Name

atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; heart diseases; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; heart diseases; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; myocardial ischemia; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; myocardial ischemia; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; diabetes mellitus; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; diabetes mellitus; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrioventricular block; death, sudden; syncope; torsades de pointes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrioventricular block; death, sudden; syncope; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

syncope, vasovagal; vasovagal syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease syncope, vasovagal; vasovagal syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Ventricular from the curated CTD Gene-Disease Associations dataset.

heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Heart Septal Defects, Atrial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Atrial from the curated CTD Gene-Disease Associations dataset.

atrial fibrillation; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Heart Septal Defects, Atrial Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects, Atrial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal death; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; heart diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy; heart failure; sudden death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy; heart failure; sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophy, left ventricular; left ventricular hypertrophy; mitral valve insufficiency; mitral valve prolapse; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, left ventricular; left ventricular hypertrophy; mitral valve insufficiency; mitral valve prolapse; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophy, left ventricular; left ventricular hypertrophy; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, left ventricular; left ventricular hypertrophy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; hypertension; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; hypertension; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Heart Septal Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects from the curated CTD Gene-Disease Associations dataset.

heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Heart Septal Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Septal Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Left ventricular noncompaction 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Left ventricular noncompaction cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Left ventricular noncompaction 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Left ventricular noncompaction 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Left ventricular noncompaction 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Left ventricular noncompaction 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Left ventricular noncompaction 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Left ventricular noncompaction 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dilated cardiomyopathy with left ventricular noncompaction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dilated cardiomyopathy with left ventricular noncompaction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LEFT VENTRICULAR NONCOMPACTION 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEFT VENTRICULAR NONCOMPACTION 2 from the curated CTD Gene-Disease Associations dataset.

LEFT VENTRICULAR NONCOMPACTION 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEFT VENTRICULAR NONCOMPACTION 1 from the curated CTD Gene-Disease Associations dataset.

left ventricular noncompaction 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular trabecula myocardium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ventricular trabecula myocardium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventricular compact myocardium morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ventricular compact myocardium morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventricular myocardium compact layer hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular myocardium compact layer hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrial heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease atrial heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

atrial heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

arrhythmias, cardiac; heart arrest; long qt syndrome; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; heart arrest; long qt syndrome; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart failure; ventricular dysfunction, left; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart failure; ventricular dysfunction, left; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart failure; hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart failure; hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart diseases; hypertension; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart diseases; hypertension; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Sudden cardiac death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sudden infant death syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sudden infant death syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Death, Sudden, Cardiac Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Death, Sudden, Cardiac from the curated CTD Gene-Disease Associations dataset.

Death, Sudden Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Death, Sudden from the curated CTD Gene-Disease Associations dataset.

Sudden Infant Death with Dysgenesis of the Testes Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sudden Infant Death with Dysgenesis of the Testes Syndrome from the curated CTD Gene-Disease Associations dataset.

Sudden Infant Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sudden Infant Death from the curated CTD Gene-Disease Associations dataset.

Death, Sudden, Cardiac Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Death, Sudden, Cardiac in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

sudden infant death syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sudden infant death syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

coronary artery disease; death, sudden; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sids/sudden infant death syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sids/sudden infant death syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac arrhythmias and sudden death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac arrhythmias and sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

staphylococcal infections; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease staphylococcal infections; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden infant death syndrome (sids) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sudden infant death syndrome (sids) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadaver; cardiovascular diseases; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadaver; cardiovascular diseases; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset of sudden infant death. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of sudden infant death. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden; pulmonary embolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long qt syndrome; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long qt syndrome; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism, inborn errors; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipid metabolism, inborn errors; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden infant death syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sudden infant death syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden cardiac death Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sudden cardiac death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

sudden death Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sudden death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

sudden cardiac death Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden cardiac death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sudden death Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Death, Sudden, Cardiac Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Death, Sudden, Cardiac phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Death, Sudden Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Death, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Sudden Infant Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Sudden Infant Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

