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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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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 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. |
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 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 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, 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. |
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. |
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. |
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. |
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. |
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. |
abnormality of the zygomatic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the zygomatic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-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. |
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. |
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. |
arch Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term arch in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
pharyngeal arch artery morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pharyngeal arch artery morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
butterfly vertebral arch Gene SetFrom HPO Gene-Disease Associations genes associated with the butterfly vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vertebral arch anomaly Gene SetFrom HPO Gene-Disease Associations genes associated with the vertebral arch anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cleft vertebral arch Gene SetFrom HPO Gene-Disease Associations genes associated with the cleft vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
rRNA-processing arch domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the rRNA-processing arch domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fused first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the fused first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pharyngeal arch arteries Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pharyngeal arch arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vertebral arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent fourth pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent fourth pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zygomatic arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zygomatic arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent vertebral arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent vertebral arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent zygomatic arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent zygomatic arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fourth pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fourth pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small second pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small second pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharyngeal arch artery hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated pharyngeal arch arteries Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated pharyngeal arch arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fourth pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fourth pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal third pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal third pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ectopic pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ectopic pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal second pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal second pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal second pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal second pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent third pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent third pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sixth pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sixth pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal third pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal third pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vertebral arch development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent sixth pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent sixth pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharyngeal arch hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharyngeal arch artery stenosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch artery stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal first pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small first pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small first pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent second pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent second pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sixth pharyngeal arch artery morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sixth pharyngeal arch artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
neural arch Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue neural arch from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
branchial arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue branchial arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
neural arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue neural arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
gill arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue gill arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Byzanthine Arch Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Byzanthine Arch Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vertebral Arch Anomaly Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vertebral Arch Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Butterfly Vertebral Arch Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Butterfly Vertebral Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
pharyngeal arch artery morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the pharyngeal arch artery morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small second pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small second pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vertebral arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vertebral arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fourth pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fourth pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal third pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal third pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pharyngeal arch artery hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vertebral arch development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal zygomatic arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zygomatic arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal first pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal first pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent second pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent second pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent pharyngeal arch arteries Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent pharyngeal arch arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent second pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent second pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent third pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent third pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mandibular dental arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mandibular dental arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fused first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fused first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent vertebral arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent vertebral arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
first pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the first pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
zygomatic arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the zygomatic arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pharyngeal arch artery stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pharyngeal arch artery stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fourth pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fourth pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sixth pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sixth pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
persistent right 6th pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the persistent right 6th pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal second pharyngeal arch artery morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal second pharyngeal arch artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal second pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal second pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal third pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal third pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch mesenchyme morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch mesenchyme morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fourth pharyngeal arch artery hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fourth pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent sixth pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sixth pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent third pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent third pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent fourth pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent fourth pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fourth pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fourth pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
third pharyngeal arch artery hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the third pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sixth pharyngeal arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sixth pharyngeal arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged first pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged first pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal maxillary dental arch morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal maxillary dental arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent fourth pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent fourth pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pharyngeal arch development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pharyngeal arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ectopic pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
second pharyngeal arch hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the second pharyngeal arch hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent sixth pharyngeal arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sixth pharyngeal arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated third pharyngeal arch artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated third pharyngeal arch artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick zygomatic arch Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick zygomatic arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vertebral arch morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal vertebral arch morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal pharyngeal arch morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal pharyngeal arch morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Pharyngeal arch mesenchyme cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pharyngeal arch mesenchyme cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Pharyngeal arch cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pharyngeal arch cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Pharyngeal arch 1 mesenchyme cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pharyngeal arch 1 mesenchyme cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
pharyngeal arch artery morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the pharyngeal arch artery morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
Neural arch Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Neural arch from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Branchial arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Branchial arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Neural arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Neural arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Gill arch Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Gill arch in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Pharyngeal arch cartilage Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Pharyngeal arch cartilage in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 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, 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. |
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 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 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 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 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 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 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 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, 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 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Aneurysm 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 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 Rupture Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aortic Rupture from the curated CTD Gene-Disease Associations dataset. |
Aortic Aneurysm, Familial Thoracic 1 Gene 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 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 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 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. |
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. |
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. |
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 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 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 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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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, 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. |
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 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 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. |
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. |
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 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 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, 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. |
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 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 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. |
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 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. |
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. |
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 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 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 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 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 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 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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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 aneurysm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aortic aneurysm 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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, 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. |
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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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 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 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. |
