Name

Familial Ventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET 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.

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.

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; 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.

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.

long qt syndrome; sinus tachycardia; tachycardia, sinus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long qt syndrome; sinus tachycardia; tachycardia, sinus 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.

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.

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.

Ventricular tachycardia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular tachycardia 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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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 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.

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 Ventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Paroxysmal Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Sustained Ventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Sustained Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Stress-Induced Polymorphic Ventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Stress-Induced Polymorphic Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Tachycardia, Polymorphic Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Tachycardia, Polymorphic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Induced Ventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Induced Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Non-Sustained Ventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Non-Sustained Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Polymorphic Ventricular Tachycardia By Ecg Finding Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Polymorphic Ventricular Tachycardia By Ecg Finding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

ventricular tachycardia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular tachycardia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Catecholaminergic polymorphic ventricular tachycardia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Catecholaminergic polymorphic ventricular tachycardia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Catecholaminergic polymorphic ventricular tachycardia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Catecholaminergic polymorphic ventricular tachycardia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Catecholaminergic polymorphic ventricular tachycardia 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Catecholaminergic polymorphic ventricular tachycardia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Catecholaminergic polymorphic ventricular tachycardia 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Catecholaminergic polymorphic ventricular tachycardia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Catecholaminergic polymorphic ventricular tachycardia 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Catecholaminergic polymorphic ventricular tachycardia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Catecholaminergic polymorphic ventricular tachycardia 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Catecholaminergic polymorphic ventricular tachycardia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Ventricular tachycardia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Catecholaminergic polymorphic ventricular tachycardia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Catecholaminergic polymorphic ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Polymorphic ventricular tachycardia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Polymorphic ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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, 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.

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.

Paroxysmal Familial Ventricular Fibrillation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Paroxysmal Familial Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Noncompaction Of Left Ventricular Myocardium, Familial Isolated, Autosomal Dominant 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial isolated arrhythmogenic right ventricular dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial isolated arrhythmogenic right ventricular dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Paroxysmal familial ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.

amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; amyloidosis, familial; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple familial trichoepithelioma and familial cylindromatosis Gene Set

From GAD Gene-Disease Associations

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

amyloidosis, familial; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Tachycardia, Paroxysmal Gene Set

From CTD Gene-Disease Associations

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

Tachycardia Gene Set

From CTD Gene-Disease Associations

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

Tachycardia, Sinus Gene Set

From CTD Gene-Disease Associations

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

Tachycardia, Supraventricular Gene Set

From CTD Gene-Disease Associations

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

Tachycardia, Ectopic Junctional Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tachycardia, Ectopic Junctional from the curated CTD Gene-Disease Associations dataset.

obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

postural tachycardia syndrome Gene Set

From GAD Gene-Disease Associations

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

atrial fibrillation; postoperative complications; tachycardia Gene Set

From GAD Gene-Disease Associations

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

tachycardia Gene Set

From GAD Gene-Disease Associations

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

tachycardia cardiomyopathy Gene Set

From GAD Gene-Disease Associations

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

tachycardia Gene Set

From GeneRIF Biological Term Annotations

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

tachycardia Gene Set

From GWASdb SNP-Phenotype Associations

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

orthostatic tachycardia Gene Set

From GWASdb SNP-Phenotype Associations

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

supraventricular tachycardia Gene Set

From GWASdb SNP-Phenotype Associations

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

postural hypotension with compensatory tachycardia Gene Set

From HPO Gene-Disease Associations

genes associated with the postural hypotension with compensatory tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal atrial tachycardia Gene Set

From HPO Gene-Disease Associations

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

orthostatic tachycardia Gene Set

From HPO Gene-Disease Associations

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

paroxysmal supraventricular tachycardia Gene Set

From HPO Gene-Disease Associations

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

supraventricular tachycardia Gene Set

From HPO Gene-Disease Associations

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

tachycardia Gene Set

From HPO Gene-Disease Associations

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

sinus tachycardia Gene Set

From HPO Gene-Disease Associations

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

tachycardia (with pheochromocytoma) Gene Set

From HPO Gene-Disease Associations

genes associated with the tachycardia (with pheochromocytoma) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Tachycardia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Postural Orthostatic Tachycardia Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Postural Orthostatic Tachycardia Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Tachycardia, Sinus Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tachycardia, Supraventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tachycardia, Ectopic Junctional Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Supraventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Supraventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