{sudden infant death syndrome, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {sudden infant death syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

sudden infant death with dysgenesis of the testes syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the sudden infant death with dysgenesis of the testes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Ventricular septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular septal defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inlet ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

left ventricular septal hypertrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the left ventricular septal hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

perimembranous ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the perimembranous ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

perimembraneous ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

inlet ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Atrial septal defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial septal defect 2 from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 4 from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 6 from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 5 from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 1 from the curated CTD Gene-Disease Associations dataset.

secundum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrial septal aneurysm Gene Set

From HPO Gene-Disease Associations

genes associated with the atrial septal aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

primum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the primum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium primum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrial septal aneurysm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrial septal aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium secundum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrial septal defect 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

Syncope Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Syncope from the curated CTD Gene-Disease Associations dataset.

syncope, vasovagal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease syncope, vasovagal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dizziness; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dizziness; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autonomic nervous system diseases; syncope, vasovagal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autonomic nervous system diseases; syncope, vasovagal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

syncope Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term syncope in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

syncope Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the syncope phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

syncope Gene Set

From HPO Gene-Disease Associations

genes associated with the syncope phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Syncope Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Syncope phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Syncope, Vasovagal Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Syncope, Vasovagal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

diabetes complications; hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; left ventricular function; blood pressure; left ventricular structure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; left ventricular function; blood pressure; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic valve insufficiency; aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic valve insufficiency; aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; ventricular fibrillation; ventricular premature complexes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; ventricular fibrillation; ventricular premature complexes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular mass; left ventricular wall thickness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular mass; left ventricular wall thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophy, left ventricular; insulin resistance; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, left ventricular; insulin resistance; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

accelerated idioventricular rhythm; arrhythmias, cardiac; myocardial infarction; reperfusion injury; tachycardia, ventricular; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease accelerated idioventricular rhythm; arrhythmias, cardiac; myocardial infarction; reperfusion injury; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy; blood flow; left ventricular function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy; blood flow; left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; hypertrophy, left ventricular; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; hypertrophy, left ventricular; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus; hypertension; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus; hypertension; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.

atrial fibrillation; brugada syndrome; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; brugada syndrome; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial ventricular junction remodeling Gene Set

From GO Biological Process Annotations

genes participating in the atrial ventricular junction remodeling biological process from the curated GO Biological Process Annotations dataset.

atrial fibrillation/atrial flutter Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation/atrial flutter in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defect Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

noncompaction Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term noncompaction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

noncompaction cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the noncompaction cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

myocardium Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term myocardium in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

pulmonary myocardium development Gene Set

From GO Biological Process Annotations

genes participating in the pulmonary myocardium development biological process from the curated GO Biological Process Annotations dataset.

abnormality of the myocardium Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the myocardium Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal atrium myocardium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal atrium myocardium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick myocardium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick myocardium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized myocardium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized myocardium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricle myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricle myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ventricle myocardium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ventricle myocardium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrium myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrium myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin myocardium Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin myocardium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin myocardium compact layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin myocardium compact layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin ventricle myocardium compact layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin ventricle myocardium compact layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal myocardium compact layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal myocardium compact layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal myocardium layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal myocardium layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

myocardium Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term myocardium in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

myocardium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue myocardium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

pulmonary venous myocardium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue pulmonary venous myocardium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

myocardium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue myocardium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heart Defects, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Defects, Congenital from the curated CTD Gene-Disease Associations dataset.

congenital heart defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dilatation, pathologic; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dilatation, pathologic; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathies; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathies; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Conotruncal heart defects Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Conotruncal heart defects phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Heart Defects, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Heart Defects, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

congenital heart defects, nonsyndromic, 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, congenital heart defects, and posterior embryotoxon Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; heart failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart failure; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart failure; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; hypertension; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; hypertension; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart failure; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart failure; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart failure; inflammation; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart failure; inflammation; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart failure; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart failure; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; heart failure; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; heart failure; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart diseases; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart diseases; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart valve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart valve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart valve diseases; rheumatic heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart valve diseases; rheumatic heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Hearing Loss, Sudden Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Sudden from the curated CTD Gene-Disease Associations dataset.

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden cardiac arrest risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sudden cardiac arrest risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term sudden in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Sudden cardiac arrest Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sudden cardiac arrest phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

sudden episodic apnea Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden episodic apnea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sudden central visual loss Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hearing Loss, Sudden Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Isolated 17,20-lyase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Isolated 17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectopia lentis, isolated autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectopia lentis, isolated autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant isolated somatotropin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Isolated growth hormone deficiency type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Isolated growth hormone deficiency type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sulfite oxidase deficiency, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sulfite oxidase deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Follicle-stimulating hormone deficiency, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Follicle-stimulating hormone deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Laron-type isolated somatotropin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperchlorhidrosis, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperchlorhidrosis, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Digital clubbing, isolated congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Digital clubbing, isolated congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated, with coloboma 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated, with coloboma 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated, with coloboma 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated, with coloboma 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microphthalmia, isolated, with coloboma 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microphthalmia, isolated, with coloboma 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mineralocorticoid deficiency, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Question mark ears, isolated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Question mark ears, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectopia lentis, isolated, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectopia lentis, isolated, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

H2AX complex, isolated from cells without IR exposure Gene Set

From CORUM Protein Complexes

proteins in the H2AX complex, isolated from cells without IR exposure protein complex from the CORUM Protein Complexes dataset.

MICROPHTHALMIA, ISOLATED 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROPHTHALMIA, ISOLATED 5 from the curated CTD Gene-Disease Associations dataset.

MICROPHTHALMIA, ISOLATED 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROPHTHALMIA, ISOLATED 7 from the curated CTD Gene-Disease Associations dataset.

MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6 from the curated CTD Gene-Disease Associations dataset.

Isolated Growth Hormone Deficiency, Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type II from the curated CTD Gene-Disease Associations dataset.

Hypoparathyroidism familial isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoparathyroidism familial isolated from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Coloboma 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 2 from the curated CTD Gene-Disease Associations dataset.

Isolated Growth Hormone Deficiency, Type IB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type IB from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Coloboma 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 5 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated 1 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated 3 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated 4 from the curated CTD Gene-Disease Associations dataset.

ACTH Deficiency, Isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ACTH Deficiency, Isolated from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated 2 from the curated CTD Gene-Disease Associations dataset.

Toenail Dystrophy, Isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toenail Dystrophy, Isolated from the curated CTD Gene-Disease Associations dataset.

Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

Hemihyperplasia, Isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemihyperplasia, Isolated from the curated CTD Gene-Disease Associations dataset.

HYPERCHLORHIDROSIS, ISOLATED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERCHLORHIDROSIS, ISOLATED from the curated CTD Gene-Disease Associations dataset.

ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

Nail dysplasia, isolated congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nail dysplasia, isolated congenital from the curated CTD Gene-Disease Associations dataset.

Cleft Palate, Isolated, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cleft Palate, Isolated, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Cataract 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 2 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Cataract 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 1 from the curated CTD Gene-Disease Associations dataset.

ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset.

Follicle-stimulating hormone deficiency, isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Follicle-stimulating hormone deficiency, isolated from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Coloboma 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 3 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Coloboma 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Coloboma 1 from the curated CTD Gene-Disease Associations dataset.

