Congenital Supravalvular Aortic Stenosis

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Results for "Congenital Supravalvular Aortic Stenosis": 1001 gene sets

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Congenital Supravalvular Aortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Supravalvular Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Aortic Stenosis, Supravalvular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Stenosis, Supravalvular from the curated CTD Gene-Disease Associations dataset.
supravalvular aortic stenosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease supravalvular aortic stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
supravalvular aortic stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease supravalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
supravalvular aortic stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease supravalvular aortic stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
supravalvular aortic stenosis Gene Set From HPO Gene-Disease Associations genes associated with the supravalvular aortic stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Aortic Stenosis, Supravalvular Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Stenosis, Supravalvular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Supravalvular Aortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supravalvular Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supravalvular aortic stenosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Supravalvular aortic stenosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Supravalvular aortic stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Supravalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
retinal arterial macroaneurysm with supravalvular pulmonic stenosis Gene Set From OMIM Gene-Disease Associations genes associated with the retinal arterial macroaneurysm with supravalvular pulmonic stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.
Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
aneurysm, ruptured; aortic aneurysm, abdominal; arterial occlusive diseases; carotid artery stenosis; carotid stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal; arterial occlusive diseases; carotid artery stenosis; carotid stenosis 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 Set From 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.
aortic valve stenosis; calcinosis; mitral valve stenosis; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis; mitral valve stenosis; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve insufficiency; aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve insufficiency; aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipids; left ventricular mass; aortic gradient; aortic valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease lipids; left ventricular mass; aortic gradient; aortic valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Congenital Stenosis Of Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Stenosis Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
apoplexy; carotid artery stenosis; carotid stenosis; hyperhomocysteinemia; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; carotid artery stenosis; carotid stenosis; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; carotid artery stenosis; carotid stenosis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; carotid artery stenosis; carotid stenosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery stenosis; carotid stenosis; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery stenosis; carotid stenosis; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery stenosis; carotid stenosis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery stenosis; carotid stenosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery stenosis; carotid stenosis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery stenosis; carotid stenosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery stenosis; carotid stenosis; graft occlusion, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery stenosis; carotid stenosis; graft occlusion, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery diseases; carotid artery stenosis; carotid stenosis; hypertension Gene Set From 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.
carotid artery stenosis; carotid stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery stenosis; carotid stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Supravalvar aortic stenosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Supravalvar aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic Stenosis, Subvalvular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Stenosis, Subvalvular from the curated CTD Gene-Disease Associations dataset.
aortic valve stenosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic valve stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
subvalvular aortic stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subvalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
aortic valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
aortic valve stenosis; Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
calcific aortic valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease calcific aortic valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis; calcinosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis Gene Set From HPO Gene-Disease Associations genes associated with the aortic valve stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
calcific aortic valve stenosis Gene Set From HPO Gene-Disease Associations genes associated with the calcific aortic valve stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Aortic Valve Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Valve Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
aortic valve stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
supravalvar aortic stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the supravalvar aortic stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
supravalvar aortic stenosis Gene Set From OMIM Gene-Disease Associations genes associated with the supravalvar aortic stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.
Aortic Valve Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Stenosis Symptomatic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Stenosis Symptomatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rheumatic Aortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonrheumatic Aortic (Valve) Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonrheumatic Aortic (Valve) Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Aortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
aortic valve stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
supravalvar aortic stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the supravalvar aortic stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Aortic valve stenosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic valve stenosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Aortic valve stenosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic valve stenosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subvalvular aortic stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subvalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Supravalvar aortic stenosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Supravalvar aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Subvalvular aortic stenosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Subvalvular aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aortic valve stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic valve stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Calcific aortic valve stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Calcific aortic valve stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension Gene Set From 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.
aortic aneurysm, thoracic; aortic rupture Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, thoracic; aortic rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; aortic rupture Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormal aortic arch and aortic arch branch attachment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thoracic Aortic Aneurysm And Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
abnormal aortic arch and aortic arch branch attachment Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Familial thoracic aortic aneurysm and aortic dissection Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial thoracic aortic aneurysm and aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bicuspid aortic valve without aortic dilation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve without aortic dilation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Congenital Stenosis Of Aqueduct Of Sylvius Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Stenosis Of Aqueduct Of Sylvius in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Subaortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Subaortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Stenosis Of Pulmonary Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Stenosis Of Pulmonary Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Stenosis Of Nasal Pyriform Aperture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Stenosis Of Nasal Pyriform Aperture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypoplasia Of Aortic Arch Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Anomaly Of Aortic Arch Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomaly Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Atresia Of Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atresia Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Heart Defects, Congenital, And Other Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyloric stenosis, infantile hypertrophic, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carotid Stenosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carotid Stenosis from the curated CTD Gene-Disease Associations dataset.
Esophageal Stenosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal Stenosis from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 5 from the curated CTD Gene-Disease Associations dataset.
Coronary Stenosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Stenosis from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic 1 from the curated CTD Gene-Disease Associations dataset.
Pyloric Stenosis, Infantile Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Carotid Stenosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Carotid Stenosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Pyloric Stenosis, Hypertrophic Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Pyloric Stenosis, Hypertrophic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
coronary stenosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease coronary stenosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
carotid stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease carotid stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
discrete subaortic stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease discrete subaortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pulmonary valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypertrophic pyloric stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypertrophic pyloric stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tracheal stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tracheal stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
coronary stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease coronary stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mitral valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mitral valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pyloric stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pyloric stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tricuspid valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tricuspid valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
carotid stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pyloric stenosis, hypertrophic Gene Set From GAD Gene-Disease Associations genes associated with the disease pyloric stenosis, hypertrophic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; diabetes complications Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; carotid stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; carotid stenosis 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 Set From 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.
carotid stenosis; lupus erythematosus, systemic; lupus nephritis Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid stenosis; lupus erythematosus, systemic; lupus nephritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; carotid stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; carotid stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial diseases; tracheal stenosis; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial diseases; tracheal stenosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary restenosis; coronary stenosis; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary restenosis; coronary stenosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; coronary stenosis; Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary stenosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; mucocutaneous lymph node syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vessel stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease vessel stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; coronary stenosis; graft occlusion, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary stenosis; graft occlusion, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal artery stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease renal artery stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary restenosis; coronary stenosis; diabetes complications Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary restenosis; coronary stenosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary occlusion; coronary stenosis; diabetes complications Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary occlusion; coronary stenosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary stenosis; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary stenosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; hypercholesterolemia; hypertension; obesity Gene Set From 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.