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

Postural Orthostatic Tachycardia Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Postural Orthostatic Tachycardia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Sinus Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Sinus Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Paroxysmal Supraventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Paroxysmal Supraventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bradycardia-Tachycardia Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bradycardia-Tachycardia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bidirectional Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bidirectional Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atrioventricular Reciprocating Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atrioventricular Reciprocating Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Re-Entrant Atrial Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Re-Entrant Atrial Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Re-Entrant Atrioventricular Tachycardia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Re-Entrant Atrioventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atrial Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atrial Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Continuous Electrocardiogram - Paroxysmal Supraventricular Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Continuous Electrocardiogram - Paroxysmal Supraventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Inappropriate Sinus Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Inappropriate Sinus Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Supraventricular Tachycardia With An Accessory Connection Mediated Pathway Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Supraventricular Tachycardia With An Accessory Connection Mediated Pathway in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Postural Hypotension With Compensatory Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Postural Hypotension With Compensatory Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Paroxysmal Atrial Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Paroxysmal Atrial Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Paroxysmal Atrial Tachycardia, Ctcae Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Paroxysmal Atrial Tachycardia, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Orthostatic Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Orthostatic Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atrial Reentry Tachycardia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atrial Reentry Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Postural orthostatic tachycardia syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Postural orthostatic tachycardia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Supraventricular tachycardia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Supraventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Tachycardia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.

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.

Ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 Association Evidence Scores

genes involed in the disease arrhythmogenic right ventricular cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association 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.

arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Association 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 2015

genes participating in the forebrain ventricular zone progenitor cell division biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of planar cell polarity pathway involved in ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations 2015

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 2015 dataset.

ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.

purkinje myocyte to ventricular cardiac muscle cell communication Gene Set

From GO Biological Process Annotations 2015

genes participating in the purkinje myocyte to ventricular cardiac muscle cell communication biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular trabecula myocardium morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular trabecula myocardium morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2015 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 2015

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 2015 dataset.

ventricular system development Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular system development biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations 2015

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 2015 dataset.

right ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the right ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular cardiac muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular septum development Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular septum development biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of ventricular cardiac muscle cell membrane depolarization Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of ventricular cardiac muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular zone neuroblast division Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular zone neuroblast division biological process from the curated GO Biological Process Annotations 2015 dataset.

planar cell polarity pathway involved in ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the planar cell polarity pathway involved in ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

left ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the left ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of planar cell polarity pathway involved in ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of planar cell polarity pathway involved in ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

atrial ventricular junction remodeling Gene Set

From GO Biological Process Annotations 2015

genes participating in the atrial ventricular junction remodeling biological process from the curated GO Biological Process Annotations 2015 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 2015

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 2015 dataset.

ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular compact myocardium morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular compact myocardium morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular cardiac myofibril assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular cardiac myofibril assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

purkinje myocyte to ventricular cardiac muscle cell signaling Gene Set

From GO Biological Process Annotations 2015

genes participating in the purkinje myocyte to ventricular cardiac muscle cell signaling biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of ventricular cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of ventricular cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular cardiac muscle cell development Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular cardiac muscle cell development biological process from the curated GO Biological Process Annotations 2015 dataset.

ventricular cardiac muscle tissue development Gene Set

From GO Biological Process Annotations 2015

genes participating in the ventricular cardiac muscle tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.

voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations 2015

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 2015 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 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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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 2014

proteins participating in the Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.

Left Ventricular Hypertrophy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Arrhythmia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Arrhythmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Fibrillation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Hypertrophy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Arrhythmogenic Right Ventricular Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Dilatation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Systolic Dysfunction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Right Ventricular Failure Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Right Ventricular Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Right Ventricular Hypertrophy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Right Ventricular Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Dilatation (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Dilatation (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Diastolic Dysfunction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Noncompaction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Noncompaction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Noncompaction Cardiomyopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Noncompaction Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Failure Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Dyssynchrony Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Dyssynchrony in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Preexcitation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Preexcitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Muscular Ventricular Septum Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Muscular Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Perimembranous Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Perimembranous Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Progressive Post Hemorrhagic Ventricular Dilatation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Progressive Post Hemorrhagic Ventricular Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Thrombus Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Thrombus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Septal Hypertrophy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Septal Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Early Repolarization Associated With Ventricular Fibrillation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Early Repolarization Associated With Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Aneurysm Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Dyssynchrony Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Dyssynchrony in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Outflow Tract Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Outflow Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Right Ventricular Dilatation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Right Ventricular Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Right Ventricular Cardiomyopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Right Ventricular Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Rapid Ventricular Response Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Rapid Ventricular Response in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Ventricular Septum Morphology Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Ventricular Septum Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pulmonary Atresia With Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pulmonary Atresia With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Membranous Ventricular Septum Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Membranous Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Severe Left Ventricular Systolic Dysfunction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Severe Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Outflow Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pulmonary Atresia With Intact Ventricular Septum Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pulmonary Atresia With Intact Ventricular Septum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Overload Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Free Wall Rupture Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Free Wall Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Right Ventricular Systolic Dysfunction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Right Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Hypoplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Right Ventricular Thrombus Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Right Ventricular Thrombus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Hypoplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Septal Rupture Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Septal Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Aneurysm Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Right Ventricular Overload Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Right Ventricular Overload in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Ventricular Septal Defects Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Ventricular Septal Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Dysfunction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Premature Ventricular Contractions Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Premature Ventricular Contractions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Remodeling Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Remodeling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Hemorrhage Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Cardiac Ventricular Function Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Cardiac Ventricular Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Arrhythmia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Arrhythmia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Auriculo-Ventricular Dissociation Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Auriculo-Ventricular Dissociation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Left Ventricular Mass Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Left Ventricular Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Right Ventricular Dysfunction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Right Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Fibrillation Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Fibrillation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Escape Rhythm Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Escape Rhythm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Morphology Of Left Ventricular Trabeculae Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Morphology Of Left Ventricular Trabeculae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Dilatation Of The Ventricular Cavity Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Dilatation Of The Ventricular Cavity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Outflow Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Morphology Of Right Ventricular Trabeculae Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Morphology Of Right Ventricular Trabeculae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Bidirectional Ventricular Ectopy Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Bidirectional Ventricular Ectopy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Left Ventricular Septal Hypertrophy Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Left Ventricular Septal Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Left Ventricular Systolic Dysfunction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Preexcitation With Multiple Accessory Pathways Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Preexcitation With Multiple Accessory Pathways in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Left Ventricular Function Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Left Ventricular Function in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Arrhythmogenic Right Ventricular Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Effort-Induced Polymorphic Ventricular Tachycardias Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Effort-Induced Polymorphic Ventricular Tachycardias in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

ventricular cardiac muscle cell development Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular cardiac muscle cell development biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular septum development Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular septum development biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

Purkinje myocyte to ventricular cardiac muscle cell signaling Gene Set

From GO Biological Process Annotations 2023

genes participating in the Purkinje myocyte to ventricular cardiac muscle cell signaling biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of ventricular cardiac muscle cell membrane depolarization Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of ventricular cardiac muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of ventricular cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of ventricular cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations 2023 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 2023

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 2023 dataset.

regulation of ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular compact myocardium morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular compact myocardium morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular trabecula myocardium morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular trabecula myocardium morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular zone neuroblast division Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular zone neuroblast division biological process from the curated GO Biological Process Annotations 2023 dataset.

Purkinje myocyte to ventricular cardiac muscle cell communication by electrical coupling Gene Set

From GO Biological Process Annotations 2023

genes participating in the Purkinje myocyte to ventricular cardiac muscle cell communication by electrical coupling biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular system development Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular system development biological process from the curated GO Biological Process Annotations 2023 dataset.

right ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the right ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular cardiac myofibril assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular cardiac myofibril assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular cardiac muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations 2023

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 2023 dataset.

left ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the left ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

ventricular cardiac muscle tissue development Gene Set

From GO Biological Process Annotations 2023

genes participating in the ventricular cardiac muscle tissue development biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

Purkinje myocyte to ventricular cardiac muscle cell communication Gene Set

From GO Biological Process Annotations 2023

genes participating in the Purkinje myocyte to ventricular cardiac muscle cell communication biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations 2023

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 2023 dataset.

gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

perimembraneous ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

thin ventricular wall Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the thin ventricular wall phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal neural tube ventricular layer morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal neural tube ventricular layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal brain ventricular system morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal brain ventricular system morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

thick ventricular wall Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the thick ventricular wall phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ventricular hypoplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

muscular ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ventricular myocardium compact layer hypoplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular myocardium compact layer hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal cortical ventricular zone morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal cortical ventricular zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ventricular cardiomyopathy Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular cardiomyopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

inlet ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ventricular premature beat Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular premature beat phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal ventricular thrombosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal ventricular thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ventricular fibrillation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular fibrillation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

double outlet right ventricle, ventricular defect committed to aorta Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

double outlet right ventricle, noncommitted ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the double outlet right ventricle, noncommitted ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

subarterial ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the subarterial ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

thick ventricular wall Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the thick ventricular wall phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

thin ventricular wall Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the thin ventricular wall phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

Human - Heart - L2 - Ventricular Cardiomyocyte Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Heart - L2 - Ventricular Cardiomyocyte cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Ventricular radial glial cell_Brain_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular radial glial cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular cardiomyocyte_Embryo_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular cardiomyocyte_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Left ventricular cell_Left ventricle_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Left ventricular cell_Left ventricle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular compact cell_Heart_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular compact cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular trabecular cell_Heart_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular trabecular cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular zone cell_Heart_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular zone cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular cell_Heart_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular cell_Heart_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular cell_Heart_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular cell_Undefined_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Ventricular cardiomyocyte_Undefined_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Ventricular cardiomyocyte_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From WikiPathways Pathways 2024

proteins participating in the Arrhythmogenic right ventricular cardiomyopathy pathway from the WikiPathways Pathways 2024 dataset.

ventricular cardiac muscle cell development Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular cardiac muscle cell development biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular septum development Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular septum development biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

Purkinje myocyte to ventricular cardiac muscle cell signaling Gene Set

From GO Biological Process Annotations 2025

genes participating in the Purkinje myocyte to ventricular cardiac muscle cell signaling biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of ventricular cardiac muscle cell membrane depolarization Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of ventricular cardiac muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular septum morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular septum morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of ventricular cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of ventricular cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular trabecula myocardium morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular trabecula myocardium morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular compact myocardium morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular compact myocardium morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular zone neuroblast division Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular zone neuroblast division biological process from the curated GO Biological Process Annotations 2025 dataset.

Purkinje myocyte to ventricular cardiac muscle cell communication by electrical coupling Gene Set

From GO Biological Process Annotations 2025

genes participating in the Purkinje myocyte to ventricular cardiac muscle cell communication by electrical coupling biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular cardiac muscle cell membrane repolarization Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular cardiac muscle cell membrane repolarization biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular system development Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular system development biological process from the curated GO Biological Process Annotations 2025 dataset.

right ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the right ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular cardiac myofibril assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular cardiac myofibril assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular cardiac muscle cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular cardiac muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

left ventricular cardiac muscle tissue morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the left ventricular cardiac muscle tissue morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

ventricular cardiac muscle tissue development Gene Set

From GO Biological Process Annotations 2025

genes participating in the ventricular cardiac muscle tissue development biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

Purkinje myocyte to ventricular cardiac muscle cell communication Gene Set

From GO Biological Process Annotations 2025

genes participating in the Purkinje myocyte to ventricular cardiac muscle cell communication biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of membrane repolarization during ventricular cardiac muscle cell action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations 2025

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 2025 dataset.

gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

Left ventricular noncompaction Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Left ventricular noncompaction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Arrhythmogenic right ventricular cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

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 2025 dataset.

Arrhythmogenic right ventricular dysplasia 11 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Left ventricular noncompaction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Left ventricular noncompaction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 5 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic left ventricular cardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic left ventricular cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 8 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 9 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 6 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 12 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 10 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 13 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Arrhythmogenic right ventricular dysplasia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Ventricular zone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Ventricular zone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Ventricular aneurysm disease specific cell type Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Ventricular aneurysm disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Arrhythmogenic right ventricular dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Arrhythmogenic right ventricular dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Arrhythmogenic right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Arrhythmogenic ventricular cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Arrhythmogenic ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Left ventricular noncompaction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Left ventricular noncompaction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Left ventricular noncompaction cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Left ventricular noncompaction cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Left ventricular hypertrophy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Left ventricular hypertrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Premature ventricular contraction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Premature ventricular contraction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Increased left ventricular wall thickness Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Increased left ventricular wall thickness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ventricular hypertrophy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ventricular hypertrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLA Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Isolated Noncompaction of the Ventricular Myocardium Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Isolated Noncompaction of the Ventricular Myocardium phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Right ventricular cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ventricular arrhythmia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ventricular arrhythmia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Abnormal morphology of left ventricular trabeculae Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Abnormal morphology of left ventricular trabeculae phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Reduced left ventricular ejection fraction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Reduced left ventricular ejection fraction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Left ventricular end-diastolic volume Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular end-diastolic volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular end-systolic volume Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular end-systolic volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular ejection fraction Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular ejection fraction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Total ventricular volume (Alzheimer's disease interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Total ventricular volume (Alzheimer's disease interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Total ventricular volume Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Total ventricular volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular mass Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular fractional shortening Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular fractional shortening phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular global radial strain Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular global radial strain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular ejection fraction (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular ejection fraction (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular mass to end-diastolic volume ratio (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular mass to end-diastolic volume ratio (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular mass (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular mass (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular end-diastolic volume (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular end-diastolic volume (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular end-systolic volume (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular end-systolic volume (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular global circumferential strain (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular global circumferential strain (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular global radial strain (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular global radial strain (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular global longitudinal strain (MTAG) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular global longitudinal strain (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular global circumferential strain Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular global circumferential strain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular mass to end-diastolic volume ratio Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular mass to end-diastolic volume ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular global longitudinal strain Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular global longitudinal strain phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Lateral ventricular volume in normal aging Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Lateral ventricular volume in normal aging phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular QRS voltage Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular QRS voltage phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular internal dimension in diastole Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular internal dimension in diastole phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular internal dimension in systole Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular internal dimension in systole phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular obstructive tract defect (inherited effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular obstructive tract defect (inherited effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular obstructive tract defect (maternal effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular obstructive tract defect (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Ventricular ectopy or supraventricular ectopy (pleiotropy) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Ventricular ectopy or supraventricular ectopy (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Ventricular ectopy Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Ventricular ectopy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular function change in anthracycline treatment Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular function change in anthracycline treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular mass x antihypertensive treatment interaction Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular mass x antihypertensive treatment interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Rate of ventricular enlargement Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Rate of ventricular enlargement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Arrhythmogenic right ventricular cardiomyopathy Gene Set

From KEGG Pathways 2026

proteins participating in the Arrhythmogenic right ventricular cardiomyopathy pathway from the KEGG Pathways 2026 dataset.

Familial Mediterranean fever Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial Mediterranean fever phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytosis, benign familial microcytic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytosis, benign familial microcytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial neonatal-infantile seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurofibromatosis, familial spinal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tumoral calcinosis, familial, hyperphosphatemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tumoral calcinosis, familial, hyperphosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Febrile seizures, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Febrile seizures, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial restrictive cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaze palsy, familial horizontal, with progressive scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hemiplegic migraine type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hemiplegic migraine type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocytosis, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Erythrocytosis, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Erythrocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Aortic aneurysm, familial thoracic 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial X-linked hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial neonatal seizures 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial neonatal seizures 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial neonatal seizures 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial neonatal seizures 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemic nephropathy, familial juvenile, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial cancer of breast Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial cancer of breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial benign pemphigus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial benign pemphigus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic pain syndrome, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperpigmentation, familial progressive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial aortopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Digital arthropathy-brachydactyly, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Digital arthropathy-brachydactyly, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic pain syndrome, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Febrile seizures, familial, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Febrile seizures, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial benign hypercalcemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial benign hypercalcemia 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.

Familial visceral amyloidosis, Ostertag type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial visceral amyloidosis, Ostertag type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dementia familial British Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial porencephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypocalciuric hypercalcemia, familial, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

familial hyperinsulinism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperinsulinemic hypoglycemia familial 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperinsulinemic hypoglycemia familial 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Febrile seizures, familial, 3b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Febrile seizures, familial, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypercholesterolemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hidradenitis suppurativa, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dementia, familial Danish Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign familial hematuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial hematuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial dysautonomia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial febrile seizures 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial febrile seizures 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fleck retina, familial benign Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fleck retina, familial benign phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial exudative vitreoretinopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial exudative vitreoretinopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial colorectal cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial colorectal cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial porphyria cutanea tarda Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial porphyria cutanea tarda phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypertrophic cardiomyopathy 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Advanced sleep phase syndrome, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonus, familial cortical Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Migraine, familial basilar Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Migraine, familial basilar phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Breast-ovarian cancer, familial 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Breast-ovarian cancer, familial 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercholanemia, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone marrow failure, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone marrow failure, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Advanced sleep phase syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Candidiasis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Candidiasis, familial, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypokalemia-hypomagnesemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypokalemia-hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenia, limb-girdle, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenia, limb-girdle, familial 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.

Atrial fibrillation, familial, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial platelet disorder with associated myeloid malignancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial erythrocytosis, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial erythrocytosis, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial medullary thyroid carcinoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial medullary thyroid carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperinsulinemic hypoglycemia, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic aneurysm, familial thoracic 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperlipidemia, familial combined Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperlipidemia, familial combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial amyloid polyneuropathy, Iowa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial amyloid polyneuropathy, Iowa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, familial adult myoclonic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial myxoma, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial myxoma, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, familial partial, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, familial partial, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, familial partial, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, familial partial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypocalciuric hypercalcemia, familial, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypocalciuric hypercalcemia, familial, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypocalciuric hypercalcemia, familial, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypocalciuric hypercalcemia, familial, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial multiple polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial juvenile gout Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypobetalipoproteinemia, familial, associated with apob32 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypobetalipoproteinemia, familial, associated with apob32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Breast-ovarian cancer, familial 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Breast-ovarian cancer, familial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary familial hypertrophic cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial type 3 hyperlipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial type 3 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tumoral calcinosis, familial, normophosphatemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tumoral calcinosis, familial, normophosphatemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cd8 deficiency, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial infantile myasthenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked familial atypical mycobacteriosis, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked familial atypical mycobacteriosis, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperthyroxinemia, familial dysalbuminemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperthyroxinemia, familial dysalbuminemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial type 5 hyperlipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial type 5 hyperlipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial renal glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial pulmonary capillary hemangiomatosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypoalphalipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial renal hypouricemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonic epilepsy, familial infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial hypoplastic, glomerulocystic kidney Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial hypoplastic, glomerulocystic kidney phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial cold urticaria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic Aneurysm, Familial Abdominal 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset.

Familial myelofibrosis Gene Set

From CTD Gene-Disease Associations

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

Nephronophthisis, familial juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset.

Eosinophilia, Familial Gene Set

From CTD Gene-Disease Associations

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

Hyperlipidemia, Familial Combined Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperlipidemia, Familial Combined from the curated CTD Gene-Disease Associations dataset.

Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic hypoglycemia, familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 6 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Pemphigus, Benign Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pemphigus, Benign Familial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.

Amyloidosis, familial visceral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyloidosis, familial visceral from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Hypertrophic, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.

Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 7 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.

Myasthenia, Familial Infantile, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Abdominal 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset.

STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease STUTTERING, FAMILIAL PERSISTENT, 1 from the curated CTD Gene-Disease Associations dataset.

Dementia, familial British Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset.

Candidiasis familial chronic mucocutaneous, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Gliosis, Familial Progressive Subcortical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.

CD8 Deficiency, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset.

Insomnia, Fatal Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Insomnia, Fatal Familial from the curated CTD Gene-Disease Associations dataset.

SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 2 from the curated CTD Gene-Disease Associations dataset.

Familial HDL deficiency Gene Set

From CTD Gene-Disease Associations

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

Familial dermographism Gene Set

From CTD Gene-Disease Associations

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

Candidiasis, Familial, 3 Gene Set

From CTD Gene-Disease Associations

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

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.

Erythrocytosis, Familial, 3 Gene Set

From CTD Gene-Disease Associations

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

Erythrocytosis, Familial, 2 Gene Set

From CTD Gene-Disease Associations

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

Visceral Myopathy, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Visceral Myopathy, Familial from the curated CTD Gene-Disease Associations dataset.

Hyperthyroidism, Familial Gestational Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperthyroidism, Familial Gestational from the curated CTD Gene-Disease Associations dataset.

Hematuria, Benign Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hematuria, Benign Familial from the curated CTD Gene-Disease Associations dataset.

SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Migraine, Familial Hemiplegic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine, Familial Hemiplegic, 3 from the curated CTD Gene-Disease Associations dataset.

FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Cancer, Familial, with In Vitro Radioresistance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cancer, Familial, with In Vitro Radioresistance from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 5 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.

Tumoral Calcinosis, Hyperphosphatemic, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tumoral Calcinosis, Hyperphosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

Hidradenitis suppurativa, familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hidradenitis suppurativa, familial from the curated CTD Gene-Disease Associations dataset.

Dementia, familial Danish Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset.

Familial medullary thyroid carcinoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial medullary thyroid carcinoma from the curated CTD Gene-Disease Associations dataset.

Interstitial Pneumonitis, Desquamative, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Interstitial Pneumonitis, Desquamative, Familial from the curated CTD Gene-Disease Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 4 from the curated CTD Gene-Disease Associations dataset.

Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.

Cirrhosis, Familial Gene Set

From CTD Gene-Disease Associations

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

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Familial Partial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Familial Partial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.

Familial Mediterranean Fever, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Mediterranean Fever, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Familial Hypophosphatemic Rickets Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.

