Name

anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pregnancy complications, hematologic; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pregnancy complications, hematologic; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; spinal dysraphism 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 Set

From 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.

alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious 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 Set

From 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.

Neural Tube Defects Gene Set

From CTD Gene-Disease Associations

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

neural tube defects; dihydropyrimidine dehydrogenase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; dihydropyrimidine dehydrogenase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects and preeclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects and preeclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects Gene Set

From GAD Gene-Disease Associations

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

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Neural Tube Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

{neural tube defects, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{neural tube defects, folate-sensitive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {neural tube defects, folate-sensitive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

neural tube defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the neural tube defects phenotype from the curated OMIM Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choline deficiency; dna damage; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thromboembolism 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 Set

From 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.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene Set

From 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.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thrombosis Gene Set

From 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.

complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria 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 Set

From 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.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism 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 Set

From 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.

complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; gastroenteritis; pregnancy complications, infectious; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; gastroenteritis; pregnancy complications, infectious; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Spinal Dysraphism Gene Set

From CTD Gene-Disease Associations

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

hyperhomocysteinemia; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal dysraphism Gene Set

From GAD Gene-Disease Associations

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

glucose metabolism disorders; obesity; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose metabolism disorders; obesity; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meningomyelocele; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meningomyelocele; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal dysraphism Gene Set

From HPO Gene-Disease Associations

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

Spinal Dysraphism Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Folic Acid Deficiency Gene Set

From CTD Gene-Disease Associations

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

folic acid deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adenoma; colorectal neoplasms; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; colorectal neoplasms; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; folic acid deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; folic acid deficiency; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; folic acid deficiency; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; folic acid deficiency; gastrointestinal neoplasms; oesophageal neoplasm Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; folic acid deficiency; gastrointestinal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; folic acid deficiency; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; folic acid deficiency; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; leukemia, lymphoid; lymphoblastic leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; leukemia, lymphoid; lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency Gene Set

From GAD Gene-Disease Associations

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

Folic Acid Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Neural tube defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neural tube defect, folate-sensitive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neural tube defect, folate-sensitive from the curated CTD Gene-Disease Associations dataset.

planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

neural tube development Gene Set

From GO Biological Process Annotations

genes participating in the neural tube development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of planar polarity involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of planar polarity involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

rostrocaudal neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the rostrocaudal neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

regulation of planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

establishment of planar polarity involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the establishment of planar polarity involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

neural tube formation Gene Set

From GO Biological Process Annotations

genes participating in the neural tube formation biological process from the curated GO Biological Process Annotations dataset.

initiation of neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the initiation of neural tube closure biological process from the curated GO Biological Process Annotations dataset.

neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the regulation of smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the neural tube closure biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in dorsal/ventral neural tube patterning Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in dorsal/ventral neural tube patterning biological process from the curated GO Biological Process Annotations dataset.

abnormality of neural tube closure Gene Set

From HPO Gene-Disease Associations

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

neural tube degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neural tube mantle layer morphology Gene Set

From 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.

open neural tube Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neural tube morphology/development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube marginal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube marginal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kinked neural tube Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neural tube ventricular layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube ventricular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed neural tube closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed neural tube closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased neural tube apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased neural tube apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

wavy neural tube Gene Set

From MPO Gene-Phenotype Associations

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

neural tube Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

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

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; brain ischemia; diabetes mellitus; heart septal defects, atrial; hypertension; intracranial thrombosis; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From 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.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; heart septal defects, atrial; stroke; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial septal defects; embolism, paradoxical; heart septal defects, atrial; migraine with aura; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Anencephaly Gene Set

From CTD Gene-Disease Associations

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

anencephaly Gene Set

From GAD Gene-Disease Associations

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

anencephaly Gene Set

From GeneRIF Biological Term Annotations

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

anencephaly Gene Set

From HPO Gene-Disease Associations

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

Anencephaly Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

anencephaly Gene Set

From MPO Gene-Phenotype Associations

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

anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set

From 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.

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Pregnancy Complications Gene Set

From CTD Gene-Disease Associations

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

Pregnancy Complications, Cardiovascular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pregnancy Complications, Cardiovascular from the curated CTD Gene-Disease Associations dataset.

birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; pre-eclampsia; pregnancy complications; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; pre-eclampsia; pregnancy complications; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; puerperal disorders; venous thrombosis Gene Set

From 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.

hiv infections; pregnancy complications, infectious; viremia; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; pregnancy complications, infectious; viremia; [x]human immunodeficiency virus disease 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 Set

From 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.

pregnancy complications, hematologic; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, hematologic; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; pre-eclampsia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, infectious; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, infectious; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis Gene Set

From 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.

malaria, falciparum; pregnancy complications, parasitic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, falciparum; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; prenatal exposure delayed effects; serotonin syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications; prenatal exposure delayed effects; serotonin syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholestasis, intrahepatic; pregnancy complications; pruritus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholestasis, intrahepatic; pregnancy complications; pruritus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nausea; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nausea; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; pregnancy complications; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

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

coronary disease; pregnancy complications, cardiovascular; premature birth; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; pregnancy complications, cardiovascular; premature birth; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; pregnancy complications; puerperal disorders; recurrence; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; pregnancy complications; puerperal disorders; recurrence; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis b; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis b; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications Gene Set

From GAD Gene-Disease Associations

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

hypertriglyceridemia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertriglyceridemia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; tic disorder; tic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications; tic disorder; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal death; pre-eclampsia; pregnancy complications; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholestasis, intrahepatic; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholestasis, intrahepatic; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hyperglycemia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperglycemia; pregnancy complications 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 Set

From 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.

coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, falciparum; placenta diseases; pregnancy complications, parasitic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, falciparum; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; pre-eclampsia; pregnancy complications, cardiovascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; pre-eclampsia; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; pregnancy complications, cardiovascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; pregnancy complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; overnutrition; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; overnutrition; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; purpura, thrombotic thrombocytopenic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, hematologic; purpura, thrombotic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; pre-eclampsia; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral palsy; pregnancy complications, infectious; virus diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral palsy; pregnancy complications, infectious; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infections; pregnancy complications, infectious; viremia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; pregnancy complications, infectious; viremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, cardiovascular; venous thrombosis Gene Set

From 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.

activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis Gene Set

From 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 Set

From 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.

pregnancy complications, hematologic; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, hematologic; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; periodontal diseases; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; periodontal diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

herpesviridae infections; kaposi sarcoma; pregnancy complications, infectious; sarcoma, kaposi Gene Set

From GAD Gene-Disease Associations

genes associated with the disease herpesviridae infections; kaposi sarcoma; pregnancy complications, infectious; sarcoma, kaposi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pre-eclampsia; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dental plaque; periodontitis; pregnancy complications; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental plaque; periodontitis; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; intrauterine growth retardation; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; thrombocythemia, essential Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications, hematologic; thrombosis Gene Set

From 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.

abortion, spontaneous; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; thrombosis Gene Set

From 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.

depression, postpartum; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depression, postpartum; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, infectious; ureaplasma infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, infectious; ureaplasma infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; venous thrombosis Gene Set

From 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.

abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; venous thrombosis Gene Set

From 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.

budd-chiari syndrome; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease budd-chiari syndrome; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; thromboembolism; venous thrombosis Gene Set

From 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.

cholestasis, intrahepatic; intrahepatic cholestasis; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholestasis, intrahepatic; intrahepatic cholestasis; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv seropositivity; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv seropositivity; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Pregnancy Complications, Infectious Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pregnancy Complications, Hematologic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pregnancy Complications, Parasitic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pregnancy Complications Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pregnancy Complications, Neoplastic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pregnancy Complications, Cardiovascular Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

dysraphism Gene Set

From GeneRIF Biological Term Annotations

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

folic acid-2783 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the folic acid-2783 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

folic acid-1790 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the folic acid-1790 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

folic acid-7201 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the folic acid-7201 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

folic acid-5844 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the folic acid-5844 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Folic Acid Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Folic Acid from the curated CTD Gene-Chemical Interactions dataset.

Folic Acid Antagonists Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Folic Acid Antagonists from the curated CTD Gene-Chemical Interactions dataset.

Folic Acid Gene Set

From DrugBank Drug Targets

interacting proteins for the Folic Acid drug from the curated DrugBank Drug Targets dataset.

folic acid in plasma and red blood cell folate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid in plasma and red blood cell folate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid-containing compound catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the folic acid-containing compound catabolic process biological process from the curated GO Biological Process Annotations dataset.

folic acid transport Gene Set

From GO Biological Process Annotations

genes participating in the folic acid transport biological process from the curated GO Biological Process Annotations dataset.

folic acid-containing compound biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the folic acid-containing compound biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

response to folic acid Gene Set

From GO Biological Process Annotations

genes participating in the response to folic acid biological process from the curated GO Biological Process Annotations dataset.

folic acid-containing compound metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the folic acid-containing compound metabolic process biological process from the curated GO Biological Process Annotations dataset.

folic acid metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the folic acid metabolic process biological process from the curated GO Biological Process Annotations dataset.

folic acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the folic acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

folic acid binding Gene Set

From GO Molecular Function Annotations

genes performing the folic acid binding molecular function from the curated GO Molecular Function Annotations dataset.

[3H]folic acid Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [3H]folic acid ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Folic acid Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Folic acid metabolite from the curated HMDB Metabolites of Enzymes dataset.

abnormal folic acid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal folic acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Folic Acid Network(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Folic Acid Network(Mus musculus) pathway from the Wikipathways Pathways dataset.

spinal canal and spinal cord meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular atrophy, spinal; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal cord compression; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal cord compression; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Spinal Cord Injury_CNS - Spinal Cord (MMHCC)_GSE16710 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Spinal Cord Injury_CNS - Spinal Cord (MMHCC)_GSE16710 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

anticoagulant complications; bleeding complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anticoagulant complications; bleeding complications 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 Set

From 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.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From 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.

folic Gene Set

From GeneRIF Biological Term Annotations

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

folic acid_homo sapiens_gpl2700_gds3656 Gene Set

From GEO Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the folic acid_homo sapiens_gpl2700_gds3656 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.

increased serum bile acid concentration during pregnancy Gene Set

From HPO Gene-Disease Associations

genes associated with the increased serum bile acid concentration during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lipid tube Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the lipid tube cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

virus tail, tube Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the virus tail, tube cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

germ tube Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the germ tube cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

pollen tube tip Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the pollen tube tip cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

lipid tube Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the lipid tube cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

pollen tube Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the pollen tube cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

polar tube Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the polar tube cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

fallopian tube endometrioid adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fallopian tube disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fallopian tube adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eustachian tube disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fallopian tube carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fallopian tube cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fallopian tube gestational choriocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fallopian tube squamous cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease fallopian tube squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

patulous eustachian tube Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fallopian tube neoplasms Gene Set

