Congenital bile acid synthesis defect type 4

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Results for "Congenital bile acid synthesis defect type 4": 1000+ gene sets

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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.
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.
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 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.
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 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 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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
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.
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.
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.
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.
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.
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.
congenital goiter and defective tg synthesis. Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital goiter and defective tg synthesis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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 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.
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.
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.
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 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.
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.
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 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 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.
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.
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.
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 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.
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.
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.
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.
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.
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 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.
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.
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.
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 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 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.
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.
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.
Gamma-aminobutyric acid synthesis Gene Set From PANTHER Pathways proteins participating in the Gamma-aminobutyric acid synthesis pathway from the PANTHER Pathways dataset.
Amino acid synthesis and interconversion (transamination) Gene Set From Reactome Pathways 2014 proteins participating in the Amino acid synthesis and interconversion (transamination) pathway from the Reactome Pathways dataset.
Synthesis of 12-eicosatetraenoic acid derivatives Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of 12-eicosatetraenoic acid derivatives pathway from the Reactome Pathways dataset.
Synthesis of 15-eicosatetraenoic acid derivatives Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of 15-eicosatetraenoic acid derivatives pathway from the Reactome Pathways dataset.
Mitochondrial fatty acid synthesis pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Mitochondrial fatty acid synthesis pathway pathway from the WikiPathways Pathways 2024 dataset.
Omega 3 omega 6 fatty acid synthesis Gene Set From WikiPathways Pathways 2024 proteins participating in the Omega 3 omega 6 fatty acid synthesis pathway from the WikiPathways Pathways 2024 dataset.
Omega 9 fatty acid synthesis Gene Set From WikiPathways Pathways 2024 proteins participating in the Omega 9 fatty acid synthesis pathway from the WikiPathways Pathways 2024 dataset.
Synthesis of 12-eicosatetraenoic acid derivatives Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of 12-eicosatetraenoic acid derivatives pathway from the Reactome Pathways 2024 dataset.
Synthesis of 15-eicosatetraenoic acid derivatives Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis of 15-eicosatetraenoic acid derivatives pathway from the Reactome Pathways 2024 dataset.
Mitochondrial aminoacyl-tRNA synthesis and branched-chain amino acid catabolism Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Mitochondrial aminoacyl-tRNA synthesis and branched-chain amino acid catabolism assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies 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.
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.
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.
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.
Type I collagen synthesis in the context of osteogenesis imperfecta Gene Set From WikiPathways Pathways 2024 proteins participating in the Type I collagen synthesis in the context of osteogenesis imperfecta pathway from the WikiPathways Pathways 2024 dataset.
albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Heart Defects, Congenital, And Other Congenital Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations 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.
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.
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.
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.
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.
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.
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 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.
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.
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 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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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-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.
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.
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-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 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 secretion Gene Set From KEGG Pathways 2026 proteins participating in the Bile secretion pathway from the KEGG Pathways 2026 dataset.
Congenital generalized lipodystrophy type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, congenital generalized, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital secretory diarrhea, chloride type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2k Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1v Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type Ix Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital order of glycosylation type 1r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital dyserythropoietic anemia, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1O Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1y Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1u Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1t Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital hyperammonemia, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital stationary night blindness, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital myopathy with fiber type disproportion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract congenital Volkmann type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder of Glycosylation, Type Io Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type Im Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type In Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.
Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.
Adrenal hyperplasia, congenital, type 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adrenal hyperplasia, congenital, type 5 from the curated CTD Gene-Disease Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIH from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 3 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 4 from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIB from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C from the curated CTD Gene-Disease Associations dataset.
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A from the curated CTD Gene-Disease Associations dataset.
congenital disorder of glycosylation type ii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation type i Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set From GAD Gene-Disease Associations genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chuvash-type congenital polycythemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chuvash-type congenital polycythemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital fibrosis of extraocular muscles type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of extraocular muscles type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyserythropoietic anemia, congenital, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the dyserythropoietic anemia, congenital, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ih Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ih phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ij Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ij phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ik Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ik phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type il Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type il phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type im Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type im phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type id Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type id phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ie Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ie phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type if Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type if phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ig Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ig phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iq Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iq phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type it Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type it phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iu Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iu phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, megaconial type Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
dyserythropoietic anemia, congenital, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the dyserythropoietic anemia, congenital, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
dyserythropoietic anemia, congenital, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the dyserythropoietic anemia, congenital, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
dyserythropoietic anemia, congenital, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the dyserythropoietic anemia, congenital, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type iw Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type iw phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type ix Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type iy Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type iy phenotype from the curated OMIM Gene-Disease Associations dataset.
?congenital disorder of glycosylation, type ir Gene Set From OMIM Gene-Disease Associations genes associated with the ?congenital disorder of glycosylation, type ir phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type in Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type in phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type io Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type io phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type ip Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type ip phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type is Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type is phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
?lipodystrophy, congenital generalized, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?lipodystrophy, congenital generalized, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iil Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iil phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iij Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iij phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iik Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iik phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iih Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iih phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iii Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iim Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iim phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iib Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iia Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iif Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iif phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iig Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iig phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iid Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iid phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital disorder of glycosylation, type iie Gene Set From OMIM Gene-Disease Associations genes associated with the congenital disorder of glycosylation, type iie phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, congenital, with fiber-type disproportion Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, congenital, with fiber-type disproportion phenotype from the curated OMIM Gene-Disease Associations dataset.
dyserythropoietic anemia, congenital, type iv Gene Set From OMIM Gene-Disease Associations genes associated with the dyserythropoietic anemia, congenital, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.
oculomotor apraxia, congenital, cogan-type Gene Set From OMIM Gene-Disease Associations genes associated with the oculomotor apraxia, congenital, cogan-type phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuromuscular disease, congenital, with uniform type 1 fiber Gene Set From OMIM Gene-Disease Associations genes associated with the neuromuscular disease, congenital, with uniform type 1 fiber phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital Fiber Type Disproportion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Fiber Type Disproportion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Eichsfeld Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eichsfeld Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fukuyama Type Congenital Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fukuyama Type Congenital Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, Congenital Dyserythropoietic, Type Ib Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Congenital Dyserythropoietic, Type Ib in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Secretory Diarrhea, Sodium Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Secretory Diarrhea, Sodium Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Congenital Methemoglobinemia Type I Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Congenital Methemoglobinemia Type I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuromuscular Disease, Congenital, With Uniform Type 1 Fiber (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progeroid Syndrome, Congenital, Petty Type Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progeroid Syndrome, Congenital, Petty Type in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hydrops Fetalis (Type Ii, Congenital) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hydrops Fetalis (Type Ii, Congenital) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe congenital neutropenia type 4 (G6PC3) Gene Set From Reactome Pathways 2024 proteins participating in the Severe congenital neutropenia type 4 (G6PC3) pathway from the Reactome Pathways 2024 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy-dystroglycanopathy type A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital disorder of glycosylation type IIm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type II Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital disorder of glycosylation type II from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type I Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital disorder of glycosylation type I from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIi Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital disorder of glycosylation type IIi from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIe Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIe in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIa Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIk Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIk in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIc Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megaconial type congenital muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megaconial type congenital muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIq Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIq in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIf Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIf in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIh Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIh in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIj Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIj in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIp Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIp in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIo Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIn Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIn in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type Ia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type Ia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type III Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type III in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIg Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIg in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIl Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIl in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IIb Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IIb in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital disorder of glycosylation type IId Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital disorder of glycosylation type IId in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type IV Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type IV in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type Ib Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type Ib in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy-dystroglycanopathy type A9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy-dystroglycanopathy type A9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
srebp control of lipid synthesis Gene Set From Biocarta Pathways proteins participating in the srebp control of lipid synthesis pathway from the Biocarta Pathways dataset.
cadmium induces dna synthesis and proliferation in macrophages Gene Set From Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset.
cholesterol synthesis rate Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol synthesis rate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
interleukin-1 beta (il-1 beta) synthesis capacity Gene Set From GAD Gene-Disease Associations genes associated with the disease interleukin-1 beta (il-1 beta) synthesis capacity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cytokine synthesis Gene Set From GAD Gene-Disease Associations genes associated with the disease cytokine synthesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
synthesis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term synthesis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
dna synthesis involved in dna repair Gene Set From GO Biological Process Annotations 2015 genes participating in the dna synthesis involved in dna repair biological process from the curated GO Biological Process Annotations 2015 dataset.
trna dihydrouridine synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the trna dihydrouridine synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
atp synthesis coupled proton transport Gene Set From GO Biological Process Annotations 2015 genes participating in the atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations 2015 dataset.
atp synthesis coupled electron transport Gene Set From GO Biological Process Annotations 2015 genes participating in the atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2015 dataset.
rrna pseudouridine synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the rrna pseudouridine synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
error-prone translesion synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the error-prone translesion synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
snrna pseudouridine synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the snrna pseudouridine synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
mrna pseudouridine synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the mrna pseudouridine synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
dna replication, synthesis of rna primer Gene Set From GO Biological Process Annotations 2015 genes participating in the dna replication, synthesis of rna primer biological process from the curated GO Biological Process Annotations 2015 dataset.
pseudouridine synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the pseudouridine synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
translesion synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the translesion synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
meiotic dna repair synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the meiotic dna repair synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
trna pseudouridine synthesis Gene Set From GO Biological Process Annotations 2015 genes participating in the trna pseudouridine synthesis biological process from the curated GO Biological Process Annotations 2015 dataset.
mitochondrial atp synthesis coupled electron transport Gene Set From GO Biological Process Annotations 2015 genes participating in the mitochondrial atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2015 dataset.
mitochondrial atp synthesis coupled proton transport Gene Set From GO Biological Process Annotations 2015 genes participating in the mitochondrial atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations 2015 dataset.
reduced beta/alpha synthesis ratio Gene Set From HPO Gene-Disease Associations genes associated with the reduced beta/alpha synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced alpha/beta synthesis ratio Gene Set From HPO Gene-Disease Associations genes associated with the reduced alpha/beta synthesis ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
imbalanced hemoglobin synthesis Gene Set From HPO Gene-Disease Associations genes associated with the imbalanced hemoglobin synthesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fructose 2,6-bisphosphate synthesis/dephosphorylation Gene Set From HumanCyc Pathways proteins participating in the fructose 2,6-bisphosphate synthesis/dephosphorylation pathway from the HumanCyc Pathways dataset.
Diphthamide synthesis DHP2, eukaryotic Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Diphthamide synthesis DHP2, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Molybdenum cofactor synthesis C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Molybdenum cofactor synthesis C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
tRNA wybutosine-synthesis Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the tRNA wybutosine-synthesis protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Synthesis of cytochrome c oxidase, Sco1/Sco2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Synthesis of cytochrome c oxidase, Sco1/Sco2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Diphthamide synthesis DPH1/DPH2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Diphthamide synthesis DPH1/DPH2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
synthesis and degradation of ketone bodies Gene Set From KEGG Pathways proteins participating in the synthesis and degradation of ketone bodies pathway from the KEGG Pathways dataset.
abnormal mitochondrial atp synthesis coupled electron transport Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrial atp synthesis coupled electron transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Vasopressin synthesis Gene Set From PANTHER Pathways proteins participating in the Vasopressin synthesis pathway from the PANTHER Pathways dataset.
ATP synthesis Gene Set From PANTHER Pathways proteins participating in the ATP synthesis pathway from the PANTHER Pathways dataset.
Histamine synthesis Gene Set From PANTHER Pathways proteins participating in the Histamine synthesis pathway from the PANTHER Pathways dataset.
Telomere C-strand synthesis initiation Gene Set From Reactome Pathways 2014 proteins participating in the Telomere C-strand synthesis initiation pathway from the Reactome Pathways dataset.
Synthesis of GDP-mannose Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of GDP-mannose pathway from the Reactome Pathways dataset.
Hypusine synthesis from eIF5A-lysine Gene Set From Reactome Pathways 2014 proteins participating in the Hypusine synthesis from eIF5A-lysine pathway from the Reactome Pathways dataset.
Synthesis of dolichyl-phosphate-glucose Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of dolichyl-phosphate-glucose pathway from the Reactome Pathways dataset.
Synthesis of PS Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PS pathway from the Reactome Pathways dataset.
Synthesis of PE Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PE pathway from the Reactome Pathways dataset.
GABA synthesis Gene Set From Reactome Pathways 2014 proteins participating in the GABA synthesis pathway from the Reactome Pathways dataset.
Translesion synthesis by DNA polymerases bypassing lesion on DNA template Gene Set From Reactome Pathways 2014 proteins participating in the Translesion synthesis by DNA polymerases bypassing lesion on DNA template pathway from the Reactome Pathways dataset.
Synthesis of IPs in the ER lumen Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of IPs in the ER lumen pathway from the Reactome Pathways dataset.
Minus-strand DNA synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Minus-strand DNA synthesis pathway from the Reactome Pathways dataset.
Synthesis of IP3 and IP4 in the cytosol Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of IP3 and IP4 in the cytosol pathway from the Reactome Pathways dataset.
Post-translational modification: synthesis of GPI-anchored proteins Gene Set From Reactome Pathways 2014 proteins participating in the Post-translational modification: synthesis of GPI-anchored proteins pathway from the Reactome Pathways dataset.
A tetrasaccharide linker sequence is required for GAG synthesis Gene Set From Reactome Pathways 2014 proteins participating in the A tetrasaccharide linker sequence is required for GAG synthesis pathway from the Reactome Pathways dataset.
Synthesis of substrates in N-glycan biosythesis Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of substrates in N-glycan biosythesis pathway from the Reactome Pathways dataset.
Viral Messenger RNA Synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Viral Messenger RNA Synthesis pathway from the Reactome Pathways dataset.
Synthesis of DNA Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of DNA pathway from the Reactome Pathways dataset.
Carnitine synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Carnitine synthesis pathway from the Reactome Pathways dataset.
Gap-filling DNA repair synthesis and ligation in GG-NER Gene Set From Reactome Pathways 2014 proteins participating in the Gap-filling DNA repair synthesis and ligation in GG-NER pathway from the Reactome Pathways dataset.
Synthesis of PIPs at the early endosome membrane Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PIPs at the early endosome membrane pathway from the Reactome Pathways dataset.
Glycogen synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Glycogen synthesis pathway from the Reactome Pathways dataset.
Synthesis of Ketone Bodies Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of Ketone Bodies pathway from the Reactome Pathways dataset.
Translesion synthesis by Pol eta Gene Set From Reactome Pathways 2014 proteins participating in the Translesion synthesis by Pol eta pathway from the Reactome Pathways dataset.
Synthesis of IPs in the nucleus Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of IPs in the nucleus 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.
Processive synthesis on the lagging strand Gene Set From Reactome Pathways 2014 proteins participating in the Processive synthesis on the lagging strand pathway from the Reactome Pathways dataset.
Synthesis of PIPs at the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PIPs at the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis of glycosylphosphatidylinositol (GPI) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of glycosylphosphatidylinositol (GPI) 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.
Translesion synthesis by HREV1 Gene Set From Reactome Pathways 2014 proteins participating in the Translesion synthesis by HREV1 pathway from the Reactome Pathways dataset.
Synthesis of PIPs at the Golgi membrane Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PIPs at the Golgi membrane 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.
Insulin effects increased synthesis of Xylulose-5-Phosphate Gene Set From Reactome Pathways 2014 proteins participating in the Insulin effects increased synthesis of Xylulose-5-Phosphate pathway from the Reactome Pathways dataset.
Synthesis of Leukotrienes (LT) and Eoxins (EX) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of Leukotrienes (LT) and Eoxins (EX) pathway from the Reactome Pathways dataset.
Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation Gene Set From Reactome Pathways 2014 proteins participating in the Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation pathway from the Reactome Pathways dataset.
Synthesis And Processing Of GAG, GAGPOL Polyproteins Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis And Processing Of GAG, GAGPOL Polyproteins pathway from the Reactome Pathways dataset.
Incretin synthesis, secretion, and inactivation Gene Set From Reactome Pathways 2014 proteins participating in the Incretin synthesis, secretion, and inactivation pathway from the Reactome Pathways dataset.
Synthesis of IP2, IP, and Ins in the cytosol Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of IP2, IP, and Ins in the cytosol pathway from the Reactome Pathways dataset.
Synthesis of PIPs at the late endosome membrane Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PIPs at the late endosome membrane pathway from the Reactome Pathways dataset.
Repair synthesis for gap-filling by DNA polymerase in TC-NER Gene Set From Reactome Pathways 2014 proteins participating in the Repair synthesis for gap-filling by DNA polymerase in TC-NER pathway from the Reactome Pathways dataset.
Transport and synthesis of PAPS Gene Set From Reactome Pathways 2014 proteins participating in the Transport and synthesis of PAPS pathway from the Reactome Pathways dataset.
Synthesis of UDP-N-acetyl-glucosamine Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of UDP-N-acetyl-glucosamine pathway from the Reactome Pathways dataset.
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) pathway from the Reactome Pathways dataset.
Synthesis of PA Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PA pathway from the Reactome Pathways dataset.
Synthesis of PC Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PC pathway from the Reactome Pathways dataset.
Synthesis of PG Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PG pathway from the Reactome Pathways dataset.
Synthesis of PI Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PI pathway from the Reactome Pathways dataset.
Synthesis of PIPs at the ER membrane Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of PIPs at the ER membrane pathway from the Reactome Pathways dataset.
GABA synthesis, release, reuptake and degradation Gene Set From Reactome Pathways 2014 proteins participating in the GABA synthesis, release, reuptake and degradation pathway from the Reactome Pathways dataset.
Synthesis of pyrophosphates in the cytosol Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of pyrophosphates in the cytosol pathway from the Reactome Pathways dataset.
Reactions specific to the complex N-glycan synthesis pathway Gene Set From Reactome Pathways 2014 proteins participating in the Reactions specific to the complex N-glycan synthesis pathway pathway from the Reactome Pathways dataset.
Reactions specific to the hybrid N-glycan synthesis pathway Gene Set From Reactome Pathways 2014 proteins participating in the Reactions specific to the hybrid N-glycan synthesis pathway pathway from the Reactome Pathways dataset.
Synthesis of Dolichyl-phosphate Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of Dolichyl-phosphate pathway from the Reactome Pathways dataset.
Processive synthesis on the C-strand of the telomere Gene Set From Reactome Pathways 2014 proteins participating in the Processive synthesis on the C-strand of the telomere pathway from the Reactome Pathways dataset.
Lagging Strand Synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Lagging Strand Synthesis pathway from the Reactome Pathways dataset.
Synthesis of Hepoxilins (HX) and Trioxilins (TrX) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of Hepoxilins (HX) and Trioxilins (TrX) pathway from the Reactome Pathways dataset.
Synthesis of diphthamide-EEF2 Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of diphthamide-EEF2 pathway from the Reactome Pathways dataset.
Glutathione synthesis and recycling Gene Set From Reactome Pathways 2014 proteins participating in the Glutathione synthesis and recycling pathway from the Reactome Pathways dataset.
Leading Strand Synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Leading Strand Synthesis pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis of Prostaglandins (PG) and Thromboxanes (TX) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of Prostaglandins (PG) and Thromboxanes (TX) pathway from the Reactome Pathways dataset.
Synthesis of Lipoxins (LX) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of Lipoxins (LX) pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
Plus-strand DNA synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Plus-strand DNA synthesis pathway from the Reactome Pathways dataset.
Synthesis of dolichyl-phosphate mannose Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of dolichyl-phosphate mannose pathway from the Reactome Pathways dataset.
Translesion synthesis by Pol zeta Gene Set From Reactome Pathways 2014 proteins participating in the Translesion synthesis by Pol zeta pathway from the Reactome Pathways dataset.
Synthesis, secretion, and deacylation of Ghrelin Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis, secretion, and deacylation of Ghrelin pathway from the Reactome Pathways dataset.
Synthesis of CL Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of CL pathway from the Reactome Pathways dataset.
Gap-filling DNA repair synthesis and ligation in TC-NER Gene Set From Reactome Pathways 2014 proteins participating in the Gap-filling DNA repair synthesis and ligation in TC-NER pathway from the Reactome Pathways dataset.
Repair synthesis of patch ~27-30 bases long by DNA polymerase Gene Set From Reactome Pathways 2014 proteins participating in the Repair synthesis of patch ~27-30 bases long by DNA polymerase pathway from the Reactome Pathways dataset.
Telomere C-strand (Lagging Strand) Synthesis Gene Set From Reactome Pathways 2014 proteins participating in the Telomere C-strand (Lagging Strand) Synthesis pathway from the Reactome Pathways dataset.
Synthesis of very long-chain fatty acyl-CoAs Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis of very long-chain fatty acyl-CoAs pathway from the Reactome Pathways dataset.
Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. Gene Set From Reactome Pathways 2014 proteins participating in the Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. pathway from the Reactome Pathways dataset.
Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) pathway from the Reactome Pathways dataset.
Biogenic Amine Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Biogenic Amine Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Triacylglyceride Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Triacylglyceride Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Prostaglandin Synthesis and Regulation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Prostaglandin Synthesis and Regulation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Synthesis and Degradation of Ketone Bodies(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Synthesis and Degradation of Ketone Bodies(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Prostaglandin Synthesis and Regulation(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Prostaglandin Synthesis and Regulation(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Biogenic Amine Synthesis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Biogenic Amine Synthesis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Synthesis and Degradation of Ketone Bodies(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Synthesis and Degradation of Ketone Bodies(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Acetylcholine Synthesis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Acetylcholine Synthesis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Acetylcholine Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Acetylcholine Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Eicosanoid Synthesis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Eicosanoid Synthesis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Triacylglyceride Synthesis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Triacylglyceride Synthesis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Eicosanoid Synthesis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Eicosanoid Synthesis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Defective Thyroglobulin Synthesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Defective Thyroglobulin Synthesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reduced Alpha/Beta Synthesis Ratio Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Alpha/Beta Synthesis Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Harmonizome 3.0

Congenital Bile Acid Synthesis Defect Type 3 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

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 Synthesis Defect 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 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 conjugation defect Gene Set

cholesterol, ldl; bile acid synthesis Gene Set

Bile acid synthesis and enterohepatic circulation Gene Set

Disorders of bile acid synthesis and biliary transport Gene Set

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

Synthetic Defect Of Bile Acids Gene Set

Adenosylcobalamin Synthesis Defect Gene Set

Thyroglobulin synthesis defect Gene Set

Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set

Acyl-CoA thioester hydrolase/bile acid-CoA amino acid N-acetyltransferase Gene Set

ABC-type bile acid transporter activity Gene Set

ABC-type bile acid transporter activity Gene Set

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

Congenital Atresia Of Extrahepatic Bile Duct Gene Set

Congenital Hypoplasia Of Bile Duct Gene Set

Congenital defect of folate absorption Gene Set

congenital septal defect Gene Set

Congenital Defect Of Skull And Scalp Gene Set

Congenital Defect Of The Pericardium Gene Set

Congenital defect of folate absorption Gene Set

congenital goiter and defective tg synthesis. Gene Set

Bile acid malabsorption, primary Gene Set

Bile Acid Malabsorption, Primary Gene Set

response to bile acid Gene Set

bile acid biosynthetic process Gene Set

cellular response to bile acid Gene Set

canalicular bile acid transport Gene Set

bile acid catabolic process Gene Set

regulation of bile acid biosynthetic process Gene Set

bile acid metabolic process Gene Set

negative regulation of bile acid biosynthetic process Gene Set

bile acid signaling pathway Gene Set

cell surface bile acid receptor signaling pathway Gene Set

intracellular bile acid receptor signaling pathway Gene Set

positive regulation of bile acid biosynthetic process Gene Set

bile acid secretion Gene Set

bile acid conjugation Gene Set

bile acid-exporting atpase activity Gene Set

bile acid transmembrane transporter activity Gene Set

bile acid receptor activity Gene Set

bile acid binding Gene Set

bile acid:sodium symporter activity Gene Set

canalicular bile acid transmembrane transporter activity Gene Set

g-protein coupled bile acid receptor activity Gene Set

increased serum bile acid concentration during pregnancy Gene Set