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Leiomyomatosis, esophageal and vulval, with nephropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leiomyomatosis, esophageal and vulval, with nephropathy from the curated CTD Gene-Disease Associations dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset. |
leiomyomatosis and renal cell cancer Gene SetFrom OMIM Gene-Disease Associations genes associated with the leiomyomatosis and renal cell cancer phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hereditary Leiomyomatosis And Renal Cell Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Leiomyomatosis And Renal Cell Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary leiomyomatosis and renal cell carcinoma pathway Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Hereditary leiomyomatosis and renal cell carcinoma pathway pathway from the WikiPathways Pathways 2024 dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
vulval paget's disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulval paget's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
vulval lichen sclerosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vulval lichen sclerosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vulval Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term vulval in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Vulval Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vulval Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vulval Cancer Metastatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vulval Cancer Metastatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vulval Paget's disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vulval Paget's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
leiomyomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leiomyomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intravenous leiomyomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intravenous leiomyomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
carcinoma, renal cell; kidney neoplasms; leiomyoma; leiomyomatosis; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; leiomyoma; leiomyomatosis; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leiomyomatosis; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leiomyomatosis; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary leiomyomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary leiomyomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leiomyomatosis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term leiomyomatosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
diffuse leiomyomatosis Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse leiomyomatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Leiomyomatosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Leiomyomatosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Leiomyomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leiomyomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intravenous Leiomyomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intravenous Leiomyomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Leiomyomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Leiomyomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leiomyomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leiomyomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intravenous leiomyomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intravenous leiomyomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diffuse peritoneal leiomyomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse peritoneal leiomyomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 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. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset. |
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy with Pretibial Epidermolysis Bullosa and Deafness from the curated CTD Gene-Disease Associations dataset. |
diabetic nephropathy and retinopathy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic nephropathy and retinopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom OMIM Gene-Disease Associations genes associated with the angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated OMIM Gene-Disease Associations dataset. |
nephropathy with pretibial epidermolysis bullosa and deafness Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephropathy with pretibial epidermolysis bullosa and deafness phenotype from the curated OMIM Gene-Disease Associations dataset. |
Nephropathy With Pretibial Epidermolysis Bullosa And Deafness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nephropathy With Pretibial Epidermolysis Bullosa And Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal and Gastric Varices Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal and Gastric Varices from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
lung cancer; colorectal cancer; esophageal cancer; head and neck cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; head and neck cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; esophageal neoplasms; head and neck neoplasms; lung neoplasms; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; esophageal neoplasms; head and neck neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; head and neck neoplasms; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; head and neck neoplasms; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD 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. |
esophageal neoplasms; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal and gastric cardia cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal and gastric cardia cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastric cardia adenocarcinoma and esophageal squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastric cardia adenocarcinoma and esophageal squamous cell carcinoma 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. |
esophageal cancer and lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer and lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer and gastric cardiac carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer and gastric cardiac carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Esophageal cancer and gastric cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer and gastric cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Esophageal and Gastric Varices Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Esophageal and Gastric Varices phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Esophageal And Gastric Varices Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal And Gastric Varices in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer and gastric cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer and gastric cancer 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. |
Hyperuricemic nephropathy, familial juvenile, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multicentric osteolysis nephropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multicentric osteolysis nephropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nephronophthisis-like nephropathy 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nephronophthisis-like nephropathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Balkan Nephropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Balkan Nephropathy from the curated CTD Gene-Disease Associations dataset. |
NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 from the curated CTD Gene-Disease Associations dataset. |
Hyperuricemic Nephropathy, Familial Juvenile 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset. |
Hypertensive Nephropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertensive Nephropathy from the curated CTD Gene-Disease Associations dataset. |
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset. |
Nephropathy, Progressive, with Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy, Progressive, with Deafness from the curated CTD Gene-Disease Associations dataset. |
familial juvenile hyperuricemic nephropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
acute urate nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute urate nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
balkan nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease balkan nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial juvenile hyperuricemic nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, diabetic; diabetes, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, diabetic; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; diabetes, type 1; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; diabetes, type 1; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; cerebrovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, basement membrane Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, basement membrane in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type 2 diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type 2 diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, congenital obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, congenital obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; peripheral vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
