| Name |
|---|
AAA1 Geneaortic aneurysm, familial abdominal 1 |
AAA2 GeneAortic aneurysm, familial abdominal 2 |
AAA4 GeneAortic aneurysm, familial abdominal, 4 |
AAT2 GeneAortic aneurysm, familial thoracic 2 |
AAT1 GeneAortic aneurysm, familial thoracic 1 |
AAA3 GeneAneurysm, familial abdominal 3 |
AOMS1 GeneAbdominal obesity-metabolic syndrome QTL1 |
AOMS2 Geneabdominal obesity-metabolic syndrome QTL2 |
ANIB11 GeneAneurysm, intracranial berry, 11 |
ANIB10 GeneAneurysm, intracranial berry, 10 |
ANIB9 GeneAneurysm, intracranial berry, 9 |
ANIB8 GeneAneurysm, intracranial berry, 8 |
ANIB5 GeneAneurysm, intracranial berry, 5 |
ANIB4 Geneaneurysm, intracranial berry 4 |
ANIB7 GeneAneurysm, intracranial berry, 7 |
ANIB6 GeneAneurysm, intracranial berry, 6 |
ANIB1 Geneaneurysm, intracranial berry 1 |
ANIB3 Geneaneurysm, intracranial berry 3 |
ANIB2 Geneaneurysm, intracranial berry 2 |
ETL6 GeneEpilepsy, familial temporal lobe, 6 |
RCM2 Genecardiomyopathy, familial restrictive, 2 |
ATFB8 GeneAtrial fibrillation, familial, 8 |
HNFJ3 GeneHyperuricemic nephropathy, familial juvenile, 3 |
GPSC Genegliosis, familial progressive subcortical |
BHD GeneBeukes familial hip dysplasia |
FAME4 GeneEpilepsy, familial adult myoclonic, 4 |
FAME3 GeneEpilepsy, familial adult myoclonic, 3 |
PFHB2 GeneProgressive familial heart block, type II |
BFIS1 Genebenign familial infantile convulsions |
HBN1 GeneProgressive familial heart block, type I, locus 1 |
ETL2 Geneepilepsy, familial temporal lobe |
FHII GeneHyperaldosteronism, familial, type II |
FCMTE2 Genefamilial cortical myoclonic tremor with epilepsy 2 |
FCMTE1 Genefamilial cortical myoclonic tremor with epilepsy 1 |
GLM4 GeneGlioma, familial, 1 |
PSHK2 GenePseudohyperkalemia, familial, 2, due to red cell leak |
VVS GeneSyncope, familial vasovagal |
BFIS4 GeneConvulsions, benign familial infantile, 4 |
ATFB1 GeneAtrial fibrillation, familial 1 |
ATFB2 Genefamilial atrial fibrillation 2 |
SXI2 GeneX inactivation, familial skewed, 2 |
BFIC2 GeneBenign familial infantile convulsions-2 |
FMTLE GeneEpilepsy, familial mesial temporal lobe |
STUT3 GeneStuttering, familial persistent, 3 |
STUT2 GeneStuttering, familial persistent 2 |
STUT1 GeneStuttering, familial persistent 1 |
STUT4 GeneStuttering, familial persistent, 4 |
BRCD1 Genecancer, familial, with in vitro radioresistance |
MGR2 GeneMigraine, familial typical, susceptibility to |
MGR3 GeneMigraine, familial, with or without aura, susceptibility to |
MFT2 GeneTrichoepithelioma, multiple familial, 2 |
FEB9 GeneFebrile convulsions, familial, 9 |
ATFB5 GeneAtrial fibrillation, familial, 5 |
HTGS GeneHypertriglyceridemia, familial |
DIP Geneinterstitial pneumonitis, desquamative, familial |
CMH21 GeneCardiomyopathy, familial hypertrophic, 21 |
CANDF1 Genecandidiasis, familial 1 |
ATPLS Geneantiphospholipid syndrome, familial |
EOS Geneeosinophilia, familial |
FEB10 GeneFebrile convulsions, familial, 10 |
LVNC2 Genenoncompaction of left ventricular myocardium, familial isolated, autosomal dominant 2 |
THCYTX GeneThrombocytosis, familial X-linked |
CMS1A1 Genemyasthenia gravis, familial infantile, 1 |
BPPV Genevestibulopathy, familial |
NKCD GeneNatural killer cell deficiency, familial isolated |
aortic aneurysm, familial abdominal, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aneurysm, ruptured; aortic aneurysm, abdominal; intracranial aneurysm; subarachnoid hemorrhage Gene SetFrom 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. |
aneurysm, ruptured; aortic aneurysm, abdominal Gene SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, ruptured; aortic aneurysm, abdominal; arterial occlusive diseases; carotid artery stenosis; carotid stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; aortic rupture Gene SetFrom 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 SetFrom 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. |
Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic Aneurysm, Familial Abdominal 2 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial abdominal 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Familial Thoracic Aortic Aneurysm And Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Thoracic Aortic Aneurysm And Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial thoracic aortic aneurysm and aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial thoracic aortic aneurysm and aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
sporadic abdominal aortic aneurysm Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Abdominal from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Abdominal Gene SetFrom 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. |
abdominal aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abdominal aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic aneurysm, abdominal; disease progression Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; lung cancer; abdominal aortic aneurysm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; disease susceptibility; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; arterial occlusive diseases Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
abdominal aortic aneurysm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abdominal aortic aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abdominal aortic aneurysm Gene SetFrom 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. |
Aortic Aneurysm, Abdominal Gene SetFrom 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. |
Dissecting Abdominal Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ruptured Abdominal Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inflammatory Abdominal Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Abdominal Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Abdominal aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abdominal aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sporadic abdominal aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sporadic abdominal aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abdominal aortic aneurysm Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abdominal aortic aneurysm phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
aneurysm, dissecting; aortic aneurysm, thoracic; Gene SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneurysm, dissecting; aortic aneurysm; cardiovascular diseases; hyperhomocysteinemia; marfan syndrome Gene SetFrom 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. |
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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, familial abdominal 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {aneurysm, familial abdominal 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Aortic aneurysm, familial thoracic 6 Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic aneurysm, familial thoracic 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic aneurysm, familial thoracic 8 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic aneurysm, familial thoracic 1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, familial thoracic 9 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aneurysm of an abdominal artery Gene SetFrom 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. |
abdominal aorta aneurysm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abdominal aorta aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abdominal aorta aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abdominal aorta aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aneurysm, ruptured; intracranial aneurysm; stroke; subarachnoid hemorrhage Gene SetFrom 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 SetFrom 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. |
differential expansion rates of small abdominal aortic aneurysms Gene SetFrom 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. |
Abdominal Aortic Atherosclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Aortic Atherosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal aortic calcification levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abdominal aortic calcification levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm, Thoracic from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Aortic Aneurysm, Thoracic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
aortic aneurysm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic aneurysm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
thoracic aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene SetFrom 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 SetFrom 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 SetFrom GWASdb SNP-Disease Associations genes associated with the disease thoracic aortic aneurysm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
aortic aneurysm Gene SetFrom 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. |
aortic aneurysm Gene SetFrom 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 SetFrom 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. |
ascending aortic aneurysm Gene SetFrom 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 SetFrom 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. |
thoracic aortic aneurysm Gene SetFrom 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. |