coronary stenosis; hypertension Gene Set From 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.
infantile hypertrophic pyloric stenosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tracheal stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease tracheal stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina, unstable; coronary stenosis; inflammation; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease angina, unstable; coronary stenosis; inflammation; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid artery stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid artery stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
convalescence; coronary stenosis; mucocutaneous lymph node syndrome; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease convalescence; coronary stenosis; mucocutaneous lymph node syndrome; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary restenosis; coronary stenosis; graft occlusion, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary restenosis; coronary stenosis; graft occlusion, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid stenosis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid stenosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; coronary stenosis; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary stenosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; coronary stenosis; diabetes complications; hypertension Gene Set From 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.
coronary stenosis; prosthesis failure Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; prosthesis failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; brain ischemia; carotid stenosis; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; brain ischemia; carotid stenosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary restenosis; coronary stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary restenosis; coronary stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infantile hypertrophic pyloric stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease infantile hypertrophic pyloric stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; coronary stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
calcinosis; cardiomyopathies; coronary stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease calcinosis; cardiomyopathies; coronary stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; carotid stenosis; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; carotid stenosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary stenosis; hypertrophy, left ventricular; sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary stenosis; hypertrophy, left ventricular; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stenosis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term stenosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
hypertrophic pyloric stenosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease hypertrophic pyloric stenosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
pyloric stenosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease pyloric stenosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
subaortic stenosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the subaortic stenosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
pyloric stenosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the pyloric stenosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
arterial stenosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the arterial stenosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
urethral stenosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the urethral stenosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
coronary artery stenosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the coronary artery stenosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
tricuspid stenosis Gene Set From HPO Gene-Disease Associations genes associated with the tricuspid stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulmonary artery stenosis Gene Set From HPO Gene-Disease Associations genes associated with the pulmonary artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lacrimal duct stenosis Gene Set From HPO Gene-Disease Associations genes associated with the lacrimal duct stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral pulmonary artery stenosis Gene Set From HPO Gene-Disease Associations genes associated with the peripheral pulmonary artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
calcific mitral stenosis Gene Set From HPO Gene-Disease Associations genes associated with the calcific mitral stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subaortic stenosis Gene Set From HPO Gene-Disease Associations genes associated with the subaortic stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subglottic stenosis Gene Set From HPO Gene-Disease Associations genes associated with the subglottic stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midnasal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the midnasal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal canal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the spinal canal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal artery stenosis Gene Set From HPO Gene-Disease Associations genes associated with the renal artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stenosis of the medullary cavity of the long bones Gene Set From HPO Gene-Disease Associations genes associated with the stenosis of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal stenosis with reduced interpedicular distance Gene Set From HPO Gene-Disease Associations genes associated with the spinal stenosis with reduced interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aqueductal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the aqueductal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
arterial stenosis Gene Set From HPO Gene-Disease Associations genes associated with the arterial stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small intestinal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the small intestinal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tracheal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the tracheal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choanal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the choanal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulmonic stenosis Gene Set From HPO Gene-Disease Associations genes associated with the pulmonic stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the anal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral arterial stenosis Gene Set From HPO Gene-Disease Associations genes associated with the peripheral arterial stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mitral stenosis Gene Set From HPO Gene-Disease Associations genes associated with the mitral stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
laryngotracheal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the laryngotracheal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
urethral stenosis Gene Set From HPO Gene-Disease Associations genes associated with the urethral stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
esophageal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the esophageal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
laryngeal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the laryngeal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ureteral stenosis Gene Set From HPO Gene-Disease Associations genes associated with the ureteral stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duodenal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the duodenal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stenosis of the external auditory canal Gene Set From HPO Gene-Disease Associations genes associated with the stenosis of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pyloric stenosis Gene Set From HPO Gene-Disease Associations genes associated with the pyloric stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cervical spinal canal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the cervical spinal canal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Carotid Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Carotid Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Discrete Subaortic Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Discrete Subaortic Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pulmonary Valve Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Valve Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Coronary Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Coronary Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Pyloric Stenosis, Hypertrophic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Pyloric Stenosis, Hypertrophic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mitral Valve Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mitral Valve Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
vascular stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vascular stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary valve stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pulmonary artery stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pulmonary artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
tricuspid valve stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the tricuspid valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pharynx stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pharynx stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spiral modiolar artery stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spiral modiolar artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart right ventricle outflow tract stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart right ventricle outflow tract stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aorta stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aorta stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
supravalvar pulmonary trunk stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the supravalvar pulmonary trunk stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart left ventricle outflow tract stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart left ventricle outflow tract stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
umbilical artery stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the umbilical artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
umbilical vein stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the umbilical vein stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebral aqueductal stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebral aqueductal stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
artery stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
larynx stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the larynx stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ureteropelvic junction stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ureteropelvic junction stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pharyngeal arch artery stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mitral valve stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mitral valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ureter stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ureter stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
esophagus stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the esophagus stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
descending aorta stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the descending aorta stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
brain ventricle stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the brain ventricle stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
coronary artery stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the coronary artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
trachea stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the trachea stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pyloric stenosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pyloric stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pyloric stenosis, infantile hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
pyloric stenosis, infantile hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the pyloric stenosis, infantile hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
diaphyseal medullary stenosis with malignant fibrous histiocytoma Gene Set From OMIM Gene-Disease Associations genes associated with the diaphyseal medullary stenosis with malignant fibrous histiocytoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hydrocephalus due to aqueductal stenosis Gene Set From OMIM Gene-Disease Associations genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.
epidermolysis bullosa, junctional, with pyloric stenosis Gene Set From OMIM Gene-Disease Associations genes associated with the epidermolysis bullosa, junctional, with pyloric stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.
{carotid stenosis, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {carotid stenosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Pulmonary Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Carotid Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Carotid Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Arterial Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Arterial Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Canal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Canal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitral Valve Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitral Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Premature Occlusive Vascular Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Premature Occlusive Vascular Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Esophageal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Calcific Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Calcific Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Internal Carotid Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Internal Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Main Coronary Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Main Coronary Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tracheal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tracheal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tricuspid Valve Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tricuspid Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rheumatic Mitral Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Mitral Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Renal Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Renal Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Carotid Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Portal Vein Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Portal Vein Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vascular Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vascular Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Stenosis Of Lumbar Region Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Stenosis Of Lumbar Region in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyloric Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyloric Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Common Carotid Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Common Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
External Carotid Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease External Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aqueductal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aqueductal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Valve Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Pulmonary Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Pulmonary Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subaortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subaortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Basilar Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Basilar Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asymptomatic Carotid Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asymptomatic Carotid Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Choanal Atresia/Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Choanal Atresia/Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inferior Vena Cava Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inferior Vena Cava Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subglottic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subglottic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diaphyseal Medullary Stenosis With Malignant Fibrous Histiocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degenerative Lumbar Spinal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degenerative Lumbar Spinal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cafe-Au-Lait Macules With Pulmonary Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cafe-Au-Lait Macules With Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diaphyseal Medullary Stenosis With Bone Malignancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diaphyseal Medullary Stenosis With Bone Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypertrophic Subaortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypertrophic Subaortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ileal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ileal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatic Duct Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Duct Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Artery Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Heart Valve Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rectal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rectal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyloric Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pyloric Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Urethral Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Urethral Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anal Stenosis, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anal Stenosis, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Midnasal Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Midnasal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cervical Spinal Canal Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Spinal Canal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Choanal Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choanal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Stenosis With Reduced Interpedicular Distance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Stenosis With Reduced Interpedicular Distance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Laryngotracheal Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Laryngotracheal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Arterial Macroaneurysm With Supravascular Pulmonic Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Arterial Macroaneurysm With Supravascular Pulmonic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cicatricial Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cicatricial Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fibrous Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrous Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rectal Stenosis, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rectal Stenosis, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
trachea stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the trachea stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
esophagus stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the esophagus stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pyloric stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pyloric stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vascular stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vascular stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pulmonary valve stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary valve stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
heart right ventricle outflow tract stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the heart right ventricle outflow tract stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
mitral valve stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the mitral valve stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pulmonary artery stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spiral modiolar artery stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spiral modiolar artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
piriform aperture stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the piriform aperture stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ureteropelvic junction stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ureteropelvic junction stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
supravalvar pulmonary trunk stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the supravalvar pulmonary trunk stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pharyngeal arch artery stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pharyngeal arch artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
larynx stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the larynx stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
artery stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
umbilical artery stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the umbilical artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
umbilical vein stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the umbilical vein stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebral aqueductal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral aqueductal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aorta stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aorta stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
foramen magnum stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the foramen magnum stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pharynx stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pharynx stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
brain ventricle stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the brain ventricle stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
descending aorta stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the descending aorta stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ureter stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ureter stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
coronary artery stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the coronary artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
tricuspid valve stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the tricuspid valve stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
external auditory canal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the external auditory canal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spinal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic canal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic canal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
choanal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the choanal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ductus venosus stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ductus venosus stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hepatic portal vein stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hepatic portal vein stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intestinal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intestinal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
jugular vein stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the jugular vein stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subglottis stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subglottis stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aorta stenosis Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the aorta stenosis phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Hypertrophic pyloric stenosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Hypertrophic pyloric stenosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Pyloric stenosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Pyloric stenosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Pyloric stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pyloric stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic pyloric stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic pyloric stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tracheal stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tracheal stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Coronary stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Coronary stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulmonary subvalvular stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary subvalvular stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Carotid stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Carotid stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mitral valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mitral valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulmonary valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diaphyseal medullary stenosis with malignant fibrous histiocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diaphyseal medullary stenosis with malignant fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tricuspid valve stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tricuspid valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired gastric outlet stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired gastric outlet stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Discrete subaortic stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Discrete subaortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Stenosis of lacrimal passage Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Stenosis of lacrimal passage in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired tear duct stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired tear duct stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hydrocephalus due to aqueductal stenosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hydrocephalus due to aqueductal stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonary valve stenosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary valve stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonic stenosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diaphyseal medullary stenosis-bone malignancy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diaphyseal medullary stenosis-bone malignancy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pyloric stenosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pyloric stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Maximum stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Maximum stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mean degree of stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean degree of stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sum of stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sum of stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Infantile hypertrophic pyloric stenosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vein graft stenosis in coronary artery bypass grafting Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vein graft stenosis in coronary artery bypass grafting phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe coronary stenosis (young age of onset interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe coronary stenosis (young age of onset interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
sporadic abdominal aortic aneurysm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the sporadic abdominal aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic aneurysm, familial thoracic 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic valve disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic valve disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic Aneurysm, Familial Abdominal 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 2 from the curated CTD Gene-Disease Associations dataset.
Aortic Valve, Calcification of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Valve, Calcification of from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 1 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Thoracic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Thoracic from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Abdominal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Abdominal from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm from the curated CTD Gene-Disease Associations dataset.
Aortic Valve Insufficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Valve Insufficiency from the curated CTD Gene-Disease Associations dataset.
Aortic Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Diseases from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 6 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 2 from the curated CTD Gene-Disease Associations dataset.
Aortic Rupture Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Rupture from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Thoracic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Thoracic 1 from the curated CTD Gene-Disease Associations dataset.
Aortic aneurysm, familial thoracic 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic aneurysm, familial thoracic 4 from the curated CTD Gene-Disease Associations dataset.
AORTIC VALVE DISEASE 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AORTIC VALVE DISEASE 1 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Familial Abdominal 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Familial Abdominal 3 from the curated CTD Gene-Disease Associations dataset.
Aortic Aneurysm, Abdominal Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Aortic Aneurysm, Abdominal in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Aortic Aneurysm, Thoracic Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Aortic Aneurysm, Thoracic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
aortic disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
aortic aneurysm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic aneurysm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
aortic valve disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic valve disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
aortic disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease aortic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
aortic aneurysm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
aortic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
aortic aneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
aortic valve insufficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
aortic atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
aortic valve prolapse Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve prolapse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
thoracic aortic aneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
abdominal aortic aneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abdominal aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
aortic valve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
H3K4me3_fibroblast of the aortic adventitia_hg19_2 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of the aortic adventitia_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
H3K4me3_fibroblast of the aortic adventitia_hg19_1 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of the aortic adventitia_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
CTCF_fibroblast of the aortic adventitia_hg19_1 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of the aortic adventitia_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
CTCF_fibroblast of the aortic adventitia_hg19_2 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of the aortic adventitia_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
coronary artery disease; aortic stiffness Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; aortic stiffness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, thoracic Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, thoracic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm, thoracic; Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, ruptured; aortic aneurysm, abdominal; intracranial aneurysm; subarachnoid hemorrhage Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic diseases; calcinosis; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic diseases; calcinosis; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; inflammation; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; inflammation; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve insufficiency; rheumatic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve insufficiency; rheumatic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, ruptured; aortic aneurysm, abdominal Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abdominal aortic aneurysm Gene Set From GAD Gene-Disease Associations genes associated with the disease abdominal aortic aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm, thoracic; hypertension Gene Set From 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.
hypertension; lung cancer; abdominal aortic aneurysm Gene Set From 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.
aortic stiffness and disease severity Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic stiffness and disease severity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; hypertension Gene Set From 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.
aortic atherosclerosis in diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic atherosclerosis in diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, abdominal aortic Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, abdominal aortic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic diseases; calcinosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic diseases; calcinosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic diseases; calcinosis; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic diseases; calcinosis; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic stiffness Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic stiffness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction Gene Set From 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.
aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; arterial occlusive diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; arterial occlusive diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic root size Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic root size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm; cardiovascular diseases; hyperhomocysteinemia; marfan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm; cardiovascular diseases; hyperhomocysteinemia; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve insufficiency; calcinosis; mitral valve insufficiency; rheumatic heart disease; tricuspid valve insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve insufficiency; calcinosis; mitral valve insufficiency; rheumatic heart disease; tricuspid valve insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic aneurysm, abdominal; arteriosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm, thoracic Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
differential expansion rates of small abdominal aortic aneurysms Gene Set From GAD Gene-Disease Associations genes associated with the disease differential expansion rates of small abdominal aortic aneurysms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term aortic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
LOX-1_OE_GDS4262_433_human_HAECT - aortic endothelial cell line - 6 Hours Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_433_human_HAECT - aortic endothelial cell line - 6 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
LOX-1_OE_GDS4262_434_human_HAECT - aortic endothelial cell line - 12 Hours Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_434_human_HAECT - aortic endothelial cell line - 12 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
LOX-1_OE_GDS4262_435_human_HAECT - aortic endothelial cell line - 24 Hours Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_435_human_HAECT - aortic endothelial cell line - 24 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
LOX-1_OE_GDS4262_432_human_HAECT - aortic endothelial cell line - 2 Hours Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LOX-1_OE_GDS4262_432_human_HAECT - aortic endothelial cell line - 2 Hours gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
aortic valve morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
aortic smooth muscle cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback biological process from the curated GO Biological Process Annotations 2015 dataset.
Abdominal aortic aneurysm Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Abdominal aortic aneurysm phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Thoracic aortic aneurysms and dissections Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Aortic-valve calcification Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Aortic-valve calcification phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Aortic root size Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Aortic root size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
abdominal aortic aneurysm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease abdominal aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
aortic disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease aortic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
thoracic aortic aneurysm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease thoracic aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
aortic valve disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease aortic valve disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
aortic aneurysm Gene Set From GWASdb SNP-Disease Associations genes associated with the disease aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of the aortic valve Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abdominal aortic aneurysm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abdominal aortic aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
aortic valve calcification Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aortic valve calcification phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
bicuspid aortic valve Gene Set From GWASdb SNP-Phenotype Associations genes associated with the bicuspid aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
aortic aneurysm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aortic aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
aortic dilatation Gene Set From GWASdb SNP-Phenotype Associations genes associated with the aortic dilatation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal branching pattern of the aortic arch Gene Set From HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic regurgitation Gene Set From HPO Gene-Disease Associations genes associated with the aortic regurgitation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic tortuosity Gene Set From HPO Gene-Disease Associations genes associated with the aortic tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic root dilatation Gene Set From HPO Gene-Disease Associations genes associated with the aortic root dilatation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right aortic arch Gene Set From HPO Gene-Disease Associations genes associated with the right aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the aortic arch Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the aortic valve Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
descending aortic aneurysm Gene Set From HPO Gene-Disease Associations genes associated with the descending aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic dissection Gene Set From HPO Gene-Disease Associations genes associated with the aortic dissection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abdominal aortic aneurysm Gene Set From HPO Gene-Disease Associations genes associated with the abdominal aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ascending aortic aneurysm Gene Set From HPO Gene-Disease Associations genes associated with the ascending aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic valve atresia Gene Set From HPO Gene-Disease Associations genes associated with the aortic valve atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ascending aortic dissection Gene Set From HPO Gene-Disease Associations genes associated with the ascending aortic dissection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
coarctation of the descending aortic arch Gene Set From HPO Gene-Disease Associations genes associated with the coarctation of the descending aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
interrupted aortic arch Gene Set From HPO Gene-Disease Associations genes associated with the interrupted aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic aneurysm Gene Set From HPO Gene-Disease Associations genes associated with the aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bicuspid aortic valve Gene Set From HPO Gene-Disease Associations genes associated with the bicuspid aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic valve calcification Gene Set From HPO Gene-Disease Associations genes associated with the aortic valve calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aortic dilatation Gene Set From HPO Gene-Disease Associations genes associated with the aortic dilatation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thoracic aortic aneurysm Gene Set From HPO Gene-Disease Associations genes associated with the thoracic aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right aortic arch with mirror image branching Gene Set From HPO Gene-Disease Associations genes associated with the right aortic arch with mirror image branching phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dissecting aortic aneurysm Gene Set From HPO Gene-Disease Associations genes associated with the dissecting aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Aortic Aneurysm, Thoracic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm, Thoracic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aortic Aneurysm, Abdominal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm, Abdominal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aortic Valve Insufficiency Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Valve Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aortic Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aortic Aneurysm Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aortic Rupture Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Rupture phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aortic Coarctation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Coarctation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
aortic valve atresia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
right aortic arch Gene Set From MPO Gene-Phenotype Associations gene mutations causing the right aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic valve anulus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic valve anulus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic arch hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
calcified aortic valve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the calcified aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic dissection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic dissection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic sinus aneurysm Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic sinus aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic sinus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic valve cusp morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic valve cusp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
double aortic arch Gene Set From MPO Gene-Phenotype Associations gene mutations causing the double aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
calcified aortic arch Gene Set From MPO Gene-Phenotype Associations gene mutations causing the calcified aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic hypertrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic arch morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thick aortic valve cusps Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thick aortic valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
interrupted aortic arch Gene Set From MPO Gene-Phenotype Associations gene mutations causing the interrupted aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic sac morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic sac morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thick aortic valve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thick aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic aneurysm Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bicuspid aortic valve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the bicuspid aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent aortic valve cusps Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent aortic valve cusps phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic arch development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cervical aortic arch Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cervical aortic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
enlarged aortic valve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the enlarged aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
interrupted aortic arch, type b Gene Set From MPO Gene-Phenotype Associations gene mutations causing the interrupted aortic arch, type b phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic valve regurgitation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic valve regurgitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
patent aortic valve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the patent aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dilated aortic sac Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated aortic sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
overriding aortic valve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the overriding aortic valve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic elastic tissue lesions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic arch coarctation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aortic arch coarctation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal aortic valve morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic valve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aortic aneurysm, familial thoracic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 7 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 8 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial thoracic 9 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, ascending, and dissection Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, ascending, and dissection phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic valve disease 2 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic valve disease 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic valve disease 1 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic valve disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic aneurysm, familial abdominal, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aortic Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term aortic in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
aortic smooth muscle Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue aortic smooth muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
aortic smooth muscle cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic smooth muscle cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
aortic endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
aortic valve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic valve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
aortic smooth muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic smooth muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
aortic endothelial cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic endothelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
porcine aortic endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue porcine aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
human aortic endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue human aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
aortic root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue aortic root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Aortic Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Aortic Morphology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bicuspid Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Dissection Rupture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Dissection Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Valve Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Valve Insufficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Coarctation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Coarctation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Valve Calcification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Descending Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Descending Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dissecting Aortic Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Right Aortic Arch (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Right Aortic Arch (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Rupture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Valve Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Senile Sclerosis Of Aortic Cusp Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Senile Sclerosis Of Aortic Cusp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Root Dilation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Root Dilation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Wall Hypertrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Wall Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dissecting Abdominal Aortic Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Root Dilatation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Root Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Angiosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Angiosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ruptured Abdominal Aortic Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ruptured Thoracic Aortic Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Thoracic Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thoracoabdominal Aortic Aneurysm, Ruptured Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thoracoabdominal Aortic Aneurysm, Ruptured in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paravalvular Aortic Regurgitation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paravalvular Aortic Regurgitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Aortic Arch Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Aortic Valve Physiology Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Valve Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degenerative Aortic Valve Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degenerative Aortic Valve Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thoracic Aortic Ectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Aortic Ectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mitral And Aortic Incompetence Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitral And Aortic Incompetence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rheumatic Aortic Regurgitation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Aortic Regurgitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Abdominal Aortic Aneurysm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interrupted Aortic Arch Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interrupted Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Right Aortic Arch With Mirror Image Branching Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Right Aortic Arch With Mirror Image Branching in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Valve Disease 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disease 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Descending Thoracic Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Descending Thoracic Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Two-Raphe Bicuspid Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Two-Raphe Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ascending Aortic Rupture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ascending Aortic Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Bicuspid Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abdominal Aortic Atherosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Aortic Atherosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mid Aortic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mid Aortic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Tortuosity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Loeys-Dietz Aortic Aneurysm Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Loeys-Dietz Aortic Aneurysm Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Valve Disease 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disease 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Intramural Haematoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortic Intramural Haematoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervical Aortic Arch Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervical Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Quadricuspid Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Quadricuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unicuspid Aortic Valve Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortic Stiffness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ascending Aortic Dissection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ascending Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ascending Aortic Dilatation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ascending Aortic Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dysplastic Aortic Valve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysplastic Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aortic Aneurysm Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aortic Arch Calcification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Arch Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dilated Aortic Root Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilated Aortic Root in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Left Aortic Arch With Retroesophageal Right Subclavian Artery Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Aortic Arch With Retroesophageal Right Subclavian Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
aortic valve morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of aortic smooth muscle cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
aortic valve development Gene Set From GO Biological Process Annotations 2023 genes participating in the aortic valve development biological process from the curated GO Biological Process Annotations 2023 dataset.
aortic valve formation Gene Set From GO Biological Process Annotations 2023 genes participating in the aortic valve formation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of aortic smooth muscle cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
overriding aortic valve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the overriding aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic arch morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
interrupted aortic arch Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the interrupted aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic arch coarctation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch coarctation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thick aortic valve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thick aortic valve cusps Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic valve morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
dilated aortic sac Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated aortic sac phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged aortic valve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic valve regurgitation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve regurgitation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic valve cusp morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve cusp morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
right aortic arch Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the right aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
calcified aortic valve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic hypertrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic hypertrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cervical aortic arch Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cervical aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double aortic arch Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic aneurysm Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic arch hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
patent aortic valve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the patent aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic dissection Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic dissection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bicuspid aortic valve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bicuspid aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic valve commissure morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve commissure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic sinus aneurysm Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic sinus aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic elastic tissue lesions Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
interrupted aortic arch, type b Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the interrupted aortic arch, type b phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic valve flow Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve flow phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic sac morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic sac morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased aortic weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased aortic weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic arch development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent aortic valve cusps Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent aortic valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
calcified aortic arch Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic valve atresia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve atresia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal aortic valve anulus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve anulus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double lumen aortic arch Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double lumen aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic valve inflammation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aortic arch dilation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch dilation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Intra-aortic hematopoietic cell_Embryo_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Intra-aortic hematopoietic cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
aortic valve morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of aortic smooth muscle cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
aortic valve development Gene Set From GO Biological Process Annotations 2025 genes participating in the aortic valve development biological process from the curated GO Biological Process Annotations 2025 dataset.
aortic valve formation Gene Set From GO Biological Process Annotations 2025 genes participating in the aortic valve formation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of aortic smooth muscle cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
Aortic disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Aortic aneurysm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic aneurysm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Thoracic aortic aneurysm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thoracic aortic aneurysm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Aortic valve disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic valve disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Aortic aneurysm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Abdominal aortic aneurysm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Abdominal aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic valve disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic valve disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Thoracic aortic aneurysm Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Thoracic aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic aneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic valve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic dissection Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic dissection in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Abdominal aortic aneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abdominal aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thoracic aortic aneurysm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic valve insufficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bicuspid aortic valve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bicuspid aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic malignant tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic malignant tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic valve disease 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve disease 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic valve prolapse Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve prolapse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aortic smooth muscle Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Aortic smooth muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic valve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic valve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic smooth muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic smooth muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic endothelial cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic endothelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic smooth muscle cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic smooth muscle cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Human aortic endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Human aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic arch Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic body Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic intima Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic intima in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Porcine aortic endothelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Porcine aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Aortic adventitial fibroblast Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic adventitial fibroblast in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Thoracic aortic aneurysm or dissection Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm or dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aortic valve disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic valve disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aortic aneurysm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated thoracic aortic aneurysm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aortic dissection Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute aortic dissection Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thoracic aortic aneurysm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal aortic valve morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal aortic valve morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aortic valve atresia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic valve atresia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sporadic abdominal aortic aneurysm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sporadic abdominal aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aortic dilatation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic dilatation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bicuspid aortic valve Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Heritable Thoracic Aortic disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Heritable Thoracic Aortic disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early age onset of sporadic thoracic aortic dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early age onset of sporadic thoracic aortic dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ascending aortic dissection Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ascending aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abdominal aortic aneurysm Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abdominal aortic aneurysm phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aortic root size Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic root size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aortic valve area Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic valve area phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thoracic aortic calcification levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic calcification levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Abdominal aortic calcification levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abdominal aortic calcification levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe aortic features in Marfan syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe aortic features in Marfan syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aortic vascular smooth muscle cell calcification in response to osteogenic stimuli Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic vascular smooth muscle cell calcification in response to osteogenic stimuli phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aortic vascular smooth muscle cell proliferation in response to IL-1 beta Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic vascular smooth muscle cell proliferation in response to IL-1 beta phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thoracic aortic aneurysms and dissections Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aortic stiffness Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic stiffness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aortic-valve calcification Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic-valve calcification phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aortic coarctation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic coarctation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bicuspid aortic valve Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal dominant form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hyperplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital human immunodeficiency virus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital human immunodeficiency virus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set From 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.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diarrhea 5, with tufting enteropathy, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 5, with tufting enteropathy, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vertical talus, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Vertical talus, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital generalized lipodystrophy type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IV, congenital neuromuscular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facial paresis, hereditary congenital, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital glucose-galactose malabsorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital glucose-galactose malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with cores Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aphakia, congenital primary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aphakia, congenital primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, congenital generalized, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital contractural arachnodactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital contractural arachnodactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital absence of salivary gland Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nystagmus 6, congenital, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Afibrinogenemia, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Afibrinogenemia, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deafness, congenital heart defects, and posterior embryotoxon Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From 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 Set From 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.
Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital amegakaryocytic thrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital amegakaryocytic thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, fast-channel Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal recessive congenital 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From 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.
Diarrhea 3, secretory sodium, congenital, syndromic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 3, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hypoplasia, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital secretory diarrhea, chloride type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Testicular anomalies with or without congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital short bowel syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From 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 Set From 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 Set From 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 Set From 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.
Congenital heart disease, multiple types, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Indifference to pain, congenital, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Indifference to pain, congenital, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, autosomal dominant 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contractural syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart defects, multiple types, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital erythropoietic porphyria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital erythropoietic porphyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
congenital neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypothyroidism, congenital, nongoitrous, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, congenital, nongoitrous, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, actin, congenital, with excess of thin myofilaments Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett syndrome, congenital variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From 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.
Congenital disorder of glycosylation type 2k Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, with excess of muscle spindles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital lactase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myotonia, autosomal recessive form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myotonia, autosomal recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 6, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From 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.
Congenital disorder of glycosylation type 1H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1v Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From 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.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, congenital, compton-north Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set From 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.
Congenital cystic disease of liver Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type Ix Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital order of glycosylation type 1r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital central hypoventilation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital ocular coloboma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital ocular coloboma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1O Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1y Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digital clubbing, isolated congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digital clubbing, isolated congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1u Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1t Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Prothrombin deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital defect of folate absorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe congenital neutropenia 4, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital aniridia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital aniridia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital hyperammonemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital exostosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamine deficiency, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leber congenital amaurosis 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leber congenital amaurosis 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Partial congenital absence of teeth Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Partial congenital absence of teeth phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive congenital ichthyosis 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myasthenic syndrome, acetazolamide-responsive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myasthenic syndrome, acetazolamide-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glaucoma, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glaucoma, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular hypertrophy-cerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Stromal Corneal Dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set From 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.
Congenital myopathy with fiber type disproportion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Hyperinsulinism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hyperinsulinism from the curated CTD Gene-Disease Associations dataset.
Cataract congenital Volkmann type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital Hypothyroidism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.
Congenital bilateral aplasia of vas deferens Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.
Congenital Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Abnormalities from the curated CTD Gene-Disease Associations dataset.
Anemia, Hemolytic, Congenital Nonspherocytic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic, Congenital Nonspherocytic from the curated CTD Gene-Disease Associations dataset.
Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 4 from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 4 from the curated CTD Gene-Disease Associations dataset.
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set From 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.
Congenital idiopathic intestinal pseudoobstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.
Vertical talus, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vertical talus, congenital from the curated CTD Gene-Disease Associations dataset.
Nystagmus 1, congenital, X- linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 1, congenital, X- linked from the curated CTD Gene-Disease Associations dataset.
Facial paresis, hereditary, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset.
Congenital anosmia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital anosmia from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 5 from the curated CTD Gene-Disease Associations dataset.
Hyperferritinemia, hereditary, with congenital cataracts Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset.
Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosiform erythroderma, Brocq congenital, nonbullous form from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Hernias, Diaphragmatic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hernias, Diaphragmatic, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.
Lethal Congenital Contracture Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Aphakia, congenital primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aphakia, congenital primary from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From 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.
Congenital thrombotic disease, due to Protein C deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
Nystagmus 2, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 2, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 3 from the curated CTD Gene-Disease Associations dataset.
Congenital contractural arachnodactyly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital contractural arachnodactyly from the curated CTD Gene-Disease Associations dataset.
Lactase Deficiency, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lactase Deficiency, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.
Nystagmus 4, congenital, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nystagmus 4, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.
Anti-plasmin deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.
Muscular dystrophy congenital, merosin negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.
Indifference to Pain, Congenital, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Indifference to Pain, Congenital, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Ptosis, Hereditary Congenital 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 1 from the curated CTD Gene-Disease Associations dataset.
Pain Insensitivity, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pain Insensitivity, Congenital from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.
Congenital amegakaryocytic thrombocytopenia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital amegakaryocytic thrombocytopenia from the curated CTD Gene-Disease Associations dataset.
Adrenal Hyperplasia, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adrenal Hyperplasia, Congenital from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.
Anemia, Hypoplastic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hypoplastic, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.
Congenital hypertrichosis lanuginosa Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital hypertrichosis lanuginosa from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 10 from the curated CTD Gene-Disease Associations dataset.
Hypothyroidism, Congenital, Nongoitrous, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 2 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, Compton-North Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 3 from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder of Glycosylation, Type Io Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital central hypoventilation syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type Im Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type In Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Zonular, with Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
Lethal congenital contracture syndrome 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.
Microcoria, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microcoria, congenital from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Anemia, Hemolytic, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic, Congenital from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.
Leber Congenital Amaurosis 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leber Congenital Amaurosis 14 from the curated CTD Gene-Disease Associations dataset.
ADRENAL HYPOPLASIA, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.
Ptosis, Hereditary Congenital 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
Diarrhea 4, Malabsorptive, Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diarrhea 4, Malabsorptive, Congenital from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.
CAPILLARY MALFORMATIONS, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CAPILLARY MALFORMATIONS, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.
Nephrosis, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephrosis, congenital from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Severe Congenital, Autosomal Dominant 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.
GLAUCOMA 3, PRIMARY CONGENITAL, C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLAUCOMA 3, PRIMARY CONGENITAL, C from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.
ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Merosin-Positive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

Congenital Supravalvular Aortic Stenosis Gene Set

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

Aortic Stenosis, Supravalvular Gene Set

supravalvular aortic stenosis Gene Set

supravalvular aortic stenosis Gene Set

alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome Gene Set

supravalvular aortic stenosis Gene Set

supravalvular aortic stenosis Gene Set

Aortic Stenosis, Supravalvular Gene Set

Supravalvular Aortic Stenosis Gene Set

Supravalvular aortic stenosis Gene Set

Supravalvular aortic stenosis Gene Set

retinal arterial macroaneurysm with supravalvular pulmonic stenosis Gene Set

Retinal Arterial Macroaneurysm With Supravalvular Pulmonic Stenosis Gene Set

aneurysm, ruptured; aortic aneurysm, abdominal; arterial occlusive diseases; carotid artery stenosis; carotid stenosis Gene Set

aortic valve stenosis; calcinosis; diabetes mellitus; hyperlipidemias; hypertension; mitral valve stenosis Gene Set

aortic valve stenosis; calcinosis; mitral valve stenosis; renal insufficiency, chronic Gene Set

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

lipids; left ventricular mass; aortic gradient; aortic valve stenosis Gene Set

Congenital Stenosis Of Aortic Valve Gene Set

apoplexy; carotid artery stenosis; carotid stenosis; hyperhomocysteinemia; stroke Gene Set

atherosclerosis; carotid artery stenosis; carotid stenosis; inflammation Gene Set

apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set

carotid artery stenosis; carotid stenosis; disease progression Gene Set

carotid artery stenosis; carotid stenosis; inflammation Gene Set

carotid artery stenosis; carotid stenosis; recurrence Gene Set

carotid artery stenosis; carotid stenosis; graft occlusion, vascular Gene Set

carotid artery diseases; carotid artery stenosis; carotid stenosis; hypertension Gene Set

carotid artery stenosis; carotid stenosis Gene Set

Supravalvar aortic stenosis Gene Set

Aortic Stenosis, Subvalvular Gene Set

aortic valve stenosis Gene Set

subvalvular aortic stenosis Gene Set

aortic valve stenosis Gene Set

aortic valve stenosis; Gene Set

aortic stenosis Gene Set

calcific aortic valve stenosis Gene Set

aortic valve stenosis; calcinosis Gene Set

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

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

aortic valve stenosis Gene Set

calcific aortic valve stenosis Gene Set

Aortic Valve Stenosis Gene Set

aortic valve stenosis Gene Set

supravalvar aortic stenosis Gene Set

supravalvar aortic stenosis Gene Set

Aortic Valve Stenosis Gene Set

Aortic Stenosis Symptomatic Gene Set

Rheumatic Aortic Stenosis Gene Set

Nonrheumatic Aortic (Valve) Stenosis Gene Set

Isolated Aortic Stenosis Gene Set

aortic valve stenosis Gene Set

supravalvar aortic stenosis Gene Set

Aortic valve stenosis Gene Set

Aortic valve stenosis Gene Set

Aortic valve stenosis Gene Set

Subvalvular aortic stenosis Gene Set

Supravalvar aortic stenosis Gene Set

Subvalvular aortic stenosis Gene Set

Aortic valve stenosis Gene Set

Calcific aortic valve stenosis Gene Set

aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension Gene Set

aortic aneurysm, thoracic; aortic rupture Gene Set

aortic aneurysm, abdominal; aortic rupture Gene Set

aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases Gene Set

abnormal aortic arch and aortic arch branch attachment Gene Set

Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene Set

abnormal aortic arch and aortic arch branch attachment Gene Set

Familial thoracic aortic aneurysm and aortic dissection Gene Set

Bicuspid aortic valve without aortic dilation Gene Set

Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) Gene Set

Congenital Stenosis Of Aqueduct Of Sylvius Gene Set

Congenital Subaortic Stenosis Gene Set

Congenital Stenosis Of Pulmonary Valve Gene Set

Congenital Stenosis Of Nasal Pyriform Aperture Gene Set

Congenital Hypoplasia Of Aortic Arch Gene Set

Congenital Anomaly Of Aortic Arch Gene Set

Congenital Atresia Of Aortic Valve Gene Set

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