retinopathy, diabetic; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease retinopathy, diabetic; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetic nephropathy; polycystic kidney disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic nephropathy; polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hyperhomocysteinemia; kidney failure, chronic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hyperhomocysteinemia; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
immunoglobin a nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease immunoglobin a nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetic nephropathy; retinopathy, diabetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic nephropathy; retinopathy, diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, diabetic; retinopathy, diabetic; neuropathy, diabetic; microalbuminuria, diabetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, diabetic; retinopathy, diabetic; neuropathy, diabetic; microalbuminuria, diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; nephropathy, diabetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; nephropathy, diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ig a nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ig a nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; diabetes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; diabetic foot; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; diabetic foot; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, diabetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; diabetes, type 2; hypertension; nephropathy, diabetic; albuminuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; diabetes, type 2; hypertension; nephropathy, diabetic; albuminuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, diabetic; blood pressure, arterial; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, diabetic; blood pressure, arterial; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reflux nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reflux nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, iga Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, iga in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple sclerosis; iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; retinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetic nephropathy; hypertensive disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetic nephropathy; hypertensive disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetic nephropathies; diabetic nephropathy; glomerulonephritis; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; glomerulonephritis; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aids-associated nephropathy; focal segmental glomsclerosis; glomerulosclerosis, focal segmental Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aids-associated nephropathy; focal segmental glomsclerosis; glomerulosclerosis, focal segmental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aids-associated nephropathy; glomerulosclerosis, focal segmental; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetic nephropathy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic nephropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; blood pressure, arterial; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; blood pressure, arterial; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
balkan nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease balkan nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
systemic lupus erythematosus; nephropathy, iga Gene SetFrom GAD Gene-Disease Associations genes associated with the disease systemic lupus erythematosus; nephropathy, iga in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, diabetic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, diabetic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; diabetic nephropathies; diabetic nephropathy; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; diabetic nephropathies; diabetic nephropathy; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
allograft nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease allograft nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadaver; diabetic nephropathies; diabetic nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadaver; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term nephropathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Type 1 diabetes nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Type 1 diabetes nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
IgA nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the IgA nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Type 2 diabetes nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Type 2 diabetes nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Nephropathy (idiopathic membranous) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Nephropathy (idiopathic membranous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
nephropathy Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the nephropathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
nephropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the nephropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
membranous nephropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the membranous nephropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Balkan Nephropathy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Balkan Nephropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
nephropathy due to cfhr5 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
nephronophthisis-like nephropathy 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephronophthisis-like nephropathy 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypertensive nephropathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypertensive nephropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
iga nephropathy, susceptibility to, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the iga nephropathy, susceptibility to, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemic nephropathy, familial juvenile 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemic nephropathy, familial juvenile 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperuricemic nephropathy, familial juvenile, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperuricemic nephropathy, familial juvenile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
nephropathy-hypertension Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephropathy-hypertension phenotype from the curated OMIM Gene-Disease Associations dataset. |
nephropathy, progressive, with deafness Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephropathy, progressive, with deafness phenotype from the curated OMIM Gene-Disease Associations dataset. |
{?membranous nephropathy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {?membranous nephropathy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{iga nephropathy, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {iga nephropathy, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Aristolochic Acid Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aristolochic Acid Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Balkan Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Balkan Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Contrast - Induced Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Contrast - Induced Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypertensive Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypertensive Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Immunoglobulin A Nephropathy (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Immunoglobulin A Nephropathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Radiation Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Radiation Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reflux Nephropathy (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reflux Nephropathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sickle Cell Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sickle Cell Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microalbuminuric Diabetic Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microalbuminuric Diabetic Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstructive Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Obstructive Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Macroalbuminuric Diabetic Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macroalbuminuric Diabetic Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bk Virus Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bk Virus Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyomavirus-Associated Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyomavirus-Associated Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Drug-Induced Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Drug-Induced Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Crystal Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Crystal Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Urate Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urate Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nephropathy Salt Wasting Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nephropathy Salt Wasting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ischemic Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperuricemic Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperuricemic Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gouty Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gouty Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Immunoglobulin A Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Immunoglobulin A Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Osteolysis, Hereditary, Of Carpal Bones With Or Without Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proteinuric Diabetic Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proteinuric Diabetic Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Amyloid Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Amyloid Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignancy-Associated Membranous Nephropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignancy-Associated Membranous Nephropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Iga Nephropathy, Susceptibility To, 3 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Iga Nephropathy, Susceptibility To, 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obstructive nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Obstructive nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial juvenile hyperuricemic nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Balkan nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Balkan nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Polyomavirus-associated nephropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Polyomavirus-associated nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
nephronophthisis-like nephropathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease nephronophthisis-like nephropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial amyloid nephropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial amyloid nephropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial juvenile hyperuricemic nephropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial juvenile hyperuricemic nephropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nephronophthisis-like nephropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nephronophthisis-like nephropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyperuricemic nephropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperuricemic nephropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
IgA nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the IgA nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Membranous nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Membranous nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Type 2 diabetes nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 2 diabetes nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Type 2 diabetes nephropathy including microalbuminuria Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 2 diabetes nephropathy including microalbuminuria phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diabetic nephropathy in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic nephropathy in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Serum galactose-deficient IgA1 levels in IgA nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Serum galactose-deficient IgA1 levels in IgA nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Type 1 diabetes nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Type 1 diabetes nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Idiopathic membranous nephropathy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic membranous nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal Achalasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal Achalasia from the curated CTD Gene-Disease Associations dataset. |
Esophageal Stenosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal Stenosis from the curated CTD Gene-Disease Associations dataset. |
Esophageal Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal Neoplasms from the curated CTD Gene-Disease Associations dataset. |
Esophageal Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal Diseases from the curated CTD Gene-Disease Associations dataset. |
Esophageal Squamous Cell Carcinoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Esophageal Squamous Cell Carcinoma from the curated CTD Gene-Disease Associations dataset. |
Esophageal Neoplasms Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Esophageal Neoplasms in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
esophageal disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease esophageal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
esophageal cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease esophageal cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
esophageal disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal adenosquamous carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal adenosquamous carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal atresia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal basaloid squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal basaloid squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mucoepidermoid esophageal carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mucoepidermoid esophageal carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal candidiasis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
esophageal varix Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease esophageal varix in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 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. |
adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; gastric cardia adenocarcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; gastric cardia adenocarcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; diarrhea; esophageal neoplasms; nausea; neutropenia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; diarrhea; esophageal neoplasms; nausea; neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal mucosal injury Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal mucosal injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; esophageal neoplasms; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; esophageal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; neoplasm recurrence, local; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; neoplasm recurrence, local; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; oropharyngolaryngeal cancers; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; oropharyngolaryngeal cancers; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; esophageal neoplasms; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; esophageal neoplasms; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; hyperglycemia; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; hyperglycemia; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cachexia; esophageal neoplasms; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cachexia; esophageal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colonic neoplasms; esophageal neoplasms; oesophageal neoplasm; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic neoplasms; esophageal neoplasms; oesophageal neoplasm; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer; bladder cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer; bladder cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; carcinoma, squamous cell; cell transformation, neoplastic; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; carcinoma, squamous cell; cell transformation, neoplastic; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; hyperplasia; metaplasia; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; hyperplasia; metaplasia; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; carcinoma, squamous cell; esophageal neoplasms; papillomavirus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; carcinoma, squamous cell; esophageal neoplasms; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; esophageal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; lung diseases; oesophageal neoplasm; postoperative complications; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; lung diseases; oesophageal neoplasm; postoperative complications; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; aneuploidy; barrett esophagus; esophageal neoplasms; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; aneuploidy; barrett esophagus; esophageal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diarrhea; esophageal neoplasms; neutropenia; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diarrhea; esophageal neoplasms; neutropenia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal adenocarcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal adenocarcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; carcinoma, squamous cell; esophageal neoplasms; laryngeal neoplasms; neoplasm invasiveness; oropharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; carcinoma, squamous cell; esophageal neoplasms; laryngeal neoplasms; neoplasm invasiveness; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chagas disease; esophageal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chagas disease; esophageal neoplasms 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. |
carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; colorectal neoplasms; esophageal neoplasms; lung neoplasms; nasopharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; colorectal neoplasms; esophageal neoplasms; lung neoplasms; nasopharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cell transformation, neoplastic; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; gastritis, atrophic; gastrointestinal neoplasms; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; gastritis, atrophic; gastrointestinal neoplasms; helicobacter infections 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. |
adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bladder neoplasm; esophageal neoplasms; leiomyoma; lung neoplasms; neoplasm of lung ; oesophageal neoplasm; urinary bladder neoplasms; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bladder neoplasm; esophageal neoplasms; leiomyoma; lung neoplasms; neoplasm of lung ; oesophageal neoplasm; urinary bladder neoplasms; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; esophageal neoplasms; hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; esophageal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; esophageal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; gastric cardia cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; gastric cardia cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tuberculosis; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tuberculosis; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; neoplasm recurrence, local; neovascularization, pathologic; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; neoplasm recurrence, local; neovascularization, pathologic; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; barrett esophagus; gastroesophageal reflux disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; barrett esophagus; gastroesophageal reflux disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; esophageal neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal atresia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal atresia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; flushing; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; flushing; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; stomach cancer; barret's esophagus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; stomach cancer; barret's esophagus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; flushing; oesophageal neoplasm; oropharyngeal neoplasms; squamous cell carcinoma; tumor of oropharynx Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; flushing; oesophageal neoplasm; oropharyngeal neoplasms; squamous cell carcinoma; tumor of oropharynx in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; neoplasm metastasis; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; neoplasm metastasis; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; gastrointestinal neoplasms; oesophageal neoplasm; pancreatic neoplasm; pancreatic neoplasms; squamous cell carcinoma; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; gastrointestinal neoplasms; oesophageal neoplasm; pancreatic neoplasm; pancreatic neoplasms; squamous cell carcinoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer; bladder cancer; warfarin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; folic acid deficiency; gastrointestinal neoplasms; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; folic acid deficiency; gastrointestinal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; gastric cardiac cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; gastric cardiac cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; cervical neoplasm; esophageal neoplasms; mammary neoplasms; oesophageal neoplasm; uterine cervical neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; cervical neoplasm; esophageal neoplasms; mammary neoplasms; oesophageal neoplasm; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; flushing; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; flushing; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; barrett's esophagus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; barrett's esophagus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal achalasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal achalasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; gastroesophageal reflux; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; gastroesophageal reflux; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; esophagitis; metaplasia; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; esophagitis; metaplasia; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; esophageal neoplasms; esophagitis, peptic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; esophagitis, peptic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; hyperhomocysteinemia; neoplasms; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; hyperhomocysteinemia; neoplasms; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; esophageal neoplasms; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; esophageal neoplasms; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; carcinoma, squamous cell; digestive system neoplasms; esophageal neoplasms; melanosis; oesophageal neoplasm; precancerous conditions; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; carcinoma, squamous cell; digestive system neoplasms; esophageal neoplasms; melanosis; oesophageal neoplasm; precancerous conditions; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; gastroesophageal reflux Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; gastroesophageal reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast cancer; colorectal cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast cancer; colorectal cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; cardiac cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; cardiac cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; carcinoma, squamous cell; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal cancer; laryngeal cancer; oropharynx cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal cancer; laryngeal cancer; oropharynx cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; tumor virus infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; papillomavirus infections; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; esophageal neoplasms; heartburn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; esophageal neoplasms; heartburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cocarcinogenesis; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal achalasia; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal achalasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal varices Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal varices in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; cell transformation, neoplastic; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cell transformation, neoplastic; esophageal neoplasms; oesophageal neoplasm; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; thoracic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis; thoracic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, adenosquamous; carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, adenosquamous; carcinoma, squamous cell; esophageal neoplasms; lymphatic metastasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; barrett esophagus; esophageal neoplasms; gastroesophageal reflux; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; esophageal cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; esophageal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lung cancer; colorectal cancer; esophageal cancer; stomach cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term esophageal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Esophageal adenocarcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal adenocarcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Esophageal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Esophageal squamous cell cancer (length of survival) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal squamous cell cancer (length of survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Esophageal cancer (squamous cell) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer (squamous cell) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Esophageal cancer (alcohol interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Esophageal cancer (alcohol interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
esophageal carcinoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease esophageal carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
esophageal disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease esophageal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
esophageal cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease esophageal cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
esophageal carcinoma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the esophageal carcinoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
esophageal neoplasm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the esophageal neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
esophageal carcinoma Gene SetFrom HPO Gene-Disease Associations genes associated with the esophageal carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spontaneous esophageal perforation Gene SetFrom HPO Gene-Disease Associations genes associated with the spontaneous esophageal perforation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
esophageal neoplasm Gene SetFrom HPO Gene-Disease Associations genes associated with the esophageal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
esophageal atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the esophageal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
esophageal varix Gene SetFrom HPO Gene-Disease Associations genes associated with the esophageal varix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
esophageal stricture Gene SetFrom HPO Gene-Disease Associations genes associated with the esophageal stricture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
esophageal stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the esophageal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Esophageal Achalasia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Esophageal Achalasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Esophageal Atresia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Esophageal Atresia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Esophageal Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Esophageal Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Esophageal Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Esophageal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal esophageal squamous epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal esophageal squamous epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
esophageal inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the esophageal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
esophageal atresia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the esophageal atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
esophageal ulcer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the esophageal ulcer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal esophageal smooth muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal esophageal smooth muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
esophageal epithelium hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the esophageal epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal esophageal epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal esophageal epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased esophageal papilloma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased esophageal papilloma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
tylosis with esophageal cancer Gene SetFrom OMIM Gene-Disease Associations genes associated with the tylosis with esophageal cancer phenotype from the curated OMIM Gene-Disease Associations dataset. |
esophageal cancer Gene SetFrom OMIM Gene-Disease Associations genes associated with the esophageal cancer phenotype from the curated OMIM Gene-Disease Associations dataset. |
esophageal squamous cell carcinoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the esophageal squamous cell carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
esophageal carcinoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the esophageal carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
esophageal squamous cell carcinoma, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the esophageal squamous cell carcinoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
esophageal carcinoma, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the esophageal carcinoma, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
esophageal cancer, somatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the esophageal cancer, somatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
barrett esophagus/esophageal adenocarcinoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the barrett esophagus/esophageal adenocarcinoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
{esophageal cancer, alcohol-related, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {esophageal cancer, alcohol-related, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
esophageal epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal squamous cell carcinoma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal squamous cell carcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal squamous epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal squamous epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal squamous cell carcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal squamous cell carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal cancer cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue esophageal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
esophageal carcinoma Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease esophageal carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
esophageal cancer Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease esophageal cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Esophageal Achalasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Achalasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Stricture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Stricture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Atresia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Varices Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Varices in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tylosis With Esophageal Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tylosis With Esophageal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iv Esophageal Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iv Esophageal Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gastro-Esophageal Reflux Disease With Esophagitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gastro-Esophageal Reflux Disease With Esophagitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Gastrointestinal Stromal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Intestinal Metaplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Intestinal Metaplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Atresia With Or Without Tracheoesophageal Fistula Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Atresia With Or Without Tracheoesophageal Fistula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage I Esophageal Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage I Esophageal Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage I Esophageal Squamous Cell Carcinoma Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage I Esophageal Squamous Cell Carcinoma Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chalasia Of Lower Esophageal Sphincter Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chalasia Of Lower Esophageal Sphincter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Spindle Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Spindle Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Squamous Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Squamous Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Neuroendocrine Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Neuroendocrine Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage, Esophageal Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage, Esophageal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Fistula Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Fistula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Barrett Esophagus/Esophageal Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Barrett Esophagus/Esophageal Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Erosions Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Erosions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Ii Esophageal Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Ii Esophageal Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Ii Esophageal Squamous Cell Carcinoma Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Ii Esophageal Squamous Cell Carcinoma Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Basaloid Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Basaloid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Adenosquamous Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Adenosquamous Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Esophageal Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Esophageal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iv Esophageal Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iv Esophageal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bleeding Esophageal Varices Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bleeding Esophageal Varices in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stage Iia Esophageal Squamous Cell Carcinoma Ajcc V7 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stage Iia Esophageal Squamous Cell Carcinoma Ajcc V7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal High Grade Intraepithelial Neoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal High Grade Intraepithelial Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Spasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Spasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Melanoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Liposarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Dysphagia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Dysphagia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Atresia With Tracheoesophageal Fistula (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Esophageal Atresia With Tracheoesophageal Fistula (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Esophageal Cancer, Alcohol-Related, Susceptibility To Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Esophageal Cancer, Alcohol-Related, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Esophageal Diverticulum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Esophageal Diverticulum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal esophageal smooth muscle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal esophageal smooth muscle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal esophageal epithelium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal esophageal epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal esophageal squamous epithelium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal esophageal squamous epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased esophageal papilloma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased esophageal papilloma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
esophageal atresia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the esophageal atresia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
esophageal epithelium hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the esophageal epithelium hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
esophageal ulcer Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the esophageal ulcer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
esophageal inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the esophageal inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
retro-esophageal left subclavian artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the retro-esophageal left subclavian artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
esophageal achalasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the esophageal achalasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Esophageal progenitor cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal progenitor cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal squamous cell_Esophageal_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal squamous cell_Esophageal_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal mucosal cell_Esophagus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal mucosal cell_Esophagus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal epithelial cell_Esophagus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal epithelial cell_Esophagus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Stratified esophageal cell_Esophagus_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Stratified esophageal cell_Esophagus_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal cell_Duodenum_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal cell_Duodenum_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal stem cell_Duodenum_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal stem cell_Duodenum_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal progenitor cell_Duodenum_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal progenitor cell_Duodenum_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal squamous cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Esophageal squamous cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Esophageal carcinoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Esophageal carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Esophageal cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Esophageal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal varix Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal varix in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal atresia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal candidiasis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal candidiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Palmoplantar keratoderma-esophageal carcinoma syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Palmoplantar keratoderma-esophageal carcinoma syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal atresia/tracheoesophageal fistula Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal atresia/tracheoesophageal fistula in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal adenosquamous carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal adenosquamous carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal basaloid squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal basaloid squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal neuroendocrine tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal neuroendocrine tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal lipoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal adenoid cystic carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal adenoid cystic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal diverticulosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal diverticulosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal tuberculosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal leukoplakia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Esophageal leukoplakia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Displacement of cardia through esophageal hiatus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Displacement of cardia through esophageal hiatus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mucoepidermoid esophageal carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mucoepidermoid esophageal carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Esophageal mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal squamous cell carcinoma cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal squamous cell carcinoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal epithelial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal epithelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal squamous cell carcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal squamous cell carcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal cancer cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal cancer cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal squamous epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal squamous epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal adenocarcinoma cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Esophageal adenocarcinoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Esophageal atresia/tracheoesophageal fistula Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Esophageal atresia/tracheoesophageal fistula phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Anophthalmia/microphthalmia-esophageal atresia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Anophthalmia/microphthalmia-esophageal atresia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ESOPHAGEAL CAN Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ESOPHAGEAL CAN phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
BARRETT ESOPHAGUS/ESOPHAGEAL ADENOCARCIN Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the BARRETT ESOPHAGUS/ESOPHAGEAL ADENOCARCIN phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Palmoplantar keratoderma-esophageal carcinoma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Palmoplantar keratoderma-esophageal carcinoma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Esophageal squamous cell carcinoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Esophageal squamous cell carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Esophageal atresia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Esophageal atresia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Esophageal adenocarcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal adenocarcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal squamous cell carcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal squamous cell carcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Barrett's esophagus or esophageal adenocarcinoma x sex interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Barrett's esophagus or esophageal adenocarcinoma x sex interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Barrett's esophagus or esophageal adenocarcinoma x sex interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Barrett's esophagus or esophageal adenocarcinoma x sex interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Barrett's esophagus or Esophageal adenocarcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Barrett's esophagus or Esophageal adenocarcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer (squamous cell) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer (squamous cell) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal cancer (alcohol interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal cancer (alcohol interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal squamous cell cancer (length of survival) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal squamous cell cancer (length of survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal adenocarcinoma x smoking interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal adenocarcinoma x smoking interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal adenocarcinoma x pack-years of smoking exposure interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal adenocarcinoma x pack-years of smoking exposure interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Esophageal adenocarcinoma x gastroesophageal reflux disease interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Esophageal adenocarcinoma x gastroesophageal reflux disease interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Survival time in esophageal squamous cell carcinoma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Survival time in esophageal squamous cell carcinoma 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone fragility with contractures, arterial rupture, and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna and fibula absence of with severe limb deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor v and factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paragangliomas and Pheochromocytomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Band-like calcification with simplified gyration and polymicrogyria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, epilepsy, and diabetes syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia and hypogonadotropic hypogonadism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
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. |
Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, juvenile, with microcornea and glucosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, deafness, and narcolepsy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile macular degeneration and hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monocyte and dendritic cell deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, hiatal hernia and nephrotic syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pancreatic agenesis and congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jervell and Lange-Nielsen syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined malonic and methylmalonic aciduria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis Gyrata syndrome of Beare and Stevenson Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aniridia, cerebellar ataxia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hereditary motor and sensory neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Craniosynostosis and dental anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, hyperphagia, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebroretinal microangiopathy with calcifications and cysts Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Generalized epilepsy and paroxysmal dyskinesia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alacrima, achalasia, and mental retardation syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, normal intelligence and immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Calcification of joints and arteries Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis and recurrent skin vesicles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutaneous telangiectasia and cancer syndrome, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pineal hyperplasia AND diabetes mellitus syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Morbid obesity and spermatogenic failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skeletal defects, genital hypoplasia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Striatal necrosis, bilateral, and progressive polyneuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sensory and autonomic neuropathy type IIA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopia, high, with cataract and vitreoretinal degeneration Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of factor V and factor VIII, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Camptodactyly, tall stature, and hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum and acne Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth deficiency and mental retardation with facial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, cochlear, with myopia and intellectual impairment Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of sialidase AND beta galactosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
calcium- and calmodulin-dependent protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mrna cleavage and polyadenylation specificity factor complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
collagen and cuticulin-based cuticle extracellular matrix part Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitochondrial sorting and assembly machinery complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Setproteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset. |
NRD complex (Nucleosome remodeling and deacetylation complex) Gene Setproteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset. |
6S methyltransferase and RG-containing Sm proteins complex Gene Setproteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset. |
Remodeling and spacing factor (RSF) complex Gene Setproteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset. |
PBAF complex (Polybromo- and BAF containing complex) Gene Setproteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset. |
Cleavage and polyadenylation factor (CPSF) Gene Setproteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Nucleic and chromatin Fanconi complex Gene Setproteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset. |
Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Setproteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset. |
Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Setproteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset. |
ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Setproteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset. |
20S methylosome and RG-containing Sm protein complex Gene Setproteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset. |
Amino Acids, Peptides, and Proteins Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset. |
Bile Acids and Salts Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset. |
Prime and Bond NT Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset. |
drospirenone and ethinyl estradiol combination Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset. |
Hypophosphatemic Rickets And Hyperparathyroidism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset. |
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset. |
Synovitis granulomatous with uveitis and cranial neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory and Motor Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Preaxial deficiency, postaxial polydactyly and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset. |
Combined Cellular And Humoral Immune Defects With Granulomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset. |
OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset. |
Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset. |
Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset. |
Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset. |
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset. |
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset. |
Microtia, Hearing Impairment, And Cleft Palate Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset. |
OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Acromegaloid features, overgrowth, cleft palate, and hernia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset. |
46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset. |
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset. |
Craniosynostosis, anal anomalies, and porokeratosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset. |
Sacral defect and anterior sacral meningocele Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset. |
Classical Lissencephalies and Subcortical Band Heterotopias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset. |
Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 1 and deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Russe type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset. |
Blepharophimosis, Ptosis, and Epicanthus Inversus Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset. |
Hypotrichosis And Recurrent Skin Vesicles Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset. |
Signs and Symptoms, Digestive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria and Homocystinuria, CblD Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblD Type from the curated CTD Gene-Disease Associations dataset. |
Head and Neck Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Head and Neck Neoplasms from the curated CTD Gene-Disease Associations dataset. |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset. |
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset. |
Cataract, Juvenile, With Microcornea And Glucosuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset. |
Venous Malformations, Multiple Cutaneous and Mucosal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset. |
BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset. |
Postoperative Nausea and Vomiting Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Postoperative Nausea and Vomiting from the curated CTD Gene-Disease Associations dataset. |
Myopathy with lactic acidosis and sideroblastic anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset. |
Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset. |
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset. |
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset. |
Hypopituitarism and septooptic 'dysplasia' Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset. |
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset. |
Aplasia of Lacrimal and Salivary Glands Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset. |
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset. |
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset. |
Calcification of Joints and Arteries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Calcification of Joints and Arteries from the curated CTD Gene-Disease Associations dataset. |
CHOANAL ATRESIA AND LYMPHEDEMA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset. |
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy, Type IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset. |
Asthma, Nasal Polyps, And Aspirin Intolerance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Asthma, Nasal Polyps, And Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Germ Cell and Embryonal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Germ Cell and Embryonal from the curated CTD Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy VI Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset. |
Cutis Gyrata Syndrome of Beare And Stevenson Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare And Stevenson from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset. |
Wounds and Injuries Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wounds and Injuries from the curated CTD Gene-Disease Associations dataset. |
Schizophrenia and Disorders with Psychotic Features Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Schizophrenia and Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset. |
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset. |
Sleep Initiation and Maintenance Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sleep Initiation and Maintenance Disorders from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria and Homocystinuria, CblF Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria and Homocystinuria, CblF Type from the curated CTD Gene-Disease Associations dataset. |
Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Cataract and cardiomyopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Generalized Epilepsy and Paroxysmal Dyskinesia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset. |
Hereditary Breast and Ovarian Cancer Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset. |
Keratosis palmoplantaris with periodontopathia and onychogryposis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratosis palmoplantaris with periodontopathia and onychogryposis from the curated CTD Gene-Disease Associations dataset. |
Intracranial Embolism and Thrombosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intracranial Embolism and Thrombosis from the curated CTD Gene-Disease Associations dataset. |
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset. |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset. |
Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset. |
Nevi and Melanomas Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nevi and Melanomas from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Attention Deficit and Disruptive Behavior Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit and Disruptive Behavior Disorders from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy dilated with Woolly hair and keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset. |
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
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. |
Juvenile macular degeneration and hypotrichosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset. |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset. |
Mullerian Aplasia and Hyperandrogenism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset. |
Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, squamous cell of head and neck Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, squamous cell of head and neck from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial and congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset. |
Extravasation of Diagnostic and Therapeutic Materials Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Extravasation of Diagnostic and Therapeutic Materials from the curated CTD Gene-Disease Associations dataset. |
Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset. |
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Knuckle pads, leuconychia and sensorineural deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Knuckle pads, leuconychia and sensorineural deafness from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Hyperekplexia and Epilepsy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperekplexia and Epilepsy from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset. |
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset. |
Iris hypoplasia and glaucoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset. |
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Sarcoma family syndrome of Li and Fraumeni Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoma family syndrome of Li and Fraumeni from the curated CTD Gene-Disease Associations dataset. |
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset. |
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset. |
Lipoid Proteinosis of Urbach and Wiethe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipoid Proteinosis of Urbach and Wiethe from the curated CTD Gene-Disease Associations dataset. |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset. |
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset. |
Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset. |
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset. |
Jervell And Lange-Nielsen Syndrome 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Jervell And Lange-Nielsen Syndrome 2 from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Glandular and Epithelial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Glandular and Epithelial from the curated CTD Gene-Disease Associations dataset. |
Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset. |
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset. |
Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset. |
Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset. |
Pyogenic arthritis, pyoderma gangrenosum, and acne Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyogenic arthritis, pyoderma gangrenosum, and acne from the curated CTD Gene-Disease Associations dataset. |
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset. |