| Name |
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Hepatic Fibrosis And Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Fibrosis And Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic iron and fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic iron and fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; biliary cirrhosis; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; biliary cirrhosis; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c; liver cirrhosis; liver cirrhosis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c; liver cirrhosis; liver cirrhosis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b; hepatitis c; lcc - liver cell carcinoma; liver cirrhosis; liver cirrhosis, alcoholic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b; hepatitis c; lcc - liver cell carcinoma; liver cirrhosis; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; liver cirrhosis, biliary; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; liver cirrhosis, biliary; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis; liver cirrhosis, alcoholic; liver failure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis; liver cirrhosis, alcoholic; liver failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; liver cirrhosis; liver cirrhosis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; liver cirrhosis; liver cirrhosis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary cirrhosis; hepatitis, autoimmune; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary cirrhosis; hepatitis, autoimmune; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic encephalopathy; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic encephalopathy; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypertension, portal; liver cirrhosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; fibrosis; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset. |
congenital hepatic fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital hepatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hepatic Fibrosis, Congenital Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Fibrosis, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Liver fibrosis (total hepatic collagen content) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis (total hepatic collagen content) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
fibrosis; pulmonary fibrosis; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; pulmonary fibrosis; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Setproteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset. |
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
esophageal and gastric varices; gastrointestinal hemorrhage; liver cirrhosis; postoperative complications; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal and gastric varices; gastrointestinal hemorrhage; liver cirrhosis; postoperative complications; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver disease, chronic and cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver disease, chronic and cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic; esophageal cancer; head and neck cancer; liver cancer; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic; esophageal cancer; head and neck cancer; liver cancer; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypermanganesemia with dystonia, polycythemia, and cirrhosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypermanganesemia with dystonia, polycythemia, and cirrhosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
plasma glucose, basal hepatic glucose and increased insulin release Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma glucose, basal hepatic glucose and increased insulin release in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lower levels of hepatic lipase activity buoyant ldl and higher hdl2 cholesterol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lower levels of hepatic lipase activity buoyant ldl and higher hdl2 cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic failure, early onset, and neurologic disorder Gene SetFrom OMIM Gene-Disease Associations genes associated with the hepatic failure, early onset, and neurologic disorder phenotype from the curated OMIM Gene-Disease Associations dataset. |
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
polycystic kidney and hepatic disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the polycystic kidney and hepatic disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene SetFrom Biocarta Pathways proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms, germ cell and embryonal; pulmonary fibrosis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; oral submucous fibrosis; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
Combined Pulmonary Fibrosis And Emphysema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Combined Pulmonary Fibrosis And Emphysema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis, Neurodegeneration, And Cerebral Angiomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis, Neurodegeneration, And Cerebral Angiomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary fibrosis and/or bone marrow failure Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis and/or bone marrow failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary fibrosis and/or bone marrow failure syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis and/or bone marrow failure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Liver fibrosis and steatohepatitis severity (MRI cT1 measure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis and steatohepatitis severity (MRI cT1 measure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Setproteins 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. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
North american indian childhood cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the North american indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Biliary Cirrhosis, Primary, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Biliary Cirrhosis, Primary, 2 from the curated CTD Gene-Disease Associations dataset. |
Liver Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Liver Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
North American Indian Childhood Cirrhosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease North American Indian Childhood Cirrhosis from the curated CTD Gene-Disease Associations dataset. |
Liver Cirrhosis, Alcoholic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Liver Cirrhosis, Alcoholic from the curated CTD Gene-Disease Associations dataset. |
Liver Cirrhosis, Experimental Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Liver Cirrhosis, Experimental from the curated CTD Gene-Disease Associations dataset. |
Liver Cirrhosis, Biliary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Liver Cirrhosis, Biliary from the curated CTD Gene-Disease Associations dataset. |
Cirrhosis, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cirrhosis, Familial from the curated CTD Gene-Disease Associations dataset. |
Biliary Cirrhosis, Primary, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Biliary Cirrhosis, Primary, 3 from the curated CTD Gene-Disease Associations dataset. |
Liver Cirrhosis, Biliary Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Liver Cirrhosis, Biliary in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
primary biliary cirrhosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease primary biliary cirrhosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
liver cirrhosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease liver cirrhosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
primary biliary cirrhosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary biliary cirrhosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alcoholic liver cirrhosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcoholic liver cirrhosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
liver cirrhosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease liver cirrhosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis; pancreatitis; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis; pancreatitis; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary biliary cirrhosis] Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary biliary cirrhosis] in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
helicobacter infections; liver cirrhosis; peptic ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease helicobacter infections; liver cirrhosis; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ascites; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ascites; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, primary biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, primary biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, alcoholic; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, alcoholic; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b; hepatitis b, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b; hepatitis b, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; liver disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary biliary cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary biliary cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; fatty liver; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; fatty liver; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic; hepatitis c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatopulmonary syndrome; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatopulmonary syndrome; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; cholangitis, sclerosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c; hiv infections; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c; hiv infections; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver failure; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver failure; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholic liver diseases; alcoholism; liver cirrhosis, alcoholic; liver diseases, alcoholic; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; alcoholism; liver cirrhosis, alcoholic; liver diseases, alcoholic; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, biliary; pruritus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, biliary; pruritus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; hepatitis c, chronic; hyperhomocysteinemia; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; hepatitis c, chronic; hyperhomocysteinemia; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis c, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; hemochromatosis; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; hemochromatosis; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms; siderosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms; siderosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthralgia; carcinoma, hepatocellular; hemochromatosis; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthralgia; carcinoma, hepatocellular; hemochromatosis; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c; iron overload; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis; liver cancer; hepatitis c, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis; liver cancer; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; liver carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; liver carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; triglycerides; cirrhosis, alcoholic; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; triglycerides; cirrhosis, alcoholic; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis, alcoholic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis, alcoholic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis c; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; cirrhosis; esophageal cancer; pancreatitis, acute Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; cirrhosis; esophageal cancer; pancreatitis, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; cirrhosis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; cirrhosis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; liver cirrhosis, alcoholic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; hepatitis type 1, autoimmune (aih-1) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; hepatitis type 1, autoimmune (aih-1) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; liver cirrhosis, alcoholic; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; liver cirrhosis, alcoholic; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; bone necrosis; liver cirrhosis; osteonecrosis; pancreatitis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; bone necrosis; liver cirrhosis; osteonecrosis; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; liver cirrhosis; liver failure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; liver cirrhosis; liver failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic; liver cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic; liver cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis; hepatocellular carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis; hepatocellular carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b; cirrhosis; liver cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b; cirrhosis; liver cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertriglyceridemia; liver cirrhosis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertriglyceridemia; liver cirrhosis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; liver cirrhosis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; liver cirrhosis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; diabetes mellitus; heart failure; hemochromatosis; lcc - liver cell carcinoma; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; diabetes mellitus; heart failure; hemochromatosis; lcc - liver cell carcinoma; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis; liver cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis; liver cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, alcoholic; pancreatitis, alcoholic; pancreatitis, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, alcoholic; pancreatitis, alcoholic; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; liver cirrhosis; obesity, morbid Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; liver cirrhosis; obesity, morbid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c; liver cirrhosis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c; liver cirrhosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; hepatitis c, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; hepatitis c, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial infections; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial infections; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b; hepatitis, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b; hepatitis, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; hepatitis c, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; hepatitis c, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis; pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c; liver cirrhosis; recurrence; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c; liver cirrhosis; recurrence; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis c, chronic; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c, chronic; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; liver carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; liver carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
avitaminosis; carcinoma, hepatocellular; fatty liver; hepatitis, chronic; hyperhomocysteinemia; lcc - liver cell carcinoma; liver cirrhosis; liver diseases; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease avitaminosis; carcinoma, hepatocellular; fatty liver; hepatitis, chronic; hyperhomocysteinemia; lcc - liver cell carcinoma; liver cirrhosis; liver diseases; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis; hepatocellular carcinoma; hepatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis; hepatocellular carcinoma; hepatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic; liver disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic; liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis; schistosomiasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis; schistosomiasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; liver cirrhosis; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; liver cirrhosis; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; liver cirrhosis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; liver cirrhosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
osteoporosis; cirrhosis, primary biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease osteoporosis; cirrhosis, primary biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; hepatitis c, chronic; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; hepatitis c, chronic; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; insulin resistance; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; liver cirrhosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; liver cirrhosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial infections; liver cirrhosis; peritonitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial infections; liver cirrhosis; peritonitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; liver carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; liver carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; hepatitis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; hepatitis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, portal; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, portal; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disease models, animal; hemochromatosis; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disease models, animal; hemochromatosis; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis, autoimmune; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis, autoimmune; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, alcoholic; alcoholism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, alcoholic; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b; hepatitis c; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b; hepatitis c; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; diabetes, gestational Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; diabetes, gestational in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver cirrhosis, alcoholic; liver diseases, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver cirrhosis, alcoholic; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; hyperhomocysteinemia; liver cirrhosis, alcoholic; protein-energy malnutrition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; hyperhomocysteinemia; liver cirrhosis, alcoholic; protein-energy malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; lcc - liver cell carcinoma; liver cirrhosis, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c, chronic; iron overload; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c, chronic; iron overload; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis c, chronic; liver cirrhosis; liver neoplasms; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis c, chronic; liver cirrhosis; liver neoplasms; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart diseases; hemochromatosis; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart diseases; hemochromatosis; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term cirrhosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Hepatitis C induced liver cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hepatitis C induced liver cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Primary biliary cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Primary biliary cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
primary biliary cirrhosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease primary biliary cirrhosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
liver cirrhosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease liver cirrhosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
biliary cirrhosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary cirrhosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
micronodular cirrhosis Gene SetFrom HPO Gene-Disease Associations genes associated with the micronodular cirrhosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary cirrhosis Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary cirrhosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cirrhosis Gene SetFrom HPO Gene-Disease Associations genes associated with the cirrhosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Liver Cirrhosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Liver Cirrhosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Liver Cirrhosis, Alcoholic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Liver Cirrhosis, Alcoholic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Liver Cirrhosis, Biliary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Liver Cirrhosis, Biliary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
liver cirrhosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the liver cirrhosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
biliary cirrhosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the biliary cirrhosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{biliary cirrhosis, primary, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {biliary cirrhosis, primary, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
biliary cirrhosis, primary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the biliary cirrhosis, primary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
biliary cirrhosis, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the biliary cirrhosis, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{cirrhosis, noncryptogenic, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {cirrhosis, noncryptogenic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cirrhosis due to liver phosphorylase kinase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the cirrhosis due to liver phosphorylase kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
cirrhosis, north american indian childhood type Gene SetFrom OMIM Gene-Disease Associations genes associated with the cirrhosis, north american indian childhood type phenotype from the curated OMIM Gene-Disease Associations dataset. |
{biliary cirrhosis, primary, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {biliary cirrhosis, primary, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cirrhosis, cryptogenic Gene SetFrom OMIM Gene-Disease Associations genes associated with the cirrhosis, cryptogenic phenotype from the curated OMIM Gene-Disease Associations dataset. |
emphysema-cirrhosis, due to aat deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
Liver Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Liver Cirrhosis, Experimental Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver Cirrhosis, Experimental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Biliary Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Biliary Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Biliary Cirrhosis, Primary, 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Biliary Cirrhosis, Primary, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Early Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Early Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Micronodular Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Micronodular Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Liver Cirrhosis, Alcoholic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver Cirrhosis, Alcoholic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Copper-Overload Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Copper-Overload Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Indian Childhood Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Compensated Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Compensated Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endemic Tyrolean Infantile Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Endemic Tyrolean Infantile Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
North American Indian Childhood Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease North American Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cirrhosis, Noncryptogenic, Susceptibility To (Finding) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cirrhosis, Noncryptogenic, Susceptibility To (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Cirrhosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cardiac Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decompensated Cirrhosis Of Liver Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decompensated Cirrhosis Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Portal Cirrhosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Portal Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
biliary cirrhosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the biliary cirrhosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
liver cirrhosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the liver cirrhosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Liver cirrhosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Liver cirrhosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcoholic liver cirrhosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Alcoholic liver cirrhosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Liver cirrhosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Liver cirrhosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alcoholic liver cirrhosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcoholic liver cirrhosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary North American Indian childhood cirrhosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary North American Indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary biliary cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Primary biliary cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hepatitis B virus-related hepatocellular carcinoma vs hepatitis B virus-related decompensated cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatitis B virus-related hepatocellular carcinoma vs hepatitis B virus-related decompensated cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cirrhosis (alcohol related) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cirrhosis (alcohol related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cirrhosis (multi-trait analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cirrhosis (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hepatitis C induced liver cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatitis C induced liver cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alcohol dependence or chronic alcoholic pancreatitis or alcohol-related liver cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alcohol dependence or chronic alcoholic pancreatitis or alcohol-related liver cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Renal-hepatic-pancreatic dysplasia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal-hepatic-pancreatic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hepatic venoocclusive disease with immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hepatic lipase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hepatic lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Porphyria, Acute Hepatic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Porphyria, Acute Hepatic from the curated CTD Gene-Disease Associations dataset. |
Hepatic Veno-Occlusive Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic venoocclusive disease with immunodeficiency from the curated CTD Gene-Disease Associations dataset. |
Hepatic Encephalopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Encephalopathy from the curated CTD Gene-Disease Associations dataset. |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset. |
Hepatic Adenomas, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Adenomas, Familial from the curated CTD Gene-Disease Associations dataset. |
Porphyrias, Hepatic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Porphyrias, Hepatic from the curated CTD Gene-Disease Associations dataset. |
Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset. |
Massive Hepatic Necrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Massive Hepatic Necrosis from the curated CTD Gene-Disease Associations dataset. |
Hepatic Insufficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Insufficiency from the curated CTD Gene-Disease Associations dataset. |
hepatic vein thrombosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic vein thrombosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hepatic angiomyolipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic angiomyolipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hepatic encephalopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hepatic vascular disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hepatic coma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic coma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hepatic tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hepatic tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sclerosing hepatic carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sclerosing hepatic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hepatic gsta1/gsta2 expression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic gsta1/gsta2 expression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic cyp3a4 expression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic cyp3a4 expression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic veno-occlusive disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic veno-occlusive disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; hematologic neoplasms; hemochromatosis; hepatic veno-occlusive disease; mammary neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; hematologic neoplasms; hemochromatosis; hepatic veno-occlusive disease; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
echinococcosis, hepatic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease echinococcosis, hepatic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low hepatic lipase activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low hepatic lipase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic artery thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatic artery thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta thalassemia; beta-thalassemia; hepatic veno-occlusive disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; hepatic veno-occlusive disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; hepatic lipase activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; hepatic lipase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatic Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term hepatic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Hepatic Cirrhosis_Liver_GSE6764 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Hepatic Cirrhosis_Liver_GSE6764 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
Hepatic Cirrhosis_Hepatic Tissue_GSE1843 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Hepatic Cirrhosis_Hepatic Tissue_GSE1843 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
regulation of hepatic stellate cell activation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hepatic stellate cell activation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hepatic duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hepatic duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
hepatic immune response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hepatic immune response biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of hepatic stellate cell activation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hepatic steatosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hepatic steatosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hepatic granulomatosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hepatic granulomatosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acute hepatic failure Gene SetFrom HPO Gene-Disease Associations genes associated with the acute hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic amyloidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic amyloidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased hepatic glycogen content Gene SetFrom HPO Gene-Disease Associations genes associated with the increased hepatic glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse hepatic steatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic arteriovenous malformation Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic necrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acute hepatic steatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the acute hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic encephalopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic periportal necrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic periportal necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic calcification Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic steatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malformation of the hepatic ductal plate Gene SetFrom HPO Gene-Disease Associations genes associated with the malformation of the hepatic ductal plate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated hepatic transaminases Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated hepatic transaminases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic vascular malformations Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic vascular malformations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hepatic vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hepatic vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic failure Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
macrovesicular hepatic steatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the macrovesicular hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic cysts Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fulminant hepatic failure Gene SetFrom HPO Gene-Disease Associations genes associated with the fulminant hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic abscesses due to immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chronic hepatic failure Gene SetFrom HPO Gene-Disease Associations genes associated with the chronic hepatic failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
microvesicular hepatic steatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the microvesicular hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Hepatic Veno-Occlusive Disease Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatic Veno-Occlusive Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hepatic Encephalopathy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatic Encephalopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Echinococcosis, Hepatic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Echinococcosis, Hepatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hepatic Vein Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatic Vein Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hepatic leukemia factor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hepatic leukemia factor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hepatic lipase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hepatic lipase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hepatic lectin, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hepatic lectin, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
multifocal hepatic necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the multifocal hepatic necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed hepatic development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed hepatic development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hepatic necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hepatic necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatic diverticulum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatic diverticulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hepatic steatosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hepatic steatosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatic portal vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatic portal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased hepatic hemangioma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased hepatic hemangioma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatic vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatic vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
focal hepatic necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the focal hepatic necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatic cord morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatic cord morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
diffuse hepatic necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the diffuse hepatic necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased susceptibility to hepatic steatosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to hepatic steatosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal-hepatic-pancreatic dysplasia 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal-hepatic-pancreatic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hepatic venoocclusive disease with immunodeficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hepatic venoocclusive disease with immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
porphyria, acute hepatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the porphyria, acute hepatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
hepatic adenoma, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the hepatic adenoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
hepatic lipase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hepatic lipase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
cpt deficiency, hepatic, type ii Gene SetFrom OMIM Gene-Disease Associations genes associated with the cpt deficiency, hepatic, type ii phenotype from the curated OMIM Gene-Disease Associations dataset. |
cpt deficiency, hepatic, type ia Gene SetFrom OMIM Gene-Disease Associations genes associated with the cpt deficiency, hepatic, type ia phenotype from the curated OMIM Gene-Disease Associations dataset. |
?renal-hepatic-pancreatic dysplasia 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?renal-hepatic-pancreatic dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hepatic Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term hepatic in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
hepatic stellate cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue hepatic stellate cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
hepatic cecum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hepatic cecum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hepatic primordium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hepatic primordium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hepatic stellate cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hepatic stellate cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hepatic artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hepatic artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hepatic stellate cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hepatic stellate cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Liver-endothelial cell of hepatic sinusoid Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Liver-endothelial cell of hepatic sinusoid relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Hepatic Form Of Wilson Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Form Of Wilson Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Methionine Adenosyltransferase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Methionine Adenosyltransferase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Angiomyolipoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Angiomyolipoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Encephalopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Vein Thrombosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Moderate Hepatic Insufficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Moderate Hepatic Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Minimal Hepatic Encephalopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Minimal Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Veno-Occlusive Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Veno-Occlusive Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Amyloidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Amyloidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Lipase Deficiency (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Lipase Deficiency (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Granuloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Granuloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Hepatic Pancreatic Dysplasia Dandy Walker Cyst Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Hepatic Pancreatic Dysplasia Dandy Walker Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Siderosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Siderosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Infarction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Calcification Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Cancer Metastatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Cancer Metastatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Hepatic Steatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Hepatic Steatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Periportal Necrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Periportal Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fulminant Hepatic Failure With Cerebral Edema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fulminant Hepatic Failure With Cerebral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Coma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Coma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Stupor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Stupor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gsd Iv, Classic Hepatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gsd Iv, Classic Hepatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Osteodystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Osteodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subacute Hepatic Necrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subacute Hepatic Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Schistosomiasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Schistosomiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Adenomas, Familial Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Adenomas, Familial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Ductular Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Ductular Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Hepatic Encephalopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal-Hepatic-Pancreatic Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal-Hepatic-Pancreatic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Hemosiderosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Hemosiderosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Accessory Hepatic Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Accessory Hepatic Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Cyst Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Cyst Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Venoocclusive Disease With Immunodeficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Venoocclusive Disease With Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Hepatic Neuroendocrine Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Hepatic Neuroendocrine Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hepatic Artery Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Elevated Hepatic Transaminase Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Hepatic Transaminase in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Microvesicular Hepatic Steatosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Microvesicular Hepatic Steatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Diffuse Hepatic Steatosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Hepatic Steatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Hepatic Glycogen Content Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Hepatic Glycogen Content in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hepatic Insufficiency Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hepatic Necrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hepatic Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Hepatic Iron Concentration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Hepatic Iron Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Hepatic Vasculature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Hepatic Vasculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Macrovesicular Hepatic Steatosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macrovesicular Hepatic Steatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hepatic Sclerosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Alkaline Phosphatase Of Hepatic Origin Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Alkaline Phosphatase Of Hepatic Origin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Malformation Of The Hepatic Ductal Plate Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Malformation Of The Hepatic Ductal Plate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hepatic Vascular Malformations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Vascular Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Massive Hepatic Necrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Massive Hepatic Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hepatic Glycogen Storage Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Glycogen Storage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hepatic Hypertrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hepatic Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
hepatic immune response Gene SetFrom GO Biological Process Annotations 2023 genes participating in the hepatic immune response biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of hepatic stellate cell activation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hepatic stellate cell activation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2023 dataset. |
increased hepatic hemangioma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hepatic hemangioma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
multifocal hepatic necrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the multifocal hepatic necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hepatic necrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hepatic necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
macrovesicular hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the macrovesicular hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
microvesicular hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the microvesicular hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed hepatic development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed hepatic development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hepatic necrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hepatic necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to diet-induced hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to diet-induced hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
diffuse hepatic necrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the diffuse hepatic necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to age-related hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to age-related hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic vein morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic vein morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic cord morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic cord morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic portal vein morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic portal vein morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to diet-induced hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to diet-induced hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic diverticulum morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic diverticulum morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to alcohol-induced hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to alcohol-induced hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic glucose production Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic glucose production phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hepatic glucose production Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hepatic glucose production phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hepatic glucose production Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hepatic glucose production phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hepatic portal vein stenosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hepatic portal vein stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic portal vein formation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic portal vein formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated hepatic portal vein Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated hepatic portal vein phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic portal vein connection Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic portal vein connection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic vein connection Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic vein connection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic portal vein thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic portal vein thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to age-related hepatic steatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to age-related hepatic steatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Ito cell (hepatic stellate cell)_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Ito cell (hepatic stellate cell)_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Ito cell (hepatic stellate cell)_Liver_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Ito cell (hepatic stellate cell)_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Liver bud hepatic cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Liver bud hepatic cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic stellate cell_Liver_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic stellate cell_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Putative hepatic stem cell_Left lobe_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Putative hepatic stem cell_Left lobe_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic stellate cell_Fetal liver_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic stellate cell_Fetal liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic stellate cell_Fetal liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic stellate cell_Fetal liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic progenitor cell_Liver_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic progenitor cell_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic progenitor cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic progenitor cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic stellate cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic stellate cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Activated hepatic stellate cell_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Activated hepatic stellate cell_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic progenitor-like cell_Pluripotent stem cell_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic progenitor-like cell_Pluripotent stem cell_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hepatic stellate cell_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hepatic stellate cell_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Liver_CT1_quiescent hepatic stellate cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Liver_CT1_quiescent hepatic stellate cell cell type from the HuBMAP ASCT+B dataset. |
Liver_CT1_quiescent hepatic stellate cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Liver_CT1_quiescent hepatic stellate cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
hepatic immune response Gene SetFrom GO Biological Process Annotations 2025 genes participating in the hepatic immune response biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of hepatic stellate cell activation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of hepatic stellate cell activation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hepatic venoocclusive disease with immunodeficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hepatic vascular disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic encephalopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic encephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic coma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic coma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic veno-occlusive disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic veno-occlusive disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial hepatic adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial hepatic adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic venoocclusive disease with immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic infarction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
renal-hepatic-pancreatic dysplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease renal-hepatic-pancreatic dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic angiomyolipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic angiomyolipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sclerosing hepatic carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sclerosing hepatic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic flexure cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hepatic flexure cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hepatic stellate cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Hepatic stellate cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Hepatic stellate cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hepatic stellate cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hepatic artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hepatic artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hepatic stellate cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hepatic stellate cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hepatic cecum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hepatic cecum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hepatic primordium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hepatic primordium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hepatic methionine adenosyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatic methionine adenosyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Renal-hepatic-pancreatic dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal-hepatic-pancreatic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatic veno-occlusive disease-immunodeficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatic veno-occlusive disease-immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatic adenomas Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatic adenomas phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Glycogen storage disorder due to hepatic glycogen synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disorder due to hepatic glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyperlipidemia due to hepatic triglyceride lipase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperlipidemia due to hepatic triglyceride lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatic cysts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatic cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Increased hepatic glycogen content Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Increased hepatic glycogen content phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatic lipid content in extreme obesity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatic lipid content in extreme obesity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fibrosis of extraocular muscles, congenital, 3b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cystic fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cystic fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oral Submucous Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Oral Submucous Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Peritoneal Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peritoneal Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Endomyocardial Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Endomyocardial Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset. |
Cystic Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cystic Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Fibrosis of Extraocular Muscles, Congenital, 3B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis of Extraocular Muscles, Congenital, 3B from the curated CTD Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles, Congenital, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 2 from the curated CTD Gene-Disease Associations dataset. |
CYSTIC FIBROSIS, MODIFIER OF, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CYSTIC FIBROSIS, MODIFIER OF, 1 from the curated CTD Gene-Disease Associations dataset. |
Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Idiopathic Pulmonary Fibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset. |
Cystic Fibrosis Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Cystic Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Idiopathic Pulmonary Fibrosis Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
cystic fibrosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cystic fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
idiopathic pulmonary fibrosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic pulmonary fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
cystic fibrosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cystic fibrosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
pulmonary fibrosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pulmonary fibrosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
cystic fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cystic fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
oral submucous fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease oral submucous fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
diffuse pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diffuse pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
localized pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease localized pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endomyocardial fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endomyocardial fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
preretinal fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease preretinal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
idiopathic pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cholestasis, intrahepatic; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; ileus; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; ileus; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; steatorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; lung diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; lung diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung neoplasms; neoplasm of lung ; pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung neoplasms; neoplasm of lung ; pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; pigeon breeders disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; pigeon breeders disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertrophy, right ventricular; pulmonary fibrosis; scleroderma, systemic; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchiectasis; cystic fibrosis; pseudomonas infections; staphylococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; fibrosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; sarcoidosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; sarcoidosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; diabetes mellitus, type 1; hyperglycemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes mellitus, type 1; hyperglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; candida Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; candida in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease child nutrition disorders; cystic fibrosis; pseudomonas infections; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital fibrosis of extraocular muscles type 2 Gene SetFrom 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. |
colonic diseases; cystic fibrosis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic diseases; cystic fibrosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chemotherapy-induced pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chemotherapy-induced pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; glomerulonephritis, iga; hepatitis c, chronic; iga glomerulonephritides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; lung diseases; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; lung diseases; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis lung disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis lung disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; sarcoidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; rhinitis; sinusitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; ileus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; disease susceptibility; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; disease susceptibility; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; retroperitoneal fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; retroperitoneal fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pancreatitis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; intussusception Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; intussusception in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; fibrosis; mouth neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; fibrosis; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; carcinoma, ductal, breast; fibrosis; invasive ductal breast carcinoma; mammary neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung allograft fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung allograft fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; disease models, animal; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; disease models, animal; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; cystic fibrosis; growth disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial infections; burkholderia infections; cystic fibrosis; pseudomonas infections; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; diabetes complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; fibrosis; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; fibrosis; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; urogenital abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; urogenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulmonary fibrosis; scleroderma, systemic; systemic scleroderma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulmonary fibrosis; scleroderma, systemic; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; protein-energy malnutrition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; protein-energy malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital fibrosis of the extraocular muscles Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital fibrosis of the extraocular muscles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; maxillary sinusitis; sinusitis, maxillary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; maxillary sinusitis; sinusitis, maxillary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; diabetes mellitus; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; diabetes mellitus; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis b, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis b, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
clonorchiasis; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease clonorchiasis; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung diseases, interstitial; pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung diseases, interstitial; pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; steatorrhea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; steatorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; lung diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; lung diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oral submucous fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; pancreatitis, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oral submucous fibrosis; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oral submucous fibrosis; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
burkholderia infections; cystic fibrosis; pseudomonas infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease burkholderia infections; cystic fibrosis; pseudomonas infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; neoplasms; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; neoplasms; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; dental caries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; dental caries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; paranasal sinus diseases; sinus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; paranasal sinus diseases; sinus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aspergillosis; cystic fibrosis; lung diseases, fungal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aspergillosis; cystic fibrosis; lung diseases, fungal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; gastrointestinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hcv-induced liver fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hcv-induced liver fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; growth disorders; nutrition disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; growth disorders; nutrition disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; cystic fibrosis; ileus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femur head necrosis; pulmonary fibrosis; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; p. aeruginosa infection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; p. aeruginosa infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; leukoplakia, oral; mouth neoplasms; oral submucous fibrosis; precancerous conditions; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; fibrosis; mammary neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; fibrosis; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; exocrine pancreatic insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; exocrine pancreatic insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis; lung diseases, interstitial; scleroderma, systemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fibrosis; lung diseases, interstitial; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
oral cancer; oral submucous fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease oral cancer; oral submucous fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
idiopathic pulmonary fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrosis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term fibrosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Cystic fibrosis severity Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Cystic fibrosis severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Idiopathic pulmonary fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hepatitis C induced liver fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
cystic fibrosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease cystic fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
idiopathic pulmonary fibrosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
pulmonary fibrosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the pulmonary fibrosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
tubulointerstitial fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pancreatic fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pancreatic fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
myocardial fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the myocardial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arterial intimal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the arterial intimal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital fibrosis of extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital fibrosis of extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
portal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the portal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retroperitoneal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the retroperitoneal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
perifollicular fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the perifollicular fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
endocardial fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the endocardial fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
periportal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the periportal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary aterial intimal fibrosis Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary aterial intimal fibrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Oral Submucous Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Oral Submucous Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cystic Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Cystic Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Idiopathic Pulmonary Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Retroperitoneal Fibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Retroperitoneal Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cystic fibrosis transmembrane conductance regulator Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cystic fibrosis transmembrane conductance regulator protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
retinal fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the retinal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cardiac interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cardiac interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cardiac fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cardiac fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
liver fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the liver fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spleen fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the spleen fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
perivascular fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the perivascular fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
urinary bladder fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the urinary bladder fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal glomerulus fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle endomysial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary interstitial fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skin fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skin fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{pulmonary fibrosis, telomere-related, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, telomere-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
cystic fibrosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the cystic fibrosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary fibrosis, idiopathic Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary fibrosis, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 3b Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3b phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis of extraocular muscles, congenital, 3a Gene SetFrom OMIM Gene-Disease Associations genes associated with the fibrosis of extraocular muscles, congenital, 3a phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pulmonary fibrosis, idiopathic, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, idiopathic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{cystic fibrosis lung disease, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {cystic fibrosis lung disease, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{meconium ileus in cystic fibrosis, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {meconium ileus in cystic fibrosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
fibrosis Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term fibrosis in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
cystic fibrosis Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease cystic fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
idiopathic pulmonary fibrosis Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis, Liver Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis, Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cardiac Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Bile Duct Gene SetFrom 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. |
Oral Submucous Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oral Submucous Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peritoneal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peritoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Interstitial Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Interstitial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Exacerbation Of Idiopathic Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Macular Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macular Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Pleura Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Pleura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Fibrosis - From Asbestos Exposure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Fibrosis - From Asbestos Exposure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Idiopathic Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arterial Intimal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arterial Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Aterial Intimal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Aterial Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nephrogenic Systemic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nephrogenic Systemic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic Idiopathic Pulmonary Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Retroperitoneal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Retroperitoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retinal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atypical Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atypical Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Classical Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Classical Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis In Children Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis Related Diabetes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis Related Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis With Meconium Ileus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis With Meconium Ileus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Liver Disease Associated With Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver Disease Associated With Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sweat Chloride Elevation Without Cystic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sweat Chloride Elevation Without Cystic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Extraocular Muscles Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Urinary Bladder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Urinary Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arterial Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arterial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ovarian Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ovarian Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Fibrosis Of The Extraocular Muscles Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Fibrosis Of The Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intimal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intimal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oesophageal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oesophageal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Corpus Cavernosum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Corpus Cavernosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystic Fibrosis Modifier 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystic Fibrosis Modifier 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Prostatic Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Prostatic Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyroid Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Portal Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Portal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tubulointerstitial Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubulointerstitial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intestinal Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intestinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Endomyocardial Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endomyocardial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Periportal Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periportal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skeletal Muscle Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibrosis Of Mesentery Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis Of Mesentery in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Myocardial Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myocardial Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibrosis Of Extraocular Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibrosis Of Extraocular Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Perifollicular Fibrosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Perifollicular Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
pulmonary fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cardiac fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cardiac interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
liver fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the liver fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle endomysial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skin fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skin fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
urinary bladder fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the urinary bladder fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
skeletal muscle fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pulmonary interstitial fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
retina fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the retina fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal glomerulus fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
perivascular fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the perivascular fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
spleen fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the spleen fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
trachea fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the trachea fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ovary fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
intestinal fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the intestinal fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
epididymis fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the epididymis fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
uterus fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the uterus fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Idiopathic pulmonary fibrosis cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Lung fibrosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Lung fibrosis pathway from the WikiPathways Pathways 2024 dataset. |
HIPK2 in kidney fibrosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the HIPK2 in kidney fibrosis pathway from the WikiPathways Pathways 2024 dataset. |
Nitric oxide metabolism in cystic fibrosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Nitric oxide metabolism in cystic fibrosis pathway from the WikiPathways Pathways 2024 dataset. |
Defective CFTR causes cystic fibrosis Gene Setproteins participating in the Defective CFTR causes cystic fibrosis pathway from the Reactome Pathways 2024 dataset. |
Cystic fibrosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cystic fibrosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital fibrosis of the extraocular muscles from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Cystic fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cystic fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Oral submucous fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oral submucous fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Renal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Preretinal fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Preretinal fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endomyocardial fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endomyocardial fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Postinflammatory pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Postinflammatory pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diffuse pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Localized pulmonary fibrosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Localized pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital fibrosis of the extraocular muscles 3A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital fibrosis of the extraocular muscles 3A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Idiopathic pulmonary fibrosis disease specific cell type Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Idiopathic pulmonary fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cystic fibrosis disease specific cell type Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cystic fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Congenital fibrosis of extraocular muscles Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fibrosis of extraocular muscles Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fibrosis of extraocular muscles phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Periportal fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Periportal fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cystic fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Idiopathic Pulmonary Fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic Pulmonary Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cystic fibrosis-gastritis-megaloblastic anemia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic fibrosis-gastritis-megaloblastic anemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diffuse interstitial pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse interstitial pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hepatorenocardiac degenerative fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatorenocardiac degenerative fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Meconium ileus in cystic fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meconium ileus in cystic fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lung disease severity in cystic fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lung disease severity in cystic fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis severity in HIV/hepatitis C co-infection Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis severity in HIV/hepatitis C co-infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis in pediatric non-alcoholic fatty acid liver disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis in pediatric non-alcoholic fatty acid liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Idiopathic pulmonary fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cystic fibrosis-related diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cystic fibrosis-related diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hepatitis C induced liver fibrosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatitis C induced liver fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Liver fibrosis in non-alcoholic fatty liver disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Liver fibrosis in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cystic fibrosis severity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cystic fibrosis severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene SetFrom Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset. |
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coloboma, uveal, with cleft lip and palate and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset. |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset. |
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety and hostility and depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vitamins and metabolites in pregnant women and neonates Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on amino acids and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene SetFrom OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset. |
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset. |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset. |
Synthesis and interconversion of nucleotide di- and triphosphates Gene Setproteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
SRF and miRs in smooth muscle differentiation and proliferation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset. |
ApoE and miR 146 in inflammation and atherosclerosis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset. |
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset. |
Somatroph axis GH and its relationship to dietary restriction and aging Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset. |
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Setproteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Setproteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset. |
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Setproteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset. |
FGFR1c and Klotho ligand binding and activation Gene Setproteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset. |
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Setproteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset. |
PI and PC transport between ER and Golgi membranes Gene Setproteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset. |
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Setproteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset. |
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Setproteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset. |
Synthesis and processing of ENV and VPU Gene Setproteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset. |
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Setproteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset. |
Transport of bile salts and organic acids, metal ions and amine compounds Gene Setproteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset. |
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Setproteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset. |
racemase and epimerase activity, acting on carbohydrates and derivatives Gene SetFrom GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Regulation of gene expression and signal transduction in immune and stress responses Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Basic cell groups and regions Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
head and face region of M1 Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
telomeres telomerase cellular aging and immortality Gene SetFrom Biocarta Pathways proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset. |
mcalpain and friends in cell motility Gene SetFrom Biocarta Pathways proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset. |
role of ppar-gamma coactivators in obesity and thermogenesis Gene SetFrom Biocarta Pathways proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset. |
il12 and stat4 dependent signaling pathway in th1 development Gene SetFrom Biocarta Pathways proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset. |
hypoxia and p53 in the cardiovascular system Gene SetFrom Biocarta Pathways proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset. |
lissencephaly gene (lis1) in neuronal migration and development Gene SetFrom Biocarta Pathways proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset. |
role of erbb2 in signal transduction and oncology Gene SetFrom Biocarta Pathways proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset. |
corticosteroids and cardioprotection Gene SetFrom Biocarta Pathways proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset. |
cyclins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
mechanism of acetaminophen activity and toxicity Gene SetFrom Biocarta Pathways proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset. |
nfat and hypertrophy of the heart Gene SetFrom Biocarta Pathways proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset. |
acetylation and deacetylation of rela in nucleus Gene SetFrom Biocarta Pathways proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset. |
thrombin signaling and protease-activated receptors Gene SetFrom Biocarta Pathways proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset. |
antigen processing and presentation Gene SetFrom Biocarta Pathways proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset. |
stathmin and breast cancer resistance to antimicrotubule agents Gene SetFrom Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset. |
role of ß-arrestins in the activation and targeting of map kinases Gene SetFrom Biocarta Pathways proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset. |
role of pi3k subunit p85 in regulation of actin organization and cell migration Gene SetFrom Biocarta Pathways proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset. |
btg family proteins and cell cycle regulation Gene SetFrom Biocarta Pathways proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset. |
control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene SetFrom Biocarta Pathways proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset. |
endocytotic role of ndk phosphins and dynamin Gene SetFrom Biocarta Pathways proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset. |
regulation of eif-4e and p70s6 kinase Gene SetFrom Biocarta Pathways proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset. |
estrogen responsive protein efp controls cell cycle and breast tumors growth Gene SetFrom Biocarta Pathways proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset. |
vegf hypoxia and angiogenesis Gene SetFrom Biocarta Pathways proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset. |
yaci and bcma stimulation of b cell immune responses Gene SetFrom Biocarta Pathways proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset. |
lck and fyn tyrosine kinases in initiation of tcr activation Gene SetFrom Biocarta Pathways proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset. |
hiv-1 nef: negative effector of fas and tnf Gene SetFrom Biocarta Pathways proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset. |
nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene SetFrom Biocarta Pathways proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset. |
ucalpain and friends in cell spread Gene SetFrom Biocarta Pathways proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset. |
ionomycin and phorbal ester signaling pathway Gene SetFrom Biocarta Pathways proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset. |
carm1 and regulation of the estrogen receptor Gene SetFrom Biocarta Pathways proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset. |
phosphoinositides and their downstream targets Gene SetFrom Biocarta Pathways proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset. |
melanocyte development and pigmentation pathway Gene SetFrom Biocarta Pathways proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset. |
akap95 role in mitosis and chromosome dynamics Gene SetFrom Biocarta Pathways proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset. |
transcription factor creb and its extracellular signals Gene SetFrom Biocarta Pathways proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset. |
visceral fat deposits and the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset. |
the igf-1 receptor and longevity Gene SetFrom Biocarta Pathways proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset. |
cdc25 and chk1 regulatory pathway in response to dna damage Gene SetFrom Biocarta Pathways proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset. |
human cytomegalovirus and map kinase pathways Gene SetFrom Biocarta Pathways proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset. |
influence of ras and rho proteins on g1 to s transition Gene SetFrom Biocarta Pathways proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset. |
proteolysis and signaling pathway of notch Gene SetFrom Biocarta Pathways proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset. |
apoptotic dna-fragmentation and tissue homeostasis Gene SetFrom Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset. |
ion channels and their functional role in vascular endothelium Gene SetFrom Biocarta Pathways proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset. |
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene SetFrom Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset. |
fosb gene expression and drug abuse Gene SetFrom Biocarta Pathways proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset. |
links between pyk2 and map kinases Gene SetFrom Biocarta Pathways proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset. |
opposing roles of aif in apoptosis and cell survival Gene SetFrom Biocarta Pathways proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset. |
degradation of the rar and rxr by the proteasome Gene SetFrom Biocarta Pathways proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset. |
cadmium induces dna synthesis and proliferation in macrophages Gene SetFrom Biocarta Pathways proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset. |
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene SetFrom Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset. |
role of brca1 brca2 and atr in cancer susceptibility Gene SetFrom Biocarta Pathways proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset. |
chrebp regulation by carbohydrates and camp Gene SetFrom Biocarta Pathways proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset. |
pten dependent cell cycle arrest and apoptosis Gene SetFrom Biocarta Pathways proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset. |
induction of apoptosis through dr3 and dr4/5 death receptors Gene SetFrom Biocarta Pathways proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset. |
CIITA-18437201-Raji B cells and iDC-human Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
VDR-23401126-LCL-AND-THP1-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
BACH1-22875853-HELA-AND-SCP4-HUMAN Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
Hypothyroidism, central, and testicular enlargement Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, mental retardation, and seizures Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vater association with macrocephaly and ventriculomegaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal hamartomas nephroblastomatosis and fetal gigantism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microtia, hearing impairment, and cleft palate Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, spastic quadriplegia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined cellular and humoral immune defects with granulomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined d-2- and l-2-hydroxyglutaric aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sinoatrial node dysfunction and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation with language impairment and autistic features Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Warts, hypogammaglobulinemia, infections, and myelokathexis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, anterior maxillary protrusion, and strabismus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile convulsions and paroxysmal choreoathetosis, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple Cutaneous and Mucosal Venous Malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy hereditary sensory and autonomic type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly with mental retardation and digital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene SetFrom 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. |
Growth retardation, developmental delay, coarse facies, and early death Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anemia sideroblastic and spinocerebellar ataxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial dysmorphism, immunodeficiency, livedo, and short stature Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, congenital heart defects, and posterior embryotoxon Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene SetFrom 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 SetFrom 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. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Iris coloboma with ptosis, hypertelorism, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Rigidity and multifocal seizure syndrome, lethal neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alopecia, neurologic defects, and endocrinopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Knuckle pads, deafness AND leukonychia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multicentric osteolysis, nodulosis and arthropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stapes ankylosis with broad thumb and toes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Noonan syndrome and Noonan-related syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, short stature, and impaired glucose metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macrocephaly, alopecia, cutis laxa, and scoliosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypomyelination and Congenital Cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy dilated with woolly hair and keratoderma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, microphthalmia and nystagmus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and anterior segment dysgenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene SetFrom 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 SetFrom 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 SetFrom 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. |