ventricular hypoplasia

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Results for "ventricular hypoplasia": 7 genes, 1003 gene sets

Name
CPVT3 Gene Ventricular tachycardia, catecholaminergic polymorphic, 3
ARVD4 Gene arrhythmogenic right ventricular* dysplasia 4*
ARVD6 Gene arrhythmogenic right ventricular* dysplasia 6*
ARVD3 Gene arrhythmogenic right ventricular* dysplasia 3*
MYL3 Gene myosin, light chain 3, alkali; ventricular, skeletal, slow MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
VEPH1 Gene ventricular zone expressed PH domain-containing 1 Predicted to enable phosphatidylinositol-5-phosphate binding activity. Involved in negative regulation of SMAD protein signal transduction and negative regulation of transforming growth factor beta receptor signaling pathway. Predicted to be located in endomembrane system. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]
LVNC2 Gene noncompaction of left ventricular* myocardium, familial isolated, autosomal dominant 2*
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 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.
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.
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.
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.
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.
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.
arrhythmogenic right ventricular dysplasia; tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophy, left ventricular; insulin resistance; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophy, left ventricular; insulin resistance; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
accelerated idioventricular rhythm; arrhythmias, cardiac; myocardial infarction; reperfusion injury; tachycardia, ventricular; ventricular fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease accelerated idioventricular rhythm; arrhythmias, cardiac; myocardial infarction; reperfusion injury; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
left ventricular hypertrophy; blood flow; left ventricular function Gene Set From GAD Gene-Disease Associations genes associated with the disease left ventricular hypertrophy; blood flow; left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophy, left ventricular; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; hypertrophy, left ventricular; ventricular remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; hypertrophy, left ventricular; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
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.
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 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.
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.
Catecholaminergic polymorphic ventricular tachycardia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Catecholaminergic polymorphic ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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 dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Paroxysmal familial ventricular fibrillation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular tachycardia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular tachycardia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Ventricular fibrillation, paroxysmal familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular tachycardia, catecholaminergic polymorphic, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
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.
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.
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.
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 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.
Ventricular Outflow Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Outflow Obstruction from the curated CTD Gene-Disease Associations dataset.
Ventricular Remodeling Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Remodeling from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Left Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Left from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.
Polymorphic catecholergic ventricular tachycardia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polymorphic catecholergic ventricular tachycardia from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Right Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Right from the curated CTD Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.
Tachycardia, Ventricular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tachycardia, Ventricular from the curated CTD Gene-Disease Associations dataset.
Hypertrophy, Left Ventricular Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Hypertrophy, Left Ventricular in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Ventricular Function, Left Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Ventricular Function, Left in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
arrhythmogenic right ventricular cardiomyopathy Gene Set From DISEASES Curated Gene-Disease 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.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
left ventricular hypertrophy; blood pressure, arterial Gene Set From GAD Gene-Disease Associations genes associated with the disease left ventricular hypertrophy; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; left ventricular function Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia; Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular dysplasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipids; left ventricular mass; aortic gradient; aortic valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lipids; left ventricular mass; aortic gradient; aortic valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; ventricular fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disease models, animal; hypertension; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease disease models, animal; hypertension; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
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.
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.
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.
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.
paroxysmal ventricular tachycardia Gene Set From HPO Gene-Disease Associations genes associated with the paroxysmal ventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right ventricular failure Gene Set From HPO Gene-Disease Associations genes associated with the right ventricular failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right ventricular cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the right ventricular cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the left ventricular outflow tract Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the left ventricular outflow tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ventricular fibrillation Gene Set From HPO Gene-Disease Associations genes associated with the ventricular fibrillation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
left ventricular hypertrophy Gene Set From HPO Gene-Disease Associations genes associated with the left ventricular hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right ventricular dilatation Gene Set From HPO Gene-Disease Associations genes associated with the right ventricular dilatation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impaired left ventricular function Gene Set From HPO Gene-Disease Associations genes associated with the impaired left ventricular function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ventricular hypertrophy Gene Set From HPO Gene-Disease Associations genes associated with the ventricular hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
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 tachycardia Gene Set From HPO Gene-Disease Associations genes associated with the ventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ventricular arrhythmia Gene Set From HPO Gene-Disease Associations genes associated with the ventricular arrhythmia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodes of ventricular tachycardia Gene Set From HPO Gene-Disease Associations genes associated with the episodes of ventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
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.
Tachycardia, Ventricular Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tachycardia, Ventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Dysfunction, Right Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Right phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Arrhythmogenic Right Ventricular Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Arrhythmogenic Right Ventricular Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
ventricular premature beat Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular premature beat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ventricular fibrillation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular fibrillation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
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.
ventricular tachycardia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular tachycardia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
double outlet right ventricle, ventricular defect committed to aorta Gene Set From MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ventricular cardiomyopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
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 aneurysm Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ventricular tachycardia, catecholaminergic polymorphic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, catecholaminergic polymorphic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, catecholaminergic polymorphic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, catecholaminergic polymorphic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular 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.
ventricular fibrillation, paroxysmal familial, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 11 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset.
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, familial, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 3 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 5 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 4 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 6 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 9 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 8 Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular fibrillation, familial, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular fibrillation, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
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.
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.
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 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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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 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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Focal dermal hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal dermal hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia type 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tibia, hypoplasia of, with polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tibia, hypoplasia of, with polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hypoplasia, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and anterior segment dysgenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia, type 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic nerve hypoplasia, bilateral Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Splenic hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Splenic hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Olivopontocerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Olivopontocerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia, type 1b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia type 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pontocerebellar hypoplasia, type 2e Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 2e phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skeletal defects, genital hypoplasia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal Dermal Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Focal Dermal Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Fibular hypoplasia and complex brachydactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.
Cartilage-hair hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset.
Leydig Cell Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leydig Cell Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Optic Nerve Hypoplasia, Bilateral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset.
Polymicrogyria With Optic Nerve Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Pontocerebellar Hypoplasia Type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2C from the curated CTD Gene-Disease Associations dataset.
Pontocerebellar Hypoplasia Type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2B from the curated CTD Gene-Disease Associations dataset.
ADRENAL HYPOPLASIA, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Anophthalmia with pulmonary hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anophthalmia with pulmonary hypoplasia from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Pontocerebellar Hypoplasia Type 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 6 from the curated CTD Gene-Disease Associations dataset.
PONTOCEREBELLAR HYPOPLASIA, TYPE 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PONTOCEREBELLAR HYPOPLASIA, TYPE 4 from the curated CTD Gene-Disease Associations dataset.
Pontocerebellar Hypoplasia Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.
Pontocerebellar Hypoplasia Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 3 from the curated CTD Gene-Disease Associations dataset.
Iris hypoplasia and glaucoma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset.
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.
Pontocerebellar Hypoplasia Type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2A from the curated CTD Gene-Disease Associations dataset.
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.
Foveal Hypoplasia and Anterior Segment Dysgenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset.
focal dermal hypoplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease focal dermal hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dental enamel hypoplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dental enamel hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
focal dermal hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal dermal hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cartilage-hair hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cartilage-hair hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pituitary hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pituitary hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dental enamel hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dental enamel hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypoplasia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term hypoplasia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
aplasia/hypoplasia involving the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
aplasia/hypoplasia of the cerebrum Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
retinal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the retinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of choroid Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the eye Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the fallopian tube Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of lymphatic vessels Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the musculature Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the uvula Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tragus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tragus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the nose Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the frontal sinuses Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
parathyroid hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the parathyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the lungs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lungs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pancreatic hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the pancreatic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the quadriceps Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the quadriceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the upper arm Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the scapulae Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the ventral pons Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the ventral pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
glenoid fossa hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the glenoid fossa hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lymph node hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the lymph node hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the skin Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of toe Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the iris Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior vertebral hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the posterior vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the lacrimal puncta Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the lacrimal puncta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the pyramidal tract Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving forearm bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the nasal bone Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the sternum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the optic nerve Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ovary Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of penis Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of penis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic disc hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the optic disc hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tarsal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the thymus Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thyroid hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the thyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ulna Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the feet Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the primary teeth Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the biceps Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the biceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the fundus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the fundus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the retina Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the odontoid process Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
calf muscle hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the calf muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the gallbladder Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the pelvis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the mandible Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the epiglottis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of metatarsal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of metatarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the uterus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
erythroid hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the erythroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the eyebrow Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the pons Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the spleen Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
breast hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the choroid Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the ciliary body Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the corpus callosum Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulmonary hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the pulmonary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the lower limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the brainstem Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the bladder Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the triceps Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the triceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the pharynx Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the pharynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the macular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pectoralis hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the pectoralis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midclavicular hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the midclavicular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal hypoplasia/aplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the femoral head Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mandibular condyle hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the mandibular condyle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting bones of the axial skeleton Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting bones of the axial skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corticospinal tract hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the corticospinal tract hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 1st metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
carpal bone hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the carpal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal ulnar hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the distal ulnar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the earlobes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the earlobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the calcaneus Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the calcaneus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 4th metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of fingers Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the radius Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of proximal fibula Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of proximal fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of deltoid muscle Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of deltoid muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the thymus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 2nd metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the skeleton Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the ulna Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the uterus Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the humerus Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the palmar creases Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the maxilla Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ribs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 1st metatarsal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the vertebral column Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
laryngeal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the laryngeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lacrimal gland hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the lacrimal gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontal bone hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the frontal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the metacarpal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nipples Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 5th metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the capital femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the ear Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the diaphragm Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the premaxilla Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebrum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 3rd toe Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the bladder Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the uvea Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the sweat glands Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
unilateral breast hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the unilateral breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thoracic hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the thoracic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the femur Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pectoralis major hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the pectoralis major hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adrenal medullary hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the adrenal medullary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the anterior segment of the eye Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of teeth Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nasal bone Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the testes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
labial hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the labial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the thorax Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the maxilla Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the optic tract Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nails Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the corpus callosum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
inferior vermis hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the inferior vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the brainstem Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the abdominal wall musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the inner ear Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the fovea Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cochlea Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the sinuses Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the semicircular canal Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the femoral head and neck Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the ear cartilage Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the ear cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
external genital hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the external genital hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the vagina Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of first ribs Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of first ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemisphere hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemisphere hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gonadal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the gonadal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the iris Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the extremities Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the nasal septum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
2nd-5th toe middle phalangeal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the 2nd-5th toe middle phalangeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the clavicles Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the sacrum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adrenocortical hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the adrenocortical hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving bones of the skull Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the ovary Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the musculature of the pelvis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized cerebral atrophy/hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tibia Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the prostate Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the prostate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of proximal radius Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of proximal radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the patella Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the lesser trochanter Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the lesser trochanter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the skeletal musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia affecting the eyelid Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the vagina Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
unilateral chest hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the unilateral chest hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the breasts Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the breasts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vertebral hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the extremities Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
shoulder muscle hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the shoulder muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the pubic bone Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the pyramidal tract Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the pancreas Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the cochlea Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the fovea Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic nerve hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the optic nerve hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cervical spine Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebellum Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the carpal bones Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adrenal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the adrenal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hemifacial hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the hemifacial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of dental enamel Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of dental enamel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the lens Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anterior pituitary hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the anterior pituitary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the external ear Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the shoulder musculature Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the frontal lobes Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the frontal lobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
scrotal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the scrotal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the radius Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the capital femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the vertebrae Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia involving the musculature of the upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intestinal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the intestinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the fallopian tube Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the tongue Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tongue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper limb muscle hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the upper limb muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
patellar hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the patellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the epiglottis Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the colon Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fibular hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the fibular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the 3rd metacarpal Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pectoral muscle hypoplasia/aplasia Gene Set From HPO Gene-Disease Associations genes associated with the pectoral muscle hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulmonary artery hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the pulmonary artery hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the macula Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of the abdominal wall musculature Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
paranasal sinus hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the paranasal sinus hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
clitoral hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the clitoral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the musculature of the thigh Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the thigh phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the phalanges of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the fibula Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
olivopontocerebellar hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the olivopontocerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axillary apocrine gland hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the axillary apocrine gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Dental Enamel Hypoplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dental Enamel Hypoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
testis hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the testis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
tongue hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the tongue hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
genital tubercle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the genital tubercle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lymphoid hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lymphoid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
palatine bone horizontal plate hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thyroid hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hindbrain hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hindbrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
midface hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the midface hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intervertebral disk hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intervertebral disk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lymph node hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lymph node hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic arch hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pituitary intermediate lobe hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pituitary intermediate lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
temporal bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
iris stroma hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the iris stroma hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ischium hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ischium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oviduct hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oviduct hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spleen hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spleen hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
radius hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the radius hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
otic vesicle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the otic vesicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
malleus hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the malleus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
maxilla hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the maxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
uterine cervix hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the uterine cervix hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
adrenal gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the adrenal gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
palatal shelf hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the palatal shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ventricle myocardium hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricle myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
leydig cell hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the leydig cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mammary gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mammary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
scrotum hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the scrotum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
diencephalon hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the diencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear ganglion hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
frontal bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the frontal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
head mesenchyme hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the head mesenchyme hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
myometrium hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the myometrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
papillary muscle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the papillary muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebellum vermis hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebellum vermis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sebaceous gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
premaxilla hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the premaxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrium myocardium hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrium myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
female preputial gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pharyngeal arch artery hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epididymis hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epididymis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
parathyroid hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the parathyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
olfactory bulb hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the olfactory bulb hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aorta hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aorta hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ethmoturbinate hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ethmoturbinate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hyoid bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hyoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pituitary gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pituitary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
parietal bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the parietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axial mesoderm hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axial mesoderm hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mesangial cell hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mesangial cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
liver hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the liver hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
palatine bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the palatine bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreas hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
gonial bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the gonial bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ear lobe hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ear lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
conotruncal ridge hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the conotruncal ridge hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
adenohypophysis hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the adenohypophysis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
alisphenoid bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the alisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vascular smooth muscle cell hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vascular smooth muscle cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hypaxial muscle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hypaxial muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
basisphenoid bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the basisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pterygoid bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pterygoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
endometrium hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the endometrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vagina hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vagina hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dorsal root ganglion hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dorsal root ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aorta tubular hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aorta tubular hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
metacarpal bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the metacarpal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axial skeleton hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axial skeleton hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
submandibular gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the submandibular gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
myocardial trabeculae hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the myocardial trabeculae hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vas deferens hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vas deferens hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebellum hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebellum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sinus venosus hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sinus venosus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney medulla hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney medulla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pubis hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pubis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ascending aorta hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ascending aorta hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mandible hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mandible hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
midbrain hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the midbrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
nasal bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the nasal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney cortex hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney cortex hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
maxillary shelf hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the maxillary shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
rathke's pouch hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the rathke's pouch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
clavicle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the clavicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sertoli cell hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sertoli cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
eyelid hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the eyelid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
turbinate hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the turbinate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vertebral body hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vertebral body hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary trunk hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary trunk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreatic acinar hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular ganglion hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
clitoris hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the clitoris hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
placental labyrinth hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the placental labyrinth hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pharyngeal arch hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ovary hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
exocrine pancreas hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ureter hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ureter hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
glossopharyngeal nerve hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the glossopharyngeal nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
telencephalon hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the telencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
forebrain hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the forebrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
scapular bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the scapular bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreatic islet hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreatic islet hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
seminal vesicle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pharynx hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pharynx hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
myocardium hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
trachea hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the trachea hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thymus cortex hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thymus cortex hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
palate bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the palate bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
inner ear hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the inner ear hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vomer bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vomer bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
meibomian gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the meibomian gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
interparietal bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the interparietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
uterus hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the uterus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
esophagus hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the esophagus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
stomach hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the stomach hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lateral prostate gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lateral prostate gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrium hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bulbourethral gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the bulbourethral gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
philtrum hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the philtrum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
presphenoid bone hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the presphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart right ventricle hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart right ventricle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
urinary bladder hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the urinary bladder hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
trabecula carnea hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the trabecula carnea hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney papillary hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney papillary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
gonadal ridge hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the gonadal ridge hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary artery hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sternum hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sternum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
otic capsule hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the otic capsule hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retina hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retina hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
prostate gland hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the prostate gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thymus hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thymus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
iris hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the iris hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Harmonizome 3.0

CPVT3 Gene

ARVD4 Gene

ARVD6 Gene

ARVD3 Gene

MYL3 Gene

VEPH1 Gene

LVNC2 Gene

ventricular hypoplasia Gene Set

Ventricular Hypoplasia Gene Set

ventricular hypoplasia Gene Set

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

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

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

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

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

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

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

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

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

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

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

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

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

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

brugada syndrome; ventricular fibrillation; ventricular premature complexes Gene Set

left ventricular mass; left ventricular wall thickness Gene Set

arrhythmogenic right ventricular dysplasia; tachycardia, ventricular Gene Set

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

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

heart septal defects, ventricular; ventricular septal defects Gene Set

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

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

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

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

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

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

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

hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

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

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

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

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

hypertension; hypertrophy, left ventricular; ventricular remodeling Gene Set

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

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

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

ventricular myocardium compact layer hypoplasia Gene Set

Left Ventricular Hypoplasia Gene Set

ventricular myocardium compact layer hypoplasia Gene Set

ventricular (matrix) zone of pons Gene Set

ventricular (matrix) zone of cerebellum Gene Set

Left ventricular noncompaction 10 Gene Set

Ventricular fibrillation Gene Set

Catecholaminergic polymorphic ventricular tachycardia Gene Set

Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

Ventricular septal defect 3 Gene Set

Ventricular septal defect 1 Gene Set

Left ventricular noncompaction cardiomyopathy Gene Set

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set

Paroxysmal familial ventricular fibrillation Gene Set

Ventricular tachycardia Gene Set

Arrhythmogenic right ventricular cardiomyopathy Gene Set

Left ventricular noncompaction 8 Gene Set

Left ventricular noncompaction 6 Gene Set

Left ventricular noncompaction 7 Gene Set

Left ventricular noncompaction 5 Gene Set

Ventricular fibrillation, paroxysmal familial, 2 Gene Set

Ventricular tachycardia, catecholaminergic polymorphic, 2 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 1 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 2 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 5 Gene Set

Left ventricular noncompaction 1 Gene Set

Dilated cardiomyopathy with left ventricular noncompaction Gene Set

Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set