Keratoacanthoma familial Gene Set

From CTD Gene-Disease Associations

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

Hepatic Adenomas, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.

Familial Wilms tumor 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Wilms tumor 2 from the curated CTD Gene-Disease Associations dataset.

Candidiasis, Familial, 1 Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic Hypoglycemia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic Hypoglycemia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic Hypoglycemia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Familial antiphospholipid syndrome Gene Set

From CTD Gene-Disease Associations

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

Amyloidosis, Familial Gene Set

From CTD Gene-Disease Associations

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

Familial paroxysmal dystonia Gene Set

From CTD Gene-Disease Associations

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

Atrial fibrillation, familial 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial fibrillation, familial 1 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 from the curated CTD Gene-Disease Associations dataset.

Hypercholanemia, Familial Gene Set

From CTD Gene-Disease Associations

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

Hyperbilirubinemia, Transient Familial Neonatal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperbilirubinemia, Transient Familial Neonatal from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 from the curated CTD Gene-Disease Associations dataset.

Meningioma, familial Gene Set

From CTD Gene-Disease Associations

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

Aortic Aneurysm, Familial Thoracic 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Thoracic 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset.

Dysautonomia, Familial Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 3 from the curated CTD Gene-Disease Associations dataset.

Familial Cold Autoinflammatory Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Cold Autoinflammatory Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Familial Adult Myoclonic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.

Prostate cancer, familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prostate cancer, familial from the curated CTD Gene-Disease Associations dataset.

Convulsions, Benign Familial Infantile, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.

Polycythemia, primary familial and congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.

PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Thoracic 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset.

Erythrocytosis, Familial, 4 Gene Set

From CTD Gene-Disease Associations

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

Hyperinsulinemic hypoglycemia, familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 3 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

Hyperinsulinemic hypoglycemia, familial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperinsulinemic hypoglycemia, familial, 7 from the curated CTD Gene-Disease Associations dataset.

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.

Hyperthyroxinemia, Familial Dysalbuminemic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperthyroxinemia, Familial Dysalbuminemic from the curated CTD Gene-Disease Associations dataset.

Aortic aneurysm, familial thoracic 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Restrictive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.

Atrial Fibrillation, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Familial cylindromatosis Gene Set

From CTD Gene-Disease Associations

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

Familial benign hypercalcemia, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial benign hypercalcemia, type 3 from the curated CTD Gene-Disease Associations dataset.

Hyperaldosteronism, Familial, Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperaldosteronism, Familial, Type II from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.

Atrial myxoma, familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial myxoma, familial from the curated CTD Gene-Disease Associations dataset.

Familial Glucocorticoid Deficiency 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset.

Tumoral Calcinosis, Normophosphatemic, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tumoral Calcinosis, Normophosphatemic, Familial from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

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

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypocalciuric hypercalcemia, familial, type 1 from the curated CTD Gene-Disease Associations dataset.

Trichoepithelioma multiple familial Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.

Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemophagocytic lymphohistiocytosis, familial, 2 from the curated CTD Gene-Disease Associations dataset.

Periodic fever, familial, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Periodic fever, familial, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset.

Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypobetalipoproteinemia, Familial, Apolipoprotein B from the curated CTD Gene-Disease Associations dataset.

Aortic Aneurysm, Familial Abdominal 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset.

Familial schizencephaly Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Fibrillation, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset.

Neurofibromatosis, Familial Spinal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.

Reticuloendotheliosis, familial, with eosinophilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Reticuloendotheliosis, familial, with eosinophilia from the curated CTD Gene-Disease Associations dataset.

SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL NEONATAL, 1 from the curated CTD Gene-Disease Associations dataset.

Advanced Sleep-Phase Syndrome, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Advanced Sleep-Phase Syndrome, Familial from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 2 from the curated CTD Gene-Disease Associations dataset.

MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.

MITRAL VALVE PROLAPSE, FAMILIAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITRAL VALVE PROLAPSE, FAMILIAL from the curated CTD Gene-Disease Associations dataset.

Progressive Familial Heart Block, Type Ib Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.

Familial dilated cardiomyopathy Gene Set

From CTD Gene-Disease Associations

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

Cholestasis, progressive familial intrahepatic 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.

Thymoma, Familial Gene Set

From CTD Gene-Disease Associations

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

Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atypical Mycobacteriosis, Familial, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

Familial Testotoxicosis Gene Set

From CTD Gene-Disease Associations

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

Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.

Hemiplegic migraine, familial type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemiplegic migraine, familial type 2 from the curated CTD Gene-Disease Associations dataset.