isolated colobomas or colobomas associated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated colobomas or colobomas associated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypothyroidism; cleft palate, isolated; thyroid agenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypothyroidism; cleft palate, isolated; thyroid agenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with or without cleft palate; cleft palate, isolated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with or without cleft palate; cleft palate, isolated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated gh deficiency (ighd) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated gh deficiency (ighd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated penile hypospadias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated penile hypospadias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term isolated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

microphthalmia, isolated 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia with isolated vitamin e deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia with isolated vitamin e deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?isolated growth hormone deficiency due to defect in ghrf Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

ectopia lentis, isolated, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectopia lentis, isolated, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

agammaglobulinemia and isolated hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the agammaglobulinemia and isolated hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with isolated growth hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with isolated growth hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated, with coloboma 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated, with coloboma 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated, with coloboma 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated, with coloboma 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia, isolated, with coloboma 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia, isolated, with coloboma 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

toenail dystrophy, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the toenail dystrophy, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

preauricular tag, isolated, autosomal dominant, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the preauricular tag, isolated, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

asplenia, isolated congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the asplenia, isolated congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

giant platelet disorder, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the giant platelet disorder, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoparathyroidism, familial isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoparathyroidism, familial isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

17,20-lyase deficiency, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the 17,20-lyase deficiency, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

cleft palate, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleft palate, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

myelokathexis, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the myelokathexis, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

growth hormone deficiency, isolated, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth hormone deficiency, isolated, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

growth hormone deficiency, isolated, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth hormone deficiency, isolated, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

growth hormone deficiency, isolated, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth hormone deficiency, isolated, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

renal hypoplasia, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal hypoplasia, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

follicle-stimulating hormone deficiency, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the follicle-stimulating hormone deficiency, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

invasive pneumococcal disease, recurrent isolated, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the invasive pneumococcal disease, recurrent isolated, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

invasive pneumococcal disease, recurrent isolated, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the invasive pneumococcal disease, recurrent isolated, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperchlorhidrosis, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperchlorhidrosis, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

digital clubbing, isolated congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the digital clubbing, isolated congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

question mark ears, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the question mark ears, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

anosmia, isolated congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the anosmia, isolated congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

death-inducing signaling complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cd95 death-inducing signaling complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cd95 death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cd95 death-inducing signaling complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cd95 death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

death-inducing signaling complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

trail death-inducing signaling complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the trail death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced protein complex from the CORUM Protein Complexes dataset.

Death-inducing signaling complex DISC (type I cells associated), stimulated Gene Set

From CORUM Protein Complexes

proteins in the Death-inducing signaling complex DISC (type I cells associated), stimulated protein complex from the CORUM Protein Complexes dataset.

Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced protein complex from the CORUM Protein Complexes dataset.

Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Death from the curated CTD Gene-Disease Associations dataset.

Fetal Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fetal Death from the curated CTD Gene-Disease Associations dataset.

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.

myocardial infarct; cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac death; cardiac morbidity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac death; cardiac morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

embryo loss; fetal death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal death; pre-eclampsia; pregnancy complications; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; brain death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; brain death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemic neuronal cell death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ischemic neuronal cell death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term death in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

regulation of death-inducing signaling complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations dataset.

regulation of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

negative regulation of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

death-inducing signaling complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations dataset.

negative regulation of neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of neuron death biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

programmed necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

modulation of programmed cell death in other organism Gene Set

From GO Biological Process Annotations

genes participating in the modulation of programmed cell death in other organism biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hydrogen peroxide-mediated programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations dataset.

neuron death Gene Set

From GO Biological Process Annotations

genes participating in the neuron death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

developmental programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the developmental programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

death Gene Set

From GO Biological Process Annotations

genes participating in the death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of neuron death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-mediated programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations dataset.

necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

ectopic germ cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the ectopic germ cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation by symbiont of host programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

cell death Gene Set

From GO Biological Process Annotations

genes participating in the cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

regulation of cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

modulation by symbiont of host programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the modulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations dataset.

modulation of programmed cell death in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the modulation of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

induction of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

host programmed cell death induced by symbiont Gene Set

From GO Biological Process Annotations

genes participating in the host programmed cell death induced by symbiont biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of death-inducing signaling complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations dataset.

autophagic cell death Gene Set

From GO Biological Process Annotations

genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

negative regulation by symbiont of host programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations dataset.

programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the programmed cell death biological process from the curated GO Biological Process Annotations dataset.

death-inducing signaling complex Gene Set

From GO Cellular Component Annotations

proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations dataset.

cd95 death-inducing signaling complex Gene Set

From GO Cellular Component Annotations

proteins localized to the cd95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations dataset.

death receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the death receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

death effector domain binding Gene Set

From GO Molecular Function Annotations

genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations dataset.

death domain binding Gene Set

From GO Molecular Function Annotations

genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations dataset.

death receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the death receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

Aging (time to death) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Aging (time to death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

time of death Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the time of death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

neonatal death Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

death in childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the death in childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

death in infancy Gene Set

From HPO Gene-Disease Associations

genes associated with the death in infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

time of death Gene Set

From HPO Gene-Disease Associations

genes associated with the time of death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

death in early adulthood Gene Set

From HPO Gene-Disease Associations

genes associated with the death in early adulthood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Brain Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Brain Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fetal Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fetal Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Death-like domain of Spt6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-like domain of Spt6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Domain of unknown function DUF2428, death-receptor-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Domain of unknown function DUF2428, death-receptor-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cell death regulator Aven Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cell death regulator Aven protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death-associated protein kinase 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-associated protein kinase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

BH3-interacting domain death agonist Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the BH3-interacting domain death agonist protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death effector domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death effector domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Caffeine-induced death protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Caffeine-induced death protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Programmed cell death protein 2, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Programmed cell death protein 2, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal interdigital cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased activation-induced cell death of t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pregnancy-related premature death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal activation-induced cell death of t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

growth retardation, developmental delay, coarse facies, and early death Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.

death Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term death in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Cell death signalling via NRAGE, NRIF and NADE Gene Set

From Reactome Pathways

proteins participating in the Cell death signalling via NRAGE, NRIF and NADE pathway from the Reactome Pathways dataset.

Stimulation of the cell death response by PAK-2p34 Gene Set

From Reactome Pathways

proteins participating in the Stimulation of the cell death response by PAK-2p34 pathway from the Reactome Pathways dataset.

Death Receptor Signalling Gene Set

From Reactome Pathways

proteins participating in the Death Receptor Signalling pathway from the Reactome Pathways dataset.

TRIF-mediated programmed cell death Gene Set

From Reactome Pathways

proteins participating in the TRIF-mediated programmed cell death pathway from the Reactome Pathways dataset.

NADE modulates death signalling Gene Set

From Reactome Pathways

proteins participating in the NADE modulates death signalling pathway from the Reactome Pathways dataset.

NRIF signals cell death from the nucleus Gene Set

From Reactome Pathways

proteins participating in the NRIF signals cell death from the nucleus pathway from the Reactome Pathways dataset.

NRAGE signals death through JNK Gene Set

From Reactome Pathways

proteins participating in the NRAGE signals death through JNK pathway from the Reactome Pathways dataset.

Programmed Cell Death Gene Set

From Reactome Pathways

proteins participating in the Programmed Cell Death pathway from the Reactome Pathways dataset.

septal nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in septal nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

septal nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in septal nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermedio-ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermedio-ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermediate part, periventricular Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermediate part, periventricular relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus, caudal (caudodorsal) part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus, caudal (caudodorsal) part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

triangular septal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in triangular septal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medial septal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medial septal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lambdoid septal zone Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lambdoid septal zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal complex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal complex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Medial septal complex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Medial septal complex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermedio-dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermedio-dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermedio-intermediate part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermedio-intermediate part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus, rostral (rostroventral) part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus, rostral (rostroventral) part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral septal nucleus, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral septal nucleus, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

medial septal nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in medial septal nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in septal region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in septal region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

septal organ Gene Set

From BioGPS Mouse Cell Type and Tissue Gene Expression Profiles

genes with high or low expression in septal organ relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.