From GAD Gene-Disease Associations

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

fallopian tube neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fallopian tube neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystadenocarcinoma, serous; fallopian tube neoplasms; precancerous conditions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystadenocarcinoma, serous; fallopian tube neoplasms; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; fallopian tube neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; fallopian tube neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chlamydia infections; fallopian tube diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chlamydia infections; fallopian tube diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chlamydia infections; fallopian tube diseases; infertility, female Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chlamydia infections; fallopian tube diseases; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; fallopian tube neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; fallopian tube neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fallopian tube neoplasms; precancerous conditions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fallopian tube neoplasms; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fallopian tube neoplasms; neoplasm invasiveness; peritoneal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fallopian tube neoplasms; neoplasm invasiveness; peritoneal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tube Gene Set

From GeneRIF Biological Term Annotations

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

embryonic heart tube anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

tube formation Gene Set

From GO Biological Process Annotations

genes participating in the tube formation biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube formation biological process from the curated GO Biological Process Annotations dataset.

respiratory tube development Gene Set

From GO Biological Process Annotations

genes participating in the respiratory tube development biological process from the curated GO Biological Process Annotations dataset.

tube closure Gene Set

From GO Biological Process Annotations

genes participating in the tube closure biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube development Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube development biological process from the curated GO Biological Process Annotations dataset.

branching morphogenesis of an epithelial tube Gene Set

From GO Biological Process Annotations

genes participating in the branching morphogenesis of an epithelial tube biological process from the curated GO Biological Process Annotations dataset.

regulation of endothelial tube morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of endothelial tube morphogenesis biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube morphogenesis biological process from the curated GO Biological Process Annotations dataset.

pulmonary artery endothelial tube morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the pulmonary artery endothelial tube morphogenesis biological process from the curated GO Biological Process Annotations dataset.

epithelial tube formation Gene Set

From GO Biological Process Annotations

genes participating in the epithelial tube formation biological process from the curated GO Biological Process Annotations dataset.

endothelial tube morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the endothelial tube morphogenesis biological process from the curated GO Biological Process Annotations dataset.

tube lumen cavitation Gene Set

From GO Biological Process Annotations

genes participating in the tube lumen cavitation biological process from the curated GO Biological Process Annotations dataset.

regulation of tube size Gene Set

From GO Biological Process Annotations

genes participating in the regulation of tube size biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube elongation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube elongation biological process from the curated GO Biological Process Annotations dataset.

epithelial tube branching involved in lung morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial tube branching involved in lung morphogenesis biological process from the curated GO Biological Process Annotations dataset.

tube development Gene Set

From GO Biological Process Annotations

genes participating in the tube development biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube left/right pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube left/right pattern formation biological process from the curated GO Biological Process Annotations dataset.

lipid tube assembly Gene Set

From GO Biological Process Annotations

genes participating in the lipid tube assembly biological process from the curated GO Biological Process Annotations dataset.

tube morphogenesis Gene Set

From GO Biological Process Annotations

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

epithelial tube morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the epithelial tube morphogenesis biological process from the curated GO Biological Process Annotations dataset.

embryonic epithelial tube formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic epithelial tube formation biological process from the curated GO Biological Process Annotations dataset.

lipid tube Gene Set

From GO Cellular Component Annotations

proteins localized to the lipid tube cellular component from the curated GO Cellular Component Annotations dataset.

fallopian tube Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in fallopian tube relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

fallopian tube Gene Set

From HPA Tissue Gene Expression Profiles

genes with high or low expression in fallopian tube relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.

fallopian tube Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in fallopian tube relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

aplasia/hypoplasia of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fallopian tube Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the fallopian tube Gene Set

From HPO Gene-Disease Associations

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

Fallopian Tube Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Fallopian Tube Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal auditory tube Gene Set

From MPO Gene-Phenotype Associations

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

absent heart tube Gene Set

From MPO Gene-Phenotype Associations

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

abnormal endocardial heart tube morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal endocardial heart tube morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart tube morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal respiratory conducting tube morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory conducting tube morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent auditory tube Gene Set

From MPO Gene-Phenotype Associations

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

sieve tube Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

tube foot Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Forebrain defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Forebrain defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Ventricular from the curated CTD Gene-Disease Associations dataset.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Heart Septal Defects Gene Set

From CTD Gene-Disease Associations

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

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Laterality Defects, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Laterality Defects, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Heart Septal Defects, Atrial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Septal Defects, Atrial from the curated CTD Gene-Disease Associations dataset.

Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.

Heart Defects, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Defects, Congenital from the curated CTD Gene-Disease Associations dataset.

Color Vision Defects Gene Set

From CTD Gene-Disease Associations

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

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

congenital heart defects Gene Set

From GAD Gene-Disease Associations

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

heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft palate and calvaria defects. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft palate and calvaria defects. 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 Set

From 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.

cardiac defects Gene Set

From GAD Gene-Disease Associations

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

birth defects Gene Set

From GAD Gene-Disease Associations

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

dilatation, pathologic; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dilatation, pathologic; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathies; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathies; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

axial skeletal defects Gene Set

From GAD Gene-Disease Associations

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

left-right laterality defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left-right laterality defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects, atrial; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, atrial; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; heart defects, congenital; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

visual field defects Gene Set

From GAD Gene-Disease Associations

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

heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; hyperhomocysteinemia; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease double outlet right ventricle; heart defects, congenital; pulmonary atresia; tetralogy of fallot; transposition of great vessels; truncus arteriosus, persistent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart defects, congenital; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart defects, congenital; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart septal defects Gene Set

From GAD Gene-Disease Associations

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

heart septal defects, ventricular; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart septal defects, ventricular; hypertension, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defects Gene Set

From GeneRIF Biological Term Annotations

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

Conotruncal heart defects Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Conotruncal heart defects phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

progressive visual field defects Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lung segmentation defects Gene Set

From HPO Gene-Disease Associations

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

pulmonary valve defects Gene Set

From HPO Gene-Disease Associations

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

mitochondrial respiratory chain defects Gene Set

From HPO Gene-Disease Associations

genes associated with the mitochondrial respiratory chain defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symmetrical, oval parietal bone defects Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical, oval parietal bone defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

forearm reduction defects Gene Set

From HPO Gene-Disease Associations

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

osteolytic defects of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric, linear skin defects Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetric, linear skin defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Heart Septal Defects, Ventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Endocardial Cushion Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heart Defects, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Color Vision Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heart Septal Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Heart Septal Defects, Atrial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

forebrain defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the forebrain defects phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.

combined cellular and humoral immune defects with granulomas Gene Set

From OMIM Gene-Disease Associations

genes associated with the combined cellular and humoral immune defects with granulomas phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, congenital heart defects, and posterior embryotoxon Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, nonsyndromic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, nonsyndromic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

pancreatic agenesis and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic agenesis and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

Defects in cobalamin (B12) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in cobalamin (B12) metabolism pathway from the Reactome Pathways dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Defects in biotin (Btn) metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in biotin (Btn) metabolism pathway from the Reactome Pathways dataset.

Neuraminidase deficiency with beta-galactosidase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia 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 Set

From 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.

blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From 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.

anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary 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 Set

From 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.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein c deficiency; protein s deficiency; venous thrombosis Gene Set

From 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.

anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.

Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.

Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set

From Reactome Pathways

proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.

neural plate Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in neural plate relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

neural Gene Set

From GeneRIF Biological Term Annotations

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

neural crest cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

ventral trunk neural crest cell migration Gene Set

From GO Biological Process Annotations

genes participating in the ventral trunk neural crest cell migration biological process from the curated GO Biological Process Annotations dataset.

neural plate morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the neural plate morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neural precursor cell proliferation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of neural precursor cell proliferation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural crest formation Gene Set

From GO Biological Process Annotations

genes participating in the neural crest formation biological process from the curated GO Biological Process Annotations dataset.

neural nucleus development Gene Set

From GO Biological Process Annotations

genes participating in the neural nucleus development biological process from the curated GO Biological Process Annotations dataset.

neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the neural precursor cell proliferation biological process from the curated GO Biological Process Annotations dataset.

neural fold formation Gene Set

From GO Biological Process Annotations

genes participating in the neural fold formation biological process from the curated GO Biological Process Annotations dataset.

neural plate mediolateral regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate mediolateral regionalization biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural crest cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of neural retina development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neural retina development biological process from the curated GO Biological Process Annotations dataset.

neural plate pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the neural plate pattern specification biological process from the curated GO Biological Process Annotations dataset.

neural plate formation Gene Set

From GO Biological Process Annotations

genes participating in the neural plate formation biological process from the curated GO Biological Process Annotations dataset.

cardiac neural crest cell migration involved in outflow tract morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations dataset.

trunk neural crest cell migration Gene Set

From GO Biological Process Annotations

genes participating in the trunk neural crest cell migration biological process from the curated GO Biological Process Annotations dataset.

negative regulation of neural crest formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of neural crest formation biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in cardiac neural crest cell differentiation involved in heart development biological process from the curated GO Biological Process Annotations dataset.

neural plate axis specification Gene Set

From GO Biological Process Annotations

genes participating in the neural plate axis specification biological process from the curated GO Biological Process Annotations dataset.

neural crest cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell fate specification biological process from the curated GO Biological Process Annotations dataset.

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

cardiac neural crest cell development involved in heart development Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell development involved in heart development biological process from the curated GO Biological Process Annotations dataset.

regulation of neural crest formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neural crest formation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural crest cell migration involved in autonomic nervous system development Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell migration involved in autonomic nervous system development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of neural precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of neural precursor cell proliferation biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural plate anterior/posterior regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations dataset.

neural crest cell migration Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell migration biological process from the curated GO Biological Process Annotations dataset.

neural fold bending Gene Set

From GO Biological Process Annotations

genes participating in the neural fold bending biological process from the curated GO Biological Process Annotations dataset.

neural crest cell development Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell development biological process from the curated GO Biological Process Annotations dataset.

neural retina development Gene Set

From GO Biological Process Annotations

genes participating in the neural retina development biological process from the curated GO Biological Process Annotations dataset.

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

cardiac neural crest cell development involved in outflow tract morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cardiac neural crest cell development involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations dataset.

convergent extension involved in neural plate elongation Gene Set

From GO Biological Process Annotations

genes participating in the convergent extension involved in neural plate elongation biological process from the curated GO Biological Process Annotations dataset.

neural plate development Gene Set

From GO Biological Process Annotations

genes participating in the neural plate development biological process from the curated GO Biological Process Annotations dataset.

neural plate regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate regionalization biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural crest cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural crest cell differentiation biological process from the curated GO Biological Process Annotations dataset.

neural crest cell migration involved in sympathetic nervous system development Gene Set

From GO Biological Process Annotations

genes participating in the neural crest cell migration involved in sympathetic nervous system development biological process from the curated GO Biological Process Annotations dataset.

neural fold elevation formation Gene Set

From GO Biological Process Annotations

genes participating in the neural fold elevation formation biological process from the curated GO Biological Process Annotations dataset.

Neural retina-specific leucine zipper protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural retina-specific leucine zipper protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural cell adhesion Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural cell adhesion protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural proliferation differentiation control-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural proliferation differentiation control-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural Wiskott-Aldrich syndrome protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural Wiskott-Aldrich syndrome protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neural chondroitin sulphate proteoglycan cytoplasmic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neural chondroitin sulphate proteoglycan cytoplasmic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal neural fold elevation formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased enteric neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased enteric neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell apoptosis Gene Set

From 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 neural crest cell physiology Gene Set

From 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 neural plate morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cranial neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cranial neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired neural crest cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired neural crest cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vagal neural crest cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vagal neural crest cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell delamination Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell delamination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent neural folds Gene Set

From MPO Gene-Phenotype Associations

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

abnormal trunk neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trunk neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cephalic neural fold morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cephalic neural fold morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal enteric neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enteric neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cranial neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cranial neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cranial neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cranial neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vagal neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vagal neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased enteric neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased enteric neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cardiac neural crest cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cardiac neural crest cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased vagal neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased vagal neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal enteric neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enteric neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired cardiac neural crest cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired cardiac neural crest cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural fold formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural fold formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cranial neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cranial neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent enteric neural crest cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent enteric neural crest cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cranial neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cranial neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural fold morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased cardiac neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cardiac neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cranial neural crest cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cranial neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased neural crest cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal enteric neural crest cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enteric neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

melanoma and neural system tumor syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the melanoma and neural system tumor syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

neural Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term neural in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

neural plate Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue neural plate from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

neural retina Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue neural retina from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

neural crest Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue neural crest from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

neural arch Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue neural arch from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

neural stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural retina Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural arch Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

embryonic neural stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue embryonic neural stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

neural crest cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue neural crest cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

neural crest-derived stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue neural crest-derived stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

neural crest Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural plate Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural cord Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

neural stem cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue neural stem cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Neural retinal development(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Neural retinal development(Mus musculus) pathway from the Wikipathways Pathways dataset.

Neural Crest Differentiation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Neural Crest Differentiation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Cholestasis, intrahepatic, of pregnancy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cholestasis, intrahepatic, of pregnancy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cholestasis of pregnancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cholestasis of pregnancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrahepatic Cholestasis of Pregnancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intrahepatic Cholestasis of Pregnancy from the curated CTD Gene-Disease Associations dataset.

Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.

Hypertension, Pregnancy-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Pregnancy-Induced from the curated CTD Gene-Disease Associations dataset.

Pregnancy, Ectopic Gene Set

From CTD Gene-Disease Associations

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

pregnancy adenoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

rhd-negative sensitized pregnancy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rhd-negative sensitized pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, second trimester Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, second trimester in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

preeclampsia; hypertension, pregnancy induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; hypertension, pregnancy induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eclampsia; hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia in pregnancy Gene Set

From GAD Gene-Disease Associations

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

pregnancy loss, recurrent; fetal loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy-induced chylomicronemia Gene Set

From GAD Gene-Disease Associations

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

pregnancy loss, recurrent; coagulation disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; rhinitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hellp syndrome; acute fatty liver of pregnancy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hellp syndrome; acute fatty liver of pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy outcome Gene Set

From GAD Gene-Disease Associations

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

pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

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

polycystic ovary syndrome; pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy-related first time venous thrombosis Gene Set

From 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.

pregnancy loss, recurrent; in vitro fertilization success Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; in vitro fertilization success in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

preeclampsia; hypertension, pregnancy induced; eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; hypertension, pregnancy induced; eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multifetal pregnancy outcome. Gene Set

From GAD Gene-Disease Associations

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

fetal loss, late; pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vasodilation during pregnancy Gene Set

From GAD Gene-Disease Associations

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

hypertension, pregnancy-induced Gene Set

From GAD Gene-Disease Associations

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

pregnancy-associated venous thromboembolism Gene Set

From GAD Gene-Disease Associations

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

hypertension, pregnancy-induced; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss Gene Set

From GAD Gene-Disease Associations

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

albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic retinopathy; obstetric labor, premature; pre-eclampsia; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic retinopathy; obstetric labor, premature; pre-eclampsia; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy induced Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent pregnancy loss Gene Set

From GAD Gene-Disease Associations

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

pregnancy Gene Set

From GeneRIF Biological Term Annotations

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

female pregnancy Gene Set

From GO Biological Process Annotations

genes participating in the female pregnancy biological process from the curated GO Biological Process Annotations dataset.

embryonic process involved in female pregnancy Gene Set

From GO Biological Process Annotations

genes participating in the embryonic process involved in female pregnancy biological process from the curated GO Biological Process Annotations dataset.

maternal process involved in female pregnancy Gene Set

From GO Biological Process Annotations

genes participating in the maternal process involved in female pregnancy biological process from the curated GO Biological Process Annotations dataset.

mammary gland branching involved in pregnancy Gene Set

From GO Biological Process Annotations

genes participating in the mammary gland branching involved in pregnancy biological process from the curated GO Biological Process Annotations dataset.

Glycemic traits (pregnancy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Glycemic traits (pregnancy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

toxemia of pregnancy Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal liver function tests during pregnancy Gene Set

From 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.

toxemia of pregnancy Gene Set

From HPO Gene-Disease Associations

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

maternal virilization in pregnancy Gene Set

From HPO Gene-Disease Associations

genes associated with the maternal virilization in pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hypertension, Pregnancy-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pregnancy, Ectopic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pregnancy in Diabetics Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Peptidase M43, pregnancy-associated plasma-A Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M43, pregnancy-associated plasma-A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

impaired mammary gland growth during pregnancy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired mammary gland growth during pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pregnancy Gene Set

From MPO Gene-Phenotype Associations

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

abnormal mammary gland growth during pregnancy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mammary gland growth during pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pregnancy-related premature death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{pregnancy loss, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.

hellp syndrome, maternal, of pregnancy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hellp syndrome, maternal, of pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, intrahepatic, of pregnancy, 1 Gene Set

From OMIM Gene-Disease Associations

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

cholestasis, intrahepatic, of pregnancy, 3 Gene Set

From OMIM Gene-Disease Associations

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

{pregnancy loss, recurrent, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypertension, pregnancy-induced} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypertension, pregnancy-induced} phenotype from the curated OMIM Gene-Disease Associations dataset.

fatty liver, acute, of pregnancy Gene Set

From OMIM Gene-Disease Associations

genes associated with the fatty liver, acute, of pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.

pregnancy Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term pregnancy in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Pyruvate dehydrogenase lipoic acid synthetase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyruvate dehydrogenase lipoic acid synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-aminobutyric acid transaminase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-aminobutyric acid transaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lysosomal acid lipase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lysosomal acid lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acid-labile subunit deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deficiency of aromatic-L-amino-acid decarboxylase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deficiency of aromatic-L-amino-acid decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lysosomal acid lipase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lysosomal acid lipase deficiency from the curated CTD Gene-Disease Associations dataset.

Aromatic amino acid decarboxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aromatic amino acid decarboxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Gamma aminobutyric acid transaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma aminobutyric acid transaminase deficiency from the curated CTD Gene-Disease Associations dataset.

acid lipase deficiency and cholesterol ester storage disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acid lipase deficiency and cholesterol ester storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ascorbic acid deficiency Gene Set

From GAD Gene-Disease Associations

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

Ascorbic Acid Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

pyruvate dehydrogenase lipoic acid synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyruvate dehydrogenase lipoic acid synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

aromatic l-amino acid decarboxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aromatic l-amino acid decarboxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

acid-labile subunit, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the acid-labile subunit, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

?lysosomal acid phosphatase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?lysosomal acid phosphatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal trigeminal nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal trigeminal nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

spinal trigeminal nucleus, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal trigeminal nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

r8 part of spinal trigeminal nucleus, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r8 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r9 part of spinal trigeminal nucleus, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r9 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r6 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r6 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, rostral dorsomedial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, rostral dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r10 part of spinal trigeminal nucleus, caudal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r10 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r6 part of spinal trigeminal nucleus, pars oralis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r6 part of spinal trigeminal nucleus, pars oralis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r3 part of spinal trigeminal sensory column, oral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r3 part of spinal trigeminal sensory column, oral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r10 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r10 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r7 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r7 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, dorsal zone Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, dorsal zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r11 part of spinal trigeminal nucleus, caudal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r11 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r5 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r5 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r7 part of spinal trigeminal nucleus, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r7 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r8 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r8 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, caudal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, interpolar part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, ventrolateral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, ventrolateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

r9 part of spinal vestibular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r9 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, ventral zone Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, ventral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Spinal nucleus of the trigeminal, oral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Spinal nucleus of the trigeminal, oral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

spinal trigeminal nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal trigeminal nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

spinal (inferior) vestibular nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in spinal (inferior) vestibular nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Neurofibromatosis, familial spinal Gene Set

From ClinVar Gene-Phenotype Associations

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

Spinal muscular atrophy, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, X-linked 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, autosomal recessive 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy, Jerash type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.

Spinal Curvatures Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy with respiratory distress 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophies of Childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.

Spinal Cord Injuries Gene Set

From CTD Gene-Disease Associations

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

Spinal Cord Diseases Gene Set

From CTD Gene-Disease Associations

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

Spinal Cord Ischemia Gene Set

From CTD Gene-Disease Associations

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

Neurofibromatosis, Familial Spinal Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.

Muscular Atrophy, Spinal Gene Set

From CTD Gene-Disease Associations

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

Spinal Cord Compression Gene Set

From CTD Gene-Disease Associations

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

Hematoma, Epidural, Spinal Gene Set

From CTD Gene-Disease Associations

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

spinal muscular atrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

spinal cord glioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adult spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

juvenile spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal stenosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intermediate spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anterior spinal artery syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cord astrocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tethered spinal cord syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cord disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cord ependymoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cord melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cord lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal chordoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal canal intradural extramedullary neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cord oligodendroglioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal cord primitive neuroectodermal neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

survival motor neuron spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

H3K4me3_astrocyte of the spinal cord_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_astrocyte of the spinal cord_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_astrocyte of the spinal cord_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_astrocyte of the spinal cord_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

CTCF_astrocyte of the spinal cord_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_astrocyte of the spinal cord_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_astrocyte of the spinal cord_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_astrocyte of the spinal cord_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tuberculosis, spinal Gene Set

From GAD Gene-Disease Associations

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

acute traumatic spinal cord injury Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute traumatic spinal cord injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; intervertebral disk displacement; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; intervertebral disk displacement; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal cord injuries Gene Set

From GAD Gene-Disease Associations

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

fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal fractures Gene Set

From GAD Gene-Disease Associations

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

fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal cord diseases; spondylosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal cord diseases; spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal cord infarction and recurrent venous thrombosis Gene Set

From 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.

acoustic neurofibromatosis; meningioma; neurofibromatosis 2; spinal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acoustic neurofibromatosis; meningioma; neurofibromatosis 2; spinal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal diseases Gene Set

From GAD Gene-Disease Associations

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

spinal muscular atrophies of childhood Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; low back pain; scoliosis; spinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; low back pain; scoliosis; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal ossification Gene Set

From GAD Gene-Disease Associations

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

fractures, spontaneous; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular atrophy, spinal Gene Set

From GAD Gene-Disease Associations

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

paralysis; sensation disorders; spinal cord injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease paralysis; sensation disorders; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

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

spinal disc degeneration Gene Set

From GAD Gene-Disease Associations

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

fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; osteoporosis; spinal injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain hypoxia; burns; hypoxia, brain; spinal cord injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain hypoxia; burns; hypoxia, brain; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cushing syndrome; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cushing syndrome; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; hip fractures; osteoporosis; spinal injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; hip fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; spinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal Gene Set

From GeneRIF Biological Term Annotations

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

Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

smoothened signaling pathway involved in spinal cord motor neuron cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations dataset.

spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

spinal cord ventral commissure morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord ventral commissure morphogenesis biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron specification Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord development Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord development biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in ventral spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification biological process from the curated GO Biological Process Annotations dataset.

negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations dataset.

commissural neuron differentiation in spinal cord Gene Set

From GO Biological Process Annotations

genes participating in the commissural neuron differentiation in spinal cord biological process from the curated GO Biological Process Annotations dataset.

spinal cord motor neuron cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in ventral spinal cord interneuron specification Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations dataset.

spinal cord association neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord association neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter involved in ventral spinal cord interneuron specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron fate commitment biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter involved in spinal cord association neuron specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord association neuron specification biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron differentiation biological process from the curated GO Biological Process Annotations dataset.

musculoskeletal movement, spinal reflex action Gene Set

From GO Biological Process Annotations

genes participating in the musculoskeletal movement, spinal reflex action biological process from the curated GO Biological Process Annotations dataset.

ventral spinal cord interneuron fate determination Gene Set

From GO Biological Process Annotations

genes participating in the ventral spinal cord interneuron fate determination biological process from the curated GO Biological Process Annotations dataset.

cell differentiation in spinal cord Gene Set

From GO Biological Process Annotations

genes participating in the cell differentiation in spinal cord biological process from the curated GO Biological Process Annotations dataset.

bmp signaling pathway involved in spinal cord dorsal/ventral patterning Gene Set

From GO Biological Process Annotations

genes participating in the bmp signaling pathway involved in spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations dataset.

dorsal spinal cord development Gene Set

From GO Biological Process Annotations

genes participating in the dorsal spinal cord development biological process from the curated GO Biological Process Annotations dataset.

spinal cord anterior/posterior patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations dataset.

spinal cord dorsal/ventral patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations dataset.

spinal cord motor neuron migration Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations dataset.

corticospinal neuron axon guidance through spinal cord Gene Set

From GO Biological Process Annotations

genes participating in the corticospinal neuron axon guidance through spinal cord biological process from the curated GO Biological Process Annotations dataset.

spinal cord development Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord development biological process from the curated GO Biological Process Annotations dataset.

spinal cord motor neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

spinal cord oligodendrocyte cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord oligodendrocyte cell fate specification biological process from the curated GO Biological Process Annotations dataset.

abnormality of the spinal cord Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

spinal rigidity Gene Set

From GWASdb SNP-Phenotype Associations

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

widening of cervical spinal canal Gene Set

From HPO Gene-Disease Associations

genes associated with the widening of cervical spinal canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic spinal processes Gene Set

From HPO Gene-Disease Associations

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

asymmetry of spinal facet joints Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetry of spinal facet joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the dorsal column of the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the dorsal column of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal rigidity Gene Set

From HPO Gene-Disease Associations

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

spinal canal stenosis Gene Set

From HPO Gene-Disease Associations

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

spinal cord compression Gene Set

From HPO Gene-Disease Associations

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

abnormality of the spinal meninges Gene Set

From HPO Gene-Disease Associations

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

spinal stenosis with reduced interpedicular distance Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal stenosis with reduced interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pallor of dorsal columns of the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the pallor of dorsal columns of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal deformities Gene Set

From HPO Gene-Disease Associations

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

abnormality of the spinal cord Gene Set

From HPO Gene-Disease Associations

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

spinal hemangioblastoma Gene Set

From HPO Gene-Disease Associations

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

spinal instability Gene Set

From HPO Gene-Disease Associations

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

spinal arteriovenous malformation Gene Set

From HPO Gene-Disease Associations

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

spinal muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

spinal cord posterior columns myelin loss Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrophy/degeneration involving the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal neurofibromas Gene Set

From HPO Gene-Disease Associations

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

symmetric spinal nerve root neurofibromas Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetric spinal nerve root neurofibromas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord lesions Gene Set

From HPO Gene-Disease Associations

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

atrophy of the spinal cord Gene Set

From HPO Gene-Disease Associations

genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord tumor Gene Set

From HPO Gene-Disease Associations

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

cervical spinal canal stenosis Gene Set

From HPO Gene-Disease Associations

genes associated with the cervical spinal canal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Spinal Muscular Atrophies of Childhood Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Cord Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spinal Osteophytosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Atrophy, Spinal Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spinal Stenosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spinal Injuries Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spinal Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spinal Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tuberculosis, Spinal Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal spinal cord dorsal column morphology Gene Set

From 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 spinal cord white matter morphology Gene Set

From 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 spinal cord dorsal horn morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord dorsal horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord grey matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord grey matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal nerve morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal spinal cord central canal morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord ventral horn morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord ventral horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spinal cord size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord interneuron morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord interneuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased spinal cord size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord ventral commissure morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord ventral commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord motor column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord lateral column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord lateral column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord lateral motor column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord lateral motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord ependymal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord ependymal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spinal cord degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal spinal cord commissure morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ventral spinal root morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ventral spinal root morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spinal cord ventral horn cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spinal cord ventral horn cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spinal hemorrhage Gene Set

From MPO Gene-Phenotype Associations

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

increased spinal cord apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased spinal cord apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal spinal cord motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal dorsal spinal root morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal dorsal spinal root morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal reflex Gene Set

From MPO Gene-Phenotype Associations

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

spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy with progressive myoclonic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, x-linked 2, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, chronic distal, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, jokela type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal spinal muscular atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, late-onset, finkel type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.

{spinal muscular atrophy, type iii, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

neurofibromatosis, familial spinal Gene Set

From OMIM Gene-Disease Associations

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

spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, x-linked 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal and bulbar muscular atrophy of kennedy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, congenital nonprogressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.

TWIK-related spinal cord K+ channel (TRESK) Gene Set

From Reactome Pathways

proteins participating in the TWIK-related spinal cord K+ channel (TRESK) pathway from the Reactome Pathways dataset.

spinal column Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal column from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

spinal cord Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal cord from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

spinal ganglion Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

spinal cord Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal cord in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

spinal ganglion Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue spinal ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

spinal column Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

anterior spinal root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

spinal nerve Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

spinal ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

spinal trigeminal tract Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

spinal muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

posterior spinal root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

spinal cord Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

spinal root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Spinal Cord Injury(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Spinal Cord Injury(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Spinal Cord Injury(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Spinal Cord Injury(Mus musculus) pathway from the Wikipathways Pathways dataset.

Postoperative Complications Gene Set

From CTD Gene-Disease Associations

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

Diabetes Complications Gene Set

From CTD Gene-Disease Associations

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

Intraoperative Complications Gene Set

From CTD Gene-Disease Associations

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

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 6 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 from the curated CTD Gene-Disease Associations dataset.

MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

diabetes complications; hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; hypertrophy, left ventricular; left ventricular hypertrophy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; retinal artery occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney diseases; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney diseases; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; postoperative complications Gene Set

From GAD Gene-Disease Associations

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

acute coronary syndrome; diabetes complications; diabetes mellitus; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; diabetes complications; diabetes mellitus; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney transplant complications Gene Set

From GAD Gene-Disease Associations

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

postoperative complications; thrombosis Gene Set

From 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.

cerebral infarction; diabetes complications; hemochromatosis; hypertension; intracranial arteriosclerosis; intracranial thrombosis Gene Set

From 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.

alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary disease; postoperative complications; thrombosis Gene Set

From 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.

activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From 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.

epilepsy; anticoagulant complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; anticoagulant complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholecystolithiasis; postoperative complications; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholecystolithiasis; postoperative complications; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

postoperative complications; systemic inflam response synd; systemic inflammatory response syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postoperative complications; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial infections; liver failure; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; liver failure; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary stenosis; diabetes complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary stenosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

postoperative complications; pulmonary embolism; pulmonary embolisms; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postoperative complications; pulmonary embolism; pulmonary embolisms; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; postoperative complications; pouchitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; postoperative complications; pouchitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; diabetes mellitus; inflammation; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; diabetes mellitus; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bleeding complications Gene Set

From GAD Gene-Disease Associations

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

heart transplant complications Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; coronary restenosis; postoperative complications; thrombosis Gene Set

From 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.

bacterial infections; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial infections; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcinosis; diabetes complications; heart valve diseases; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcinosis; diabetes complications; heart valve diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; hypertension; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; hypertension; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anticoagulant complications Gene Set

From GAD Gene-Disease Associations

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

cholelithiasis; obesity, morbid; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholelithiasis; obesity, morbid; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; coronary thrombosis; diabetes complications; hypertension; mitral valve stenosis; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; coronary thrombosis; diabetes complications; hypertension; mitral valve stenosis; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; carotid artery diseases; diabetes complications; dyslipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; carotid artery diseases; diabetes complications; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary restenosis; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary restenosis; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; diabetes complications; diabetes mellitus, type 1; infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; diabetes complications; diabetes mellitus, type 1; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial ischemia; nervous system diseases; postoperative complications; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial ischemia; nervous system diseases; postoperative complications; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension/complications* Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension/complications* in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes complications; fatty liver; fatty liver, alcoholic; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes complications; fatty liver; fatty liver, alcoholic; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.