Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4021662
Disease: Abnormal endocardium morphology
Abnormal endocardium morphology 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4021546
Disease: Abnormal mitochondria in muscle tissue
Abnormal mitochondria in muscle tissue 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4023612
Disease: Abnormality of cellular immune system
Abnormality of cellular immune system 		0.100 GeneticVariation CLINVAR

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4023166
Disease: Abnormality of T cell physiology
Abnormality of T cell physiology 		0.100 GeneticVariation CLINVAR

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4025785
Disease: Abnormality of the foot musculature
Abnormality of the foot musculature 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		0.100 GeneticVariation CLINVAR

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4024604
Disease: Amyotrophy of ankle musculature
Amyotrophy of ankle musculature 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0151942
Disease: Arterial thrombosis
Arterial thrombosis 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.430 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015

2018
Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.430 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C1843697
Disease: Axial muscle weakness
Axial muscle weakness 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0231616
Disease: Beevor's sign
Beevor's sign 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C1839666
Disease: Calf muscle pseudohypertrophy
Calf muscle pseudohypertrophy 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		0.100 Biomarker HPO

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.500 GeneticVariation CLINVAR

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.500 CausalMutation CLINVAR

Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		0.490 GeneticVariation CLINVAR Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure. 21750094

2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		0.490 CausalMutation CLINVAR Haplotype sharing test maps genes for familial cardiomyopathies. 20573160

2011