| Name |
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abnormality of the lacrimal duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lacrimal duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal duct obstruction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal duct obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal duct aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal duct aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal duct stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal duct stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplastic lacrimal duct Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic lacrimal duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal duct atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal duct atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Lacrimal Duct Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Duct Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malformed Lacrimal Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malformed Lacrimal Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lacrimal Duct Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Lacrimal Duct Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lacrimal Duct Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lacrimal Duct Defect Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Duct Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lacrimal duct obstruction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal duct obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
abnormality of the lacrimal punctum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lacrimal punctum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lacrimal gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lacrimal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intrahepatic bile duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of The Intrahepatic Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Intrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lacrimal Apparatus Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lacrimal Apparatus Diseases 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. |
acute inflammation of lacrimal passage Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute inflammation of lacrimal passage in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal system cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mixed lacrimal gland cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed lacrimal gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal gland adenoid cystic carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal gland adenoid cystic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal gland mucoepidermoid carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal gland mucoepidermoid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal apparatus disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal apparatus disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic inflammation of lacrimal passage Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic inflammation of lacrimal passage in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal gland carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal gland carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal gland adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal gland adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal gland cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lacrimal gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lacrimal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term lacrimal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
lacrimal gland development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lacrimal gland development biological process from the curated GO Biological Process Annotations 2015 dataset. |
lacrimal gland aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal gland aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the lacrimal puncta Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the lacrimal puncta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent lacrimal punctum Gene SetFrom HPO Gene-Disease Associations genes associated with the absent lacrimal punctum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
malformed lacrimal ducts Gene SetFrom HPO Gene-Disease Associations genes associated with the malformed lacrimal ducts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal gland hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplastic/hypoplastic lacrimal glands Gene SetFrom HPO Gene-Disease Associations genes associated with the aplastic/hypoplastic lacrimal glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal gland inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lacrimal gland inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lacrimal gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lacrimal bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lacrimal gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent lacrimal glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent lacrimal glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lacrimal apparatus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal apparatus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lacrimal gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lacrimal gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aplasia of lacrimal and salivary glands Gene SetFrom OMIM Gene-Disease Associations genes associated with the aplasia of lacrimal and salivary glands phenotype from the curated OMIM Gene-Disease Associations dataset. |
lacrimal gland acinar cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue lacrimal gland acinar cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Eye-epithelial cell of lacrimal sac Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-epithelial cell of lacrimal sac relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-lacrimal gland functional unit cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-lacrimal gland functional unit cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pleomorphic Adenoma Of Lacrimal Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pleomorphic Adenoma Of Lacrimal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of Lacrimal And Salivary Glands Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of Lacrimal And Salivary Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lacrimal Puncta, Absence Of Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Puncta, Absence Of in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lacrimal Mucocele Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Mucocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Lymphoepithelial Lesion Of Lacrimal Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Lymphoepithelial Lesion Of Lacrimal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lacrimal Gland Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Enlarged Lacrimal Glands Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlarged Lacrimal Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lacrimal Gland Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Gland Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lacrimal Gland Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Gland Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplastic/Hypoplastic Lacrimal Glands Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplastic/Hypoplastic Lacrimal Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ectopic Lacrimal Punctum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ectopic Lacrimal Punctum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
lacrimal gland development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lacrimal gland development biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal lacrimal bone morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal bone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small lacrimal bone Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small lacrimal bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent lacrimal glands Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent lacrimal glands phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
lacrimal gland inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the lacrimal gland inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent exorbital lacrimal gland Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent exorbital lacrimal gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lacrimal gland morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
lacrimal gland atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the lacrimal gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lacrimal gland physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal exorbital lacrimal gland morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal exorbital lacrimal gland morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lacrimal gland branching morphogenesis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland branching morphogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent intraorbital lacrimal gland Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent intraorbital lacrimal gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
lacrimal gland hypertrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the lacrimal gland hypertrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged lacrimal gland Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged lacrimal gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased lacrimal gland apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased lacrimal gland apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lacrimal gland innervation pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lacrimal gland development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lacrimal gland development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Lacrimal gland germ epithelial cell_Lacrimal gland_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Lacrimal gland germ epithelial cell_Lacrimal gland_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
lacrimal gland development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lacrimal gland development biological process from the curated GO Biological Process Annotations 2025 dataset. |
Lacrimal apparatus disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal apparatus disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acute inflammation of lacrimal passage Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute inflammation of lacrimal passage in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aplasia of lacrimal and salivary glands Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aplasia of lacrimal and salivary glands in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal gland adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal gland adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal gland carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal gland carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal system cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal gland cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal gland mucoepidermoid carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal gland mucoepidermoid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal gland adenoid cystic carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal gland adenoid cystic carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chronic inflammation of lacrimal passage Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic inflammation of lacrimal passage in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Stenosis of lacrimal passage Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Stenosis of lacrimal passage in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chronic lacrimal gland enlargement Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic lacrimal gland enlargement in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mixed lacrimal gland cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed lacrimal gland cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Prolapse of lacrimal gland Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Prolapse of lacrimal gland in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal gland squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lacrimal gland squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lacrimal gland acinar cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Lacrimal gland acinar cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Bile Duct Neoplasms Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bile Duct Neoplasms from the curated CTD Gene-Disease Associations dataset. |
Bile Duct Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bile Duct Diseases from the curated CTD Gene-Disease Associations dataset. |
Persistent Mullerian duct syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Persistent Mullerian duct syndrome 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. |
Adenoma, Bile Duct Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adenoma, Bile Duct from the curated CTD Gene-Disease Associations dataset. |
bile duct disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bile duct disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bile duct disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bile duct disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
bile duct mucoepidermoid carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct mucoepidermoid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bile duct adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bile duct adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
common bile duct disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease common bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bile duct sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bile duct carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
extrahepatic bile duct carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrahepatic bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
extrahepatic bile duct adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrahepatic bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bile duct disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bile duct cystadenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct cystadenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
breast duct papilloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast duct papilloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
collecting duct carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease collecting duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bile duct cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bile duct cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cholelithiasis; biliary duct stone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholelithiasis; biliary duct stone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma; carcinoma; common bile duct neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; carcinoma; common bile duct neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bile duct neoplasms; gallbladder neoplasms; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; gallbladder neoplasms; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary duct stones; biliary tract cancer; gallbladder cancer; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bile duct neoplasms; biliary calculi; gallstones Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; biliary calculi; gallstones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; cholangitis, sclerosing; dna damage; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, pancreatic ductal; common bile duct neoplasms; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, pancreatic ductal; common bile duct neoplasms; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bile duct neoplasms; cholangiocarcinoma; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bile duct neoplasms; cholangiocarcinoma; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
duct Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term duct in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
common bile duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the common bile duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
mullerian duct regression Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mullerian duct regression biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of apoptotic process involved in metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of apoptotic process involved in metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
dichotomous subdivision of terminal units involved in mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dichotomous subdivision of terminal units involved in mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
paramesonephric duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the paramesonephric duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
nephric duct elongation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nephric duct elongation biological process from the curated GO Biological Process Annotations 2015 dataset. |
lateral sprouting involved in mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lateral sprouting involved in mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
bmp signaling pathway involved in nephric duct formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bmp signaling pathway involved in nephric duct formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
intrahepatic bile duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intrahepatic bile duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
outer medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
branching involved in mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the branching involved in mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric cortical collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
epithelial cell proliferation involved in mammary gland duct elongation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the epithelial cell proliferation involved in mammary gland duct elongation biological process from the curated GO Biological Process Annotations 2015 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
hepatic duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hepatic duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
mesonephric duct formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mesonephric duct formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
nephric duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nephric duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
nephric duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nephric duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of apoptotic process involved in metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of apoptotic process involved in metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
branch elongation involved in mammary gland duct branching Gene SetFrom GO Biological Process Annotations 2015 genes participating in the branch elongation involved in mammary gland duct branching biological process from the curated GO Biological Process Annotations 2015 dataset. |
mesonephric duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mesonephric duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
pronephric duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pronephric duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
mammary duct terminal end bud growth Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mammary duct terminal end bud growth biological process from the curated GO Biological Process Annotations 2015 dataset. |
mesonephric duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mesonephric duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
nephric duct formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nephric duct formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
tertiary branching involved in mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the tertiary branching involved in mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of branching involved in mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of branching involved in mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cortical collecting duct development biological process from the curated GO Biological Process Annotations 2015 dataset. |
bile duct disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease bile duct disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
bile duct proliferation Gene SetFrom HPO Gene-Disease Associations genes associated with the bile duct proliferation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nasolacrimal duct obstruction Gene SetFrom HPO Gene-Disease Associations genes associated with the nasolacrimal duct obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absence of stensen duct Gene SetFrom HPO Gene-Disease Associations genes associated with the absence of stensen duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Bile Duct Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Bile Duct Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Common Bile Duct Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Common Bile Duct Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
small endolymphatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasolacrimal duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasolacrimal duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endolymphatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endolymphatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct intercalated cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct intercalated cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated endolymphatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal extrahepatic bile duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal extrahepatic bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased prostate gland duct number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased prostate gland duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sublingual duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sublingual duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct principal cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct principal cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney collecting duct atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
failure of mullerian duct regression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the failure of mullerian duct regression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
wolffian duct degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the wolffian duct degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mullerian duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mullerian duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bile duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased kidney collecting duct number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased kidney collecting duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent endolymphatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hepatic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hepatic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mullerian duct degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mullerian duct degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated bile duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated bile duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal papillary duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal papillary duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated pancreatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated pancreatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bile duct development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
bile duct hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the bile duct hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bile duct physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bile duct physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal salivary gland duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal salivary gland duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent nasolacrimal duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent nasolacrimal duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent sublingual duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent sublingual duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short endolymphatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal wolffian duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal wolffian duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
bile duct proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the bile duct proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal submandibular duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal submandibular duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
bile duct inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the bile duct inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mammary gland duct hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mammary gland duct hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal common bile duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal common bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cystic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cystic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated kidney collecting duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated kidney collecting duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thoracic duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thoracic duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intrahepatic bile duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intrahepatic bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
microtia with nasolacrimal duct imperforation and eye coloboma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microtia with nasolacrimal duct imperforation and eye coloboma phenotype from the curated OMIM Gene-Disease Associations dataset. |
persistent mullerian duct syndrome, type i Gene SetFrom OMIM Gene-Disease Associations genes associated with the persistent mullerian duct syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset. |
persistent mullerian duct syndrome, type ii Gene SetFrom OMIM Gene-Disease Associations genes associated with the persistent mullerian duct syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset. |
cochlear duct Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cochlear duct from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
mammary duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue mammary duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
m-1 collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue m-1 collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ejaculatory duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ejaculatory duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
parotid gland duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue parotid gland duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ejaculatory duct epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ejaculatory duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
pancreatic duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue pancreatic duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
submandibular gland duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue submandibular gland duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
papillary duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue papillary duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
salivary duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue salivary duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
bile duct cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile duct cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
bile duct epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
cortical collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cortical collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
collecting duct cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue collecting duct cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
cochlear duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cochlear duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
bile duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue bile duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
cortical collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cortical collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
sublingual gland duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue sublingual gland duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
venom duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue venom duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
parotid gland duct epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue parotid gland duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Salivary_Gland-duct epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Salivary_Gland-duct epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Congenital Atresia Of Extrahepatic Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atresia Of Extrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Proliferation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Advanced Bile Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Advanced Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Collecting Duct Carcinoma Of The Kidney Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Collecting Duct Carcinoma Of The Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Carcinoma Of Extrahepatic Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Carcinoma Of Extrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Adenoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Adenoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Cystadenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Cystadenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Liver And Intrahepatic Bile Duct Epithelial Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver And Intrahepatic Bile Duct Epithelial Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Liver And Intrahepatic Bile Duct Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Liver And Intrahepatic Bile Duct Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Persistent Mullerian Duct Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Persistent Mullerian Duct Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Persistent Mullerian Duct Syndrome, Type Ii Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Persistent Mullerian Duct Syndrome, Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infiltrating Duct Carcinoma Of Female Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infiltrating Duct Carcinoma Of Female Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Extrahepatic Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Extrahepatic Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Salivary Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Salivary Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infiltrating Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infiltrating Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Cancer Resectable Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Cancer Resectable in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Moderate Pancreatic Duct Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Moderate Pancreatic Duct Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stricture