Synthetic Defect Of Bile Acids

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Results for "Synthetic Defect Of Bile Acids": 13 genes, 717 gene sets

Name
MPDU1 Gene mannose-P-dolichol utilization defect* 1* This gene encodes an endoplasmic reticulum membrane protein that is required for utilization of the mannose donor mannose-P-dolichol in the synthesis of lipid-linked oligosaccharides and glycosylphosphatidylinositols. Mutations in this gene result in congenital disorder of glycosylation type If. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]
IGAT Gene Immune response to synthetic* polypeptide--IRGAT*
ASD1 Gene atrial septal defect* 1*
IGLP1 Gene immune response to synthetic* polypeptides 1*
IGLP2 Gene immune response to synthetic* polypeptides 2*
AVSD1 Gene atrioventricular septal defect* 1*
GBA2 Gene glucosidase, beta (bile* acid) 2* This gene encodes a microsomal beta-glucosidase that catalyzes the hydrolysis of bile acid 3-O-glucosides as endogenous compounds. Studies to determine subcellular localization of this protein in the liver indicated that the enzyme was mainly enriched in the microsomal fraction where it appeared to be confined to the endoplasmic reticulum. This putative transmembrane protein is thought to play a role in carbohydrate transport and metabolism. [provided by RefSeq, Jul 2008]
GPBAR1 Gene G protein-coupled bile* acid receptor 1* This gene encodes a member of the G protein-coupled receptor (GPCR) superfamily. This enzyme functions as a cell surface receptor for bile acids. Treatment of cells expressing this GPCR with bile acids induces the production of intracellular cAMP, activation of a MAP kinase signaling pathway, and internalization of the receptor. The receptor is implicated in the suppression of macrophage functions and regulation of energy homeostasis by bile acids. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]
SLC10A2 Gene solute carrier family 10 (sodium/bile* acid cotransporter), member 2* This gene encodes a sodium/bile acid cotransporter. This transporter is the primary mechanism for uptake of intestinal bile acids by apical cells in the distal ileum. Bile acids are the catabolic product of cholesterol metabolism, so this protein is also critical for cholesterol homeostasis. Mutations in this gene cause primary bile acid malabsorption (PBAM); muatations in this gene may also be associated with other diseases of the liver and intestines, such as familial hypertriglyceridemia (FHTG). [provided by RefSeq, Mar 2010]
SLC10A6 Gene solute carrier family 10 (sodium/bile* acid cotransporter), member 6* Predicted to enable bile acid:sodium symporter activity. Predicted to be involved in bile acid and bile salt transport. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]
BAATP1 Gene bile acid CoA: amino acid N-acyltransferase pseudogene 1
BAAT Gene bile acid CoA:amino acid N-acyltransferase The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
SLC10A1 Gene solute carrier family 10 (sodium/bile* acid cotransporter), member 1* The protein encoded by this gene belongs to the sodium/bile acid cotransporter family, which are integral membrane glycoproteins that participate in the enterohepatic circulation of bile acids. Two homologous transporters are involved in the reabsorption of bile acids; the ileal sodium/bile acid cotransporter with an apical cell localization that absorbs bile acids from the intestinal lumen, bile duct and kidney, and the liver-specific sodium/bile acid cotransporter, represented by this protein, that is found in the basolateral membranes of hepatocytes. Bile acids are the catabolic product of cholesterol metabolism, hence this protein is important for cholesterol homeostasis. [provided by RefSeq, Oct 2011]
Synthetic Defect Of Bile Acids Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Synthetic Defect Of Bile Acids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol pathway from the Reactome Pathways dataset.
Synthesis of bile acids and bile salts Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of bile acids and bile salts pathway from the Reactome Pathways dataset.
Synthesis of bile acids and bile salts via 24-hydroxycholesterol Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of bile acids and bile salts via 24-hydroxycholesterol pathway from the Reactome Pathways dataset.
Synthesis of bile acids and bile salts via 27-hydroxycholesterol Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of bile acids and bile salts via 27-hydroxycholesterol pathway from the Reactome Pathways dataset.
Synthesis of bile acids and bile salts Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of bile acids and bile salts pathway from the Reactome Pathways 2024 dataset.
Synthesis of bile acids and bile salts via 24-hydroxycholesterol Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of bile acids and bile salts via 24-hydroxycholesterol pathway from the Reactome Pathways 2024 dataset.
Synthesis of bile acids and bile salts via 27-hydroxycholesterol Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of bile acids and bile salts via 27-hydroxycholesterol pathway from the Reactome Pathways 2024 dataset.
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol pathway from the Reactome Pathways 2024 dataset.
Bile Acids and Salts Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.
Recycling of bile acids and salts Gene Set From Reactome Pathways 2014 proteins participating in the Recycling of bile acids and salts pathway from the Reactome Pathways dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Enterohepatic circulation of bile acids Gene Set From WikiPathways Pathways 2024 proteins participating in the Enterohepatic circulation of bile acids pathway from the WikiPathways Pathways 2024 dataset.
Recycling of bile acids and salts Gene Set From Reactome Pathways 2024 proteins participating in the Recycling of bile acids and salts pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
bile acid and bile salt transport Gene Set From GO Biological Process Annotations 2015 genes participating in the bile acid and bile salt transport biological process from the curated GO Biological Process Annotations 2015 dataset.
Bile acid and bile salt metabolism Gene Set From Reactome Pathways 2014 proteins participating in the Bile acid and bile salt metabolism pathway from the Reactome Pathways dataset.
bile acid and bile salt transport Gene Set From GO Biological Process Annotations 2023 genes participating in the bile acid and bile salt transport biological process from the curated GO Biological Process Annotations 2023 dataset.
Bile acid and bile salt metabolism Gene Set From Reactome Pathways 2024 proteins participating in the Bile acid and bile salt metabolism pathway from the Reactome Pathways 2024 dataset.
bile acid and bile salt transport Gene Set From GO Biological Process Annotations 2025 genes participating in the bile acid and bile salt transport biological process from the curated GO Biological Process Annotations 2025 dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile acid synthesis defect, congenital, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.
Bile acid synthesis defect, congenital, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.
congenital bile acid synthesis defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile acid synthesis defect, congenital, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
bile acid synthesis defect, congenital, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
bile acid synthesis defect, congenital, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
bile acid synthesis defect, congenital, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid synthesis defect, congenital, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.
Bile Acid Synthesis Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Acid Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Bile Acid Synthesis Defect Type 3 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Bile Acid Synthesis Defect Type 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital bile acid synthesis defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bile acid synthesis defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital bile acid synthesis defect 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital bile acid synthesis defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital bile acid synthesis defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bile acid synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bile acid conjugation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bile acid conjugation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FSL-1 lipoprotein, synthetic Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical FSL-1 lipoprotein, synthetic from the curated CTD Gene-Chemical Interactions dataset.
IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGAT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGAT from the curated CTD Gene-Disease Associations dataset.
synthetic hemodialysis graft failure Gene Set From GAD Gene-Disease Associations genes associated with the disease synthetic hemodialysis graft failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
synthetic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term synthetic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Abuse Of Synthetic Cathinone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abuse Of Synthetic Cathinone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synthetic smooth muscle cell_Heart_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Synthetic smooth muscle cell_Heart_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
ESTROGENS, CONJUGATED SYNTHETIC A Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ESTROGENS, CONJUGATED SYNTHETIC A drug from theDGIdb Drug Targets 2026 dataset.
SYNTHETIC CONJUGATED ESTROGENS, A Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SYNTHETIC CONJUGATED ESTROGENS, A drug from theDGIdb Drug Targets 2026 dataset.
SYNTHETIC CONJUGATED ESTROGENS, B Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SYNTHETIC CONJUGATED ESTROGENS, B drug from theDGIdb Drug Targets 2026 dataset.
SECRETIN HUMAN, SYNTHETIC Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SECRETIN HUMAN, SYNTHETIC drug from theDGIdb Drug Targets 2026 dataset.
SECRETIN SYNTHETIC PORCINE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SECRETIN SYNTHETIC PORCINE drug from theDGIdb Drug Targets 2026 dataset.
Hydroxyeicosatetraenoic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Hydroxyeicosatetraenoic Acids from the curated CTD Gene-Chemical Interactions dataset.
Hydroxy Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Hydroxy Acids from the curated CTD Gene-Chemical Interactions dataset.
Fibric Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fibric Acids from the curated CTD Gene-Chemical Interactions dataset.
Aminosalicylic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Aminosalicylic Acids from the curated CTD Gene-Chemical Interactions dataset.
Amino Acids, Peptides, and Proteins Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids, Omega-6 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids, Omega-6 from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids, Volatile Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids, Volatile from the curated CTD Gene-Chemical Interactions dataset.
Phosphorous Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Phosphorous Acids from the curated CTD Gene-Chemical Interactions dataset.
thiosulfinic acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical thiosulfinic acids from the curated CTD Gene-Chemical Interactions dataset.
Sulfenic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Sulfenic Acids from the curated CTD Gene-Chemical Interactions dataset.
Hydroxamic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Hydroxamic Acids from the curated CTD Gene-Chemical Interactions dataset.
Linoleic Acids, Conjugated Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Linoleic Acids, Conjugated from the curated CTD Gene-Chemical Interactions dataset.
Carboxylic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Carboxylic Acids from the curated CTD Gene-Chemical Interactions dataset.
Dicarboxylic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Dicarboxylic Acids from the curated CTD Gene-Chemical Interactions dataset.
Coumaric Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Coumaric Acids from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids, Nonesterified Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids, Nonesterified from the curated CTD Gene-Chemical Interactions dataset.
Anacardic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Anacardic Acids from the curated CTD Gene-Chemical Interactions dataset.
Pentanoic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Pentanoic Acids from the curated CTD Gene-Chemical Interactions dataset.
Arachidonic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Arachidonic Acids from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids, Monounsaturated Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids, Monounsaturated from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids from the curated CTD Gene-Chemical Interactions dataset.
Phthalic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Phthalic Acids from the curated CTD Gene-Chemical Interactions dataset.
Heptanoic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Heptanoic Acids from the curated CTD Gene-Chemical Interactions dataset.
Boric Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Boric Acids from the curated CTD Gene-Chemical Interactions dataset.
Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Acids from the curated CTD Gene-Chemical Interactions dataset.
Linolenic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Linolenic Acids from the curated CTD Gene-Chemical Interactions dataset.
Pteroylpolyglutamic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Pteroylpolyglutamic Acids from the curated CTD Gene-Chemical Interactions dataset.
Phosphatidic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Phosphatidic Acids from the curated CTD Gene-Chemical Interactions dataset.
Nicotinic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Nicotinic Acids from the curated CTD Gene-Chemical Interactions dataset.
Sialic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Sialic Acids from the curated CTD Gene-Chemical Interactions dataset.
Docosahexaenoic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Docosahexaenoic Acids from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids, Unsaturated Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids, Unsaturated from the curated CTD Gene-Chemical Interactions dataset.
Isonicotinic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Isonicotinic Acids from the curated CTD Gene-Chemical Interactions dataset.
Aristolochic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Aristolochic Acids from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids, Essential Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids, Essential from the curated CTD Gene-Chemical Interactions dataset.
Fatty Acids, Omega-3 Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Fatty Acids, Omega-3 from the curated CTD Gene-Chemical Interactions dataset.
Sulfinic Acids Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Sulfinic Acids from the curated CTD Gene-Chemical Interactions dataset.
BETA-AMINO ACIDS, RENAL TRANSPORT OF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BETA-AMINO ACIDS, RENAL TRANSPORT OF from the curated CTD Gene-Disease Associations dataset.
Docosahexaenoic Acids Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Docosahexaenoic Acids in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
docosahexaenoic acids Gene Set From GAD Gene-Disease Associations genes associated with the disease docosahexaenoic acids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polyunsaturated fatty acids Gene Set From GAD Gene-Disease Associations genes associated with the disease polyunsaturated fatty acids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acids Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term acids in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2015 genes performing the endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2015 dataset.
endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2015 genes performing the endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2015 dataset.
exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2015 genes performing the exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
elevated long chain fatty acids Gene Set From HPO Gene-Disease Associations genes associated with the elevated long chain fatty acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
elevated plasma branched chain amino acids Gene Set From HPO Gene-Disease Associations genes associated with the elevated plasma branched chain amino acids phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Large neutral amino acids transporter small subunit 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Large neutral amino acids transporter small subunit 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
decreased liver free fatty acids level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal free fatty acids level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal circulating free fatty acids level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased liver free fatty acids level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased liver free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
[polyunsaturated fatty acids plasma level qtl1] Gene Set From OMIM Gene-Disease Associations genes associated with the [polyunsaturated fatty acids plasma level qtl1] phenotype from the curated OMIM Gene-Disease Associations dataset.
Fatty acids Gene Set From Reactome Pathways 2014 proteins participating in the Fatty acids pathway from the Reactome Pathways dataset.
Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) pathway from the Reactome Pathways dataset.
mitochondrial fatty acid beta-oxidation of unsaturated fatty acids Gene Set From Reactome Pathways 2014 proteins participating in the mitochondrial fatty acid beta-oxidation of unsaturated fatty acids pathway from the Reactome Pathways dataset.
Synthesis of 5-eicosatetraenoic acids Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of 5-eicosatetraenoic acids pathway from the Reactome Pathways dataset.
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) pathway from the Reactome Pathways dataset.
Transport of fatty acids Gene Set From Reactome Pathways 2014 proteins participating in the Transport of fatty acids pathway from the Reactome Pathways dataset.
Beta-oxidation of very long chain fatty acids Gene Set From Reactome Pathways 2014 proteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways dataset.
Conjugation of carboxylic acids Gene Set From Reactome Pathways 2014 proteins participating in the Conjugation of carboxylic acids pathway from the Reactome Pathways dataset.
mitochondrial fatty acid beta-oxidation of saturated fatty acids Gene Set From Reactome Pathways 2014 proteins participating in the mitochondrial fatty acid beta-oxidation of saturated fatty acids pathway from the Reactome Pathways dataset.
Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion Gene Set From Reactome Pathways 2014 proteins participating in the Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion pathway from the Reactome Pathways dataset.
Free fatty acids regulate insulin secretion Gene Set From Reactome Pathways 2014 proteins participating in the Free fatty acids regulate insulin secretion pathway from the Reactome Pathways dataset.
Transport of inorganic cations/anions and amino acids/oligopeptides Gene Set From Reactome Pathways 2014 proteins participating in the Transport of inorganic cations/anions and amino acids/oligopeptides pathway from the Reactome Pathways dataset.
Metabolism of amino acids and derivatives Gene Set From Reactome Pathways 2014 proteins participating in the Metabolism of amino acids and derivatives pathway from the Reactome Pathways dataset.
Elevated Plasma Branched Chain Amino Acids Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Plasma Branched Chain Amino Acids in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
clearance of foreign intracellular nucleic acids Gene Set From GO Biological Process Annotations 2023 genes participating in the clearance of foreign intracellular nucleic acids biological process from the curated GO Biological Process Annotations 2023 dataset.
endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2023 genes performing the endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2023 dataset.
exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2023 genes performing the exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2023 dataset.
endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2023 genes performing the endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal circulating free fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased circulating free fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased circulating free fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased saturated fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased saturated fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased unsaturated fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased unsaturated fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased unsaturated fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased unsaturated fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased saturated fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased saturated fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased liver free fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased liver free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal free fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased liver free fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased liver free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased muscle free fatty acids level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased muscle free fatty acids level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased circulating free fatty acids level Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased circulating free fatty acids level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
increased circulating free fatty acids level Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased circulating free fatty acids level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
4 hydroxytamoxifen dexamethasone and retinoic acids regulation of p27 expression Gene Set From WikiPathways Pathways 2024 proteins participating in the 4 hydroxytamoxifen dexamethasone and retinoic acids regulation of p27 expression pathway from the WikiPathways Pathways 2024 dataset.
Methionine metabolism leading to sulfur amino acids and related disorders Gene Set From WikiPathways Pathways 2024 proteins participating in the Methionine metabolism leading to sulfur amino acids and related disorders pathway from the WikiPathways Pathways 2024 dataset.
Fatty acids and lipoproteins transport in hepatocytes Gene Set From WikiPathways Pathways 2024 proteins participating in the Fatty acids and lipoproteins transport in hepatocytes pathway from the WikiPathways Pathways 2024 dataset.
Omega 6 fatty acids in senescence Gene Set From WikiPathways Pathways 2024 proteins participating in the Omega 6 fatty acids in senescence pathway from the WikiPathways Pathways 2024 dataset.
Amino acids regulate mTORC1 Gene Set From Reactome Pathways 2024 proteins participating in the Amino acids regulate mTORC1 pathway from the Reactome Pathways 2024 dataset.
Beta-oxidation of very long chain fatty acids Gene Set From Reactome Pathways 2024 proteins participating in the Beta-oxidation of very long chain fatty acids pathway from the Reactome Pathways 2024 dataset.
Conjugation of carboxylic acids Gene Set From Reactome Pathways 2024 proteins participating in the Conjugation of carboxylic acids pathway from the Reactome Pathways 2024 dataset.
Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion Gene Set From Reactome Pathways 2024 proteins participating in the Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion pathway from the Reactome Pathways 2024 dataset.
Fatty acids Gene Set From Reactome Pathways 2024 proteins participating in the Fatty acids pathway from the Reactome Pathways 2024 dataset.
Free fatty acids regulate insulin secretion Gene Set From Reactome Pathways 2024 proteins participating in the Free fatty acids regulate insulin secretion pathway from the Reactome Pathways 2024 dataset.
Intracellular metabolism of fatty acids regulates insulin secretion Gene Set From Reactome Pathways 2024 proteins participating in the Intracellular metabolism of fatty acids regulates insulin secretion pathway from the Reactome Pathways 2024 dataset.
Metabolism of amino acids and derivatives Gene Set From Reactome Pathways 2024 proteins participating in the Metabolism of amino acids and derivatives pathway from the Reactome Pathways 2024 dataset.
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) pathway from the Reactome Pathways 2024 dataset.
Synthesis of 5-eicosatetraenoic acids Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of 5-eicosatetraenoic acids pathway from the Reactome Pathways 2024 dataset.
Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) pathway from the Reactome Pathways 2024 dataset.
Transport of fatty acids Gene Set From Reactome Pathways 2024 proteins participating in the Transport of fatty acids pathway from the Reactome Pathways 2024 dataset.
Transport of inorganic cations/anions and amino acids/oligopeptides Gene Set From Reactome Pathways 2024 proteins participating in the Transport of inorganic cations/anions and amino acids/oligopeptides pathway from the Reactome Pathways 2024 dataset.
mitochondrial fatty acid beta-oxidation of saturated fatty acids Gene Set From Reactome Pathways 2024 proteins participating in the mitochondrial fatty acid beta-oxidation of saturated fatty acids pathway from the Reactome Pathways 2024 dataset.
mitochondrial fatty acid beta-oxidation of unsaturated fatty acids Gene Set From Reactome Pathways 2024 proteins participating in the mitochondrial fatty acid beta-oxidation of unsaturated fatty acids pathway from the Reactome Pathways 2024 dataset.
clearance of foreign intracellular nucleic acids Gene Set From GO Biological Process Annotations 2025 genes participating in the clearance of foreign intracellular nucleic acids biological process from the curated GO Biological Process Annotations 2025 dataset.
endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2025 genes performing the endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2025 dataset.
exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2025 genes performing the exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2025 dataset.
endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters Gene Set From GO Molecular Function Annotations 2025 genes performing the endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Hyperinsulinemia x saturated fatty acids interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hyperinsulinemia x saturated fatty acids interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Homeostasis model assessment of insulin resistance x saturated fatty acids interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance x saturated fatty acids interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Biosynthesis of unsaturated fatty acids Gene Set From KEGG Pathways 2026 proteins participating in the Biosynthesis of unsaturated fatty acids pathway from the KEGG Pathways 2026 dataset.
OMEGA-3 FATTY ACIDS Gene Set From DGIdb Drug Targets 2026 interacting proteins for the OMEGA-3 FATTY ACIDS drug from theDGIdb Drug Targets 2026 dataset.
Bile acid malabsorption, primary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bile acid malabsorption, primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bile Duct Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile Duct Neoplasms from the curated CTD Gene-Disease Associations dataset.
Bile Duct Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile Duct Diseases from the curated CTD Gene-Disease Associations dataset.
Bile Acid Malabsorption, Primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bile Acid Malabsorption, Primary from the curated CTD Gene-Disease Associations dataset.
Adenoma, Bile Duct Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adenoma, Bile Duct from the curated CTD Gene-Disease Associations dataset.
bile duct disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bile duct disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bile duct disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bile duct disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
bile duct mucoepidermoid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct mucoepidermoid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile duct adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile duct adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile reflux Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile reflux in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
common bile duct disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease common bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile duct sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile duct carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
extrahepatic bile duct carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrahepatic bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
extrahepatic bile duct adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrahepatic bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile duct disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile duct cystadenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct cystadenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile duct cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bile lipid composition and cholesterol gallstone Gene Set From GAD Gene-Disease Associations genes associated with the disease bile lipid composition and cholesterol gallstone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoma; carcinoma; common bile duct neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoma; carcinoma; common bile duct neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; gallbladder neoplasms; gallstones Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; gallbladder neoplasms; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesterol, ldl; bile acid synthesis Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; bile acid synthesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease alagille syndrome; paucity of interlobular bile ducts (pilbd); pulmonary valve stenosis; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; biliary calculi; gallstones Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; biliary calculi; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, pancreatic ductal; common bile duct neoplasms; pancreatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, pancreatic ductal; common bile duct neoplasms; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile duct neoplasms; cholangiocarcinoma; Gene Set From GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bile Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term bile in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
response to bile acid Gene Set From GO Biological Process Annotations 2015 genes participating in the response to bile acid biological process from the curated GO Biological Process Annotations 2015 dataset.
common bile duct development Gene Set From GO Biological Process Annotations 2015 genes participating in the common bile duct development biological process from the curated GO Biological Process Annotations 2015 dataset.
bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
cellular response to bile acid Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to bile acid biological process from the curated GO Biological Process Annotations 2015 dataset.
intrahepatic bile duct development Gene Set From GO Biological Process Annotations 2015 genes participating in the intrahepatic bile duct development biological process from the curated GO Biological Process Annotations 2015 dataset.
canalicular bile acid transport Gene Set From GO Biological Process Annotations 2015 genes participating in the canalicular bile acid transport biological process from the curated GO Biological Process Annotations 2015 dataset.
bile acid catabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the bile acid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
bile acid metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the bile acid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
bile acid signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the bile acid signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
cell surface bile acid receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the cell surface bile acid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
intracellular bile acid receptor signaling pathway Gene Set From GO Biological Process Annotations 2015 genes participating in the intracellular bile acid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
bile acid secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the bile acid secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
bile acid conjugation Gene Set From GO Biological Process Annotations 2015 genes participating in the bile acid conjugation biological process from the curated GO Biological Process Annotations 2015 dataset.
bile acid-exporting atpase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the bile acid-exporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
bile acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the bile acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
bile acid receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the bile acid receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
bile acid binding Gene Set From GO Molecular Function Annotations 2015 genes performing the bile acid binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
bile-salt sulfotransferase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the bile-salt sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
bile acid:sodium symporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the bile acid:sodium symporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
canalicular bile acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the canalicular bile acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
g-protein coupled bile acid receptor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the g-protein coupled bile acid receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
bile duct disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease bile duct disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
abnormality of the intrahepatic bile duct Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased serum bile acid concentration during pregnancy Gene Set From HPO Gene-Disease Associations genes associated with the increased serum bile acid concentration during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced number of intrahepatic bile ducts Gene Set From HPO Gene-Disease Associations genes associated with the reduced number of intrahepatic bile ducts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased serum bile acid concentration Gene Set From HPO Gene-Disease Associations genes associated with the increased serum bile acid concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bile duct proliferation Gene Set From HPO Gene-Disease Associations genes associated with the bile duct proliferation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Bile Duct Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bile Duct Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Common Bile Duct Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Common Bile Duct Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
bile acid biosynthesis, neutral pathway Gene Set From HumanCyc Pathways proteins participating in the bile acid biosynthesis, neutral pathway pathway from the HumanCyc Pathways dataset.
Putative sodium bile acid cotransporter Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Putative sodium bile acid cotransporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Bile salt export pump Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Bile salt export pump protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Acyl-CoA thioester hydrolase/bile acid-CoA amino acid N-acetyltransferase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-CoA thioester hydrolase/bile acid-CoA amino acid N-acetyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Bile acid:sodium symporter Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Bile acid:sodium symporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Bile acid:sodium symporter/arsenical resistance protein Acr3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Bile acid:sodium symporter/arsenical resistance protein Acr3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
bile acid biosynthesis Gene Set From KEGG Pathways proteins participating in the bile acid biosynthesis pathway from the KEGG Pathways dataset.
abnormal extrahepatic bile duct morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal extrahepatic bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile salt homeostasis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile salt homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile duct morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased bile salt level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased bile salt level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dilated bile duct Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated bile duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile composition Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile composition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile duct development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bile duct hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the bile duct hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile duct physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bile duct proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the bile duct proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bile duct inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the bile duct inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal common bile duct morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal common bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile color Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile color phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile canaliculus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile canaliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal intrahepatic bile duct morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal intrahepatic bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bile salt level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bile salt level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
bile acid malabsorption, primary Gene Set From OMIM Gene-Disease Associations genes associated with the bile acid malabsorption, primary phenotype from the curated OMIM Gene-Disease Associations dataset.
Bile salt and organic anion SLC transporters Gene Set From Reactome Pathways 2014 proteins participating in the Bile salt and organic anion SLC transporters pathway from the Reactome Pathways dataset.
bile Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue bile from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
bile ductule Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile ductule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
bile canaliculus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile canaliculus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
bile duct cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile duct cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
bile duct epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
bile Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
bile duct Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Drug Induction of Bile Acid Pathway(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Drug Induction of Bile Acid Pathway(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Congenital Atresia Of Extrahepatic Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atresia Of Extrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Proliferation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrosis Of Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Advanced Bile Duct Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Advanced Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Carcinoma Of Extrahepatic Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Carcinoma Of Extrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Adenoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Cystadenocarcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Cystadenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Liver And Intrahepatic Bile Duct Epithelial Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Liver And Intrahepatic Bile Duct Epithelial Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Liver And Intrahepatic Bile Duct Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Liver And Intrahepatic Bile Duct Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Tumor Of Extrahepatic Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Extrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Acid Diarrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Acid Diarrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Cancer Resectable Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Cancer Resectable in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stricture Of Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stricture Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metastatic Bile Duct Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Reflux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Reflux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Acid Malabsorption Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Acid Malabsorption in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Bile Duct Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypoplasia Of Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Intrahepatic Bile Duct Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Intrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Bile Duct Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Adenocarcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Duct Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Acid Malabsorption, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Acid Malabsorption, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Perinatal Jaundice Due To Inspissated Bile Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Perinatal Jaundice Due To Inspissated Bile Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bile Acid Coa Ligase Deficiency And Defective Amidation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bile Acid Coa Ligase Deficiency And Defective Amidation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Increased Serum Bile Acid Concentration During Pregnancy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Serum Bile Acid Concentration During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Common Bile Duct Calculi Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Common Bile Duct Calculi in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Serum Bile Acid Concentration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Serum Bile Acid Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Reduced Number Of Intrahepatic Bile Ducts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Number Of Intrahepatic Bile Ducts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
bile acid secretion Gene Set From GO Biological Process Annotations 2023 genes participating in the bile acid secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
bile acid metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the bile acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
canalicular bile acid transport Gene Set From GO Biological Process Annotations 2023 genes participating in the canalicular bile acid transport biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of bile acid secretion Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of bile acid secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of bile acid metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of bile acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
response to bile acid Gene Set From GO Biological Process Annotations 2023 genes participating in the response to bile acid biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
cellular response to bile acid Gene Set From GO Biological Process Annotations 2023 genes participating in the cellular response to bile acid biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of bile acid secretion Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of bile acid secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
bile acid conjugation Gene Set From GO Biological Process Annotations 2023 genes participating in the bile acid conjugation biological process from the curated GO Biological Process Annotations 2023 dataset.
cell surface bile acid receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the cell surface bile acid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
intracellular bile acid receptor signaling pathway Gene Set From GO Biological Process Annotations 2023 genes participating in the intracellular bile acid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of bile acid metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of bile acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of bile acid metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of bile acid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
ABC-type bile acid transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the ABC-type bile acid transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
canalicular bile acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the canalicular bile acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
bile acid binding Gene Set From GO Molecular Function Annotations 2023 genes performing the bile acid binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
bile-salt sulfotransferase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the bile-salt sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
bile acid:sodium symporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the bile acid:sodium symporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
G protein-coupled bile acid receptor activity Gene Set From GO Molecular Function Annotations 2023 genes performing the G protein-coupled bile acid receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal bile duct development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile duct development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile salt homeostasis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile salt homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile salt level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile salt level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased bile salt level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased bile salt level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile canaliculus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile canaliculus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile duct morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bile duct epithelium hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct epithelium hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile composition Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile composition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bile duct inflammation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile secretion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
dilated bile duct Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated bile duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bile duct proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
bile duct hyperplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile color Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile color phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal intrahepatic bile duct morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intrahepatic bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased bile salt level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased bile salt level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal extrahepatic bile duct morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal extrahepatic bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal common bile duct morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal common bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bile duct epithelium morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile duct epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal interlobular bile duct morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interlobular bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Drug induction of bile acid pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Drug induction of bile acid pathway pathway from the WikiPathways Pathways 2024 dataset.
Bile acid synthesis and enterohepatic circulation Gene Set From WikiPathways Pathways 2024 proteins participating in the Bile acid synthesis and enterohepatic circulation pathway from the WikiPathways Pathways 2024 dataset.
Disorders of bile acid synthesis and biliary transport Gene Set From WikiPathways Pathways 2024 proteins participating in the Disorders of bile acid synthesis and biliary transport pathway from the WikiPathways Pathways 2024 dataset.
NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis Gene Set From Reactome Pathways 2024 proteins participating in the NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis pathway from the Reactome Pathways 2024 dataset.
bile acid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the bile acid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
bile acid secretion Gene Set From GO Biological Process Annotations 2025 genes participating in the bile acid secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
canalicular bile acid transport Gene Set From GO Biological Process Annotations 2025 genes participating in the canalicular bile acid transport biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of bile acid secretion Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of bile acid secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of bile acid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of bile acid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
nuclear receptor-mediated bile acid signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the nuclear receptor-mediated bile acid signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
response to bile acid Gene Set From GO Biological Process Annotations 2025 genes participating in the response to bile acid biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
cellular response to bile acid Gene Set From GO Biological Process Annotations 2025 genes participating in the cellular response to bile acid biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of bile acid biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of bile acid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of bile acid secretion Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of bile acid secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
bile acid conjugation Gene Set From GO Biological Process Annotations 2025 genes participating in the bile acid conjugation biological process from the curated GO Biological Process Annotations 2025 dataset.
adenylate cyclase-activating G protein-coupled bile acid receptor signaling pathway Gene Set From GO Biological Process Annotations 2025 genes participating in the adenylate cyclase-activating G protein-coupled bile acid receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of bile acid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of bile acid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of bile acid metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of bile acid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
ABC-type bile acid transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the ABC-type bile acid transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
bile acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the bile acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
canalicular bile acid transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the canalicular bile acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
bile acid binding Gene Set From GO Molecular Function Annotations 2025 genes performing the bile acid binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
bile acid nuclear receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the bile acid nuclear receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
bile-salt sulfotransferase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the bile-salt sulfotransferase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
bile acid:sodium symporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the bile acid:sodium symporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
G protein-coupled bile acid receptor activity Gene Set From GO Molecular Function Annotations 2025 genes performing the G protein-coupled bile acid receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
bile acid-gated sodium channel activity Gene Set From GO Molecular Function Annotations 2025 genes performing the bile acid-gated sodium channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Bile duct disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bile duct cancer Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bile duct adenocarcinoma Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct adenocarcinoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bile duct carcinoma Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct carcinoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Bile duct disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Bile duct disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Common bile duct disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Common bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile reflux Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile reflux in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct cystadenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct cystadenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extrahepatic bile duct carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrahepatic bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Squamous cell bile duct carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Squamous cell bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrahepatic bile duct adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct mucinous adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct mucinous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct mucoepidermoid carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct mucoepidermoid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct signet ring cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct signet ring cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Common bile duct neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Common bile duct neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extrahepatic bile duct adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrahepatic bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrahepatic bile duct cystadenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic bile duct cystadenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct cystadenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct cystadenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extrahepatic bile duct adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrahepatic bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct rhabdomyosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Perforation of bile duct Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Perforation of bile duct in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile duct carcinoma in situ Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct carcinoma in situ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bile Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Bile from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Bile duct Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bile canaliculus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile canaliculus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bile duct epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bile ductule Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile ductule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bile Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bile duct cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile duct cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Bile duct cancer Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bile duct cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal intrahepatic bile duct morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal intrahepatic bile duct morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bile acid malabsorption Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bile acid malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary bile acid biosynthesis Gene Set From KEGG Pathways 2026 proteins participating in the Primary bile acid biosynthesis pathway from the KEGG Pathways 2026 dataset.
Bile secretion Gene Set From KEGG Pathways 2026 proteins participating in the Bile secretion pathway from the KEGG Pathways 2026 dataset.
Dandy-Walker like malformation with atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Protan defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiac conduction defect, nonspecific Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiac conduction defect, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutral 1 amino acid transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular septal defect 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular septal defect 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ventricular septal defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Laron-type isolated somatotropin defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neural tube defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucose-6-phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Iodotyrosine deiodination defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iodotyrosine deiodination defect 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.
Renal carnitine transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect 5 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.
Erythrocyte lactate transporter defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Erythrocyte lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrial septal defect 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrial septal defect 3 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.
Congenital defect of folate absorption Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oocyte maturation defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oocyte maturation defect 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.
Iodotyrosyl coupling defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Iodotyrosyl coupling defect 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.
Sacral defect and anterior sacral meningocele Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele 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.
Cardiac Conduction Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiac Conduction Defect from the curated CTD Gene-Disease Associations dataset.
Atrial septal defect 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial septal defect 2 from the curated CTD Gene-Disease Associations dataset.
ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset.
Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome 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.
Atrial Septal Defect 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 4 from the curated CTD Gene-Disease Associations dataset.
Atrioventricular Canal Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrioventricular Canal Defect from the curated CTD Gene-Disease Associations dataset.
Neural tube defect, folate-sensitive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neural tube defect, folate-sensitive from the curated CTD Gene-Disease Associations dataset.
Atrial Septal Defect 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 6 from the curated CTD Gene-Disease Associations dataset.
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT 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.
Atrial Septal Defect 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 5 from the curated CTD Gene-Disease Associations dataset.
Atrial Septal Defect 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrial Septal Defect 1 from the curated CTD Gene-Disease Associations dataset.
Erythrocyte Lactate Transporter Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrocyte Lactate Transporter Defect 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.
ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.
atrial heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease atrial heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcohol-related birth defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrioventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrial heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
qualitative platelet defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
human spermatogenic defect Gene Set From GAD Gene-Disease Associations genes associated with the disease human spermatogenic defect in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
defect Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term defect in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
conotruncal defect Gene Set From GWASdb SNP-Phenotype Associations genes associated with the conotruncal defect phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
thyroid hormone receptor defect Gene Set From HPO Gene-Disease Associations genes associated with the thyroid hormone receptor defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midline defect of mandible Gene Set From HPO Gene-Disease Associations genes associated with the midline defect of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vertebral segmentation defect Gene Set From HPO Gene-Disease Associations genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene Set From HPO Gene-Disease Associations genes associated with the electron transfer flavoprotein-ubiquinone oxidoreductase defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
secundum atrial septal defect Gene Set From HPO Gene-Disease Associations genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dynein arm defect of respiratory motile cilia Gene Set From HPO Gene-Disease Associations genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
inlet ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thyroid defect in oxidation and organification of iodide Gene Set From HPO Gene-Disease Associations genes associated with the thyroid defect in oxidation and organification of iodide phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
adrenocorticotropin (acth) receptor (acthr) defect Gene Set From HPO Gene-Disease Associations genes associated with the adrenocorticotropin (acth) receptor (acthr) defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sacral segmentation defect Gene Set From HPO Gene-Disease Associations genes associated with the sacral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abdominal wall defect Gene Set From HPO Gene-Disease Associations genes associated with the abdominal wall defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
visual field defect Gene Set From HPO Gene-Disease Associations genes associated with the visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene Set From HPO Gene-Disease Associations genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscular ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
defect in the atrial septum Gene Set From HPO Gene-Disease Associations genes associated with the defect in the atrial septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital septal defect Gene Set From HPO Gene-Disease Associations genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skull defect Gene Set From HPO Gene-Disease Associations genes associated with the skull defect 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.
cervical segmentation defect Gene Set From HPO Gene-Disease Associations genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrioventricular canal defect Gene Set From HPO Gene-Disease Associations genes associated with the atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
perimembranous ventricular septal defect Gene Set From HPO Gene-Disease Associations genes associated with the perimembranous ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midline defect of the nose Gene Set From HPO Gene-Disease Associations genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete atrioventricular canal defect Gene Set From HPO Gene-Disease Associations genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large central visual field defect Gene Set From HPO Gene-Disease Associations genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
conotruncal defect Gene Set From HPO Gene-Disease Associations genes associated with the conotruncal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
primum atrial septal defect Gene Set From HPO Gene-Disease Associations genes associated with the primum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Mannose-P-dolichol utilization defect 1 protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mannose-P-dolichol utilization defect 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
atrial septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
perimembraneous ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
inlet ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
double outlet right ventricle with atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
iodide oxidation defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
aorticopulmonary septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
double outlet right ventricle, ventricular defect committed to aorta Gene Set From MPO Gene-Phenotype Associations gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular ventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ostium primum atrial septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ostium secundum atrial septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype 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.
schizophrenia, neurophysiologic defect in Gene Set From OMIM Gene-Disease Associations genes associated with the schizophrenia, neurophysiologic defect in phenotype from the curated OMIM Gene-Disease Associations dataset.
{atrioventricular septal defect, susceptibility to, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 1} 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.
erythrocyte lactate transporter defect Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocyte lactate transporter defect phenotype from the curated OMIM Gene-Disease Associations dataset.
natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set From OMIM Gene-Disease Associations genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular septal defect 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular septal defect 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
selective t-cell defect Gene Set From OMIM Gene-Disease Associations genes associated with the selective t-cell defect 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.
atrial septal defect 6 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 5 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 4 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 3 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 2 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 1 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 9 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrial septal defect 8 Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular septal defect 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiac conduction defect, nonspecific Gene Set From OMIM Gene-Disease Associations genes associated with the cardiac conduction defect, nonspecific 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.
{atrioventricular septal defect, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
oocyte maturation defect Gene Set From OMIM Gene-Disease Associations genes associated with the oocyte maturation defect 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.
atrioventricular septal defect 3 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 4 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
atrioventricular septal defect 5 Gene Set From OMIM Gene-Disease Associations genes associated with the atrioventricular septal defect 5 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.
atrial septal defect 7, with or without av conduction defects Gene Set From OMIM Gene-Disease Associations genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia 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.
{cardiac conduction defect, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {cardiac conduction defect, susceptibility to} 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.
Histidinuria Renal Tubular Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histidinuria Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Carnitine Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Carnitine Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aortopulmonary Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aortopulmonary Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrial Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ostium Secundum Atrial Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ostium Secundum Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcohol Related Birth Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcohol Related Birth Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glucose-6-Phosphate Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucose-6-Phosphate Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ventilatory Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Calvarial Skull Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Calvarial Skull Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Single Ventricle Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Single Ventricle Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Defect Of Skull And Scalp Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Defect Of Skull And Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Sinus Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Sinus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Ventricular Septum Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Perimembranous Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Perimembranous Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triple Gene Defect Alpha Thalassemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triple Gene Defect Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Defect Of Vertebral Segmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Defect Of Vertebral Segmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glycosylphosphatidylinositol Biosynthesis Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glycosylphosphatidylinositol Biosynthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Conduction Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patent Or Persistent Ostium Secundum Defect (Type Ii) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patent Or Persistent Ostium Secundum Defect (Type Ii) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Patent Or Persistent Sinus Venosus Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Patent Or Persistent Sinus Venosus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Antibody Deficiency Due To Defect In Cd19 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Due To Defect In Cd19 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Conotruncal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Conotruncal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obstructive Ventilatory Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Defect Of Atrioventricular Canal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Defect Of Atrioventricular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transitional Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transitional Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Bundle Branch System Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Bundle Branch System Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Midline Defect Of The Nose Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Midline Defect Of The Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Hormone Plasma Membrane Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Plasma Membrane Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Defect Of Articular Cartilage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Defect Of Articular Cartilage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thoracoabdominal Wall Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thoracoabdominal Wall Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Atresia With Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Atresia With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Membranous Ventricular Septum Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Membranous Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Defect Of The Pericardium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Defect Of The Pericardium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Insulin Receptor, Defect In Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Insulin Receptor, Defect In in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iodide Transport Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iodide Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neural Tube Defect, Folate-Sensitive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neural Tube Defect, Folate-Sensitive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adenosylcobalamin Synthesis Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adenosylcobalamin Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oocyte Maturation Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oocyte Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sacral Defect And Anterior Sacral Meningocele Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sacral Defect And Anterior Sacral Meningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Tubular Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Valvular Defect, Developmental Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Valvular Defect, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ulnar-Fibular Ray Defect And Brachydactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ulnar-Fibular Ray Defect And Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Conduction Defect, Nonprogressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Defect, Nonprogressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fibrinolytic Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fibrinolytic Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erythrocyte Lactate Transporter Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erythrocyte Lactate Transporter Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mondini Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mondini Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Heart Defect, Tongue Hamartoma And Polysyndactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defect, Tongue Hamartoma And Polysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mucociliary Clearance Defect Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mucociliary Clearance Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adrenocorticotropin Receptor Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adrenocorticotropin Receptor Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Color Vision Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Color Vision Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Maturation Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Restrictive Ventilatory Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restrictive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Heart Defect (In Some Patients) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Heart Defect (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cardiac Conduction Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Glaucomatous Visual Field Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glaucomatous Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dynein Arm Defect Of Respiratory Motile Cilia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dynein Arm Defect Of Respiratory Motile Cilia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Iris Transillumination Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iris Transillumination Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Iodide Organification Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iodide Organification Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cervical Segmentation Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Segmentation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Lacrimal Duct Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Duct Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Large Central Visual Field Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Unbalanced Atrioventricular Canal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unbalanced Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Afferent Pupillary Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Afferent Pupillary Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventral Septal Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventral Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thyroid Defect In Oxidation And Organification Of Iodide Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thyroid Defect In Oxidation And Organification Of Iodide in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Activating Thyroid-Stimulating Hormone Receptor Defect Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Activating Thyroid-Stimulating Hormone Receptor Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
perimembraneous ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double outlet right ventricle with atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrial septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ostium secundum atrial septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
complete atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
muscular ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ostium primum atrial septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
inlet ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
aorticopulmonary septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
iodide oxidation defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
partial atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double outlet right ventricle, ventricular defect committed to aorta Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
double outlet right ventricle, noncommitted ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the double outlet right ventricle, noncommitted ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subarterial ventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subarterial ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
repair of mitotic kinetochore microtubule attachment defect Gene Set From GO Biological Process Annotations 2025 genes participating in the repair of mitotic kinetochore microtubule attachment defect biological process from the curated GO Biological Process Annotations 2025 dataset.
Atrial heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Atrial heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Heart septal defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neural tube defect Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neural tube defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neural tube defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neural tube defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrioventricular septal defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Glycosylphosphatidylinositol biosynthesis defect 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Glycosylphosphatidylinositol biosynthesis defect 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to thrombin defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Qualitative platelet defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Joubert syndrome with orofaciodigital defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Joubert syndrome with orofaciodigital defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked thrombophilia due to factor IX defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked thrombophilia due to factor IX defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrial heart septal defect 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrial heart septal defect 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Developmental cardiac valvular defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Developmental cardiac valvular defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hypotrichosis-lymphedema-telangiectasia-renal defect syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to thrombomodulin defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombomodulin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nerve fibre bundle defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nerve fibre bundle defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thyroglobulin synthesis defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroglobulin synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iodotyrosine deiodination defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital defect of folate absorption Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neutral 1 amino acid transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thrombophilia due to thrombin defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to thrombin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iris transillumination defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iris transillumination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hepatoencephalopathy due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatoencephalopathy due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrial septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrial septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal mitochondrial disease due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal mitochondrial disease due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal carnitine transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glucose-6-phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Phosphate transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peroxisome biogenesis disorder due to PEX1 defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peroxisome biogenesis disorder due to PEX1 defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Laron- somatotropin defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Laron- somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Color vision defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Color vision defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Protan defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iodotyrosyl coupling defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MPV17-related mitochondrial DNA maintenance defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MPV17-related mitochondrial DNA maintenance defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neural tube defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Gastrointestinal defect and immunodeficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gastrointestinal defect and immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial atrioventricular septal defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Single Ventricle Defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Single Ventricle Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Heart defect - tongue hamartoma - polysyndactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Heart defect - tongue hamartoma - polysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metabolic myopathy due to lactate transporter defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Methylmalonic acidemia due to transcobalamin receptor defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic acidemia due to transcobalamin receptor defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sacral defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sacral defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ulnar/fibula ray defect-brachydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ulnar/fibula ray defect-brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to defect in CD3-gamma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to defect in CD3-gamma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thyroid Hormonogenesis Defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroid Hormonogenesis Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Oocyte maturation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycosylphosphatidylinositol biosynthesis defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycosylphosphatidylinositol biosynthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inherited oocyte maturation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrioventricular septal defect and common atrioventricular junction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrioventricular septal defect and common atrioventricular junction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive retinal dystrophy due to retinol transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiac valvular defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiac valvular defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile arthritis due to defect in LA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile arthritis due to defect in LA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Female infertility due to zona pellucida defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility due to zona pellucida defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Left ventricular obstructive tract defect (inherited effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (inherited effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Left ventricular obstructive tract defect (maternal effect) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Left ventricular obstructive tract defect (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

MPDU1 Gene

IGAT Gene

ASD1 Gene

IGLP1 Gene

IGLP2 Gene

AVSD1 Gene

GBA2 Gene

GPBAR1 Gene

SLC10A2 Gene

SLC10A6 Gene

BAATP1 Gene

BAAT Gene

SLC10A1 Gene

Synthetic Defect Of Bile Acids Gene Set

Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol Gene Set

Synthesis of bile acids and bile salts Gene Set

Synthesis of bile acids and bile salts via 24-hydroxycholesterol Gene Set

Synthesis of bile acids and bile salts via 27-hydroxycholesterol Gene Set

Synthesis of bile acids and bile salts Gene Set

Synthesis of bile acids and bile salts via 24-hydroxycholesterol Gene Set

Synthesis of bile acids and bile salts via 27-hydroxycholesterol Gene Set

Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol Gene Set

Bile Acids and Salts Gene Set

Recycling of bile acids and salts Gene Set

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

Enterohepatic circulation of bile acids Gene Set

Recycling of bile acids and salts Gene Set

Transport of bile salts and organic acids, metal ions and amine compounds Gene Set

bile acid and bile salt transport Gene Set

Bile acid and bile salt metabolism Gene Set

bile acid and bile salt transport Gene Set

Bile acid and bile salt metabolism Gene Set

bile acid and bile salt transport Gene Set

Bile acid synthesis defect, congenital, 1 Gene Set

Bile acid synthesis defect, congenital, 2 Gene Set

Bile acid synthesis defect, congenital, 2 Gene Set

Bile acid synthesis defect, congenital, 4 Gene Set

Bile acid synthesis defect, congenital, 1 Gene Set

congenital bile acid synthesis defect Gene Set

bile acid synthesis defect, congenital, 1 Gene Set

bile acid synthesis defect, congenital, 3 Gene Set

bile acid synthesis defect, congenital, 2 Gene Set

bile acid synthesis defect, congenital, 4 Gene Set

Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set

Bile Acid Synthesis Defect Gene Set

Congenital Bile Acid Synthesis Defect Type 3 Gene Set

Congenital bile acid synthesis defect Gene Set

Congenital bile acid synthesis defect 2 Gene Set

Congenital bile acid synthesis defect Gene Set

Congenital bile acid synthesis defect 5 Gene Set

Congenital bile acid synthesis defect 2 Gene Set

Congenital bile acid synthesis defect 3 Gene Set

Congenital bile acid synthesis defect 1 Gene Set

Congenital bile acid synthesis defect Gene Set

Bile acid conjugation defect Gene Set

FSL-1 lipoprotein, synthetic Gene Set

IMMUNE RESPONSE TO SYNTHETIC POLYPEPTIDE--IRGAT Gene Set

synthetic hemodialysis graft failure Gene Set

synthetic Gene Set

Abuse Of Synthetic Cathinone Gene Set

Synthetic smooth muscle cell_Heart_Human Gene Set

ESTROGENS, CONJUGATED SYNTHETIC A Gene Set

SYNTHETIC CONJUGATED ESTROGENS, A Gene Set

SYNTHETIC CONJUGATED ESTROGENS, B Gene Set

SECRETIN HUMAN, SYNTHETIC Gene Set

SECRETIN SYNTHETIC PORCINE Gene Set

Hydroxyeicosatetraenoic Acids Gene Set

Hydroxy Acids Gene Set

Fibric Acids Gene Set

Aminosalicylic Acids Gene Set

Amino Acids, Peptides, and Proteins Gene Set

Fatty Acids, Omega-6 Gene Set

Fatty Acids, Volatile Gene Set

Phosphorous Acids Gene Set

thiosulfinic acids Gene Set

Sulfenic Acids Gene Set

Hydroxamic Acids Gene Set

Linoleic Acids, Conjugated Gene Set

Carboxylic Acids Gene Set