Name

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 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.

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, 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.

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.

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.

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.

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 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 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 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 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 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 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, 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, 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.

thoracic aortic aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

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.

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.

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.

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.

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.

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.

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 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, 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.

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 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, 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, 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, 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.

thoracic aorta aneurysm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thoracic aorta aneurysm phenotype in transgenic mice from the MPO Gene-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.

aneurysm, ruptured; intracranial aneurysm; stroke; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneurysm, ruptured; intracranial aneurysm; stroke; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneurysm, ruptured; intracranial aneurysm; recurrence; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneurysm, ruptured; intracranial aneurysm; recurrence; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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, 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 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 Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

aortic aneurysm Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

aortic aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

abdominal aortic aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 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 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.

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 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 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 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 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 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.

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.

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 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.

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 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.

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.

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 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.

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, 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 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 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.

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.

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 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.

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.

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.

{aneurysm, familial abdominal 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {aneurysm, familial abdominal 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

albuminuria; amyloidosis, familial; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

multiple familial trichoepithelioma and familial cylindromatosis Gene Set

From GAD Gene-Disease Associations

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

amyloidosis, familial; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

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

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

From GAD Gene-Disease Associations

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

Asphyxiating thoracic dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thoracic Diseases Gene Set

From CTD Gene-Disease Associations

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

Asphyxiating Thoracic Dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asphyxiating Thoracic Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

thoracic cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

asphyxiating thoracic dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease asphyxiating thoracic dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

thoracic cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease thoracic cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

thoracic benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

thoracic cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

thoracic outlet syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

thoracic disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

asphyxiating thoracic dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; thoracic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; thoracic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thoracic Gene Set

From GeneRIF Biological Term Annotations

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

thoracic cancer Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease thoracic cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

anterior beaking of thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bifid thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thoracic cavity Gene Set

From HPO Gene-Disease Associations

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

anterior beaking of lower thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of lower thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dilatation of the descending thoracic aorta Gene Set

From HPO Gene-Disease Associations

genes associated with the dilatation of the descending thoracic aorta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thoracic hemivertebrae Gene Set

From HPO Gene-Disease Associations

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

thoracic hypoplasia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thoracic spine Gene Set

From HPO Gene-Disease Associations

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

lower thoracic interpediculate narrowness Gene Set

From HPO Gene-Disease Associations

genes associated with the lower thoracic interpediculate narrowness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thoracic platyspondyly Gene Set

From HPO Gene-Disease Associations

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

lower thoracic kyphosis Gene Set

From HPO Gene-Disease Associations

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

thoracic kyphosis Gene Set

From HPO Gene-Disease Associations

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

thoracic scoliosis Gene Set

From HPO Gene-Disease Associations

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

anterior concavity of thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior concavity of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Thoracic Injuries Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Thoracic Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal thoracic aorta morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal descending thoracic aorta morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal descending thoracic aorta morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thoracic cage morphology Gene Set

From MPO Gene-Phenotype Associations

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

thoracic vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thoracic vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased thoracic vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased thoracic vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged thoracic cavity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged thoracic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thoracic cavity morphology Gene Set

From MPO Gene-Phenotype Associations

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

small thoracic cage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small thoracic cage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small thoracic cavity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small thoracic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thoracic vertebrae morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal thoracic cage shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal thoracic cage shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thoracic vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thoracic vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

calcified thoracic aorta Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the calcified thoracic aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased thoracic vertebrae number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased thoracic vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thoracic duct morphology Gene Set

From MPO Gene-Phenotype Associations

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

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 9 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 8 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 2 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

thoracic leg Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thoracic ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

thoracic spine Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Aneurysm, Ruptured Gene Set

From CTD Gene-Disease Associations

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

Aneurysm, Intracranial Berry, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 8 from the curated CTD Gene-Disease Associations dataset.

Aneurysm Gene Set

From CTD Gene-Disease Associations

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

Aneurysm, Intracranial Berry, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 3 from the curated CTD Gene-Disease Associations dataset.

Aneurysm, Intracranial Berry, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 9 from the curated CTD Gene-Disease Associations dataset.

Coronary Aneurysm Gene Set

From CTD Gene-Disease Associations

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

Aneurysm, Intracranial Berry, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 4 from the curated CTD Gene-Disease Associations dataset.

Aneurysm, intracranial berry, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, intracranial berry, 2 from the curated CTD Gene-Disease Associations dataset.

Aneurysm, Dissecting Gene Set

From CTD Gene-Disease Associations

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

Intracranial Aneurysm Gene Set

From CTD Gene-Disease Associations

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

Aneurysm, Intracranial Berry, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 10 from the curated CTD Gene-Disease Associations dataset.

Aneurysm, Intracranial Berry, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 6 from the curated CTD Gene-Disease Associations dataset.

Aneurysm, Intracranial Berry, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 7 from the curated CTD Gene-Disease Associations dataset.

Aneurysm, Intracranial Berry, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aneurysm, Intracranial Berry, 1 from the curated CTD Gene-Disease Associations dataset.

Intracranial Aneurysm Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Intracranial Aneurysm in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

intracranial aneurysm Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease intracranial aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

splenic artery aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intracranial aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

coronary aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

heart aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

subclavian artery aneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intracranial aneurysm; stroke Gene Set

From GAD Gene-Disease Associations

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

intracranial aneurysm; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intracranial aneurysm Gene Set

From GAD Gene-Disease Associations

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

brain aneurysm Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral infarction; intracranial aneurysm; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneurysm, dissecting Gene Set

From GAD Gene-Disease Associations

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

congenital ductus arteriosus aneurysm Gene Set

From GAD Gene-Disease Associations

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

aneurysm; vasospasm, intracranial Gene Set

From GAD Gene-Disease Associations

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

aneurysm, intracranial Gene Set

From GAD Gene-Disease Associations

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

aneurysm, ruptured; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneurysm, ruptured; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; intracranial aneurysm Gene Set

From GAD Gene-Disease Associations

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

coronary aneurysm; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary aneurysm; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneurysm Gene Set

From GeneRIF Biological Term Annotations

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

Intracranial aneurysm Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Intracranial aneurysm phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

intracranial aneurysm Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease intracranial aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

cerebral aneurysm Gene Set

From GWASdb SNP-Phenotype Associations

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

aneurysm Gene Set

From GWASdb SNP-Phenotype Associations

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

cerebral aneurysm Gene Set

From HPO Gene-Disease Associations

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

pulmonary artery aneurysm Gene Set

From HPO Gene-Disease Associations

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

aneurysm Gene Set

From HPO Gene-Disease Associations

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

celiac artery aneurysm Gene Set

From HPO Gene-Disease Associations

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

atrial septal aneurysm Gene Set

From HPO Gene-Disease Associations

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

aneurysm of an abdominal artery Gene Set

From HPO Gene-Disease Associations

genes associated with the aneurysm of an abdominal artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mesenteric artery aneurysm Gene Set

From HPO Gene-Disease Associations

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

ventricular aneurysm Gene Set

From HPO Gene-Disease Associations

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

Aneurysm, Ruptured Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Aneurysm Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heart Aneurysm Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Coronary Aneurysm Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Aneurysm, Dissecting Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Intracranial Aneurysm Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abdominal aorta aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

ascending aorta aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

intracranial aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

coronary artery aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

brain aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

atrial septal aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

ventricular aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

heart right ventricle aneurysm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aneurysm, intracranial berry, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

{aneurysm, intracranial berry, 10} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {aneurysm, intracranial berry, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.

aneurysm, intracranial berry, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

aneurysm, intracranial berry, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

aneurysm, intracranial berry, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

aneurysm, intracranial berry, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

aneurysm, intracranial berry, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

aneurysm, intracranial berry, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

aneurysm, intracranial berry, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the aneurysm, intracranial berry, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

{aneurysm, intracranial berry, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {aneurysm, intracranial berry, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{aneurysm, intracranial berry, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {aneurysm, intracranial berry, 9} phenotype from the curated OMIM 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 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 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 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 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 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 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 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 Assocation Evidence Scores

genes involed in the disease supravalvular aortic stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

aortic valve stenosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease aortic valve stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

aortic disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

aortic valve disease Gene Set

From DISEASES Curated Gene-Disease Assocation 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 Assocation Evidence Scores

genes associated with the disease aortic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

aortic disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 valve insufficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Assocation 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 Assocation 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.

supravalvular aortic stenosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

subvalvular aortic stenosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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 Assocation 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 disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

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.

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.

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 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 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.

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 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 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.

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.

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 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; 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 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 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 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 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.

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.

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.

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

genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations dataset.

aortic smooth muscle cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback biological process from the curated GO Biological Process Annotations 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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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 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 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.

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 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.

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.

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.

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.

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.

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.

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 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.

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 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.

Familial Mediterranean fever Gene Set

From ClinVar Gene-Phenotype Associations

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

Thrombocytosis, benign familial microcytic Gene Set

From ClinVar Gene-Phenotype Associations

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

Benign familial neonatal-infantile seizures Gene Set

From ClinVar Gene-Phenotype Associations

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

Neurofibromatosis, familial spinal Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 6 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Tumoral calcinosis, familial, hyperphosphatemic Gene Set

From ClinVar Gene-Phenotype Associations

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

Febrile seizures, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial restrictive cardiomyopathy 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Gaze palsy, familial horizontal, with progressive scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hemiplegic migraine type 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hemiplegic migraine type 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hemiplegic migraine type 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Erythrocytosis, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Erythrocytosis, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Erythrocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial X-linked hypophosphatemic vitamin D refractory rickets Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Benign familial neonatal seizures 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Benign familial neonatal seizures 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperuricemic nephropathy, familial juvenile, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial cancer of breast Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial benign pemphigus Gene Set

From ClinVar Gene-Phenotype Associations

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

Episodic pain syndrome, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperpigmentation, familial progressive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial aortopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Digital arthropathy-brachydactyly, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Episodic pain syndrome, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Febrile seizures, familial, 11 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial benign hypercalcemia Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial fibrillation, familial, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial visceral amyloidosis, Ostertag type Gene Set

From ClinVar Gene-Phenotype Associations

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

Dementia familial British Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial porencephaly Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 15 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 12 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

familial hyperinsulinism Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperinsulinemic hypoglycemia familial 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Febrile seizures, familial, 3b Gene Set

From ClinVar Gene-Phenotype Associations

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

Paroxysmal familial ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypercholesterolemia Gene Set

From ClinVar Gene-Phenotype Associations

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

Hidradenitis suppurativa, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Dementia, familial Danish Gene Set

From ClinVar Gene-Phenotype Associations

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

Progressive familial intrahepatic cholestasis 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Progressive familial intrahepatic cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Benign familial hematuria Gene Set

From ClinVar Gene-Phenotype Associations

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

Progressive familial heart block type 1A Gene Set

From ClinVar Gene-Phenotype Associations

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

Progressive familial heart block type 1B Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial dysautonomia Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial febrile seizures 8 Gene Set

From ClinVar Gene-Phenotype Associations

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

Fleck retina, familial benign Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked familial exudative vitreoretinopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial colorectal cancer Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial porphyria cutanea tarda Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypertrophic cardiomyopathy 20 Gene Set

From ClinVar Gene-Phenotype Associations

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

Progressive familial intrahepatic cholestasis 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Advanced sleep phase syndrome, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Myoclonus, familial cortical Gene Set

From ClinVar Gene-Phenotype Associations

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

Migraine, familial basilar Gene Set

From ClinVar Gene-Phenotype Associations

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

Breast-ovarian cancer, familial 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypercholanemia, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Bone marrow failure, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Advanced sleep phase syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Candidiasis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Candidiasis, familial, 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypokalemia-hypomagnesemia Gene Set

From ClinVar Gene-Phenotype Associations

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

Myasthenia, limb-girdle, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial fibrillation, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial fibrillation, familial, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial fibrillation, familial, 11 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial fibrillation, familial, 17 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial fibrillation, familial, 16 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial fibrillation, familial, 15 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hemophagocytic lymphohistiocytosis, familial, 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Ventricular fibrillation, paroxysmal familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial platelet disorder with associated myeloid malignancy Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial erythrocytosis, 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial medullary thyroid carcinoma Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperinsulinemic hypoglycemia, familial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperlipidemia, familial combined Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial amyloid polyneuropathy, Iowa type Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial fibrillation, familial, 14 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From ClinVar Gene-Phenotype Associations

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

Epilepsy, familial adult myoclonic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial myxoma, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Lipodystrophy, familial partial, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

Lipodystrophy, familial partial, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypocalciuric hypercalcemia, familial, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypocalciuric hypercalcemia, familial, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial multiple polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial juvenile gout Gene Set

From ClinVar Gene-Phenotype Associations

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

Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypobetalipoproteinemia, familial, associated with apob32 Gene Set

From ClinVar Gene-Phenotype Associations

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

Breast-ovarian cancer, familial 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Atrial fibrillation, familial, 7 Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Primary familial hypertrophic cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial type 3 hyperlipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

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

Tumoral calcinosis, familial, normophosphatemic Gene Set

From ClinVar Gene-Phenotype Associations

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

Cd8 deficiency, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial infantile myasthenia Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked familial atypical mycobacteriosis, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperthyroxinemia, familial dysalbuminemic Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial type 5 hyperlipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

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

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial renal glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial pulmonary capillary hemangiomatosis Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypoalphalipoproteinemia Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial renal hypouricemia Gene Set

From ClinVar Gene-Phenotype Associations

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

HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

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

Myoclonic epilepsy, familial infantile Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial hypoplastic, glomerulocystic kidney Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial cold urticaria Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial myelofibrosis Gene Set

From CTD Gene-Disease Associations

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

Nephronophthisis, familial juvenile Gene Set

From CTD Gene-Disease Associations

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

Eosinophilia, Familial Gene Set

From CTD Gene-Disease Associations

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

Hyperlipidemia, Familial Combined Gene Set

From CTD Gene-Disease Associations

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

Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set

From CTD Gene-Disease Associations

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

Hyperinsulinemic hypoglycemia, familial, 6 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Pemphigus, Benign Familial Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Restrictive, 1 Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 9 Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 8 Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 2 Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 6 Gene Set

From CTD Gene-Disease Associations

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

Amyloidosis, familial visceral Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Hypertrophic, Familial Gene Set

From CTD Gene-Disease Associations

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

Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 8 Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 7 Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 6 Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 4 Gene Set

From CTD Gene-Disease Associations

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

Cholestasis, progressive familial intrahepatic 1 Gene Set

From CTD Gene-Disease Associations

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

Cholestasis, progressive familial intrahepatic 2 Gene Set

From CTD Gene-Disease Associations

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

Myasthenia, Familial Infantile, 1 Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 4 Gene Set

From CTD Gene-Disease Associations

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

STUTTERING, FAMILIAL PERSISTENT, 1 Gene Set

From CTD Gene-Disease Associations

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

Dementia, familial British Gene Set

From CTD Gene-Disease Associations

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

Candidiasis familial chronic mucocutaneous, autosomal recessive Gene Set

From CTD Gene-Disease Associations

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

Gliosis, Familial Progressive Subcortical Gene Set

From CTD Gene-Disease Associations

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

CD8 Deficiency, Familial Gene Set

From CTD Gene-Disease Associations

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

Insomnia, Fatal Familial Gene Set

From CTD Gene-Disease Associations

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

SEIZURES, BENIGN FAMILIAL NEONATAL, 2 Gene Set

From CTD Gene-Disease Associations

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

Familial HDL deficiency Gene Set

From CTD Gene-Disease Associations

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

Familial dermographism Gene Set

From CTD Gene-Disease Associations

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

Candidiasis, Familial, 3 Gene Set

From CTD Gene-Disease Associations

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

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

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

Erythrocytosis, Familial, 3 Gene Set

From CTD Gene-Disease Associations

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

Erythrocytosis, Familial, 2 Gene Set

From CTD Gene-Disease Associations

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

Visceral Myopathy, Familial Gene Set

From CTD Gene-Disease Associations

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

Hyperthyroidism, Familial Gestational Gene Set

From CTD Gene-Disease Associations

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

Hematuria, Benign Familial Gene Set

From CTD Gene-Disease Associations

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

SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 2 Gene Set

From CTD Gene-Disease Associations

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

Migraine, Familial Hemiplegic, 3 Gene Set

From CTD Gene-Disease Associations

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

FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

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

Cancer, Familial, with In Vitro Radioresistance Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 5 Gene Set

From CTD Gene-Disease Associations

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

Hypoparathyroidism familial isolated Gene Set

From CTD Gene-Disease Associations

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

Tumoral Calcinosis, Hyperphosphatemic, Familial Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 3 Gene Set

From CTD Gene-Disease Associations

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

Hidradenitis suppurativa, familial Gene Set

From CTD Gene-Disease Associations

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

Dementia, familial Danish Gene Set

From CTD Gene-Disease Associations

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

Familial medullary thyroid carcinoma Gene Set

From CTD Gene-Disease Associations

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

Interstitial Pneumonitis, Desquamative, Familial Gene Set

From CTD Gene-Disease Associations

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

Hemophagocytic lymphohistiocytosis, familial, 4 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Cirrhosis, Familial Gene Set

From CTD Gene-Disease Associations

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

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From CTD Gene-Disease Associations

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

Lipodystrophy, Familial Partial Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Restrictive, 3 Gene Set

From CTD Gene-Disease Associations

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

Familial Mediterranean Fever, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

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

Familial Hypophosphatemic Rickets Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 3 Gene Set

From CTD Gene-Disease Associations

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

Keratoacanthoma familial Gene Set

From CTD Gene-Disease Associations

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

Hepatic Adenomas, Familial Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 10 Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 13 Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 15 Gene Set

From CTD Gene-Disease Associations

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

Familial Wilms tumor 2 Gene Set

From CTD Gene-Disease Associations

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

Candidiasis, Familial, 1 Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 9 Gene Set

From CTD Gene-Disease Associations

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

Hyperinsulinemic Hypoglycemia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

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

Hyperinsulinemic Hypoglycemia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

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

Familial antiphospholipid syndrome Gene Set

From CTD Gene-Disease Associations

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

Amyloidosis, Familial Gene Set

From CTD Gene-Disease Associations

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

Familial paroxysmal dystonia Gene Set

From CTD Gene-Disease Associations

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

Atrial fibrillation, familial 1 Gene Set

From CTD Gene-Disease Associations

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

EPILEPSY, FAMILIAL TEMPORAL LOBE, 3 Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Hypercholanemia, Familial Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Hyperbilirubinemia, Transient Familial Neonatal Gene Set

From CTD Gene-Disease Associations

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

EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 Gene Set

From CTD Gene-Disease Associations

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

Meningioma, familial Gene Set

From CTD Gene-Disease Associations

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

Dysautonomia, Familial Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 1 Gene Set

From CTD Gene-Disease Associations

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

Hemophagocytic lymphohistiocytosis, familial, 3 Gene Set

From CTD Gene-Disease Associations

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

Familial Cold Autoinflammatory Syndrome 2 Gene Set

From CTD Gene-Disease Associations

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

Epilepsy, Familial Adult Myoclonic, 3 Gene Set

From CTD Gene-Disease Associations

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

Prostate cancer, familial Gene Set

From CTD Gene-Disease Associations

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

Convulsions, Benign Familial Infantile, 4 Gene Set

From CTD Gene-Disease Associations

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

Polycythemia, primary familial and congenital Gene Set

From CTD Gene-Disease Associations

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

PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set

From CTD Gene-Disease Associations

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

Erythrocytosis, Familial, 4 Gene Set

From CTD Gene-Disease Associations

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

Hyperinsulinemic hypoglycemia, familial, 3 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Hyperinsulinemic hypoglycemia, familial, 7 Gene Set

From CTD Gene-Disease Associations

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

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.

Hyperthyroxinemia, Familial Dysalbuminemic Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Restrictive, 2 Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 5 Gene Set

From CTD Gene-Disease Associations

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

Familial cylindromatosis Gene Set

From CTD Gene-Disease Associations

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

Familial benign hypercalcemia, type 3 Gene Set

From CTD Gene-Disease Associations

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

Hyperaldosteronism, Familial, Type II Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 11 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Atrial myxoma, familial Gene Set

From CTD Gene-Disease Associations

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

Familial Glucocorticoid Deficiency 1 Gene Set

From CTD Gene-Disease Associations

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

Tumoral Calcinosis, Normophosphatemic, Familial Gene Set

From CTD Gene-Disease Associations

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

MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

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

Hypocalciuric hypercalcemia, familial, type 1 Gene Set

From CTD Gene-Disease Associations

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

Trichoepithelioma multiple familial Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 10 Gene Set

From CTD Gene-Disease Associations

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

EPILEPSY, FAMILIAL TEMPORAL LOBE, 1 Gene Set

From CTD Gene-Disease Associations

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

EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set

From CTD Gene-Disease Associations

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

Hemophagocytic lymphohistiocytosis, familial, 2 Gene Set

From CTD Gene-Disease Associations

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

Periodic fever, familial, autosomal dominant Gene Set

From CTD Gene-Disease Associations

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

VENTRICULAR TACHYCARDIA, FAMILIAL Gene Set

From CTD Gene-Disease Associations

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

Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

Hypobetalipoproteinemia, Familial, Apolipoprotein B Gene Set

From CTD Gene-Disease Associations

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

Familial schizencephaly Gene Set

From CTD Gene-Disease Associations

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

Atrial Fibrillation, Familial, 2 Gene Set

From CTD Gene-Disease Associations

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

HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set

From CTD Gene-Disease Associations

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

Neurofibromatosis, Familial Spinal Gene Set

From CTD Gene-Disease Associations

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

Reticuloendotheliosis, familial, with eosinophilia Gene Set

From CTD Gene-Disease Associations

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

SEIZURES, BENIGN FAMILIAL NEONATAL, 1 Gene Set

From CTD Gene-Disease Associations

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

Advanced Sleep-Phase Syndrome, Familial Gene Set

From CTD Gene-Disease Associations

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

MIGRAINE, FAMILIAL HEMIPLEGIC, 2 Gene Set

From CTD Gene-Disease Associations

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

MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set

From CTD Gene-Disease Associations

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

MITRAL VALVE PROLAPSE, FAMILIAL Gene Set

From CTD Gene-Disease Associations

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

Progressive Familial Heart Block, Type Ib Gene Set

From CTD Gene-Disease Associations

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

Familial dilated cardiomyopathy Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 3 Gene Set

From CTD Gene-Disease Associations

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

Thymoma, Familial Gene Set

From CTD Gene-Disease Associations

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

Atypical Mycobacteriosis, Familial, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

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

Familial Testotoxicosis Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Hemiplegic migraine, familial type 2 Gene Set

From CTD Gene-Disease Associations

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

Hemiplegic migraine, familial type 1 Gene Set

From CTD Gene-Disease Associations

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

Familial apoceruloplasmin deficiency Gene Set

From CTD Gene-Disease Associations

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

HYPERCHOLESTEROLEMIA, FAMILIAL Gene Set

From CTD Gene-Disease Associations

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

Amyloid Neuropathies, Familial Gene Set

From CTD Gene-Disease Associations

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

CANDIDIASIS, FAMILIAL, 2 Gene Set

From CTD Gene-Disease Associations

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

Familial Mediterranean Fever Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 7 Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 6 Gene Set

From CTD Gene-Disease Associations

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

Febrile Convulsions, Familial, 1 Gene Set

From CTD Gene-Disease Associations

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

Cerebral Amyloid Angiopathy, Familial Gene Set

From CTD Gene-Disease Associations

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

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set

From CTD Gene-Disease Associations

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

Hypobetalipoproteinemia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

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

Stuttering, Familial Persistent 2 Gene Set

From CTD Gene-Disease Associations

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

Trichoepithelioma, Multiple Familial, 2 Gene Set

From CTD Gene-Disease Associations

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

Epilepsy, Familial Temporal Lobe, 4 Gene Set

From CTD Gene-Disease Associations

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

MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set

From CTD Gene-Disease Associations

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

Cardiomyopathy, Familial Hypertrophic, 14 Gene Set

From CTD Gene-Disease Associations

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

familial mediterranean fever Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial adenomatous polyposis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial hyperlipidemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial hemiplegic migraine Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial atrial fibrillation Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial lipoprotein lipase deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial periodic paralysis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial lipoprotein lipase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial hypertriglyceridemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

benign familial infantile epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial adenomatous polyposis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial combined hyperlipidemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial renal oncocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fatal familial insomnia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial mediterranean fever Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial nephrotic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial glomangioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial hyperlipidemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial hypercholesterolemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial periodic paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

benign familial neonatal epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial partial lipodystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial hemiplegic migraine Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial visceral amyloidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial atrial fibrillation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial medullary thyroid carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial renal papillary carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial retinoblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial adenomatous polyposis. Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

familial mediterranean fever; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

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

mild familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

familial atypical progressive supranuclear palsy Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

familial or sporadic prostate cancer. Gene Set

From GAD Gene-Disease Associations

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

familial distal renal tubular acidosis Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

familial defective apolipoprotein b100. Gene Set

From GAD Gene-Disease Associations

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

asthma; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

familial hypercholesterolaemia Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

amyloidosis, familial; cerebral hemorrhage; cerebral hemorrhages Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

amyloid neuropathies; amyloid neuropathies, familial Gene Set

From GAD Gene-Disease Associations

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

early-onset familial alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

abdomen, acute; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

familial dysbetalipoproteinemia Gene Set

From GAD Gene-Disease Associations

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

familial defective apolipoprotein b Gene Set

From GAD Gene-Disease Associations

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

familial amyloid polyneuropathy. Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease (familial) Gene Set

From GAD Gene-Disease Associations

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

mild familial hypercholesterolaemia Gene Set

From GAD Gene-Disease Associations

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

familial combined hyperlipidemia Gene Set

From GAD Gene-Disease Associations

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

endogenous hypertriglyceridemia and familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

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

familial age-related macular degeneration Gene Set

From GAD Gene-Disease Associations

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

familial premature myocardial infarction. Gene Set

From GAD Gene-Disease Associations

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

familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

late onset of familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

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

familial amyloidotic polyneuropathy. Gene Set

From GAD Gene-Disease Associations

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

amyloid neuropathies, familial Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

amyloidosis; familial mediterranean fever; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

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

premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set

From GAD Gene-Disease Associations

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

body weight; familial mediterranean fever; recurrence Gene Set

From GAD Gene-Disease Associations

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

familial male-limited precocious puberty. Gene Set

From GAD Gene-Disease Associations

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

familial combined hyperlipidaemia. Gene Set

From GAD Gene-Disease Associations

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

amyloidosis; familial mediterranean fever; inflammation Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

familial early onset psoriasis. Gene Set

From GAD Gene-Disease Associations

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

familial hypobetalipoproteinemia Gene Set

From GAD Gene-Disease Associations

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

familial amyotrophic lateral sclerosis. Gene Set

From GAD Gene-Disease Associations

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

familial amyloid polyneuropathy in a hungarian family. Gene Set

From GAD Gene-Disease Associations

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

familial melanoma Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

rapidly progressive familial amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

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

arthritis, juvenile rheumatoid; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; coronary artery disease; hyperlipidemia, familial combined; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

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

familial hypocalciuric hypercalcemia Gene Set

From GAD Gene-Disease Associations

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

familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

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

familial hyperinsulinism. Gene Set

From GAD Gene-Disease Associations

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

familial glucocorticoid deficiency Gene Set

From GAD Gene-Disease Associations

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

familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

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

late onset familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

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

arthritis; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

familial amyloid polyneuropathy Gene Set

From GAD Gene-Disease Associations

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

familial hypercholesterolemia. Gene Set

From GAD Gene-Disease Associations

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

familial partial lipodystrophy Gene Set

From GAD Gene-Disease Associations

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

familial amyloidotic polyneuropathy type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial amyloidotic polyneuropathy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; infertility, male Gene Set

From GAD Gene-Disease Associations

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

familial liver adenomatosis Gene Set

From GAD Gene-Disease Associations

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

diarrhea; familial mediterranean fever; pain; stomatitis, aphthous Gene Set

From GAD Gene-Disease Associations

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

breast cancer, familial Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

familial hypertrophic cardiomyopathy. Gene Set

From GAD Gene-Disease Associations

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

familial cataract Gene Set

From GAD Gene-Disease Associations

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

amyloid neuropathies, familial; constipation; diarrhea; gastrointestinal diseases; nausea; vomiting Gene Set

From GAD Gene-Disease Associations

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

amyloidosis; arthritis, rheumatoid; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

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

amyloidosis; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; hyperlipidemia, familial combined; metabolic syndrome x; mixed hyperlipidemia Gene Set

From GAD Gene-Disease Associations

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

creutzfeldt-jakob disease; creutzfeldt-jakob syndrome; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

blood pressure; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

amyloidosis; atherosclerosis; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

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

creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial exudative vitreoretinopathy Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, hypertrophic, familial Gene Set

From GAD Gene-Disease Associations

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

amyloidosis; arthritis, rheumatoid; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

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

familial dysautonomia Gene Set

From GAD Gene-Disease Associations

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

familial alzheimer's disease associated Gene Set

From GAD Gene-Disease Associations

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

familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

greenland familial cholestasis Gene Set

From GAD Gene-Disease Associations

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

familial diabetes insipidus Gene Set

From GAD Gene-Disease Associations

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

familial erythrocytosis Gene Set

From GAD Gene-Disease Associations

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

familial bronchiectasis. Gene Set

From GAD Gene-Disease Associations

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

arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set

From GAD Gene-Disease Associations

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

familial non-ret c cell hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial non-ret c cell hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypertension of early onset. Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

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

familial mediterranean fever; hyper-igd syndrome Gene Set

From GAD Gene-Disease Associations

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

familial mediterranean fever; fever Gene Set

From GAD Gene-Disease Associations

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

familial Gene Set

From GeneRIF Biological Term Annotations

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

Familial combined hyperlipidaemia_Blood monocyte_GSE11393 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Familial combined hyperlipidaemia_Blood monocyte_GSE11393 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Familial combined hyperlipidaemia_lymphoblast_GSE1010 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Familial combined hyperlipidaemia_lymphoblast_GSE1010 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Familial hypophosphataemic rickets_Renal Tissue_GSE868 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Familial hypophosphataemic rickets_Renal Tissue_GSE868 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Parkinson's disease (familial) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Parkinson's disease (familial) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

familial hypertriglyceridemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

familial atrial fibrillation Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease familial atrial fibrillation in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

familial predisposition Gene Set

From HPO Gene-Disease Associations

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

Hyperlipidemia, Familial Combined Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Paralyses, Familial Periodic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cardiomyopathy, Hypertrophic, Familial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Familial Mediterranean Fever Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Lipodystrophy, Familial Partial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Amyloidosis, Familial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Dysautonomia, Familial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Amyloid Neuropathies, Familial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Insomnia, Fatal Familial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

epilepsy, familial focal, with variable foci Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial focal, with variable foci phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperparathyroidism, familial primary Gene Set

From OMIM Gene-Disease Associations

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

{atrial fibrillation, familial, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrial fibrillation, familial, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{breast-ovarian cancer, familial, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {breast-ovarian cancer, familial, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

digital arthropathy-brachydactyly, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the digital arthropathy-brachydactyly, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive familial heart block, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial basilar Gene Set

From OMIM Gene-Disease Associations

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

insomnia, fatal familial Gene Set

From OMIM Gene-Disease Associations

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

dysautonomia, familial Gene Set

From OMIM Gene-Disease Associations

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

febrile seizures, familial, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

combined hyperlipidemia, familial Gene Set

From OMIM Gene-Disease Associations

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

familial cold-induced inflammatory syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the familial cold-induced inflammatory syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial temporal lobe, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial temporal lobe, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypobetalipoproteinemia, familial, 2 Gene Set

From OMIM Gene-Disease Associations

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

febrile seizures, familial, 3a Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 3a phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, familial danish Gene Set

From OMIM Gene-Disease Associations

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

cardiomyopathy, familial hypertrophic 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

[igg receptor i, phagocytic, familial deficiency of] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [igg receptor i, phagocytic, familial deficiency of] phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperuricemic nephropathy, familial juvenile 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperuricemic nephropathy, familial juvenile 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{breast-ovarian cancer, familial, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {breast-ovarian cancer, familial, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperaldosteronism, familial, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperaldosteronism, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperinsulinemic hypoglycemia, familial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperinsulinemic hypoglycemia, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperinsulinemic hypoglycemia, familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperinsulinemic hypoglycemia, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperinsulinemic hypoglycemia, familial, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperinsulinemic hypoglycemia, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperinsulinemic hypoglycemia, familial, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperinsulinemic hypoglycemia, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperinsulinemic hypoglycemia, familial, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperinsulinemic hypoglycemia, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperinsulinemic hypoglycemia, familial, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperinsulinemic hypoglycemia, familial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

?epilepsy, familial adult myoclonic, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epilepsy, familial adult myoclonic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

?candidiasis, familial, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?candidiasis, familial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

[fleck retina, familial benign] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fleck retina, familial benign] phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

candidiasis, familial, 6, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the candidiasis, familial, 6, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

carpal tunnel syndrome, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the carpal tunnel syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial fibrillation, familial, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial fibrillation, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial fibrillation, familial, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial fibrillation, familial, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial fibrillation, familial, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial fibrillation, familial, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial fibrillation, familial, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial fibrillation, familial, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial fibrillation, familial, 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial fibrillation, familial, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial fibrillation, familial, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial fibrillation, familial, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial fibrillation, familial, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial fibrillation, familial, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

medullary thyroid carcinoma, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the medullary thyroid carcinoma, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercholesterolemia, familial, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercholesterolemia, familial, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular fibrillation, paroxysmal familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, familial hypertrophic, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, familial hypertrophic, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

acne inversa, familial, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the acne inversa, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

endometrial cancer, familial Gene Set

From OMIM Gene-Disease Associations

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

hyperbilirubinemia, familial transient neonatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperbilirubinemia, familial transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, familial, nonspecific Gene Set

From OMIM Gene-Disease Associations

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

hyperuricemic nephropathy, familial juvenile 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperuricemic nephropathy, familial juvenile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperuricemic nephropathy, familial juvenile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperuricemic nephropathy, familial juvenile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperaldosteronism, familial, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperaldosteronism, familial, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, familial partial, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, familial partial, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, familial partial, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, familial partial, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hemophagocytic lymphohistiocytosis, familial, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemophagocytic lymphohistiocytosis, familial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

hemophagocytic lymphohistiocytosis, familial, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemophagocytic lymphohistiocytosis, familial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyloidosis, familial visceral Gene Set

From OMIM Gene-Disease Associations

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

migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

hematuria, familial benign Gene Set

From OMIM Gene-Disease Associations

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

hematuria, benign familial Gene Set

From OMIM Gene-Disease Associations

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

dementia, familial british Gene Set

From OMIM Gene-Disease Associations

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

pseudohyperkalemia, familial, 2, due to red cell leak Gene Set

From OMIM Gene-Disease Associations

genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenia, limb-girdle, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenia, limb-girdle, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

hemophagocytic lymphohistiocytosis, familial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemophagocytic lymphohistiocytosis, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hemophagocytic lymphohistiocytosis, familial, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemophagocytic lymphohistiocytosis, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

[erythrocytosis, familial, 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [erythrocytosis, familial, 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, familial, with neuroserpin inclusion bodies Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, familial typical, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, familial typical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperpigmentation, familial progressive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary hypertension, familial primary, 1, with or without hht Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, familial, due to decreased release of plat Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.

cylindromatosis, familial Gene Set

From OMIM Gene-Disease Associations

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

dyskinesia, familial, with facial myokymia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskinesia, familial, with facial myokymia phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic pain syndrome, familial, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic pain syndrome, familial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic pain syndrome, familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic pain syndrome, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoparathyroidism, familial isolated Gene Set

From OMIM Gene-Disease Associations

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

gastrointestinal stromal tumor, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the gastrointestinal stromal tumor, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

hemophagocytic lymphohistiocytosis, familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemophagocytic lymphohistiocytosis, familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

febrile seizures, familial, 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the febrile seizures, familial, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

advanced sleep phase syndrome, familial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the advanced sleep phase syndrome, familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

stuttering, familial persistent, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuttering, familial persistent, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocytosis, familial, 4 Gene Set

From OMIM Gene-Disease Associations

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

erythrocytosis, familial, 3 Gene Set

From OMIM Gene-Disease Associations

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

erythrocytosis, familial, 2 Gene Set

From OMIM Gene-Disease Associations

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

hypercholesterolemia, familial, 3 Gene Set

From OMIM Gene-Disease Associations

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

x inactivation, familial skewed, 2 Gene Set