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. |
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. |
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. |
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. |
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 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 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 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. |
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. |
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. |
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. |
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 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 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. |
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. |
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. |
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. |
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 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. |
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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of glucagon secretion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrin secretion abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
torsion abnormality; vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormality Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of vitamin metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endometrium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forearm bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the integument Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin d metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stomach Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of connective tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cellular immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hearing abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of oral mucosa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urethra Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of brain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endocrine system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cerebral artery Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the breast Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the autonomic nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
eeg abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femur Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin a metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the calf Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the carotid arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of retinal arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the kidney Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circle of willis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hand Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pituitary gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the myocardium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cell cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of von willebrand factor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thrombocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of neutrophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hip bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the iris Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
mesangial abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin b metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the adrenal glands Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the respiratory system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the musculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral white matter Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the duodenum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the astrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of basophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the male genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of facial skeleton Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gingiva Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lung Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating hormone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the placenta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ankles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the heart valves Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of aromatic amino acid family metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the prostate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of digit Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the testis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental eruption Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the clavicle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of homocysteine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the knees Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coronary arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin adnexa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pleura Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of interleukin secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of tryptophan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of head or neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mandible Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of humoral immunity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neurodevelopmental abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of taste sensation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skeletal system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thorax Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thyroid gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdomen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrospinal fluid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
behavioral abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the oral cavity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cholesterol metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of granulocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the fundus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forebrain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the tongue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebrae Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the spinal cord Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vascular skin abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of refraction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood volume homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dna repair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nose Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of erythrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of liposaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating protein level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
prenatal maternal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humeral diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
phenotypic abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uterus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the metaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the common coagulation pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fatty-acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genitourinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cytokine secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
growth abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the choroid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the globe Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of radial diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear ossicles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the monocyte/macrophage lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb joint Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uvea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality 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. |
abnormality of the esophagus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retina Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the penis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood circulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the radius Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of urine homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the costochondral junction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral cortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone marrow cell morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the liver Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fluid regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pylorus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of adipose tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior pituitary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nasopharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intervertebral disk Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stapes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gallbladder Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
generalized abnormality of skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glial cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ulna Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lymphocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mouth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vitamin b12 metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genital system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humerus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of complement system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
chorioretinal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sulfur amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating cortisol level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prothrombin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of coagulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cervical spine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carboxylic acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skeletal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lens Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body weight Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of temperature regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the systemic arterial tree Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the rib cage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin e metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retinal vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of ion homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of macrophages Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of calcium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body height Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of polysaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intrinsic pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eosinophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the macula Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of epidermal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of higher mental function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ribs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nucleobase metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the forearm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of purine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of serum cytokine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating leptin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nephron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nephron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating glucocorticoid level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the falx cerebri Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of gastrointestinal vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choanae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choanae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the immune system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reticulocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of von willebrand factor Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebellar peduncle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the gingiva Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the gingiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lung Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lung phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vena cava Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of sharpey fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metacarpophalangeal joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intrahepatic bile duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fluid regulation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of secondary sexual hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pineal gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the crus of the helix Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acetabulum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acetabulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sense of smell Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of permanent molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the achilles tendon Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the myocardium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of complement system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of blood glucose concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal tubule Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the shoulder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the shoulder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chromosome condensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prostaglandin metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neurodevelopmental abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of connective tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thumb phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alanine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atlantoaxial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the atlantoaxial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lower limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thrombocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thrombocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior pituitary Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vestibulocochlear nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of binocular vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thyroid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forebrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forebrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cerebral artery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choroid plexus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choroid plexus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating protein level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the seventh cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the labia minora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the lymphoid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized abnormality of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the glial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aryepiglottic fold Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prothrombin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the subungual region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal collecting system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acoustic reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubulointerstitial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dental pulp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cysteine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |