Name

hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Methionine adenosyltransferase deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methionine adenosyltransferase deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methionine adenosyltransferase deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Methionine Adenosyltransferase Deficiency Gene Set

From CTD Gene-Disease Associations

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

methionine adenosyltransferase i/iii deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease methionine adenosyltransferase i/iii deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

methionine adenosyltransferase deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) Gene Set

From Reactome Pathways

proteins participating in the Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD) pathway from the Reactome Pathways dataset.

methionine adenosyltransferase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the methionine adenosyltransferase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

methionine adenosyltransferase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

methionine adenosyltransferase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the methionine adenosyltransferase complex cellular component from the curated GO Cellular Component Annotations dataset.

methionine adenosyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the methionine adenosyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

methionine adenosyltransferase regulator activity Gene Set

From GO Molecular Function Annotations

genes performing the methionine adenosyltransferase regulator activity molecular function from the curated GO Molecular Function Annotations dataset.

Methionine adenosyltransferase 2 subunit beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Methionine adenosyltransferase 2 subunit beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

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

From CTD Gene-Disease Associations

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

demyelination Gene Set

From GAD Gene-Disease Associations

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

demyelination Gene Set

From GeneRIF Biological Term Annotations

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

segmental peripheral demyelination/remyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the segmental peripheral demyelination/remyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cns demyelination Gene Set

From HPO Gene-Disease Associations

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

symmetrical progressive peripheral demyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse demyelination of the cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse demyelination of the cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe demyelination of the white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the severe demyelination of the white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

segmental peripheral demyelination Gene Set

From HPO Gene-Disease Associations

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

patchy demyelination of subcortical white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy demyelination of subcortical white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral demyelination Gene Set

From HPO Gene-Disease Associations

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

symmetric peripheral demyelination Gene Set

From HPO Gene-Disease Associations

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

demyelination Gene Set

From MPO Gene-Phenotype Associations

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

brain concussion; brain injuries; brain ischemia Gene Set

From GAD Gene-Disease Associations

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

adenosyltransferase Gene Set

From GeneRIF Biological Term Annotations

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

cob(i)yrinic acid a,c-diamide adenosyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the cob(i)yrinic acid a,c-diamide adenosyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

Adenosylcobalamin biosynthesis, ATP:cob(I)alamin adenosyltransferase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenosylcobalamin biosynthesis, ATP:cob(I)alamin adenosyltransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP:cob(I)alamin adenosyltransferase, PduO-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP:cob(I)alamin adenosyltransferase, PduO-type protein domain from the InterPro Predicted Protein Domain Annotations 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.

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.

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to protein S deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency due to ADA deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HNSHA due to aldolase A deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia due to hexokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex I deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocysteinemia due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to ficolin 3 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermethioninemia due to adenosine kinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria due to MTHFR deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome due to mitochondrial complex II deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, severe, due to leptin deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenylate kinase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.

Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.

Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.

Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Severe combined immunodeficiency due to adenosine deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset.

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.

Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.

Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Metachromatic Leukodystrophy due to Saposin B Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

{chronic infections, due to mbl deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {chronic infections, due to mbl deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to hrg deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to hrg deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to il2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to phosphofructokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

nephropathy due to cfhr5 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease, autosomal, due to deficiency of cyba Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset.

?isolated growth hormone deficiency due to defect in ghrf Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to heparin cofactor ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

glucocorticoid deficiency, due to acth unresponsiveness Gene Set

From OMIM Gene-Disease Associations

genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to purine nucleoside phosphorylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione peroxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

lacticacidemia due to pdx1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the lacticacidemia due to pdx1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, due to umph1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

homocystinuria due to mthfr deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria due to mthfr deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency due to ada deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cirrhosis due to liver phosphorylase kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the cirrhosis due to liver phosphorylase kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

metachromatic leukodystrophy due to sap-b deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the metachromatic leukodystrophy due to sap-b deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, morbid, due to leptin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, morbid, due to leptin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome, due to cox deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome, due to cox deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperammonemia due to carbonic anhydrase va deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to g6pd deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to adenylate kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to adenylate kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to antithrombin iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocytosis due to bisphosphoglycerate mutase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocytosis due to bisphosphoglycerate mutase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

aica-ribosiduria due to atic deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the aica-ribosiduria due to atic deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo i deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial cox4 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic granulomatous disease due to deficiency of ncf-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the chronic granulomatous disease due to deficiency of ncf-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia due to adenosine kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia due to adenosine kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to cytochrome c oxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to cytochrome c oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration due to cerebral folate transport deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to ficolin 3 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to ficolin 3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome due to mitochondrial complex 1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to triosephosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to triosephosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{resistance to malaria due to g6pd deficiency} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {resistance to malaria due to g6pd deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to hexokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to hexokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to cpt ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

emphysema-cirrhosis, due to aat deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoaldosteronism, congenital, due to cmo ii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?male infertility due to acrosin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy due to myoadenylate deaminase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set

From Reactome Pathways

proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.

L-methionine sulfoximine-4070 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the L-methionine sulfoximine-4070 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

L-methionine sulfoximine-2470 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the L-methionine sulfoximine-2470 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

L-methionine sulfoximine-4151 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the L-methionine sulfoximine-4151 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

L-methionine sulfoximine-2831 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the L-methionine sulfoximine-2831 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methionine selenoxide Gene Set

From CTD Gene-Chemical Interactions

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

Methionine Gene Set

From CTD Gene-Chemical Interactions

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

Methionine Sulfoximine Gene Set

From CTD Gene-Chemical Interactions

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

D-Methionine Gene Set

From DrugBank Drug Targets

interacting proteins for the D-Methionine drug from the curated DrugBank Drug Targets dataset.

Methionine Sulfoxide Gene Set

From DrugBank Drug Targets

interacting proteins for the Methionine Sulfoxide drug from the curated DrugBank Drug Targets dataset.

L-Methionine Gene Set

From DrugBank Drug Targets

interacting proteins for the L-Methionine drug from the curated DrugBank Drug Targets dataset.

methionine Gene Set

From GeneRIF Biological Term Annotations

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

methionine biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the methionine biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

peptidyl-methionine modification Gene Set

From GO Biological Process Annotations

genes participating in the peptidyl-methionine modification biological process from the curated GO Biological Process Annotations dataset.

l-methionine biosynthetic process from methylthioadenosine Gene Set

From GO Biological Process Annotations

genes participating in the l-methionine biosynthetic process from methylthioadenosine biological process from the curated GO Biological Process Annotations dataset.

l-methionine biosynthetic process from s-adenosylmethionine Gene Set

From GO Biological Process Annotations

genes participating in the l-methionine biosynthetic process from s-adenosylmethionine biological process from the curated GO Biological Process Annotations dataset.

methionine metabolic process Gene Set

From GO Biological Process Annotations

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

s-adenosyl-l-methionine transport Gene Set

From GO Biological Process Annotations

genes participating in the s-adenosyl-l-methionine transport biological process from the curated GO Biological Process Annotations dataset.

methionine transport Gene Set

From GO Biological Process Annotations

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

n-terminal peptidyl-methionine acetylation Gene Set

From GO Biological Process Annotations

genes participating in the n-terminal peptidyl-methionine acetylation biological process from the curated GO Biological Process Annotations dataset.

l-methionine biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the l-methionine biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

s-adenosyl-l-methionine transmembrane transport Gene Set

From GO Biological Process Annotations

genes participating in the s-adenosyl-l-methionine transmembrane transport biological process from the curated GO Biological Process Annotations dataset.

l-methionine salvage Gene Set

From GO Biological Process Annotations

genes participating in the l-methionine salvage biological process from the curated GO Biological Process Annotations dataset.

protein initiator methionine removal Gene Set

From GO Biological Process Annotations

genes participating in the protein initiator methionine removal biological process from the curated GO Biological Process Annotations dataset.

peptide-methionine (r)-s-oxide reductase activity Gene Set

From GO Molecular Function Annotations

genes performing the peptide-methionine (r)-s-oxide reductase activity molecular function from the curated GO Molecular Function Annotations dataset.

[methionine synthase] reductase activity Gene Set

From GO Molecular Function Annotations

genes performing the [methionine synthase] reductase activity molecular function from the curated GO Molecular Function Annotations dataset.

methionine-trna ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the methionine-trna ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

s-adenosyl-l-methionine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the s-adenosyl-l-methionine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

peptide-methionine (s)-s-oxide reductase activity Gene Set

From GO Molecular Function Annotations

genes performing the peptide-methionine (s)-s-oxide reductase activity molecular function from the curated GO Molecular Function Annotations dataset.

methionine synthase activity Gene Set

From GO Molecular Function Annotations

genes performing the methionine synthase activity molecular function from the curated GO Molecular Function Annotations dataset.

methionine-r-sulfoxide reductase activity Gene Set

From GO Molecular Function Annotations

genes performing the methionine-r-sulfoxide reductase activity molecular function from the curated GO Molecular Function Annotations dataset.

l-methionine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-methionine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

methionine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the methionine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

methionine benzimidazole 6 Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the methionine benzimidazole 6 ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Plasma homocysteine levels (post-methionine load test) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Plasma homocysteine levels (post-methionine load test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

N-Acetyl-L-methionine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the N-Acetyl-L-methionine metabolite from the curated HMDB Metabolites of Enzymes dataset.

Methionine sulfoxide Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Methionine sulfoxide metabolite from the curated HMDB Metabolites of Enzymes dataset.

L-Methionine Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the L-Methionine metabolite from the curated HMDB Metabolites of Enzymes dataset.

abnormality of methionine metabolism Gene Set

From HPO Gene-Disease Associations

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

decreased methionine synthase activity Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased methionine synthase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

methionine salvage Gene Set

From HumanCyc Pathways

proteins participating in the methionine salvage pathway from the HumanCyc Pathways dataset.

methionine degradation Gene Set

From HumanCyc Pathways

proteins participating in the methionine degradation pathway from the HumanCyc Pathways dataset.

S-adenosyl-L-methionine biosynthesis Gene Set

From HumanCyc Pathways

proteins participating in the S-adenosyl-L-methionine biosynthesis pathway from the HumanCyc Pathways dataset.

superpathway of methionine degradation Gene Set

From HumanCyc Pathways

proteins participating in the superpathway of methionine degradation pathway from the HumanCyc Pathways dataset.

Vitamin B12-dependent methionine synthase, activation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vitamin B12-dependent methionine synthase, activation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-adenosyl-L-methionine dependent methyltransferase, Mett10D, predicted Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-adenosyl-L-methionine dependent methyltransferase, Mett10D, predicted protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase M24A, methionine aminopeptidase, subfamily 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M24A, methionine aminopeptidase, subfamily 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Bin3-type S-adenosyl-L-methionine binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Bin3-type S-adenosyl-L-methionine binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Methionine-tRNA ligase, type 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Methionine-tRNA ligase, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase M24A, methionine aminopeptidase, subfamily 2, binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M24A, methionine aminopeptidase, subfamily 2, binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-adenosyl-L-methionine-dependent methyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-adenosyl-L-methionine-dependent methyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase M24A, methionine aminopeptidase, subfamily 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M24A, methionine aminopeptidase, subfamily 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

S-adenosyl-L-methionine-dependent methyltransferase, MraW, recognition domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the S-adenosyl-L-methionine-dependent methyltransferase, MraW, recognition domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptide methionine sulphoxide reductase MsrA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide methionine sulphoxide reductase MsrA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cobalamin-dependent methionine synthase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cobalamin-dependent methionine synthase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase M24, methionine aminopeptidase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase M24, methionine aminopeptidase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Putative S-adenosyl-L-methionine-dependent methyltransferase MidA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Putative S-adenosyl-L-methionine-dependent methyltransferase MidA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptide methionine sulphoxide reductase MrsB Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide methionine sulphoxide reductase MrsB protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Methionine tRNA Formyltransferase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Methionine tRNA Formyltransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptide methionine sulfoxide reductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptide methionine sulfoxide reductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

methionine metabolism Gene Set

From KEGG Pathways

proteins participating in the methionine metabolism pathway from the KEGG Pathways dataset.

Methionine biosynthesis Gene Set

From PANTHER Pathways

proteins participating in the Methionine biosynthesis pathway from the PANTHER Pathways dataset.

Methionine salvage pathway Gene Set

From Reactome Pathways

proteins participating in the Methionine salvage pathway pathway from the Reactome Pathways dataset.

brain infarction; brain ischemia Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; brain infarction; brain ischemia; coronary artery disease; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain damage, chronic; brain injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain damage, chronic; brain injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; brain injuries Gene Set

From GAD Gene-Disease Associations

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

brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; brain ischemia; cerebrovascular disorders; hypertension; leukoaraiosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain concussion; brain injuries; unconsciousness Gene Set

From GAD Gene-Disease Associations

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

brain edema; brain hemorrhage, traumatic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; brain hemorrhage, traumatic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asphyxia neonatorum; brain ischemia; hypoxia-ischemia, brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asphyxia neonatorum; brain ischemia; hypoxia-ischemia, brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain infarction; brain ischemia; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain damage, chronic; hypoxia-ischemia, brain; infant, newborn, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain damage, chronic; hypoxia-ischemia, brain; infant, newborn, diseases 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.

apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

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.

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.

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; 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.

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.

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.

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.

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.

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.

Megaloblastic anemia due to inborn errors of metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to activated protein C resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to thrombomodulin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to defect in cd3-zeta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset.

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.

Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset.

Thrombophilia due to Activated Protein C Resistance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia due to Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in CD3-Zeta Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.

thrombocytopenia due to platelet alloimmunization Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pneumoconiosis due to talc Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary spastic paraparesis due to a frame shift mutat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depressed suicide; suicide due to depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

due Gene Set

From GeneRIF Biological Term Annotations

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

anemia due to reduced life span of red cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anemia due to reduced life span of red cells Gene Set

From HPO Gene-Disease Associations

genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

restricted neck movement due to contractures Gene Set

From HPO Gene-Disease Associations

genes associated with the restricted neck movement due to contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic rhinitis due to narrow nasal airway Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

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

osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bowing of limbs due to multiple fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis leading to amputation due to slow healing fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

weakness due to upper motor neuron dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

self-mutilation of tongue and lips due to involuntary movements Gene Set

From HPO Gene-Disease Associations

genes associated with the self-mutilation of tongue and lips due to involuntary movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

respiratory insufficiency due to defective ciliary clearance Gene Set

From HPO Gene-Disease Associations

genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent infections due to aspiration Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chronic hepatitis due to cryptospridium infection Gene Set

From HPO Gene-Disease Associations

genes associated with the chronic hepatitis due to cryptospridium infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subperiosteal erosions due to secondary hyperparathyroidism Gene Set

From HPO Gene-Disease Associations

genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

painless fractures due to injury Gene Set

From HPO Gene-Disease Associations

genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hepatic abscesses due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cellulitis due to immunodeficiency Gene Set

From HPO Gene-Disease Associations

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

decreased sweating due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intermittent episodes of respiratory insufficiency due to muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

orthostatic hypotension due to autonomic dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombomodulin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder due to p2rx1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercholesterolemia, due to ligand-defective apo b Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercholesterolemia, due to ligand-defective apo b phenotype from the curated OMIM Gene-Disease Associations dataset.

disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene Set

From OMIM Gene-Disease Associations

genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset.

hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset.

hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

omphalocele due to duplication of 1p31.3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset.

gigantism due to ghrf hypersecretion Gene Set

From OMIM Gene-Disease Associations

genes associated with the gigantism due to ghrf hypersecretion phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

{drug-induced liver injury due to flucloxacillin} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {drug-induced liver injury due to flucloxacillin} phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to activated protein c resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to activated protein c resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

?male pseudohermaphroditism due to defective lh Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset.

hydrocephalus due to aqueductal stenosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to elevated hrg Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to elevated hrg phenotype from the curated OMIM Gene-Disease Associations dataset.

thalassemia due to hb lepore Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia due to hb lepore phenotype from the curated OMIM Gene-Disease Associations dataset.

rickets due to defect in vitamin d 25-hydroxylation Gene Set

From OMIM Gene-Disease Associations

genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria due to transcobalamin receptor defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.

{thrombophilia, susceptibility to, due to factor v leiden} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {thrombophilia, susceptibility to, due to factor v leiden} phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to defect in mapbp-interacting protein Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, familial, due to ttf-1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperfibrinolysis, familial, due to increased release of plat Gene Set

From OMIM Gene-Disease Associations

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

hemosiderosis, systemic, due to aceruloplasminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemosiderosis, systemic, due to aceruloplasminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Brain stem Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Iron accumulation in brain Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iron accumulation in brain phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brain small vessel disease with hemorrhage Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurodegeneration with brain iron accumulation 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurodegeneration with brain iron accumulation 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscle eye brain disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurodegeneration with brain iron accumulation 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurodegeneration with brain iron accumulation 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurodegeneration with brain iron accumulation 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurodegeneration with brain iron accumulation 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neurodegeneration with brain iron accumulation 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neurodegeneration with brain iron accumulation 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kir4.1-alpha-1-syntrophin complex, whole brain lysate Gene Set

From CORUM Protein Complexes

proteins in the Kir4.1-alpha-1-syntrophin complex, whole brain lysate protein complex from the CORUM Protein Complexes dataset.

Kir4.1-dystrophin complex, whole brain lysate Gene Set

From CORUM Protein Complexes

proteins in the Kir4.1-dystrophin complex, whole brain lysate protein complex from the CORUM Protein Complexes dataset.

PS1-E-cadherin-catenin complex, brain Gene Set

From CORUM Protein Complexes

proteins in the PS1-E-cadherin-catenin complex, brain protein complex from the CORUM Protein Complexes dataset.

Brain-derived dystrobrevin-syntrophin complex Gene Set

From CORUM Protein Complexes

proteins in the Brain-derived dystrobrevin-syntrophin complex protein complex from the CORUM Protein Complexes dataset.

Kir4.1-beta-dystroglycan complex, whole brain lysate Gene Set

From CORUM Protein Complexes

proteins in the Kir4.1-beta-dystroglycan complex, whole brain lysate protein complex from the CORUM Protein Complexes dataset.

Pick Disease of the Brain Gene Set

From CTD Gene-Disease Associations

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

Hypoxia, Brain Gene Set

From CTD Gene-Disease Associations

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

Hypoxia-Ischemia, Brain Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoxia-Ischemia, Brain from the curated CTD Gene-Disease Associations dataset.

Brain Stem Infarctions Gene Set

From CTD Gene-Disease Associations

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

Brain Edema Gene Set

From CTD Gene-Disease Associations

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

MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.

Brain Infarction Gene Set

From CTD Gene-Disease Associations

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

PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY from the curated CTD Gene-Disease Associations dataset.

Brain Stem Neoplasms Gene Set

From CTD Gene-Disease Associations

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

Brain Neoplasms Gene Set

From CTD Gene-Disease Associations

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

NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A from the curated CTD Gene-Disease Associations dataset.

Brain Small Vessel Disease with Hemorrhage Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Brain Damage, Chronic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Damage, Chronic from the curated CTD Gene-Disease Associations dataset.

Brain Ischemia Gene Set

From CTD Gene-Disease Associations

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

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Brain Diseases Gene Set

From CTD Gene-Disease Associations

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

Brain Injuries Gene Set

From CTD Gene-Disease Associations

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

Brain Diseases, Metabolic Gene Set

From CTD Gene-Disease Associations

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

Brain Abscess Gene Set

From CTD Gene-Disease Associations

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

HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS from the curated CTD Gene-Disease Associations dataset.

NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B from the curated CTD Gene-Disease Associations dataset.

Neurodegeneration with brain iron accumulation (NBIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neurodegeneration with brain iron accumulation (NBIA) from the curated CTD Gene-Disease Associations dataset.

Brain Diseases, Metabolic, Inborn Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Diseases, Metabolic, Inborn from the curated CTD Gene-Disease Associations dataset.

Brain Mapping Gene Set

From dbGAP Gene-Trait Associations

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

Natriuretic Peptide, Brain Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Natriuretic Peptide, Brain in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Brain Waves Gene Set

From dbGAP Gene-Trait Associations

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

Brain Gene Set

From dbGAP Gene-Trait Associations

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

brain disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

brain infarction Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

brain cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

brain disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

brain stem infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain stem astrocytic neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain ischemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain glioblastoma multiforme Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain glioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain germinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain stem cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain stem glioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain ependymoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain compression Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain oligodendroglioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain angioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain sarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain injuries; dementia, vascular; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; dementia, vascular; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain morphology Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; meningioma Gene Set

From GAD Gene-Disease Associations

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

astrocytoma; brain neoplasms Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms Gene Set

From GAD Gene-Disease Associations

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

brain tumors Gene Set

From GAD Gene-Disease Associations

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

anoxia; brain injuries; hypotension Gene Set

From GAD Gene-Disease Associations

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

astrocytoma; brain neoplasms; neoplasm invasiveness Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

astrocytoma; brain neoplasms; glioblastoma Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; foramen ovale, patent; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; foramen ovale, patent; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; recurrence; stroke Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; breast neoplasms; laryngeal neoplasm; laryngeal neoplasms; mammary neoplasms; neoplasms; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; breast neoplasms; laryngeal neoplasm; laryngeal neoplasms; mammary neoplasms; neoplasms; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; heart diseases; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; heart diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; stroke, lacunar; atherothrombotic brain infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; stroke, lacunar; atherothrombotic brain infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

traumatic brain imjury Gene Set

From GAD Gene-Disease Associations

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

brain lesion load Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; glioma; oligodendroglioma Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; intracranial arteriosclerosis; stroke Gene Set

From GAD Gene-Disease Associations

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

arteriosclerosis; brain ischemia; carotid artery diseases; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; brain ischemia; carotid artery diseases; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; brain infarction; hypertension Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; hypertension; stroke Gene Set

From GAD Gene-Disease Associations

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

astrocytoma; brain neoplasms; oligodendroglioma Gene Set

From GAD Gene-Disease Associations

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

brain Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; inflammation Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

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

astrocytoma; brain neoplasms; meningeal neoplasms; meningioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease astrocytoma; brain neoplasms; meningeal neoplasms; meningioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

traumatic brain injury. Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; hyperhomocysteinemia; stroke Gene Set

From GAD Gene-Disease Associations

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

apoplexy; atherosclerosis; brain ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atherosclerosis; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; carotid artery stenosis; carotid stenosis; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain activity Gene Set

From GAD Gene-Disease Associations

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

brain damage, chronic; hypertension; myocardial ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain damage, chronic; hypertension; myocardial ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; inflammation; stroke Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; stroke Gene Set

From GAD Gene-Disease Associations

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

myocardial infarct; brain infarction Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; carotid stenosis Gene Set

From GAD Gene-Disease Associations

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

brain atrophy Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; stroke; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; stroke Gene Set

From GAD Gene-Disease Associations

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

brain receptor-binding characteristics Gene Set

From GAD Gene-Disease Associations

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

brain aging Gene Set

From GAD Gene-Disease Associations

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

atrial fibrillation; brain ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; carotid artery diseases; hemochromatosis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; carotid artery diseases; hemochromatosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; diabetes complications; hypertension; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; diabetes complications; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; intracranial thrombosis; ischemic attack, transient; migraine disorders; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; diabetes mellitus; hemiplegia; hypercholesterolemia; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; stroke; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; stroke; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain tumor Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; hypertension; osteoporosis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; hypertension; osteoporosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases Gene Set

From GAD Gene-Disease Associations

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

brain ischemia Gene Set

From GAD Gene-Disease Associations

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

amphetamine-related disorders; brain diseases, metabolic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders; brain diseases, metabolic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; hemangioma, cavernous, central nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; hemangioma, cavernous, central nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries; hypopituitarism Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain infarction; recurrence; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain infarction; recurrence; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; brain death Gene Set

From GAD Gene-Disease Associations

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

myocardial infarction; brain infarction Gene Set

From GAD Gene-Disease Associations

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

brain lesions or calcifications Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; intracranial arterial diseases; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; intracranial arterial diseases; stroke 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.

hypoxia-ischemia, brain; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypoxia-ischemia, brain; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries; nerve degeneration Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; carotid artery diseases; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; carotid artery diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; abeta load in brain Gene Set

From GAD Gene-Disease Associations

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

brain hemorrhage Gene Set

From GAD Gene-Disease Associations

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

brain injuries; fatigue; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; fatigue; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

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

atrial fibrillation; brain ischemia; coronary thrombosis; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; brain ischemia; coronary thrombosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

astrocytoma; brain neoplasms; ependymoma; glioma; neoplasm metastasis; oligodendroglioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease astrocytoma; brain neoplasms; ependymoma; glioma; neoplasm metastasis; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; stroke; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries; wounds, penetrating Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; wounds, penetrating in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; carotid artery diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; carotid artery diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphasia; brain ischemia; cardiovascular diseases; cerebral hemorrhage; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

brain imaging Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; coronary disease; stroke Gene Set

From GAD Gene-Disease Associations

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

brain aneurysm Gene Set

From GAD Gene-Disease Associations

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

asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; brain neoplasms; eczema; glioma; hay fever; hypersensitivity; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; diabetes mellitus; intracranial arteriosclerosis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; diabetes mellitus; intracranial arteriosclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; cerebral arterial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cerebral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; hyperlipidemias; hypertension; intracranial arteriosclerosis; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain function Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; hyperhomocysteinemia; intracranial arterial diseases; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain cancer Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; cardiovascular diseases; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

atrophy; brain diseases Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral hemorrhage; stroke Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; glioblastoma; oligodendroglioma Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; diabetes mellitus; hyperlipidemias; myocardial infarction; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain mapping Gene Set

From GAD Gene-Disease Associations

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

brain injury, chronic Gene Set

From GAD Gene-Disease Associations

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

brain infarction; Gene Set

From GAD Gene-Disease Associations

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

brain injuries; intracranial hypertension Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; intracranial hemorrhages; stroke Gene Set

From GAD Gene-Disease Associations

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

anoxia; asphyxia; brain ischemia; disease models, animal; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; asphyxia; brain ischemia; disease models, animal; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; hypoxia-ischemia, brain; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; hypoxia-ischemia, brain; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain hemorrhage; stroke, ischemic Gene Set

From GAD Gene-Disease Associations

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

brain injuries; epilepsy, post-traumatic; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; epilepsy, post-traumatic; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amnesia; brain injuries Gene Set

From GAD Gene-Disease Associations

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

childhood brain tumors ; residential insecticide exposure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; ischemic attack, transient; stroke; thrombosis; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; glioblastoma; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; glioblastoma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain hemorrhage; cerebrovascular disease; thrombosis, deep vein Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain hemorrhage; cerebrovascular disease; thrombosis, deep vein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; occupational diseases Gene Set

From GAD Gene-Disease Associations

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

brain diseases; mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult brain tumors Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral arterial diseases; intracranial embolism; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cerebral arterial diseases; intracranial embolism; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; dementia; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; dementia; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; inflammation Gene Set

From GAD Gene-Disease Associations

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

brain injuries; memory disorders Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cerebral infarction Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; encephalitis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; encephalitis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atrial fibrillation; brain ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atrial fibrillation; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

normalized brain volume, multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease normalized brain volume, multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aphasia; aphasia, nos; apoplexy; brain ischemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphasia; aphasia, nos; apoplexy; brain ischemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries; inflammation; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; inflammation; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; meningioma; nervous system neoplasms; neurilemmoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; meningioma; nervous system neoplasms; neurilemmoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; inflammation; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; oligodendroglioma Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; coronary disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; coronary disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; diabetes mellitus; genetic diseases, inborn; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; intracranial embolism and thrombosis; sinus thrombosis, intracranial; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; glioma; meningioma; neuroma, acoustic; neuromas, acoustic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; glioma; meningioma; neuroma, acoustic; neuromas, acoustic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; dementia Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; intracranial hemorrhages; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; intracranial hemorrhages; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood brain tumor Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; glioblastoma Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; cerebral infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; glioma; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; glioma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; intracranial hemorrhages; myocardial infarction; stroke; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; hemorrhage Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; subarachnoid hemorrhage; vasospasm, intracranial Gene Set

From GAD Gene-Disease Associations

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

brain injuries; closed head injuries; head injuries, closed Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; closed head injuries; head injuries, closed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; ischemic attack, transient; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; ischemic attack, transient; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; hypertension; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

natriuretic peptide, brain Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; glioma; meningeal neoplasms; meningioma; neuroma, acoustic; neuromas, acoustic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; glioma; meningeal neoplasms; meningioma; neuroma, acoustic; neuromas, acoustic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; glioma; meningeal neoplasms; meningioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; glioma; meningeal neoplasms; meningioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; cadasil; cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; dementia, vascular; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; dementia, vascular; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain electrical response Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebral hemorrhage; cerebral hemorrhages; hypertension; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; cardiovascular diseases; coronary disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; coronary artery disease; intracranial arteriosclerosis; myocardial infarction; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cerebrovascular accident; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cerebrovascular accident; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; intracranial hemorrhages; stroke; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

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

brain edema; infarction, middle cerebral artery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; infarction, middle cerebral artery in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; meningioma; neurilemmoma Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; brain ischemia; carotid stenosis; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; brain ischemia; carotid stenosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; atrophy; brain diseases Gene Set

From GAD Gene-Disease Associations

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

brain edema; cerebral hemorrhage; Gene Set

From GAD Gene-Disease Associations

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

brain injuries; seizures Gene Set

From GAD Gene-Disease Associations

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

altered brain levels of apolipoprotein e Gene Set

From GAD Gene-Disease Associations

genes associated with the disease altered brain levels of apolipoprotein e in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; hyperlipidemias; stroke Gene Set

From GAD Gene-Disease Associations

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

astrocytoma; brain neoplasms; glioma; oligodendroglioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease astrocytoma; brain neoplasms; glioma; oligodendroglioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

athletic injuries; brain concussion; Gene Set

From GAD Gene-Disease Associations

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

brain structure Gene Set

From GAD Gene-Disease Associations

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

volumetric brain mri Gene Set

From GAD Gene-Disease Associations

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

brain hemorrhage; stroke; stroke, lacunar Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain concussion Gene Set

From GAD Gene-Disease Associations

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

brain infarction; carotid artery diseases; intracranial thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; carotid artery diseases; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; glioma Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; hyperhomocysteinemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; hyperhomocysteinemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

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

brain injuries; cerebrovascular disorders; migraine disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; cerebrovascular disorders; migraine disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; infarction, middle cerebral artery; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; infarction, middle cerebral artery; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; brain atrophy Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; hypoxia-ischemia, brain Gene Set

From GAD Gene-Disease Associations

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

frontal brain electrical asymmetry Gene Set

From GAD Gene-Disease Associations

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

brain infarction; intracranial arteriosclerosis Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; intracranial hemorrhages; stroke Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; diabetes mellitus; hyperlipidemias; hypertension; intracranial embolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; diabetes mellitus; hyperlipidemias; hypertension; intracranial embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; brain ischemia; recurrence Gene Set

From GAD Gene-Disease Associations

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

athletic injuries; brain concussion Gene Set

From GAD Gene-Disease Associations

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

brain imaging in schizophrenia (interaction) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain imaging in schizophrenia (interaction) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries; dementia Gene Set

From GAD Gene-Disease Associations

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

brain Gene Set

From GeneRIF Biological Term Annotations

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

Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE9857 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE9857 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Huntington's Disease_CNS - Brain (MMHCC)_GSE857 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Huntington's Disease_CNS - Brain (MMHCC)_GSE857 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Turner Syndrome_CNS - Brain (MMHCC)_GSE1606 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Turner Syndrome_CNS - Brain (MMHCC)_GSE1606 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE3583 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE3583 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Alexander Disease_CNS - Brain - Olfactory Bulb (MMHCC)_GSE977 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Alexander Disease_CNS - Brain - Olfactory Bulb (MMHCC)_GSE977 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Astrocytoma_CNS - Brain (MMHCC)_GSE4290 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Astrocytoma_CNS - Brain (MMHCC)_GSE4290 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Down Syndrome_CNS - Brain - Cerebellum (MMHCC)_GSE1611 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Down Syndrome_CNS - Brain - Cerebellum (MMHCC)_GSE1611 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Huntington's Disease_CNS - Brain - Cerebellum (MMHCC)_GSE3248 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Huntington's Disease_CNS - Brain - Cerebellum (MMHCC)_GSE3248 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Schizophrenia_CNS - Brain - Cerebellum (MMHCC)_GSE4036 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Schizophrenia_CNS - Brain - Cerebellum (MMHCC)_GSE4036 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Alzheimer's Disease_CNS - Brain - Hippocampus (MMHCC)_GSE1297 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Alzheimer's Disease_CNS - Brain - Hippocampus (MMHCC)_GSE1297 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE5786 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE5786 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE7958 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE7958 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Dehydration_CNS - Brain - Hypothalamus (MMHCC)_GSE4130 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Dehydration_CNS - Brain - Hypothalamus (MMHCC)_GSE4130 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE9375 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Huntington's Disease_CNS - Brain - Striatum (MMHCC)_GSE9375 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Oligodendroglioma_CNS - Brain (MMHCC)_GSE2223 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Oligodendroglioma_CNS - Brain (MMHCC)_GSE2223 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Gamma-hydroxybutyric acidaemia_CNS - Brain - Hippocampus (MMHCC)_GSE2866 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Gamma-hydroxybutyric acidaemia_CNS - Brain - Hippocampus (MMHCC)_GSE2866 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Senescence_CNS - Brain - Hippocampus (MMHCC)_GSE5078 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Senescence_CNS - Brain - Hippocampus (MMHCC)_GSE5078 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

ALDH1A2_KO_GDS4836_290_mouse_anterior embryonic brain Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the ALDH1A2_KO_GDS4836_290_mouse_anterior embryonic brain gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

ALDH1A2_KO_GDS4836_289_mouse_posterior embryonic brain Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the ALDH1A2_KO_GDS4836_289_mouse_posterior embryonic brain gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

midbrain-hindbrain boundary maturation during brain development Gene Set

From GO Biological Process Annotations

genes participating in the midbrain-hindbrain boundary maturation during brain development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

brain renin-angiotensin system Gene Set

From GO Biological Process Annotations

genes participating in the brain renin-angiotensin system biological process from the curated GO Biological Process Annotations dataset.

establishment of glial blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of glial blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

maintenance of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the maintenance of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

negative regulation of establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

brain morphogenesis Gene Set

From GO Biological Process Annotations

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

brain segmentation Gene Set

From GO Biological Process Annotations

genes participating in the brain segmentation biological process from the curated GO Biological Process Annotations dataset.

brain-derived neurotrophic factor receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the brain-derived neurotrophic factor receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

brain development Gene Set

From GO Biological Process Annotations

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

lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

brain-derived neurotrophic factor binding Gene Set

From GO Molecular Function Annotations

genes performing the brain-derived neurotrophic factor binding molecular function from the curated GO Molecular Function Annotations dataset.

brain-derived neurotrophic factor-activated receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the brain-derived neurotrophic factor-activated receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

brain Gene Set

From GTEx Tissue Gene Expression Profiles

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

Brain structure (temporal lobe volume) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Brain structure (temporal lobe volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis--Brain Glutamate Levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Brain structure (hippocampal volume) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Brain structure (hippocampal volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Brain lesion load Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Brain lesion load phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Normalized brain volume Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Normalized brain volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Brain imaging in schizophrenia (interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Brain imaging in schizophrenia (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Brain cytoarchitecture Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Event-related brain oscillations Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Event-related brain oscillations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Volumetric brain MRI Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Volumetric brain MRI phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Brain connectivity Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

5-HTT brain serotonin transporter levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the 5-HTT brain serotonin transporter levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Brain structure Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

brain glioma Gene Set

From GWASdb SNP-Disease Associations

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

brain ischemia Gene Set

From GWASdb SNP-Disease Associations

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

brain cancer Gene Set

From GWASdb SNP-Disease Associations

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

brain disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of brain morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

brain Gene Set

From HPA Tissue Gene Expression Profiles

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

brain abscess Gene Set

From HPO Gene-Disease Associations

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

global brain atrophy Gene Set

From HPO Gene-Disease Associations

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

brain atrophy Gene Set

From HPO Gene-Disease Associations

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

brain stem compression Gene Set

From HPO Gene-Disease Associations

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

abnormality of brain morphology Gene Set

From HPO Gene-Disease Associations

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

brain very small Gene Set

From HPO Gene-Disease Associations

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

calcification of the small brain vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the calcification of the small brain vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Brain Injury, Chronic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Pick Disease of the Brain Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Pick Disease of the Brain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Brain Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Concussion Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hypoxia, Brain Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hypoxia-Ischemia, Brain Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Edema Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Infarction Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Stem Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Damage, Chronic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Ischemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Hemorrhage, Traumatic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Brain Injuries Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

GPCR, family 2, brain-specific angiogenesis inhibitor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GPCR, family 2, brain-specific angiogenesis inhibitor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Brain-derived neurotrophic factor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Brain-derived neurotrophic factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Brain/reproductive organ-expressed protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Brain/reproductive organ-expressed protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription elongation factor A-like/Brain expressed X-linked-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription elongation factor A-like/Brain expressed X-linked-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Brain protein I3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Brain protein I3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Natriuretic peptide, brain type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Natriuretic peptide, brain type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Brain-expressed X-linked protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Brain-expressed X-linked protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Brain acid soluble protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Brain acid soluble protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal brain development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain white matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brain vacuoles Gene Set

From MPO Gene-Phenotype Associations

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

increased brain sterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain meninges morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent brain internal capsule Gene Set

From MPO Gene-Phenotype Associations

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

brain vascular congestion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain iron level Gene Set

From MPO Gene-Phenotype Associations

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

absent brain ventricles Gene Set

From MPO Gene-Phenotype Associations

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

delayed brain development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain wave pattern Gene Set

From MPO Gene-Phenotype Associations

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

brain atrophy Gene Set

From MPO Gene-Phenotype Associations

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

decreased brain size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain ventricular system morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain ventricular system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain ventricle size Gene Set

From MPO Gene-Phenotype Associations

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

brain inflammation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal blood-brain barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-brain barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

collapsed brain ventricles Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain copper level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain weight Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain ependyma motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain ependyma motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain ependyma morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased brain cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain zinc level Gene Set

From MPO Gene-Phenotype Associations

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

brain aneurysm Gene Set

From MPO Gene-Phenotype Associations

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

increased brain tumor incidence Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain vasculature morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased brain sterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain size Gene Set

From MPO Gene-Phenotype Associations

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

absent brain ependyma motile cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent brain ependyma motile cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain pia mater morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain pia mater morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain ventricle morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased brain weight Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain ependyma motile cilium physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged brain ventricles Gene Set

From MPO Gene-Phenotype Associations

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

decreased brain zinc level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain commissure morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased susceptibility to ischemic brain injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to ischemic brain injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dilated brain ventricles Gene Set

From MPO Gene-Phenotype Associations

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

decreased brain internal capsule size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased brain internal capsule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased brain size Gene Set

From MPO Gene-Phenotype Associations

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

increased brain copper level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain interneuron morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain internal capsule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain internal capsule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased brain cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased brain weight Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain dura mater morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain dura mater morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

brain ventricle stenosis Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to ischemic brain injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ischemic brain injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased brain copper level Gene Set

From MPO Gene-Phenotype Associations

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

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic destruction of the brain, subependymal calcification, and cataracts 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.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

brain tumor-polyposis syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain tumor-polyposis syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration with brain iron accumulation 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration with brain iron accumulation 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration with brain iron accumulation 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration with brain iron accumulation 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration with brain iron accumulation 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration with brain iron accumulation 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration with brain iron accumulation 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration with brain iron accumulation 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration with brain iron accumulation 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration with brain iron accumulation 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

{intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{prostate cancer/brain cancer susceptibility, somatic} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {prostate cancer/brain cancer susceptibility, somatic} phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

[creatine kinase, brain type, ectopic expression of] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [creatine kinase, brain type, ectopic expression of] phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

dopamine receptor d2, reduced brain density of Gene Set

From OMIM Gene-Disease Associations

genes associated with the dopamine receptor d2, reduced brain density of phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

neurodegeneration with brain iron accululation 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the neurodegeneration with brain iron accululation 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

brain Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Fetal Brain Male Gene Set

From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles

genes with high or low DNA methylation in Fetal Brain Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.

H3K4me1_Fetal Brain Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me1_Fetal Brain histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K9me3_Fetal Brain Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9me3_Fetal Brain histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27me3_Fetal Brain Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27me3_Fetal Brain histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me3_Fetal Brain Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_Fetal Brain histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K36me3_Fetal Brain Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K36me3_Fetal Brain histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A7IQ-01A-21R-A34F-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A7IQ-01A-21R-A34F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DB-A75K-01A-11R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DB-A75K-01A-11R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-A5TT-01A-11R-A28M-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-A5TT-01A-11R-A28M-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DH-5141-01A-01R-1470-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DH-5141-01A-01R-1470-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-CS-5390-01A-02R-1470-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-CS-5390-01A-02R-1470-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7692-01A-12R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7692-01A-12R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-8167-01A-11R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-8167-01A-11R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-6397-02A-12R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-6397-02A-12R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-CS-4942-01A-01R-1470-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-CS-4942-01A-01R-1470-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7676-01A-11R-2403-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7676-01A-11R-2403-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-8182-01A-11R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-8182-01A-11R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-CS-4938-01B-11R-1896-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-CS-4938-01B-11R-1896-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-A87Q-01A-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-A87Q-01A-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-8165-01A-11R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-8165-01A-11R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-8186-01A-11R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-8186-01A-11R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A7R4-01A-12R-A34R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A7R4-01A-12R-A34R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-7637-01A-11R-2090-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-7637-01A-11R-2090-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DB-A64W-01A-11R-A29R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DB-A64W-01A-11R-A29R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TM-A84J-01A-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TM-A84J-01A-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DB-A75L-01A-11R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DB-A75L-01A-11R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-P5-A5F0-01A-11R-A28M-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-P5-A5F0-01A-11R-A28M-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A7QX-01A-11R-A34F-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A7QX-01A-11R-A34F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DH-A66B-01A-11R-A29R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DH-A66B-01A-11R-A29R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-CS-5397-01A-01R-1896-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-CS-5397-01A-01R-1896-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-WY-A85E-01A-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-WY-A85E-01A-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DH-A7UU-01A-12R-A34F-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DH-A7UU-01A-12R-A34F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-A60J-01A-11R-A28M-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-A60J-01A-11R-A28M-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-E1-A7YK-01A-11R-A34F-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-E1-A7YK-01A-11R-A34F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A7J1-01A-21R-A34R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A7J1-01A-21R-A34R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DB-A64X-01A-11R-A29R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DB-A64X-01A-11R-A29R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-E1-A7YO-01A-11R-A34F-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-E1-A7YO-01A-11R-A34F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-A74O-01A-11R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-A74O-01A-11R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-A5RA-01A-11R-A28M-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-A5RA-01A-11R-A28M-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-IK-8125-01A-11R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-IK-8125-01A-11R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7856-01A-11R-2403-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7856-01A-11R-2403-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7879-01A-11R-2403-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7879-01A-11R-2403-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HW-7490-01A-11R-2027-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HW-7490-01A-11R-2027-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7681-01A-11R-2403-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7681-01A-11R-2403-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RN-01A-11R-A33Z-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RN-01A-11R-A33Z-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-A7T8-01A-21R-A34R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-A7T8-01A-21R-A34R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-QH-A6X5-01A-12R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-QH-A6X5-01A-12R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A7J3-01A-21R-A34R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A7J3-01A-21R-A34R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-5871-01A-12R-1708-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-5871-01A-12R-1708-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7478-01A-11R-2027-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7478-01A-11R-2027-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-E1-5311-01A-01R-1470-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-E1-5311-01A-01R-1470-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-7634-01A-11R-2090-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-7634-01A-11R-2090-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-8111-01A-11R-2404-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-8111-01A-11R-2404-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DB-5280-01A-01R-1470-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DB-5280-01A-01R-1470-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RI-01A-11R-A33Z-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RI-01A-11R-A33Z-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-CS-6670-01A-11R-1896-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-CS-6670-01A-11R-1896-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7475-01A-11R-2027-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7475-01A-11R-2027-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TM-A7C3-01A-11R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TM-A7C3-01A-11R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-6542-01A-11R-1896-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-6542-01A-11R-1896-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-6403-01A-11R-1708-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-6403-01A-11R-1708-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-5854-01A-11R-1708-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-5854-01A-11R-1708-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-A76O-01A-11R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-A76O-01A-11R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-P5-A5ET-01A-11R-A27Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-P5-A5ET-01A-11R-A27Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7687-01A-11R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7687-01A-11R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A6TX-01A-21R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A6TX-01A-21R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RV-01A-21R-A34F-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RV-01A-21R-A34F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A6U5-01A-12R-A33Z-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A6U5-01A-12R-A33Z-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7680-01A-11R-2256-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7680-01A-11R-2256-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-5963-02A-12R-A29R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-5963-02A-12R-A29R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TM-A84O-01A-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TM-A84O-01A-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-A60L-01A-12R-A31N-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-FG-A60L-01A-12R-A31N-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-7603-01A-21R-2090-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-7603-01A-21R-2090-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-QH-A6XC-01A-12R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-QH-A6XC-01A-12R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RV-02A-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RV-02A-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DH-A669-01A-12R-A31N-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DH-A669-01A-12R-A31N-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-6396-01A-11R-1708-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-6396-01A-11R-1708-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-VW-A8FI-01A-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-VW-A8FI-01A-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-R8-A6MO-01A-11R-A33Z-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-R8-A6MO-01A-11R-A33Z-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-E1-A7YS-01A-11R-A34F-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-E1-A7YS-01A-11R-A34F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-A5TP-01A-11R-A28M-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-A5TP-01A-11R-A28M-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-QH-A6XA-01A-12R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-QH-A6XA-01A-12R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-HT-A74L-01A-11R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-HT-A74L-01A-11R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-7304-01A-12R-2090-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-7304-01A-12R-2090-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-QH-A65R-01A-21R-A31N-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-QH-A65R-01A-21R-A31N-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DB-5275-01A-01R-1470-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DB-5275-01A-01R-1470-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A7R8-01A-11R-A34R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A7R8-01A-11R-A34R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RM-01A-11R-A33Z-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RM-01A-11R-A33Z-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-CS-6668-01A-11R-1896-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-CS-6668-01A-11R-1896-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-VM-A8CD-01A-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-VM-A8CD-01A-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-R8-A6ML-01A-11R-A32Q-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-R8-A6ML-01A-11R-A32Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RJ-01A-11R-A33Z-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-TQ-A7RJ-01A-11R-A33Z-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DB-A4XB-01A-11R-A26U-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DB-A4XB-01A-11R-A26U-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-E1-5304-01A-01R-1470-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-E1-5304-01A-01R-1470-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-S9-A7R7-01A-11R-A34R-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-S9-A7R7-01A-11R-A34R-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-FG-A4MT-02A-11R-A29R-07 Gene Set