Dandy-Walker like malformation with atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

septal periplasm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the septal periplasm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset.

Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome from the curated CTD Gene-Disease Associations dataset.

septal myocardial infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease septal myocardial infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atrioventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pronounced septal hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pronounced septal hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

septal Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term septal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

absent nasal septal cartilage Gene Set

From HPO Gene-Disease Associations

genes associated with the absent nasal septal cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric septal hypertrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetric septal hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

partial atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle with atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aorticopulmonary septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

complete atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{atrioventricular septal defect, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{atrioventricular septal defect, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

lateral septal area Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue lateral septal area in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

ventral septal area Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ventral septal area in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

septal area Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue septal area in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Forebrain defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Forebrain defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Neural Tube Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neural Tube Defects from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Laterality Defects, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Laterality Defects, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.

Color Vision Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Color Vision Defects from the curated CTD Gene-Disease Associations dataset.

cleft palate and calvaria defects. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft palate and calvaria defects. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; dihydropyrimidine dehydrogenase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; dihydropyrimidine dehydrogenase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

axial skeletal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease axial skeletal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left-right laterality defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left-right laterality defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects and preeclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects and preeclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

visual field defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease visual field defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defects Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term defects in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

progressive visual field defects Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lung segmentation defects Gene Set

From HPO Gene-Disease Associations

genes associated with the lung segmentation defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary valve defects Gene Set

From HPO Gene-Disease Associations

genes associated with the pulmonary valve defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mitochondrial respiratory chain defects Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial respiratory chain defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symmetrical, oval parietal bone defects Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical, oval parietal bone defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

forearm reduction defects Gene Set

From HPO Gene-Disease Associations

genes associated with the forearm reduction defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric, linear skin defects Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetric, linear skin defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Endocardial Cushion Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Endocardial Cushion Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Color Vision Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Color Vision Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neural Tube Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neural Tube Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

forebrain defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the forebrain defects phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, folate-sensitive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, folate-sensitive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.

combined cellular and humoral immune defects with granulomas Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined cellular and humoral immune defects with granulomas phenotype from the curated OMIM Gene-Disease Associations dataset.

neural tube defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the neural tube defects phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Defects in cobalamin (B12) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in cobalamin (B12) metabolism pathway from the Reactome Pathways dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Defects in biotin (Btn) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in biotin (Btn) metabolism pathway from the Reactome Pathways dataset.

ventricular (matrix) zone of pons Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in ventricular (matrix) zone of pons relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

ventricular (matrix) zone of cerebellum Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in ventricular (matrix) zone of cerebellum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Catecholaminergic polymorphic ventricular tachycardia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Catecholaminergic polymorphic ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal familial ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular tachycardia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular fibrillation, paroxysmal familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular tachycardia, catecholaminergic polymorphic, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertrophy, Left Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrophy, Left Ventricular from the curated CTD Gene-Disease Associations dataset.

Paroxysmal ventricular fibrillation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal ventricular fibrillation from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 from the curated CTD Gene-Disease Associations dataset.

Ventricular Premature Complexes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Premature Complexes from the curated CTD Gene-Disease Associations dataset.

Ventricular Dysfunction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Dysfunction from the curated CTD Gene-Disease Associations dataset.

Ventricular Fibrillation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Fibrillation from the curated CTD Gene-Disease Associations dataset.

Hypertrophy, Right Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrophy, Right Ventricular from the curated CTD Gene-Disease Associations dataset.

Ventricular Outflow Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Outflow Obstruction from the curated CTD Gene-Disease Associations dataset.

Ventricular Remodeling Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Remodeling from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Ventricular Dysfunction, Left Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Dysfunction, Left from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.

Polymorphic catecholergic ventricular tachycardia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polymorphic catecholergic ventricular tachycardia from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

Ventricular Dysfunction, Right Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Dysfunction, Right from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Tachycardia, Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tachycardia, Ventricular from the curated CTD Gene-Disease Associations dataset.

