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abnormal thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormal Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
abnormal thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Abnormal thrombosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal thrombosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; pulmonary embolism; pulmonary embolisms; stroke; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis; recurrence; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis; recurrence; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; intracranial thrombosis; lupus erythematosus, systemic; systemic lupus erythematosus; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; intracranial thrombosis; lupus erythematosus, systemic; systemic lupus erythematosus; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; hyperhomocysteinemia; intracranial thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; hyperhomocysteinemia; intracranial thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombophilia; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombophilia; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; intracranial thrombosis; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; intracranial thrombosis; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney diseases; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney diseases; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thromboembolism; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thromboembolism; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
puerperal disorders; sinus thrombosis, intracranial; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease puerperal disorders; sinus thrombosis, intracranial; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intracranial thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intracranial thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal atrial thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal atrial thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glomerular capillary thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glomerular capillary thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placental thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placental thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cardiac thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cardiac thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lung thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lung thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal venous thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal venous thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney venous thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney venous thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal arterial thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal arterial thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ventricular thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ventricular thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic portal vein thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic portal vein thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Coronary Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Venous Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Venous Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Sinus Thrombosis, Intracranial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sinus Thrombosis, Intracranial from the curated CTD Gene-Disease Associations dataset. |
Intracranial Embolism and Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Sagittal Sinus Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sagittal Sinus Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Carotid Artery Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carotid Artery Thrombosis from the curated CTD Gene-Disease Associations dataset. |
PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset. |
Intracranial Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Embolism and Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset. |
Venous Thrombosis Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Venous Thrombosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
intracranial sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intracranial sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intracranial thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intracranial thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cavernous sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cavernous sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sagittal sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sagittal sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hepatic vein thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic vein thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
portal vein thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease portal vein thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
coronary thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease coronary thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
carotid artery thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease carotid artery thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lateral sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lateral sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infection; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infection; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary thrombosis; graft occlusion, vascular; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary thrombosis; graft occlusion, vascular; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
deep venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease deep venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; puerperal disorders; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; puerperal disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis; antiphospholipid syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis; antiphospholipid syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postoperative complications; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thromboembolism; venous thrombosis; vitamin b deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thromboembolism; venous thrombosis; vitamin b deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral vascular diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral vascular diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; coronary disease; postoperative complications; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary disease; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; foramen ovale, patent; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; foramen ovale, patent; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhage; thromboembolism; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhage; thromboembolism; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
budd-chiari syndrome; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease budd-chiari syndrome; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pulmonary; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
severe childhood thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease severe childhood thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein s deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhage; thrombosis; von willebrand disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhage; thrombosis; von willebrand disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart diseases; myocardial infarction; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart diseases; myocardial infarction; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis, venous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis, venous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dyspnea; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dyspnea; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mesenteric vascular occlusion; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mesenteric vascular occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; heart diseases; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; heart diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
massive thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease massive thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrence and early onset of venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrence and early onset of venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carotid artery diseases; cerebrovascular disorders; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid artery diseases; cerebrovascular disorders; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; thrombophilia; thrombosis; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thrombophilia; thrombosis; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
seizures; thrombosis, deep vein; systemic sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease seizures; thrombosis, deep vein; systemic sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; myocardial ischemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; myocardial ischemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; coronary restenosis; postoperative complications; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary restenosis; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; myeloproliferative disorders; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; myeloproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperplasia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperplasia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; thrombocythemia, essential; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; thrombocythemia, essential; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
idiopathic deep venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic deep venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intracranial thrombosis; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intracranial thrombosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; coronary thrombosis; diabetes complications; hypertension; mitral valve stenosis; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; coronary thrombosis; diabetes complications; hypertension; mitral valve stenosis; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhage; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhage; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary artery disease; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; thrombocythemia, hemorrhagic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antiphospholipid syndrome; arteriosclerosis; lupus erythematosus, systemic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arteriosclerosis; lupus erythematosus, systemic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antiphospholipid syndrome; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary restenosis; myocardial infarction; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary restenosis; myocardial infarction; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ischemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ischemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein deficiency; recurrence; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein deficiency; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; coronary thrombosis; hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary thrombosis; hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intracranial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary thrombosis; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary thrombosis; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
venous thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis, deep vein; pulmonary thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis, deep vein; pulmonary thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; cardiovascular diseases; hypertension; myocardial ischemia; pulmonary embolism; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
varicose ulcer; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease varicose ulcer; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intracranial thrombosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intracranial thrombosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; brain ischemia; coronary thrombosis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; brain ischemia; coronary thrombosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
puerperal disorders; sinus thrombosis, intracranial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease puerperal disorders; sinus thrombosis, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central nervous system vascular malformations; intracranial arteriovenous malformations; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central nervous system vascular malformations; intracranial arteriovenous malformations; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal and gastric varices; gastrointestinal hemorrhage; liver cirrhosis; postoperative complications; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal and gastric varices; gastrointestinal hemorrhage; liver cirrhosis; postoperative complications; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal cord infarction and recurrent venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal cord infarction and recurrent venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stroke, ischemic; cerebrovascular disease; thrombosis, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stroke, ischemic; cerebrovascular disease; thrombosis, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; activated protein c resistance; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; recurrence; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; recurrence; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; pulmonary embolism; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; pulmonary embolism; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; osteonecrosis; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; osteonecrosis; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; postthrombotic syndrome; varicose veins; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; postthrombotic syndrome; varicose veins; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammatory bowel disease, nos; inflammatory bowel diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammatory bowel disease, nos; inflammatory bowel diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor vii deficiency; peripheral vascular diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor vii deficiency; peripheral vascular diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; cerebral infarction; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; cerebral infarction; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; coronary disease; inflammation; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; inflammation; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombocytopenia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombocytopenia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis, deep vein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial and venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial and venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy-related first time venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy-related first time venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft occlusion, vascular; kidney failure, chronic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft occlusion, vascular; kidney failure, chronic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; intracranial embolism and thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; intracranial embolism and thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antiphospholipid syndrome; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leucocytosis; leukocytosis; thrombocythemia, hemorrhagic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leucocytosis; leukocytosis; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombophilia; thrombosis; varicose veins Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombophilia; thrombosis; varicose veins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
death, sudden; pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease death, sudden; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus, systemic; systemic lupus erythematosus; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; systemic lupus erythematosus; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; carotid artery thrombosis; intracranial arteriosclerosis; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; carotid artery thrombosis; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein c deficiency; protein s deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
budd-chiari syndrome; myeloproliferative disorders; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease budd-chiari syndrome; myeloproliferative disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leg injuries; pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leg injuries; pulmonary embolism; pulmonary embolisms; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; hyperhomocysteinemia; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; hyperhomocysteinemia; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bilateral iliac vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bilateral iliac vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coagulation protein disorders; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coagulation protein disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain hemorrhage; cerebrovascular disease; thrombosis, deep vein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain hemorrhage; cerebrovascular disease; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thromboembolism; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thromboembolism; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postoperative complications; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postoperative complications; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; myeloproliferative disorders; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; myeloproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sinus thrombosis, intracranial; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sinus thrombosis, intracranial; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, cardiovascular; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent deep-vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent deep-vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary hypertension; thrombosis, deep vein; pulmonary thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
phlebitis; pulmonary embolism; varicose veins; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease phlebitis; pulmonary embolism; varicose veins; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; coronary thrombosis; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; coronary thrombosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft occlusion, vascular; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft occlusion, vascular; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis; thrombocythemia, essential; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis; thrombocythemia, essential; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
previous first episodes of deep-vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease previous first episodes of deep-vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial ischemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial ischemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
retinal vein occlusion; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis, deep vein; behcet's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis, deep vein; behcet's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; hyperhomocysteinemia; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; hyperhomocysteinemia; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; hyperhomocysteinemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; infection; neoplasms; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; infection; neoplasms; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; intracranial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
retinal vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease retinal vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus, systemic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic artery thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic artery thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postoperative complications; pulmonary embolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postoperative complications; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
splanchnic vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease splanchnic vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; thrombosis, deep vein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; liver cirrhosis; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; liver cirrhosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; pregnancy complications, hematologic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrence; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrence; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
metabolic diseases; migraine disorders; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease metabolic diseases; migraine disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis and resistance to activated protein c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis and resistance to activated protein c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
occlusive artery disease and deep vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease occlusive artery disease and deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; coronary thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; brain ischemia; carotid stenosis; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; brain ischemia; carotid stenosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; venous thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphoproliferative disorders; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute coronary syndrome; cardiovascular diseases; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; cardiovascular diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sudden; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein c deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antiphospholipid syndrome; hemorrhage; recurrence; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; hemorrhage; recurrence; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrinogen; thrombosis, venous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrinogen; thrombosis, venous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina, unstable; coronary thrombosis; inflammation; myocardial infarction; recurrence; syndrome; unstable angina Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina, unstable; coronary thrombosis; inflammation; myocardial infarction; recurrence; syndrome; unstable angina in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombocythemia, essential; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombocythemia, essential; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; thromboembolism, venous; thrombosis, deep vein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; thromboembolism, venous; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain infarction; carotid artery diseases; intracranial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain infarction; carotid artery diseases; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid; myeloid leukemia; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid; myeloid leukemia; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; hyperhomocysteinemia; ischemia; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; hyperhomocysteinemia; ischemia; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; inflammation; mouth neoplasms; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; inflammation; mouth neoplasms; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis; varicose ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombosis; varicose ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antiphospholipid syndrome; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
seizures; thrombosis, deep vein Gene SetFrom GAD Gene-Disease Associations genes associated with the disease seizures; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombocythemia, essential; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease thrombocythemia, essential; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial ischemia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial ischemia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
thrombosis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term thrombosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
coronary thrombosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease coronary thrombosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
deep venous thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the deep venous thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
deep venous thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the deep venous thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral venous thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral venous thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
venous thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the venous thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arterial thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the arterial thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent deep vein thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent deep vein thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Coronary Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Coronary Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Venous Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Venous Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Carotid Artery Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carotid Artery Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Intracranial Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Intracranial Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Sinus Thrombosis, Intracranial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sinus Thrombosis, Intracranial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Intracranial Embolism and Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Intracranial Embolism and Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Upper Extremity Deep Vein Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Upper Extremity Deep Vein Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hepatic Vein Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatic Vein Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
thrombosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thrombosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
atrial thrombosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrial thrombosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased clearance of atrial thrombosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased clearance of atrial thrombosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
glomerular capillary thrombosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the glomerular capillary thrombosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney thrombosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney thrombosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{venous thrombosis, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {venous thrombosis, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{deep venous thrombosis, protection against} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {deep venous thrombosis, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{venous thrombosis, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {venous thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombosis, hyperhomocysteinemic Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombosis, hyperhomocysteinemic phenotype from the curated OMIM Gene-Disease Associations dataset. |
Deep Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Deep Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Portal Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Portal Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Splanchnic Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Splanchnic Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Large-Artery Atherosclerosis (Embolus/Thrombosis) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Large-Artery Atherosclerosis (Embolus/Thrombosis) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coronary Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coronary Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Capillary Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Capillary Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carotid Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carotid Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Middle Cerebral Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Middle Cerebral Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tumour Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tumour Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Venous Sinus Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Venous Sinus Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Arterial Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Arterial Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sinus Thrombosis, Intracranial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sinus Thrombosis, Intracranial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cancer-Associated Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cancer-Associated Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retinal Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retinal Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Deep Venous Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Deep Venous Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Basilar Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Basilar Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prosthetic Valve Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prosthetic Valve Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Mesenteric Arterial Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Mesenteric Arterial Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Petrous Sinus Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Petrous Sinus Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Extremity Deep Vein Thrombosis, Primary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Extremity Deep Vein Thrombosis, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrial Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrial Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Postoperative Deep Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Postoperative Deep Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Postpartum Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Postpartum Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sagittal Sinus Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sagittal Sinus Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Allograft Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Allograft Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Common Carotid Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Common Carotid Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
External Carotid Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease External Carotid Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Internal Carotid Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Internal Carotid Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Deep Vein Thrombosis Of Lower Limb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Deep Vein Thrombosis Of Lower Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lateral Sinus Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lateral Sinus Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neonatal Thrombosis Of Cerebral Venous Sinus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Thrombosis Of Cerebral Venous Sinus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Superior Mesenteric Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Superior Mesenteric Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intracranial Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Embolism And Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Embolism And Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Embolism And Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Embolism And Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intracranial Embolism And Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Embolism And Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Axillary Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Axillary Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Superior Vena Cava Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Superior Vena Cava Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Left Atrial Appendage Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Left Atrial Appendage Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subclinical Leaflet Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subclinical Leaflet Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Artery Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Artery Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cavernous Sinus Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cavernous Sinus Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Venous Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Venous Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Arterial Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Arterial Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Portal Vein Thrombosis, Ctcae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Portal Vein Thrombosis, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Venous Thrombosis, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Venous Thrombosis, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mesenteric Venous Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mesenteric Venous Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Deep Vein Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Deep Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
increased susceptibility to induced thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to induced thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to induced thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to induced thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
COVID 19 thrombosis and anticoagulation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the COVID 19 thrombosis and anticoagulation pathway from the WikiPathways Pathways 2024 dataset. |
Thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Portal vein thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Portal vein thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cavernous sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cavernous sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intracranial sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intracranial sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intracranial thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intracranial thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Coronary thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Coronary thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sagittal sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sagittal sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Carotid artery thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Carotid artery thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lateral sinus thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lateral sinus thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Deep venous thrombosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Deep venous thrombosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Venous thrombosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Venous thrombosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Stent thrombosis in response to clopidogrel treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Stent thrombosis in response to clopidogrel treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thrombosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thrombosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Plasma factor V levels in venous thrombosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma factor V levels in venous thrombosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Plasma factor V levels in venous thrombosis (conditioned on rs6027) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Plasma factor V levels in venous thrombosis (conditioned on rs6027) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thyroid hormone metabolism, abnormal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reflex, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Neutrophil Chemotactic Response, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Thyroid Hormone Metabolism, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset. |
abnormal retinal correspondence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormal splicing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal; brugada syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal urogenital development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal fibrin polymerization and thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormal cannabidiol Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eating behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal leukocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal iris pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bleeding Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair quantity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal ekg Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal monocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neutrophil cell number Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal facial shape Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal joint morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal genital system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal respiratory system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal muscle tone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal diaphysis morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal spermatogenesis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hemoglobin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of hand bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone structure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal branching pattern of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal maternal serum screening Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rod and cone electroretinograms Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal albumin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enchondral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet membrane protein expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondria in muscle tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal placental size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal placental size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal central microtubular pair morphology of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet granules Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal subcutaneous fat tissue distribution Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lung lobation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lung lobation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal flash visual evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine phosphate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal drinking behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal drinking behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal fear/anxiety-related behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal corticomedullary differentiation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal humeral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delayed hypersensitivity skin test Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein n-linked glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal echocardiogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal echocardiogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum ferritin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axial skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal calcification of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal testosterone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal speech discrimination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal genital system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal liver function tests during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal trabecular bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metacarpal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metacarpal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal t3/t4 ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal posturing Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal posturing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal natural killer cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal immunoglobulin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal monocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal monocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrial arrangement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrial arrangement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating renin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating renin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal folds Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pancreas size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pancreas size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine sodium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine sodium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vestibulo-ocular reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vestibulo-ocular reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral pedicle morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tendon morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tendon morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal leukocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal leukocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spermatogenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine potassium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine potassium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary light reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pyramidal signs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pyramidal signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pigmentation of the oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of incisors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal localization of kidney Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal localization of kidney phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal elasticity of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet volume Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vas deferens morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vas deferens morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle tone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle tone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lower motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ciliary motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ciliary motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metatarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metatarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal st segment Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sweat homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal base Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pelvis bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of the pubic bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal isoelectric focusing of serum transferrin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal isoelectric focusing of serum transferrin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hemoglobin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hemoglobin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal concentration of calcium in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal emotion/affect behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal epiphyseal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine cytology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine cytology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal palmar dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal palmar dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal csf lactate level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal csf lactate level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal joint morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal joint morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral segmentation and fusion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal oral glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal oral glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone collagen fibril morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delivery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delivery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal middle ear reflexes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal middle ear reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cervical curvature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cervical curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal auditory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal activity of mitochondrial respiratory chain Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal location of ears Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal location of ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cns myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eating behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eating behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ventriculo-arterial connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ventriculo-arterial connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anterior horn cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper to lower segment ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal form of the vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine output Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal blistering of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal diaphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal diaphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cholesterol homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cholesterol homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine citrate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine citrate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of the palpebral fissures Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of the palpebral fissures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair quantity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair quantity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anatomic location of the heart Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anatomic location of the heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iron deposition in mitochondria Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iron deposition in mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating aldosterone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating aldosterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating creatinine level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine chloride concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine chloride concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vascular physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal heart morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal heart morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair laboratory examination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lymphocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lymphocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal conjugate eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pulmonary lymphatics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pulmonary lymphatics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pattern of respiration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair whorl Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal connection of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage collagen Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage collagen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical stump bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical stump bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal social behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal social behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical gyration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical gyration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum iron Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum iron phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of permanent teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sex determination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sex determination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal prolactin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal prolactin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory epithelium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory epithelium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axonemal organization of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal foot bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neutrophil cell number Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cone-mediated electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cone-mediated electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal basal ganglia mri signal intensity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sensory nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle glycogen content Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal appendicular skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of erythroid precursors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine magnesium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine magnesium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rapid eye movement (rem) sleep Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ekg Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ekg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal levels of creatine kinase in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ejaculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ejaculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary electrolyte concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary electrolyte concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal trabeculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal trabeculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical cord blood vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal head movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal head movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acquired abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facility in opposing the shoulders Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facility in opposing the shoulders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal migration of corneal endothelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal intraocular pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the frontal region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the frontal region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary sulfate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary sulfate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spatial orientation of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spatial orientation of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rib ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sternal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the occiput Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the occiput phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal vascular invasion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal vascular invasion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enzyme/coenzyme activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral action potential amplitude Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Reflex, Abnormal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex, Abnormal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spindle assembly abnormal protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle assembly abnormal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein male abnormal 21-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Abnormal spindle-like microcephaly-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Abnormal spindle-like microcephaly-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal clitoris morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal clitoris morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung volume Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basilar membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basilar membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural fold elevation formation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensory capabilities/reflexes/nociception Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory capabilities/reflexes/nociception phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to anesthetic Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to anesthetic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal trigeminal ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal trigeminal ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response waveform shape Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal photoreceptor layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bradykinin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bradykinin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal derived definitive erythrocyte cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paravertebral ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paravertebral ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasal cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasal cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary sex determination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus stratum lacunosum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus stratum lacunosum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gallbladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ectomesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ectomesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone marrow cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zona glomerulosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zona glomerulosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal surfactant secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal surfactant secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum fastigial nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum fastigial nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal social/conspecific interaction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal social/conspecific interaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tooth morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neutrophil differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vomer bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vomer bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endplate potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endplate potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sagittal suture morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sagittal suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal semicircular canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal semicircular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal estrous cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive t cell differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive t cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular endothelial cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic neuron innervation pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanosome transport Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanosome transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inferior colliculus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inferior colliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tongue muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tongue muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal inner nuclear layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to methamphetamine Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to methamphetamine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal macrophage derived foam cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage derived foam cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left atrium weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal malleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal malleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala vestibuli morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala vestibuli morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pupillary reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pupillary reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interdigital cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal schwann cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal schwann cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior definitive endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior definitive endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal protein reabsorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal habenula morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal habenula morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic tissue morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal laryngeal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal laryngeal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasma membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneocyte envelope morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneocyte envelope morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primordial ovarian follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland dorsolateral lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular nerve morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal melanocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parametrial fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parametrial fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal effector t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal effector t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal roof plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal roof plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone healing Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone healing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rhombomere 4 morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rhombomere 4 morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart right ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal snout morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal snout morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic disc morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic disc morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parasympathetic ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parasympathetic ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blinking Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blinking phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellar molecular layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal efferent ductules of testis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal efferent ductules of testis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal periocular mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal periocular mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pancreatic peptide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal frontonasal prominence morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal frontonasal prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gas homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gas homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestinal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestinal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis papillary layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis papillary layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cellular replicative senescence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal throat morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal throat morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasolacrimal duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasolacrimal duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations 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. |
abnormal loop of henle descending limb morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal loop of henle descending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visual acuity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sulfate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parturition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala tympani morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala tympani morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external urethral orifice morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external urethral orifice morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chorioallantoic fusion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chorioallantoic fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell dendrite morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell dendrite morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lens development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lens development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary diverticulum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary diverticulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal arteriole morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal arteriole morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal outer hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic endocrine progenitor cell proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rosenthal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rosenthal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enterocyte apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal glomerulus basement membrane thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal superior vagus ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal superior vagus ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanoblast morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanoblast morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal single cell response threshold Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal single cell response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis reticular layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis reticular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body height Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body height phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic stalk morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural tube mantle layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural tube mantle layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior cardinal vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal tubule epithelial cell primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intramembranous bone ossification Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear distance/ position Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal maxillary sinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal otic vesicle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node b cell domain morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node b cell domain morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasmacytoid dendritic cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal rod cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal digestive system development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory summating potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paired-pulse inhibition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype 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 retinal ganglion cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postnatal growth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postnatal growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal miniature inhibitory postsynaptic currents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal miniature inhibitory postsynaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axillary lymph node morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axillary lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal costal cartilage morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal costal cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chemokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum posterior vermis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thalamus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thalamus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medulla air spaces Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zigzag hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zigzag hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal xenobiotic induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pons morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pons morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell anergy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somite size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somite size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic acinar cell zymogen granule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic acinar cell zymogen granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal meibomian gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal meibomian gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum vermis lobule ii morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule ii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tubuloglomerular feedback response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b wave amplitude Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine organic cation level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine organic cation level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory bulb granule cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory bulb granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lumbar dorsal root ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lumbar dorsal root ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensorimotor gating Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensorimotor gating phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatic sensory system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatic sensory system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coccygeal vertebrae morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coccygeal vertebrae morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cell chemotaxis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cell chemotaxis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural crest cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axon pruning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axon pruning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pinna reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pinna reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glomerular capillary morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glomerular capillary morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hind foot hair pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spinal cord dorsal column morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord dorsal column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coronary vessel morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coronary vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mucous neck cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mucous neck cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pre-pro b cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pre-pro b cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sertoli cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sertoli cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior primitive streak morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior primitive streak morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endolymphatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endolymphatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary respiratory rate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gestational length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gestational length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thymus medulla morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thymus medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal cone cell inner segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood gas level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood gas level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal suprachiasmatic nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal suprachiasmatic nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cortical plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cortical plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hormone-sensitive lipase activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hormone-sensitive lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male germ cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male germ cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal epididymis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal epididymis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal object recognition memory Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal catecholamine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal catecholamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basal lamina morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basal lamina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal respiration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal respiration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vagina development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vagina development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skeletal muscle fiber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skeletal muscle fiber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal forced expiratory flow rates Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal forced expiratory flow rates phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal right lung morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lateral nasal prominence morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lateral nasal prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sarcolemma morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sarcolemma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vertebral lamina morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebral lamina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine crypts of lieberkuhn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postimplantation uterine environment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postimplantation uterine environment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spinal cord white matter morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal cone bipolar cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal cone bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placenta size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cajal body morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cajal body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd8-positive, gamma-delta intraepithelial t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd8-positive, gamma-delta intraepithelial t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural crest cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cornea morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cornea morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteoblast physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoblast physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auchene hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auchene hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal t-helper 17 cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 17 cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterine horn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterine horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body temperature Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal atrium myocardium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal atrium myocardium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasma cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hyperactivated sperm motility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hyperactivated sperm motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endometrium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endometrium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eosinophil differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eosinophil differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating estradiol level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anxiety-related response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anxiety-related response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal conditioned emotional response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal conditioned emotional response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neurocranium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neurocranium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating glucagon level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal functional residual capacity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal functional residual capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mesendoderm development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mesendoderm development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pyruvate kinase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pyruvate kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intraepithelial t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intraepithelial t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal immune system organ morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal immune system organ morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal right lung middle lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung middle lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal survival Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal survival phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovulation cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovulation cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct intercalated cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct intercalated cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mucociliary clearance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mucociliary clearance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hyoid bone body morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hyoid bone body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic beta cell mass Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic beta cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal transitional stage t1 b cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal transitional stage t1 b cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zona fasciculata morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zona fasciculata morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary vitreous morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary vitreous morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin absorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulp cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulp cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dosage compensation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dosage compensation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymphatic vessel morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymphatic vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cellular extravasation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cellular extravasation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myeloid leukocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myeloid leukocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interferon secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interferon secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motor nerve collateral sprouting Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motor nerve collateral sprouting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal submandibular gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal submandibular gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skin condition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skin condition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glycogen homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glycogen homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dosage compensation, by inactivation of x chromosome Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dosage compensation, by inactivation of x chromosome phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paired-pulse facilitation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paired-pulse facilitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary vascular resistance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal manchette morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal manchette morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrial proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrial proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal peripheral nervous system regeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peripheral nervous system regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thromboxane level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thromboxane level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal type iv hypersensitivity reaction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal type iv hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |