy : Awareness and decision-making in changing scenarios.
28005231
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Identification of a novel hypertrophic cardiomyopathy-associated mutation using targeted next-generation sequencing.
28498465
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors.
28202948
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.
28449774
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy: Revisiting the Gene-Dose Effect.
28420666
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy.
29029073
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage.
29121657
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Genetic anticipation in a special form of hypertrophic cardiomyopathy with sudden cardiac death in a family with 74 members across 5 generations.
28296734
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing.
28790153
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Hypertrophic Cardiomyopathy
0.800
GeneticVariation
CLINVAR
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
27532257
2017
×
Entrez Id:
7139
Gene Symbol:
TNNT2
TNNT2
Hypertrophic Cardiomyopathy
0.800
CausalMutation
CLINVAR
Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models.
28735292
2017