Hypertrophy, Left Ventricular Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Hypertrophy, Left Ventricular in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Ventricular Function, Left Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Ventricular Function, Left in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease arrhythmogenic right ventricular cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease arrhythmogenic right ventricular cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; left ventricular function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; left ventricular mass; aortic gradient; aortic valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; left ventricular mass; aortic gradient; aortic valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disease models, animal; hypertension; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disease models, animal; hypertension; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; left ventricular mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension and left ventricular mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension and left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular cardiomyopathy/dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular cardiomyopathy/dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; recurrence; shock; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; recurrence; shock; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired left ventricular function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease impaired left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; cardiomyopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; cardiomyopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular mass; renin activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular mass; renin activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; hypertension; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; hypertension; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ventricular arrhythmia, malignant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ventricular arrhythmia, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; ventricular premature complexes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; ventricular premature complexes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy; sodium, urinary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy; sodium, urinary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; hypertrophy, left ventricular; leopard syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; hypertrophy, left ventricular; leopard syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; left ventricular structure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ventricular assist devices complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ventricular assist devices complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatigue; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; inflammation; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; inflammation; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ventricular function, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ventricular function, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophy, left ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular mass in male athletes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular mass in male athletes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypercholesterolemia; myocardial infarction; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypercholesterolemia; myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular structure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary stenosis; hypertrophy, left ventricular; sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary stenosis; hypertrophy, left ventricular; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; ventricular remodeling Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

the extent of exercise-induced left ventricular growth in endurance athletes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease the extent of exercise-induced left ventricular growth in endurance athletes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ventricular Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ventricular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Ventricular hypertrophy_Myocardial tissue_GSE4678 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Ventricular hypertrophy_Myocardial tissue_GSE4678 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Arrhythmogenic Right Ventricular Cardiomyopathy_Myocardial tissue_GSE4120 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Arrhythmogenic Right Ventricular Cardiomyopathy_Myocardial tissue_GSE4120 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

OTX2_KO_GSE27630_51_mouse_brain (fourth ventricular choroid plexus, E13) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the OTX2_KO_GSE27630_51_mouse_brain (fourth ventricular choroid plexus, E13) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

Otx2_KO_GDS4440_143_mouse_fourth ventricular choroid plexus tissue Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the Otx2_KO_GDS4440_143_mouse_fourth ventricular choroid plexus tissue gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

OTX2_KO_GDS4440_424_mouse_brain (fourth ventricular choroid plexus) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the OTX2_KO_GDS4440_424_mouse_brain (fourth ventricular choroid plexus) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

forebrain ventricular zone progenitor cell division Gene Set

From GO Biological Process Annotations

genes participating in the forebrain ventricular zone progenitor cell division biological process from the curated GO Biological Process Annotations dataset.

negative regulation of planar cell polarity pathway involved in ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of planar cell polarity pathway involved in ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

purkinje myocyte to ventricular cardiac muscle cell communication Gene Set

From GO Biological Process Annotations

genes participating in the purkinje myocyte to ventricular cardiac muscle cell communication biological process from the curated GO Biological Process Annotations dataset.

regulation of ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations dataset.

positive regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

ventricular system development Gene Set

From GO Biological Process Annotations

genes participating in the ventricular system development biological process from the curated GO Biological Process Annotations dataset.

regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

right ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the right ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle cell differentiation biological process from the curated GO Biological Process Annotations dataset.

ventricular septum development Gene Set

From GO Biological Process Annotations

genes participating in the ventricular septum development biological process from the curated GO Biological Process Annotations dataset.

regulation of ventricular cardiac muscle cell membrane depolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ventricular cardiac muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations dataset.

ventricular zone neuroblast division Gene Set

From GO Biological Process Annotations

genes participating in the ventricular zone neuroblast division biological process from the curated GO Biological Process Annotations dataset.

planar cell polarity pathway involved in ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the planar cell polarity pathway involved in ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

left ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the left ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of planar cell polarity pathway involved in ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of planar cell polarity pathway involved in ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

negative regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac myofibril assembly Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac myofibril assembly biological process from the curated GO Biological Process Annotations dataset.

ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

purkinje myocyte to ventricular cardiac muscle cell signaling Gene Set

From GO Biological Process Annotations

genes participating in the purkinje myocyte to ventricular cardiac muscle cell signaling biological process from the curated GO Biological Process Annotations dataset.

regulation of ventricular cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ventricular cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle cell development Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle cell development biological process from the curated GO Biological Process Annotations dataset.

ventricular cardiac muscle tissue development Gene Set

From GO Biological Process Annotations

genes participating in the ventricular cardiac muscle tissue development biological process from the curated GO Biological Process Annotations dataset.

voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

Left ventricular mass Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Left ventricular mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Total ventricular volume Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Total ventricular volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

ventricular fibrillation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the ventricular fibrillation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

ventricular arrhythmia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the ventricular arrhythmia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

ventricular hypertrophy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the ventricular hypertrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the left ventricular outflow tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

left ventricular hypertrophy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the left ventricular hypertrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

impaired left ventricular function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the impaired left ventricular function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

ventricular extrasystoles Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular extrasystoles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ventricular septum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the ventricular septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular preexcitation with multiple accessory pathways Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular preexcitation with multiple accessory pathways phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular hypertrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the right ventricular hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal ventricular tachycardia Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal ventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular failure Gene Set

From HPO Gene-Disease Associations

genes associated with the right ventricular failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular cardiomyopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the right ventricular cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the left ventricular outflow tract Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the left ventricular outflow tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular fibrillation Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular fibrillation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

left ventricular hypertrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the left ventricular hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular dilatation Gene Set

From HPO Gene-Disease Associations

genes associated with the right ventricular dilatation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired left ventricular function Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired left ventricular function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular hypertrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular outlet obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the right ventricular outlet obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular escape rhythms Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular escape rhythms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular tachycardia Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular arrhythmia Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular arrhythmia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

episodes of ventricular tachycardia Gene Set

From HPO Gene-Disease Associations

genes associated with the episodes of ventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bidirectional ventricular ectopy Gene Set

From HPO Gene-Disease Associations

genes associated with the bidirectional ventricular ectopy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

effort-induced polymorphic ventricular tachycardias Gene Set

From HPO Gene-Disease Associations

genes associated with the effort-induced polymorphic ventricular tachycardias phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular aneurysm Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular preexcitation Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular preexcitation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hypertrophy, Left Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hypertrophy, Left Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Premature Complexes Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Premature Complexes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Dysfunction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Fibrillation Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Fibrillation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hypertrophy, Right Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hypertrophy, Right Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Outflow Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Outflow Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Dysfunction, Left Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Dysfunction, Left phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Tachycardia, Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Tachycardia, Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Dysfunction, Right Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Dysfunction, Right phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Arrhythmogenic Right Ventricular Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

ventricular premature beat Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular premature beat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular fibrillation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular fibrillation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain ventricular system morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain ventricular system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular tachycardia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular tachycardia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle, ventricular defect committed to aorta Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular cardiomyopathy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cortical ventricular zone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cortical ventricular zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube ventricular layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube ventricular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick ventricular wall Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick ventricular wall phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin ventricular wall Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin ventricular wall phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular aneurysm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular fibrillation, paroxysmal familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, idiopathic Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular fibrillation, familial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular fibrillation, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term ventricular in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

ventricular zone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ventricular zone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) pathway from the Wikipathways Pathways dataset.

ventricular tachycardia; hypertrophic cardiomyopathy Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease ventricular tachycardia; hypertrophic cardiomyopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

ventricular tachycardia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease ventricular tachycardia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Paroxysmal atrial fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal atrial fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.