dissecting aortic aneurysm Gene SetFrom HPO Gene-Disease Associations genes associated with the dissecting aortic aneurysm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Aortic Aneurysm, Thoracic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aortic Aneurysm, Thoracic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aortic Aneurysm Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the aortic aneurysm, ascending, and dissection phenotype from the curated OMIM Gene-Disease Associations dataset. |
Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dissecting Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ruptured Thoracic Aortic Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Thoracic Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracoabdominal Aortic Aneurysm, Ruptured Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracoabdominal Aortic Aneurysm, Ruptured in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loeys-Dietz Aortic Aneurysm Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loeys-Dietz Aortic Aneurysm Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Aneurysm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
aortic aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic sinus aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic sinus aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Aortic aneurysm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic aneurysm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thoracic aortic aneurysm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Thoracic aortic aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thoracic aortic aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thoracic aortic aneurysm or dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm or dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Isolated thoracic aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thoracic aortic aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
aortic valve insufficiency; aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
abnormal aortic arch and aortic arch branch attachment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Bicuspid aortic valve without aortic dilation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve without aortic dilation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
abdominal pain; amyloidosis; arthritis; familial mediterranean fever; fever Gene SetFrom 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 Bicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Abdominal obesity metabolic syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abdominal obesity metabolic syndrome from the curated CTD Gene-Disease Associations dataset. |
Obesity, Abdominal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Obesity, Abdominal from the curated CTD Gene-Disease Associations dataset. |
Abdominal Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abdominal Pain from the curated CTD Gene-Disease Associations dataset. |
Fibromatosis, Abdominal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibromatosis, Abdominal from the curated CTD Gene-Disease Associations dataset. |
Abdominal Fat Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Abdominal Fat in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Aorta, Abdominal Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Aorta, Abdominal in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Intra-Abdominal Fat Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Intra-Abdominal Fat in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
hemangioma of intra-abdominal structure Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hemangioma of intra-abdominal structure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abdominal tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abdominal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adiposity and abdominal obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adiposity and abdominal obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intra-abdominal fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intra-abdominal fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipocyte size, large subcutaneous abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipocyte size, large subcutaneous abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; metabolic syndrome x; obesity, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; obesity, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aorta, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aorta, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal adiposity and hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal adiposity and hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complications after major abdominal operations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complications after major abdominal operations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
metabolic syndrome x; obesity, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease metabolic syndrome x; obesity, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenomatous polyposis coli; fibromatosis, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; fibromatosis, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity, abdominal; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity, abdominal; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance and intra-abdominal fat thickness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance and intra-abdominal fat thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal pain; dyspepsia; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal pain; dyspepsia; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal pain; irritable bowel syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abdominal pain; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abdominal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abdominal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
dilatation of the abdominal aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the dilatation of the abdominal aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abdominal symptom Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abdominal symptom phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdominal organs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abdominal wall muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal wall muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hernia of the abdominal wall Gene SetFrom HPO Gene-Disease Associations genes associated with the hernia of the abdominal wall phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial abdominal muscle agenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the partial abdominal muscle agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal symptom Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal symptom phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal colic Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal colic phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal wall defect Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal wall defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal situs inversus Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal situs inversus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal pain Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the abdominal wall Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the abdominal wall phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dilatation of the abdominal aorta Gene SetFrom HPO Gene-Disease Associations genes associated with the dilatation of the abdominal aorta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abdominal distention Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal distention phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of abdominal situs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of abdominal situs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the abdominal musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the abdominal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic abdominal pain Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic abdominal pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the abdominal organs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the abdominal organs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Fibromatosis, Abdominal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fibromatosis, Abdominal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Abdominal Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Abdominal Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Abdominal Pain Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Abdominal Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Obesity, Abdominal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Obesity, Abdominal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
decreased abdominal adipose tissue amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased abdominal adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abdominal situs ambiguus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abdominal situs ambiguus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal abdominal aorta morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal abdominal aorta morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal abdominal lymph node morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal abdominal lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abdominal situs inversus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abdominal situs inversus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal abdominal wall morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal abdominal wall morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased abdominal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased abdominal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased abdominal fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased abdominal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
herniated abdominal wall Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the herniated abdominal wall phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal abdominal fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal abdominal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abdominal obesity-metabolic syndrome 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the abdominal obesity-metabolic syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
abdominal obesity-metabolic syndrome 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the abdominal obesity-metabolic syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?abdominal obesity-metabolic syndrome 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?abdominal obesity-metabolic syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
abdominal obesity-metabolic syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the abdominal obesity-metabolic syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
abdominal adipose tissue Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue abdominal adipose tissue from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
abdominal ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue abdominal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
thoracico-abdominal ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue thoracico-abdominal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
abdominal muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue abdominal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
abdominal adipose tissue Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue abdominal adipose tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
abdominal aorta Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue abdominal aorta in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Abdominal Sepsis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Sepsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Obesity-Metabolic Syndrome 3 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Obesity-Metabolic Syndrome 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intra-Abdominal Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intra-Abdominal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Abdominal Wall Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Abdominal Wall in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibromatosis, Abdominal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibromatosis, Abdominal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Cryptorchidism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Cryptorchidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Abscess Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Abscess in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Migraine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Migraine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Adhesions Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Adhesions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Tuberculosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Tuberculosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Obesity Metabolic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Obesity Metabolic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Extra-Abdominal Fibromatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Extra-Abdominal Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Compartment Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Compartment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complicated Intra-Abdominal Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complicated Intra-Abdominal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Obesity-Metabolic Syndrome 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Obesity-Metabolic Syndrome 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastases To Abdominal Cavity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastases To Abdominal Cavity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abdominal Cocoon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abdominal Cocoon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Abdominal Wall Musculature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Abdominal Wall Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Bloating Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Bloating in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acute Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Symptom Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Symptom in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Colic Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Colic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Tenderness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Tenderness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Wall Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Wall Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Abdominal Wall Musculature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Abdominal Wall Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Discomfort Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Discomfort in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Partial Abdominal Muscle Agenesis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Abdominal Muscle Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Pain In Children Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Pain In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nonspecific Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonspecific Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Cramps Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Cramps in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Functional Abdominal Pain Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Functional Abdominal Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Situs Ambiguus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Situs Ambiguus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dilated Superficial Abdominal Veins Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilated Superficial Abdominal Veins in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Mass Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Mass in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lower Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lower Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
herniated abdominal wall Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the herniated abdominal wall phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal abdominal wall morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal abdominal wall morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal abdominal fat pad morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal abdominal fat pad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased abdominal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased abdominal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased abdominal adipose tissue amount Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased abdominal adipose tissue amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased abdominal fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased abdominal fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased abdominal adipose tissue amount Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased abdominal adipose tissue amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abdominal situs ambiguus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abdominal situs ambiguus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abdominal situs abnormality Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abdominal situs abnormality phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal abdominal aorta morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal abdominal aorta morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abdominal situs inversus Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abdominal situs inversus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal abdominal lymph node morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal abdominal lymph node morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal abdominal muscle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal abdominal muscle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in abdominal region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in abdominal region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal abdominal wall morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal abdominal wall morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Abdominal obesity-metabolic syndrome Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Abdominal obesity-metabolic syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal obesity-metabolic syndrome 1 Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Abdominal obesity-metabolic syndrome 1 in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abdominal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal obesity-metabolic syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abdominal obesity-metabolic syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal obesity-metabolic syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abdominal obesity-metabolic syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal obesity-metabolic syndrome 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Abdominal obesity-metabolic syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hemangioma of intra-abdominal structure Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hemangioma of intra-abdominal structure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abdominal adipose tissue Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Abdominal adipose tissue from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Abdominal adipose tissue Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Abdominal adipose tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Abdominal aorta Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Abdominal aorta in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Abdominal muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Abdominal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Abdominal ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Abdominal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
thoracico-abdominal ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue thoracico-abdominal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Abdominal obesity-metabolic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abdominal obesity-metabolic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abdominal subcutaneous adipose tissue volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Abdominal subcutaneous adipose tissue volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aneurysm, Ruptured Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aneurysm, Intracranial Berry, 8 from the curated CTD Gene-Disease Associations dataset. |
Aneurysm Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aneurysm from the curated CTD Gene-Disease Associations dataset. |
Aneurysm, Intracranial Berry, 3 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aneurysm, Dissecting from the curated CTD Gene-Disease Associations dataset. |
Intracranial Aneurysm Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom DISEASES Experimental Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom DISEASES Text-mining Gene-Disease Association 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GWASdb SNP-Phenotype Associations genes associated with the cerebral aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aneurysm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aneurysm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
cerebral aneurysm Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
mesenteric artery aneurysm Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
ascending aorta aneurysm Gene SetFrom 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 SetFrom 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 SetFrom MPO Gene-Phenotype Associations gene mutations causing the coronary artery aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aneurysm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
brain aneurysm Gene SetFrom 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 SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrial septal aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thoracic aorta aneurysm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thoracic aorta aneurysm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricular aneurysm Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the {aneurysm, intracranial berry, 9} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Intracranial Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coronary Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coronary Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ruptured Cerebral Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ruptured Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Aneurysm Of Ascending Aorta Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Aneurysm Of Ascending Aorta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bronchial Artery Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bronchial Artery Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dissecting Aneurysm Of The Thoracic Aorta Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dissecting Aneurysm Of The Thoracic Aorta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Arterial Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Arterial Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aneurysm, Intracranial Berry, 1 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aneurysm, Intracranial Berry, 1 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Saccular Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Saccular Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrial Septal Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrial Septal Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Left Ventricular Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonruptured Congenital Cerebral Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonruptured Congenital Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fusiform Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fusiform Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arterial Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arterial Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vertebral Artery Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vertebral Artery Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vascular Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vascular Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vein Of Galen Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vein Of Galen Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonruptured Cerebral Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonruptured Cerebral Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carotid Artery Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carotid Artery Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sinus Of Valsalva Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sinus Of Valsalva Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Berry Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Berry Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Giant Intracranial Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Giant Intracranial Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mycotic Aneurysm, Intracranial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mycotic Aneurysm, Intracranial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Calcified Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Calcified Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Retinal Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Retinal Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ventricular Aneurysm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ventricular Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aneurysm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pulmonary Artery Aneurysm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pulmonary Artery Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
heart right ventricle aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the heart right ventricle aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
coronary artery aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the coronary artery aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
intracranial aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the intracranial aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
brain aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the brain aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to induced aneurysm formation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to induced aneurysm formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ascending aorta aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ascending aorta aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to induced aneurysm formation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to induced aneurysm formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
atrial septal aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the atrial septal aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thoracic aorta aneurysm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thoracic aorta aneurysm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Intracranial aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Intracranial aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Coronary aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Coronary aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Heart aneurysm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Heart aneurysm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intracranial aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intracranial aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intracranial berry aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intracranial berry aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Heart aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Heart aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Coronary aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Coronary aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Splenic artery aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Splenic artery aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Subclavian artery aneurysm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subclavian artery aneurysm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intracranial berry aneurysm 12 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intracranial berry aneurysm 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ventricular aneurysm disease specific cell type Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ventricular aneurysm disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Congenital aneurysm of ascending aorta Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital aneurysm of ascending aorta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aneurysm-osteoarthritis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aneurysm-osteoarthritis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Brain aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Brain aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ascending tubular aorta aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ascending tubular aorta aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aneurysm of descending aorta Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aneurysm of descending aorta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mycotic Aneurysm Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mycotic Aneurysm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Intracranial aneurysm Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intracranial aneurysm phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Coronary artery aneurysm in Kawasaki disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery aneurysm in Kawasaki disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Supravalvar aortic stenosis Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Valve Insufficiency from the curated CTD Gene-Disease Associations dataset. |
Aortic Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Diseases from the curated CTD Gene-Disease Associations dataset. |
Aortic Rupture Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease supravalvular aortic stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic valve stenosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic valve stenosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic valve disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease aortic valve disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
aortic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease aortic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
aortic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve insufficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic atherosclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve prolapse Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve prolapse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
supravalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease supravalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
subvalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subvalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aortic valve disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
H3K4me3_fibroblast of the aortic adventitia_hg19_2 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis; diabetes mellitus; hyperlipidemias; hypertension; mitral valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GO Biological Process Annotations 2015 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback biological process from the curated GO Biological Process Annotations 2015 dataset. |
Thoracic aortic aneurysms and dissections Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Aortic-valve calcification Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the supravalvar aortic stenosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
aortic Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Abnormal Aortic Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Supravalvular Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Supravalvular Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Dissection Rupture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Dissection Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Insufficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Coarctation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Coarctation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Calcification Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Descending Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Descending Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Right Aortic Arch (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Right Aortic Arch (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Rupture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Senile Sclerosis Of Aortic Cusp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Senile Sclerosis Of Aortic Cusp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Root Dilation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Root Dilation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Wall Hypertrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Wall Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Root Dilatation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Root Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Angiosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Angiosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Stenosis Of Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Stenosis Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paravalvular Aortic Regurgitation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paravalvular Aortic Regurgitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Aortic Valve Physiology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Aortic Valve Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Degenerative Aortic Valve Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Degenerative Aortic Valve Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thoracic Aortic Ectasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thoracic Aortic Ectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mitral And Aortic Incompetence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mitral And Aortic Incompetence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Sclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Stenosis Symptomatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Stenosis Symptomatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rheumatic Aortic Regurgitation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Aortic Regurgitation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Interrupted Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Interrupted Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Anomaly Of Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomaly Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Right Aortic Arch With Mirror Image Branching Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Right Aortic Arch With Mirror Image Branching in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rheumatic Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Supravalvular Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Supravalvular Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Disease 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disease 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Descending Thoracic Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Descending Thoracic Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Two-Raphe Bicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Two-Raphe Bicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ascending Aortic Rupture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ascending Aortic Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonrheumatic Aortic (Valve) Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonrheumatic Aortic (Valve) Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mid Aortic Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mid Aortic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Isolated Aortic Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Isolated Aortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Atresia Of Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atresia Of Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Tortuosity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Valve Disease 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Valve Disease 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Intramural Haematoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aortic Intramural Haematoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical Aortic Arch Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Quadricuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Quadricuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Unicuspid Aortic Valve Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Unicuspid Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aortic Stiffness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ascending Aortic Dissection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ascending Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ascending Aortic Dilatation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ascending Aortic Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dysplastic Aortic Valve Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysplastic Aortic Valve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aortic Arch Calcification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aortic Arch Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dilated Aortic Root Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilated Aortic Root in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Left Aortic Arch With Retroesophageal Right Subclavian Artery Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Aortic Arch With Retroesophageal Right Subclavian Artery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
aortic valve morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
aortic valve development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the aortic valve development biological process from the curated GO Biological Process Annotations 2023 dataset. |
aortic valve formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the aortic valve formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
overriding aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the overriding aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
interrupted aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the interrupted aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic arch coarctation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch coarctation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick aortic valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick aortic valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated aortic sac Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated aortic sac phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve regurgitation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve regurgitation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve cusp morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve cusp morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
right aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the right aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
calcified aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic hypertrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic hypertrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cervical aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cervical aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
double aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the double aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
patent aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the patent aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic dissection Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic dissection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
bicuspid aortic valve Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the bicuspid aortic valve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve commissure morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve commissure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic elastic tissue lesions Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic elastic tissue lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
interrupted aortic arch, type b Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the interrupted aortic arch, type b phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve flow Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve flow phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic sac morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic sac morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased aortic weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased aortic weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic arch development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent aortic valve cusps Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent aortic valve cusps phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
calcified aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve atresia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve atresia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
supravalvar aortic stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the supravalvar aortic stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal aortic valve anulus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal aortic valve anulus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
double lumen aortic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the double lumen aortic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic valve inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic valve inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
aortic arch dilation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the aortic arch dilation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Intra-aortic hematopoietic cell_Embryo_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Intra-aortic hematopoietic cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
aortic valve morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the aortic valve morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
aortic valve development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the aortic valve development biological process from the curated GO Biological Process Annotations 2025 dataset. |
aortic valve formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the aortic valve formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of aortic smooth muscle cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Aortic disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic valve disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic valve disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Supravalvular aortic stenosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Supravalvular aortic stenosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic valve stenosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aortic valve stenosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Aortic disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve stenosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic valve stenosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Aortic valve disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic dissection Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic dissection in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic atherosclerosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Supravalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Supravalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve insufficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bicuspid aortic valve disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bicuspid aortic valve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic malignant tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic malignant tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve disease 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve disease 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Subvalvular aortic stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subvalvular aortic stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic valve prolapse Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aortic valve prolapse in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aortic smooth muscle Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Aortic smooth muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic root Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic valve Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic valve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic smooth muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic smooth muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic endothelial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic endothelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic smooth muscle cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic smooth muscle cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Human aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Human aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic body Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic body in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic intima Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic intima in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Porcine aortic endothelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Porcine aortic endothelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic adventitial fibroblast Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Aortic adventitial fibroblast in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Aortic valve disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic valve disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Supravalvar aortic stenosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Supravalvar aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal aortic valve morphology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal aortic valve morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic valve atresia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic valve atresia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Subvalvular aortic stenosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Subvalvular aortic stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic dilatation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aortic dilatation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bicuspid aortic valve Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Heritable Thoracic Aortic disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Heritable Thoracic Aortic disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early age onset of sporadic thoracic aortic dissections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early age onset of sporadic thoracic aortic dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ascending aortic dissection Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Ascending aortic dissection phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aortic valve stenosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic valve stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Calcific aortic valve stenosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Calcific aortic valve stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic root size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic root size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic valve area Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic valve area phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thoracic aortic calcification levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic calcification levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Severe aortic features in Marfan syndrome Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe aortic features in Marfan syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic vascular smooth muscle cell calcification in response to osteogenic stimuli Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic vascular smooth muscle cell calcification in response to osteogenic stimuli phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic vascular smooth muscle cell proliferation in response to IL-1 beta Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic vascular smooth muscle cell proliferation in response to IL-1 beta phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thoracic aortic aneurysms and dissections Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thoracic aortic aneurysms and dissections phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic stiffness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic stiffness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic-valve calcification Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic-valve calcification phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic coarctation Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic coarctation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bicuspid aortic valve Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bicuspid aortic valve phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Familial Mediterranean fever Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocytosis, familial, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocytosis, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocytosis, familial, 2 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Benign familial neonatal seizures 1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial aortopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial aortopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Digital arthropathy-brachydactyly, familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial porencephaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial porencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypertrophic cardiomyopathy 17 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the familial hyperinsulinism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperinsulinemic hypoglycemia familial 3 Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypercholesterolemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypercholesterolemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hidradenitis suppurativa, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hidradenitis suppurativa, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dementia, familial Danish Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial dysautonomia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial febrile seizures 8 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoclonus, familial cortical phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Migraine, familial basilar Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercholanemia, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone marrow failure, familial Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Candidiasis, familial, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Candidiasis, familial, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypokalemia-hypomagnesemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial infantile myasthenia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial pulmonary capillary hemangiomatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial hypoalphalipoproteinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial hypoalphalipoproteinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial renal hypouricemia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Familial cold urticaria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Familial myelofibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial myelofibrosis from the curated CTD Gene-Disease Associations dataset. |
Nephronophthisis, familial juvenile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset. |
Eosinophilia, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eosinophilia, Familial from the curated CTD Gene-Disease Associations dataset. |
Hyperlipidemia, Familial Combined Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset. |
Familial dermographism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial dermographism from the curated CTD Gene-Disease Associations dataset. |
Candidiasis, Familial, 3 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratoacanthoma familial from the curated CTD Gene-Disease Associations dataset. |
Hepatic Adenomas, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial antiphospholipid syndrome from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Familial from the curated CTD Gene-Disease Associations dataset. |
Familial paroxysmal dystonia Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Meningioma, familial from the curated CTD Gene-Disease Associations dataset. |
Dysautonomia, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset. |
HYPERCHOLESTEROLEMIA, FAMILIAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERCHOLESTEROLEMIA, FAMILIAL from the curated CTD Gene-Disease Associations dataset. |
Amyloid Neuropathies, Familial Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial mediterranean fever from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial adenomatous polyposis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial adenomatous polyposis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial hyperlipidemia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hyperlipidemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial hemiplegic migraine Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial hemiplegic migraine from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial atrial fibrillation Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial atrial fibrillation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial juvenile hyperuricemic nephropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
familial lipoprotein lipase deficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |