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hypertension and esrd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension and esrd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
end- stage renal disease (esrd) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease end- stage renal disease (esrd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esrd Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term esrd in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; hypertension; hypertension, pulmonary; tricuspid valve insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; hypertension; hypertension, pulmonary; tricuspid valve insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension induced by pregnancy; hypertension, pregnancy-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, portal; hypertension, pulmonary; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, portal; hypertension, pulmonary; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
hypertension and obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension and obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type ii diabetes and hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type ii diabetes and hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension and left ventricular mass Gene SetFrom 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. |
abdominal adiposity and hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal adiposity and hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hyperpotassemia And Hypertension, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperpotassemia And Hypertension, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypertension and brachydactyly syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertension and brachydactyly syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Idiopathic and/or familial pulmonary arterial hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic and/or familial pulmonary arterial hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diastolic blood pressure response to thiazide and thiazide-like diuretics in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure response to thiazide and thiazide-like diuretics in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure response to thiazide and thiazide-like diuretics in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure response to thiazide and thiazide-like diuretics in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary hypertension, primary, fenfluramine-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, fenfluramine-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertension, Pulmonary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Pulmonary from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Portal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Portal from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Renovascular Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Renovascular from the curated CTD Gene-Disease Associations dataset. |
Hypertension Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension from the curated CTD Gene-Disease Associations dataset. |
Intracranial Hypertension Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Hypertension from the curated CTD Gene-Disease Associations dataset. |
Ocular Hypertension Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ocular Hypertension from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Essential Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Essential from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Diastolic, Resistance to Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Diastolic, Resistance to from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Pregnancy-Induced Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Pregnancy-Induced from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Malignant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Malignant from the curated CTD Gene-Disease Associations dataset. |
Brachydactyly with hypertension Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brachydactyly with hypertension from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Renal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Renal from the curated CTD Gene-Disease Associations dataset. |
PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset. |
Renal Failure, Progressive, with Hypertension Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Failure, Progressive, with Hypertension from the curated CTD Gene-Disease Associations dataset. |
Hypertension Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hypertension in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
primary pulmonary hypertension Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary pulmonary hypertension from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hypertension Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hypertension from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
essential hypertension Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease essential hypertension in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
hypertension Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease hypertension in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
malignant renovascular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
benign essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease benign essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intracranial hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intracranial hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant secondary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
secondary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary pulmonary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary pulmonary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
portal hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease portal hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ocular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ocular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
renal hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
renovascular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; inflammation; obesity; sleep apnea, obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; inflammation; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypertension; subarachnoid hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; overweight; weight gain; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; overweight; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; hypertension, renovascular; renal artery obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension, renovascular; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pre-eclampsia; pregnancy complications; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pre-eclampsia; pregnancy complications; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; hypertension; nephrosclerosis; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension; nephrosclerosis; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene SetFrom 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. |
hypertension, renal; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, renal; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hypertension; obesity, localized Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension; obesity, localized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; hypertension; hypertrophy, left ventricular; left ventricular hypertrophy Gene SetFrom 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. |
hyperlipidemias; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
preeclampsia; hypertension, gestational Gene SetFrom GAD Gene-Disease Associations genes associated with the disease preeclampsia; hypertension, gestational in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
preeclampsia; hypertension, pregnancy induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease preeclampsia; hypertension, pregnancy induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pre-eclampsia; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; stroke, lacunar; atherothrombotic brain infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; stroke, lacunar; atherothrombotic brain infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; hypertension; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; cerebral infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; cerebral infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; left ventricular function Gene SetFrom 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. |
atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina pectoris; hypertension; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; brain infarction; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; brain infarction; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; cholesterol, hdl; cholesterol, ldl; hypertension; lipoproteins; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; cholesterol, hdl; cholesterol, ldl; hypertension; lipoproteins; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; metabolic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; hypertension; renal artery obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
erythropoietin induced hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease erythropoietin induced hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cough; coughing; hypertension; nephritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cough; coughing; hypertension; nephritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eclampsia; hypertension, pregnancy-induced; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary heart disease; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary heart disease; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; diabetes mellitus, type 2; hypercholesterolemia; hyperlipidemias; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus, type 2; hypercholesterolemia; hyperlipidemias; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity- associated hypertension ??????? Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity- associated hypertension ??????? in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibromuscular dysplasia; hypertension; renal artery obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibromuscular dysplasia; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
calcinosis; diabetes complications; heart valve diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease calcinosis; diabetes complications; heart valve diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes complications; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes complications; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; coronary thrombosis; diabetes complications; hypertension; mitral valve stenosis; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; coronary thrombosis; diabetes complications; hypertension; mitral valve stenosis; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
connective tissue diseases; hypertension, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease connective tissue diseases; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; hypertension; glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; hypertension; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain damage, chronic; hypertension; myocardial ischemia; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain damage, chronic; hypertension; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; hypercapnia; hypertension, pulmonary; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic retinopathy; hyperglycemia; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic retinopathy; hyperglycemia; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; diabetes mellitus; genetic predisposition to disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus; genetic predisposition to disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetic angiopathies; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic angiopathies; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; metabolic syndrome x; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; carotid artery diseases; hemochromatosis; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; carotid artery diseases; hemochromatosis; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension/complications* Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension/complications* in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; metabolic syndrome x; overweight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; metabolic syndrome x; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; nephrotic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; diabetes complications; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; diabetes complications; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart diseases; hypercholesterolemia; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart diseases; hypercholesterolemia; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis, iga; hypertension; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; hypertension; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disease models, animal; hypertension; hypertrophy, left ventricular Gene SetFrom 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. |
cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; diabetes, type 2; hypertension; cancer; depression; dementia; cerebrovascular disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; diabetes, type 2; hypertension; cancer; depression; dementia; cerebrovascular disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hypertension; osteoporosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hypertension; osteoporosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african Gene SetFrom GAD Gene-Disease Associations genes associated with the disease african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv; hypertension; nephrotic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv; hypertension; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; intracranial arteriosclerosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, renal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; cardiovascular diseases; hypertension; migraine disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; cardiovascular diseases; hypertension; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; cardiovascular diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; cardiovascular diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; dyslipidemias; hypertension; metabolic syndrome x; obesity; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; dyslipidemias; hypertension; metabolic syndrome x; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; diabetes mellitus; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; diabetes mellitus; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hypertension; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; cardiovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; cardiovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary restenosis; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary restenosis; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; heart diseases; hypertension; hypertrophy, left ventricular Gene SetFrom 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. |
hypertension; dyslipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; dyslipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced; pre-eclampsia; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral hemorrhage; cerebral hemorrhages; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pre-eclampsia; pregnancy complications, cardiovascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pre-eclampsia; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; beta-glucuronidase; anaphylactoid purpura Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; beta-glucuronidase; anaphylactoid purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypercholesterolemia; hypertension; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypercholesterolemia; hypertension; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; sleep apnea, obstructive; snoring Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; sleep apnea, obstructive; snoring in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypertension; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pregnancy complications, cardiovascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; exercise Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; exercise in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; polycythemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; endometrial neoplasms; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; endometrial neoplasms; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; coronary artery disease; heart failure; hypertension; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary artery disease; heart failure; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hypertriglyceridemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; hypertension 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; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; glucose tolerance; insulin; hematology indices Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; glucose tolerance; insulin; hematology indices in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; insulin resistance; metabolic syndrome x; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperlipidemias; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperlipidemias; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; hypertension; macular degeneration; prostatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension; macular degeneration; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; hypertension; fabry's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; hypertension; fabry's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; retinal artery occlusion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic; nephrosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; nephrosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carotid artery diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary stenosis; hypercholesterolemia; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary stenosis; hypercholesterolemia; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; heart disease, ischemic; hypertension; left ventricular hypertrophy Gene SetFrom 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. |
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris; apoplexy; cardiovascular diseases; diabetes mellitus; hyperlipidemias; hypertension; myocardial infarction; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; diabetes complications; hypercholesterolemia; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; diabetes complications; hypercholesterolemia; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; lung cancer; abdominal aortic aneurysm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; lung cancer; abdominal aortic aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain injuries; intracranial hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain injuries; intracranial hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; polycythemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary stenosis; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary stenosis; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; diabetes mellitus; hypertension; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus; hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; left ventricular hypertrophy Gene SetFrom 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. |
preeclampsia; hypertension, pregnancy induced; eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease preeclampsia; hypertension, pregnancy induced; eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bradycardia; glaucoma, open-angle; ocular hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bradycardia; glaucoma, open-angle; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; heart failure; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; h. pylori infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; h. pylori infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; triglycerides; hypertension; glucose tolerance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; triglycerides; hypertension; glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; hypertension; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; hypertension; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; insulin; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; coronary artery disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; coronary artery disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; hypertension; hypertrophy, left ventricular Gene SetFrom 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. |
cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
edema; hypertension; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease edema; hypertension; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hypertension; insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hypertrophy, left ventricular; left ventricular hypertrophy Gene SetFrom 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. |
hypertension; obesity; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hyperaldosteronism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; hyperaldosteronism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hypertension; insulin; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; preeclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; preeclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, cirrhotic portal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, cirrhotic portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; kidney failure; kidney; failure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; kidney failure; kidney; failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carotid artery diseases; hypertension; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hypertension; insulin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; insulin; metabolic syndrome; hypertriglyceridemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; insulin; metabolic syndrome; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; diabetes, type 2; hypertension; nephropathy, diabetic; albuminuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; diabetes, type 2; hypertension; nephropathy, diabetic; albuminuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral amyloid angiopathy; cerebral hemorrhage; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetic nephropathies; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetic nephropathies; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gitelman syndrome; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gitelman syndrome; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; diabetes mellitus; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; diabetes mellitus; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; insulin; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hypotension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; hypotension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glomerulonephritis; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glomerulonephritis; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
grade ii hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease grade ii hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; leukoaraiosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; leukoaraiosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic; hypertension; hypertrophic cardiomyopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertension; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; diabetes complications; diabetes mellitus; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; diabetes complications; diabetes mellitus; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; autonomic nervous system dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; autonomic nervous system dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, childhood acute; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hypertension; diabetes, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; hypertension; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; benazepril Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; benazepril in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; calcinosis; diabetes mellitus; hyperlipidemias; hypertension; mitral valve stenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis; diabetes mellitus; hyperlipidemias; hypertension; mitral valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
essential hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease essential hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dyslipidemias; fatty liver; hypertension; insulin resistance; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dyslipidemias; fatty liver; hypertension; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; diabetic angiopathies; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; diabetic angiopathies; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute coronary syndrome; coronary stenosis; diabetes complications; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; coronary stenosis; diabetes complications; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dyslipidemias; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dyslipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; hypertension; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; hypertension; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; cardiovascular diseases; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; cardiovascular diseases; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
triglycerides; hypertension; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease triglycerides; hypertension; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; renal sodium handling Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; renal sodium handling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hypertension; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hypertrophy, left ventricular Gene SetFrom 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. |
cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hyperlipidemias; hypertension; obesity; sleep apnea, obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; diabetes mellitus; dyslipidemias; hypertension; obesity; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus; dyslipidemias; hypertension; obesity; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; renal disease, end stage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; renal disease, end stage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hypertension; atherosclerosis; cerebrovascular disease; dyslipemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension; atherosclerosis; cerebrovascular disease; dyslipemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebrovascular disorders; foramen ovale, patent; hyperhomocysteinemia; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; foramen ovale, patent; hyperhomocysteinemia; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
down syndrome; heart defects, congenital; hypertension, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; atherosclerosis; heart diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; atherosclerosis; heart diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute coronary syndrome; dyslipidemias; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; dyslipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; myocardial infarction; stroke; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; myocardial infarction; stroke; thrombophilia 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 SetFrom 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. |
aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cough; coughing; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cough; coughing; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes complications; hypercholesterolemia; hypertension; myocardial infarction; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes complications; hypercholesterolemia; hypertension; myocardial infarction; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; hypertension; hypotension; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; hypertension; hypotension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gaucher disease; hypertension, pulmonary; necrosis; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gaucher disease; hypertension, pulmonary; necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypercholesterolemia; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; left ventricular structure Gene SetFrom 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. |
diabetes, type 2; hypertension; insulin; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; diabetic angiopathies; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; diabetic angiopathies; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension ; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension(c14.907.489)/genetics; (c23.550.291.687.500) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension(c14.907.489)/genetics; (c23.550.291.687.500) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension (young onset) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension (young onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, open-angle; low tension glaucoma; ocular hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, open-angle; low tension glaucoma; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; atherosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, portal; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, portal; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; dna damage; hypertension; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; dna damage; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; diabetes mellitus; hypercholesterolemia; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; nephrosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; nephrosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; stroke, ischemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart failure; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; cardiovascular diseases; diabetes mellitus, type 2; hypertension; kidney diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; cardiovascular diseases; diabetes mellitus, type 2; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; hemorrhage; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hypertrophy, left ventricular; ventricular remodeling Gene SetFrom 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. |
diabetes mellitus, type 2; diabetic nephropathies; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; diabetic nephropathies; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart anomalies, congenital; pulmonary hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart anomalies, congenital; pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; inflammation; ventricular remodeling Gene SetFrom 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. |
adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dyslipidemias; metabolic syndrome x; obesity; renal hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dyslipidemias; metabolic syndrome x; obesity; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; renal dysfunction, posttransplantation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; renal dysfunction, posttransplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; retinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; kidney diseases; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; kidney diseases; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hypertension; diabetes, type 1; albuminuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1; albuminuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; ventricular remodeling Gene SetFrom 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. |
arthritis, rheumatoid; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; kallikrein activity, urinary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; kallikrein activity, urinary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cognitive ability ; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cognitive ability ; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; coronary disease; factor xii deficiency; hypercholesterolemia; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; factor xii deficiency; hypercholesterolemia; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; hypertension; albuminuria; glycohemoglobin a1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; hypertension; albuminuria; glycohemoglobin a1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, open-angle; ocular hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, open-angle; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension; obesity; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carotid artery diseases; carotid artery stenosis; carotid stenosis; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; carotid artery stenosis; carotid stenosis; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic; lupus erythematosus, systemic; lupus nephritis; nephritis sle; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; lupus erythematosus, systemic; lupus nephritis; nephritis sle; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hyperlipidemias; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial hypertension of early onset. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; hypertension; intracranial arteriosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; hypertension; intracranial arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hypotension, orthostatic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; hypotension, orthostatic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; hyperlipidemias; hypertension; intracranial embolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; hyperlipidemias; hypertension; intracranial embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, gestational Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, gestational in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart septal defects, ventricular; hypertension, pulmonary Gene SetFrom 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. |
albuminuria; diabetes mellitus; hypertension; hypertrophy, left ventricular; left ventricular hypertrophy Gene SetFrom 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. |
birth weight; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term hypertension in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Response to diuretic therapy in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to diuretic therapy in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hypertension risk in short sleep duration Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
hypertension Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease hypertension in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
hypertension Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hypertension phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypertension associated with pheochromocytoma Gene SetFrom HPO Gene-Disease Associations genes associated with the hypertension associated with pheochromocytoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
portal hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the portal hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
maternal hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the maternal hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renovascular hypertension Gene SetFrom HPO Gene-Disease Associations genes associated with the renovascular hypertension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Hypertension, Pulmonary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Pulmonary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Portal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Portal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Intracranial Hypertension Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Intracranial Hypertension phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Ocular Hypertension Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Ocular Hypertension phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Pregnancy-Induced Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Pregnancy-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Renovascular Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Renovascular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Malignant Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Malignant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Renal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Renal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
hypertension Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary hypertension Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
salt-resistant hypertension Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the salt-resistant hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ocular hypertension Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ocular hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
salt-sensitive hypertension Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the salt-sensitive hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
portal hypertension Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the portal hypertension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{low renin hypertension, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {low renin hypertension, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{?hypertension, essential} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {?hypertension, essential} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, salt-sensitive} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, salt-sensitive} phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 7} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 7} phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 5} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, salt-sensitive essential, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, salt-sensitive essential, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
nephropathy-hypertension Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephropathy-hypertension phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, familial primary, 1, with or without hht Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypertension, essential Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypertension, essential phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, insulin resistance-related, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, insulin resistance-related, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 6} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
?hypertension, salt-resistant Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?hypertension, salt-resistant phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 4} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypertension with brachydactyly Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypertension with brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, diastolic, resistance to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, diastolic, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 8} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, pregnancy-induced} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, pregnancy-induced} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary hypertension, neonatal, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, neonatal, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, essential, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, essential, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypertension Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term hypertension in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Idiopathic Pulmonary Arterial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Arterial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Essential Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Essential Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ocular Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ocular Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Borderline Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Borderline Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Thromboembolic Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Thromboembolic Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diastolic Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diastolic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Genetic Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Genetic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Altitude Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Altitude Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Isolated Systolic Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Isolated Systolic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Maternal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Maternal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neurogenic Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neurogenic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Orthostatic Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Orthostatic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Persistent Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Persistent Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Portal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Portal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Sclerosis With Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Sclerosis With Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Associated Pulmonary Arterial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Associated Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renin Induced Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renin Induced Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Primary Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Primary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Pulmonary Arterial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sporadic Primary Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Primary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uncomplicated Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uncomplicated Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low-Renin Essential Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low-Renin Essential Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pre-Eclampsia Added To Pre-Existing Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pre-Eclampsia Added To Pre-Existing Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renin-Dependent Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renin-Dependent Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uncontrolled Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uncontrolled Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intra-Abdominal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intra-Abdominal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intracranial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Renin Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High Renin Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Systolic Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Systolic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
White Coat Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease White Coat Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
End Stage Renal Disease Due To Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease End Stage Renal Disease Due To Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intraoperative Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intraoperative Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endocrine Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endocrine Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Hypertension, Primary, Dexfenfluramine-Associated Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Hypertension, Primary, Dexfenfluramine-Associated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Pulmonary Arterial Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renoprival Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renoprival Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Supine Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Supine Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Venous Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Venous Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Group 3 Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Group 3 Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Portal Hypertension, Noncirrhotic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Portal Hypertension, Noncirrhotic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Postcapillary Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Postcapillary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Failure, Progressive, With Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Failure, Progressive, With Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paroxysmal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paroxysmal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rebound Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rebound Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Essential Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Essential Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypertension Complicated Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypertension Complicated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Non-Cirrhotic Portal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Cirrhotic Portal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Kallikrein Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Kallikrein Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Precapillary Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Precapillary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypertension, Resistant To Conventional Therapy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypertension, Resistant To Conventional Therapy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High-Renin Essential Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Renin Essential Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Cirrhotic Portal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Cirrhotic Portal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ocular Hypertension, Bilateral Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ocular Hypertension, Bilateral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pregnancy Associated Hypertension Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy Associated Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hypertension Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Hypertension Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Transient Hypertension Of Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Hypertension Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pulmonary hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
salt-resistant hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the salt-resistant hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ocular hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ocular hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
salt-sensitive hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the salt-sensitive hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
portal hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the portal hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to hypertension Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to hypertension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Hypertension Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hypertension from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Primary pulmonary hypertension Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Primary pulmonary hypertension from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Pulmonary hypertension Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pulmonary hypertension from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hypertension Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Hypertension in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pulmonary hypertension Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Pulmonary hypertension in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ocular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ocular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intracranial hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intracranial hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Portal hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Portal hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pulmonary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary pulmonary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary pulmonary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renovascular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renal hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Secondary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Benign essential hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign essential hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant renovascular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant secondary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Benign secondary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Benign renovascular hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign renovascular hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pulmonary hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Portal hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Portal hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary arterial hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary arterial hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary pulmonary hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary pulmonary hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
HYPERTENSION RESISTANT TO CONVENTIONAL THER Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the HYPERTENSION RESISTANT TO CONVENTIONAL THER phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Essential hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Essential hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Isolated systolic hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated systolic hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary arterial hypertension associated Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary arterial hypertension associated phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Brachydactyly-arterial hypertension syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Brachydactyly-arterial hypertension syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SOX17-related pulmonary arterial hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SOX17-related pulmonary arterial hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Heritable pulmonary arterial hypertension Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Heritable pulmonary arterial hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Essential hypertension (time to event) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Essential hypertension (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
White matter hyperintensity volume x hypertension interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensity volume x hypertension interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
White matter hyperintensity volume (adjusted for hypertension) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter hyperintensity volume (adjusted for hypertension) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure response to hydrochlorothiazide in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure response to hydrochlorothiazide in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure response to hydrochlorothiazide in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure response to hydrochlorothiazide in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cardiovascular disease in hypertension (ACE inhibitor interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular disease in hypertension (ACE inhibitor interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cardiovascular disease in hypertension (calcium channel blocker interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cardiovascular disease in hypertension (calcium channel blocker interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Myocardial infarction in hypertension (calcium channel blocker interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Myocardial infarction in hypertension (calcium channel blocker interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Resistance to antihypertensive treatment in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Resistance to antihypertensive treatment in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure night-to-day ratio in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure night-to-day ratio in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure night-to-day ratio in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure night-to-day ratio in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Uric acid elevation in response to thiazide-like diuretic in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Uric acid elevation in response to thiazide-like diuretic in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure in young-onset hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure in young-onset hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to diuretic therapy in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to diuretic therapy in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to chemotherapy in breast cancer (hypertension) (bevacizumab) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to chemotherapy in breast cancer (hypertension) (bevacizumab) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hypertension in type 2 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Resistant hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Resistant hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hypertension risk in short sleep duration Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hypertension (young onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertension (young onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulmonary arterial hypertension (without BMPR2 mutations) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary arterial hypertension (without BMPR2 mutations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Change in glucose in response to thiazide diuretic treatment in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Change in glucose in response to thiazide diuretic treatment in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alzheimer's disease in hypertension-negative individuals Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease in hypertension-negative individuals phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alzheimer's disease in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Idiopathic intracranial hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic intracranial hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulmonary arterial hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulmonary arterial hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to beta blocker use in hypertension (systolic blood pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to beta blocker use in hypertension (systolic blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bevacizumab-induced hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bevacizumab-induced hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bevacizumab-induced composite toxicity (either hypertension or proteinuria) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bevacizumab-induced composite toxicity (either hypertension or proteinuria) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene SetFrom Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset. |
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coloboma, uveal, with cleft lip and palate and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom 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. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset. |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene SetFrom 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. |
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset. |
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety and hostility and depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vitamins and metabolites in pregnant women and neonates Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on amino acids and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene SetFrom OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset. |
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset. |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset. |
Synthesis and interconversion of nucleotide di- and triphosphates Gene Setproteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
SRF and miRs in smooth muscle differentiation and proliferation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset. |
ApoE and miR 146 in inflammation and atherosclerosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset. |
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset. |
Somatroph axis GH and its relationship to dietary restriction and aging Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset. |
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Setproteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset. |
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Setproteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset. |
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Setproteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset. |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Setproteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset. |
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Setproteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset. |
Transport of bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset. |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Regulation of gene expression and signal transduction in immune and stress responses Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Basic cell groups and regions Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
head and face region of M1 Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
telomeres telomerase cellular aging and immortality Gene SetFrom Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset. |
mcalpain and friends in cell motility Gene SetFrom Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset. |
role of ppar-gamma coactivators in obesity and thermogenesis Gene SetFrom Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset. |
il12 and stat4 dependent signaling pathway in th1 development Gene SetFrom Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset. |
hypoxia and p53 in the cardiovascular system Gene SetFrom Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset. |
lissencephaly gene (lis1) in neuronal migration and development Gene SetFrom Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset. |
role of erbb2 in signal transduction and oncology Gene SetFrom Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset. |
corticosteroids and cardioprotection Gene SetFrom Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset. |
cyclins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
mechanism of acetaminophen activity and toxicity Gene SetFrom Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset. |
nfat and hypertrophy of the heart Gene SetFrom Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset. |
acetylation and deacetylation of rela in nucleus Gene SetFrom Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset. |
thrombin signaling and protease-activated receptors Gene SetFrom Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset. |
antigen processing and presentation Gene SetFrom Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset. |
stathmin and breast cancer resistance to antimicrotubule agents Gene SetFrom Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset. |
role of ß-arrestins in the activation and targeting of map kinases Gene SetFrom Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset. |
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene SetFrom Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset. |
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene SetFrom Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset. |
btg family proteins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene SetFrom Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset. |
endocytotic role of ndk phosphins and dynamin Gene SetFrom Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset. |
regulation of eif-4e and p70s6 kinase Gene SetFrom Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset. |
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene SetFrom Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset. |
vegf hypoxia and angiogenesis Gene SetFrom Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset. |
yaci and bcma stimulation of b cell immune responses Gene SetFrom Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset. |
lck and fyn tyrosine kinases in initiation of tcr activation Gene SetFrom Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset. |
hiv-1 nef: negative effector of fas and tnf Gene SetFrom Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset. |
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene SetFrom Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset. |
ucalpain and friends in cell spread Gene SetFrom Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset. |
ionomycin and phorbal ester signaling pathway Gene SetFrom Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset. |
carm1 and regulation of the estrogen receptor Gene SetFrom Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset. |
phosphoinositides and their downstream targets Gene SetFrom Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset. |
melanocyte development and pigmentation pathway Gene SetFrom Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset. |
akap95 role in mitosis and chromosome dynamics Gene SetFrom Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset. |
transcription factor creb and its extracellular signals Gene SetFrom Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset. |
visceral fat deposits and the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset. |
the igf-1 receptor and longevity Gene SetFrom Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset. |
cdc25 and chk1 regulatory pathway in response to dna damage Gene SetFrom Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset. |
human cytomegalovirus and map kinase pathways Gene SetFrom Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset. |
influence of ras and rho proteins on g1 to s transition Gene SetFrom Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset. |
proteolysis and signaling pathway of notch Gene SetFrom Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset. |
apoptotic dna-fragmentation and tissue homeostasis Gene SetFrom Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset. |
ion channels and their functional role in vascular endothelium Gene SetFrom Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset. |
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene SetFrom Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset. |
fosb gene expression and drug abuse Gene SetFrom Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset. |
links between pyk2 and map kinases Gene SetFrom Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset. |
opposing roles of aif in apoptosis and cell survival Gene SetFrom Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset. |
degradation of the rar and rxr by the proteasome Gene SetFrom Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset. |
cadmium induces dna synthesis and proliferation in macrophages Gene SetFrom Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset. |
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene SetFrom Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset. |
role of brca1 brca2 and atr in cancer susceptibility Gene SetFrom Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset. |
chrebp regulation by carbohydrates and camp Gene SetFrom Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset. |
pten dependent cell cycle arrest and apoptosis Gene SetFrom Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset. |
induction of apoptosis through dr3 and dr4/5 death receptors Gene SetFrom Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset. |
CIITA-18437201-Raji B cells and iDC-human Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
VDR-23401126-LCL-AND-THP1-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
Hypothyroidism, central, and testicular enlargement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, mental retardation, and seizures Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vater association with macrocephaly and ventriculomegaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal hamartomas nephroblastomatosis and fetal gigantism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene SetFrom 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. |
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microtia, hearing impairment, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, spastic quadriplegia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined cellular and humoral immune defects with granulomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined d-2- and l-2-hydroxyglutaric aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sinoatrial node dysfunction and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation with language impairment and autistic features Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, anterior maxillary protrusion, and strabismus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile convulsions and paroxysmal choreoathetosis, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple Cutaneous and Mucosal Venous Malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy hereditary sensory and autonomic type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly with mental retardation and digital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth retardation, developmental delay, coarse facies, and early death Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anemia sideroblastic and spinocerebellar ataxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, congenital heart defects, and posterior embryotoxon Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rigidity and multifocal seizure syndrome, lethal neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alopecia, neurologic defects, and endocrinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Knuckle pads, deafness AND leukonychia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene SetFrom 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. |
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multicentric osteolysis, nodulosis and arthropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stapes ankylosis with broad thumb and toes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene SetFrom 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. |
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, short stature, and impaired glucose metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination and Congenital Cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy dilated with woolly hair and keratoderma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom 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. |
Cataract, microphthalmia and nystagmus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and anterior segment dysgenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone fragility with contractures, arterial rupture, and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna and fibula absence of with severe limb deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor v and factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paragangliomas and Pheochromocytomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Band-like calcification with simplified gyration and polymicrogyria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, epilepsy, and diabetes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia and hypogonadotropic hypogonadism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, juvenile, with microcornea and glucosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, deafness, and narcolepsy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile macular degeneration and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monocyte and dendritic cell deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, hiatal hernia and nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pancreatic agenesis and congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined malonic and methylmalonic aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis Gyrata syndrome of Beare and Stevenson Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aniridia, cerebellar ataxia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hereditary motor and sensory neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniosynostosis and dental anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, hyperphagia, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebroretinal microangiopathy with calcifications and cysts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Generalized epilepsy and paroxysmal dyskinesia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alacrima, achalasia, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, normal intelligence and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Calcification of joints and arteries Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis and recurrent skin vesicles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pineal hyperplasia AND diabetes mellitus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Morbid obesity and spermatogenic failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skeletal defects, genital hypoplasia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Striatal necrosis, bilateral, and progressive polyneuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sensory and autonomic neuropathy type IIA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopia, high, with cataract and vitreoretinal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of factor V and factor VIII, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Camptodactyly, tall stature, and hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum and acne Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth deficiency and mental retardation with facial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, cochlear, with myopia and intellectual impairment Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of sialidase AND beta galactosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Setproteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset. |
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Setproteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset. |
6S methyltransferase and RG-containing Sm proteins complex Gene Setproteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset. |
Remodeling and spacing factor (RSF) complex Gene Setproteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset. |
PBAF complex (Polybromo- and BAF containing complex) Gene Setproteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset. |
Cleavage and polyadenylation factor (CPSF) Gene Setproteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Nucleic and chromatin Fanconi complex Gene Setproteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset. |
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Setproteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset. |
20S methylosome and RG-containing Sm protein complex Gene Setproteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset. |
Amino Acids, Peptides, and Proteins Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset. |
Bile Acids and Salts Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset. |
Prime and Bond NT Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset. |
drospirenone and ethinyl estradiol combination Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset. |
Hypophosphatemic Rickets And Hyperparathyroidism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset. |
Synovitis granulomatous with uveitis and cranial neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory and Motor Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Preaxial deficiency, postaxial polydactyly and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset. |
Combined Cellular And Humoral Immune Defects With Granulomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset. |
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset. |
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset. |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset. |
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset. |
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset. |
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset. |
Microtia, Hearing Impairment, And Cleft Palate Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset. |
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Acromegaloid features, overgrowth, cleft palate, and hernia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset. |
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset. |
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset. |
Craniosynostosis, anal anomalies, and porokeratosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset. |
Sacral defect and anterior sacral meningocele Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset. |
Classical Lissencephalies and Subcortical Band Heterotopias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 1 and deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Russe type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset. |
Blepharophimosis, Ptosis, and Epicanthus Inversus Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset. |
Hypotrichosis And Recurrent Skin Vesicles Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset. |
Signs and Symptoms, Digestive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria and Homocystinuria, CblD Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset. |
Head and Neck Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset. |
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset. |
Cataract, Juvenile, With Microcornea And Glucosuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset. |
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset. |
Venous Malformations, Multiple Cutaneous and Mucosal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset. |
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset. |
Postoperative Nausea and Vomiting Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset. |
Myopathy with lactic acidosis and sideroblastic anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset. |
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset. |
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene SetFrom 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. |
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset. |
Hypopituitarism and septooptic 'dysplasia' Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset. |
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset. |
Aplasia of Lacrimal and Salivary Glands Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset. |
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset. |
Calcification of Joints and Arteries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset. |
CHOANAL ATRESIA AND LYMPHEDEMA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset. |