Hemiplegic migraine, familial type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemiplegic migraine, familial type 1 from the curated CTD Gene-Disease Associations dataset.

Familial apoceruloplasmin deficiency Gene Set

From CTD Gene-Disease Associations

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

HYPERCHOLESTEROLEMIA, FAMILIAL Gene Set

From CTD Gene-Disease Associations

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

Amyloid Neuropathies, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyloid Neuropathies, Familial from the curated CTD Gene-Disease Associations dataset.

CANDIDIASIS, FAMILIAL, 2 Gene Set

From CTD Gene-Disease Associations

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

Familial Mediterranean Fever Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 7 from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Febrile Convulsions, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Febrile Convulsions, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Cerebral Amyloid Angiopathy, Familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Amyloid Angiopathy, Familial from the curated CTD Gene-Disease Associations dataset.

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.

Hypobetalipoproteinemia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

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

Stuttering, Familial Persistent 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stuttering, Familial Persistent 2 from the curated CTD Gene-Disease Associations dataset.

Trichoepithelioma, Multiple Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Familial Temporal Lobe, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Familial Temporal Lobe, 4 from the curated CTD Gene-Disease Associations dataset.

MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy, Familial Hypertrophic, 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.

familial mediterranean fever Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial adenomatous polyposis Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial hyperlipidemia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial hemiplegic migraine Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial atrial fibrillation Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial lipoprotein lipase deficiency Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial periodic paralysis Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease familial periodic paralysis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial lipoprotein lipase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial hypertriglyceridemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

benign familial infantile epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial melanoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial adenomatous polyposis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial adenomatous polyposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial combined hyperlipidemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial combined hyperlipidemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial renal oncocytoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

fatal familial insomnia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease fatal familial insomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial mediterranean fever Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial mediterranean fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial nephrotic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial glomangioma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial hyperlipidemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial hypercholesterolemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial periodic paralysis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial periodic paralysis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial meningioma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

benign familial neonatal epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease benign familial neonatal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial partial lipodystrophy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial partial lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial hemiplegic migraine Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial hemiplegic migraine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial visceral amyloidosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial visceral amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial atrial fibrillation Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial medullary thyroid carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial medullary thyroid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial renal papillary carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial retinoblastoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

familial adenomatous polyposis. Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; familial mediterranean fever; rheumatoid arthritis; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mild familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

familial atypical progressive supranuclear palsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial or sporadic prostate cancer. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial or sporadic prostate cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial distal renal tubular acidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

familial defective apolipoprotein b100. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b100. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypercholesterolaemia Gene Set

From GAD Gene-Disease Associations

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

familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; glomerulonephritis, iga; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloid neuropathies; amyloid neuropathies, familial Gene Set

From GAD Gene-Disease Associations

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

early-onset familial alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abdomen, acute; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abdomen, acute; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

familial dysbetalipoproteinemia Gene Set

From GAD Gene-Disease Associations

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

familial defective apolipoprotein b Gene Set

From GAD Gene-Disease Associations

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

familial amyloid polyneuropathy. Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease (familial) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease (familial) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mild familial hypercholesterolaemia Gene Set

From GAD Gene-Disease Associations

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

familial combined hyperlipidemia Gene Set

From GAD Gene-Disease Associations

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

endogenous hypertriglyceridemia and familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial age-related macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial premature myocardial infarction. Gene Set

From GAD Gene-Disease Associations

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

familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

late onset of familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial amyloidotic polyneuropathy. Gene Set

From GAD Gene-Disease Associations

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

amyloid neuropathies, familial Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperlipidemia, familial combined; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; crohn disease; familial mediterranean fever; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial defective apolipoprotein b-100 in a chinese man Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial defective apolipoprotein b-100 in a chinese man in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; familial mediterranean fever; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; familial mediterranean fever; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial male-limited precocious puberty. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial combined hyperlipidaemia. Gene Set

From GAD Gene-Disease Associations

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

amyloidosis; familial mediterranean fever; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fam hyperbetalipoproteinaemia; hyperlipidemia, familial combined; hyperlipoproteinemia type ii; hypertriglyceridemia; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cryopyrin-associated periodic syndromes; familial mediterranean fever; mevalonate kinase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial early onset psoriasis. Gene Set

From GAD Gene-Disease Associations

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

familial hypobetalipoproteinemia Gene Set

From GAD Gene-Disease Associations

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