Of Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stricture Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Bile Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Hyperplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Hypoplasia Of Bile Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Bile Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infiltrating Duct And Lobular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infiltrating Duct And Lobular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Salivary Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Salivary Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Acquired Nasolacrimal Duct Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Nasolacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bile Duct Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bile Duct Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pancreatic Duct Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Duct Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Accessory Hepatic Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Accessory Hepatic Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bilateral Arterial Duct Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Arterial Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Common Bile Duct Calculi Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Common Bile Duct Calculi in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Pancreatic Duct Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Pancreatic Duct Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Obstruction Of Nasolacrimal Duct Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Obstruction Of Nasolacrimal Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absence Of Stensen Duct Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Stensen Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
mesonephric duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mesonephric duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
BMP signaling pathway involved in nephric duct formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the BMP signaling pathway involved in nephric duct formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
nephric duct morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the nephric duct morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
nephric duct formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the nephric duct formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
branching involved in mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the branching involved in mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
mesonephric duct morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mesonephric duct morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
outer medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of apoptotic process involved in metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of apoptotic process involved in metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric cortical collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
nephric duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the nephric duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of apoptotic process involved in metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of apoptotic process involved in metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2023 dataset. |
absent endolymphatic duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent endolymphatic duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Wolffian duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Wolffian duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bile duct development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile duct development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cystic duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cystic duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endolymphatic duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endolymphatic duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal submandibular duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal submandibular duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Mullerian duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Mullerian duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
failure of Mullerian duct regression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of Mullerian duct regression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney collecting duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney collecting duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal papillary duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal papillary duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney collecting duct epithelium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney collecting duct epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased prostate gland duct number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased prostate gland duct number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal salivary gland duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal salivary gland duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated kidney collecting duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated kidney collecting duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated pancreatic duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated pancreatic duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bile duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
bile duct epithelium hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct epithelium hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal nasolacrimal duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nasolacrimal duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated pulmonary alveolar duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated pulmonary alveolar duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased kidney collecting duct number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased kidney collecting duct number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Wolffian duct degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the Wolffian duct degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated endolymphatic duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated endolymphatic duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
kidney collecting duct atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
bile duct inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated bile duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated bile duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
bile duct proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short endolymphatic duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short endolymphatic duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
mammary gland duct hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the mammary gland duct hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary gland duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal branching involved in alveolar duct morphogenesis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal branching involved in alveolar duct morphogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pulmonary alveolar duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pulmonary alveolar duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Mullerian duct degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the Mullerian duct degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent sublingual duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent sublingual duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
bile duct hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the bile duct hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent nasolacrimal duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent nasolacrimal duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intrahepatic bile duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intrahepatic bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thoracic duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thoracic duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal extrahepatic bile duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal extrahepatic bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mammary duct terminal end bud morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary duct terminal end bud morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small endolymphatic duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small endolymphatic duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney collecting duct intercalated cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney collecting duct intercalated cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal common bile duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal common bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney collecting duct principal cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney collecting duct principal cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sublingual duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sublingual duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Mullerian duct topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Mullerian duct topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Wolffian duct connection Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Wolffian duct connection phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hepatic duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hepatic duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal Wolffian duct topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Wolffian duct topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular saccule duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular saccule duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bile duct epithelium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile duct epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased mammary duct terminal end bud number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mammary duct terminal end bud number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal interlobular bile duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal interlobular bile duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Kidney - L2 - Cortical Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Cortical Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Cortical Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Cortical Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Inner Medullary Collecting Duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Outer Medullary Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Outer Medullary Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Outer Medullary Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Outer Medullary Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Cortical Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Cortical Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Cortical Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Cortical Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Inner Medullary Collecting Duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Inner Medullary Collecting Duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Outer Medullary Collecting Duct Intercalated Type A Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Outer Medullary Collecting Duct Intercalated Type A cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Outer Medullary Collecting Duct Principal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Outer Medullary Collecting Duct Principal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - L4 - SMG duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L4 - SMG duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - Finest - SMG duct Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - Finest - SMG duct cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mullerian duct epithelial cell_Endometrium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Mullerian duct epithelial cell_Endometrium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Collecting duct intercalated cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Collecting duct intercalated cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Collecting duct principal cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Collecting duct principal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Collecting duct transient cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Collecting duct transient cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Collecting duct & Ureteric Bud cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Collecting duct & Ureteric Bud cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Collecting Duct Principal Cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Collecting Duct Principal Cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Salivary duct cell_Salivary duct_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Salivary duct cell_Salivary duct_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Formation of the nephric duct Gene Setproteins participating in the Formation of the nephric duct pathway from the Reactome Pathways 2024 dataset. |
Respiratory system_CT1_airway submucosal gland ciliated duct cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Respiratory system_CT1_airway submucosal gland ciliated duct cell cell type from the HuBMAP ASCT+B dataset. |
Respiratory system_CT1_airway submucosal gland duct basal cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Respiratory system_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B dataset. |
Respiratory system_CT1_airway submucosal gland collecting duct epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Respiratory system_CT1_airway submucosal gland collecting duct epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Trachea_CT1_airway submucosal gland collecting duct epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Trachea_CT1_airway submucosal gland collecting duct epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Trachea_CT1_airway submucosal gland duct basal cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Trachea_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Cortical Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Cortical Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Inner Medullary Collecting Duct Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Inner Medullary Collecting Duct Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Collecting Duct Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Collecting Duct Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Collecting Duct Intercalated Cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Collecting Duct Intercalated Cell cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B dataset. |
Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type B Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type B cell type from the HuBMAP ASCT+B dataset. |
Extrapulmonary bronchus_CT1_airway submucosal gland duct ciliated cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland duct ciliated cell cell type from the HuBMAP ASCT+B dataset. |
Extrapulmonary bronchus_CT1_airway submucosal gland collecting duct epithelial cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland collecting duct epithelial cell cell type from the HuBMAP ASCT+B dataset. |
Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B dataset. |
Extrapulmonary bronchus_CT1_airway submucosal gland collecting duct epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland collecting duct epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Extrapulmonary bronchus_CT1_airway submucosal gland duct ciliated cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Extrapulmonary bronchus_CT1_airway submucosal gland duct ciliated cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Collecting Duct Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Collecting Duct Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Collecting Duct Intercalated Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Collecting Duct Intercalated Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type B Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Cortical Collecting Duct Intercalated Cell Type B cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Cortical Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Cortical Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Inner Medullary Collecting Duct Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Inner Medullary Collecting Duct Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Intercalated Cell Type A cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Kidney_CT1_Outer Medullary Collecting Duct Principal Cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Kidney_CT1_Outer Medullary Collecting Duct Principal Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Respiratory system_CT1_airway submucosal gland ciliated duct cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Respiratory system_CT1_airway submucosal gland ciliated duct cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Respiratory system_CT1_airway submucosal gland collecting duct epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Respiratory system_CT1_airway submucosal gland collecting duct epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Respiratory system_CT1_airway submucosal gland duct basal cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Respiratory system_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Trachea_CT1_airway submucosal gland collecting duct epithelial cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Trachea_CT1_airway submucosal gland collecting duct epithelial cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Trachea_CT1_airway submucosal gland duct basal cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Trachea_CT1_airway submucosal gland duct basal cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
mesonephric duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mesonephric duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
nephric duct formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the nephric duct formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
nephric duct morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the nephric duct morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
branching involved in mammary gland duct morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the branching involved in mammary gland duct morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
mesonephric duct morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mesonephric duct morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
outer medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the outer medullary collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
inner medullary collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of apoptotic process involved in metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of apoptotic process involved in metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric cortical collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric cortical collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
nephric duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the nephric duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of apoptotic process involved in metanephric collecting duct development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of apoptotic process involved in metanephric collecting duct development biological process from the curated GO Biological Process Annotations 2025 dataset. |
Bile duct disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Bile duct cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Bile duct adenocarcinoma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct adenocarcinoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Bile duct carcinoma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Bile duct carcinoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Bile duct disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Bile duct disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Common bile duct disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Common bile duct disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Collecting duct carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Collecting duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct cystadenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct cystadenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Extrahepatic bile duct carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrahepatic bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bartholin's duct cyst Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bartholin's duct cyst in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Persistent Mullerian duct syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent Mullerian duct syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intrahepatic gall duct cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic gall duct cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Squamous cell bile duct carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Squamous cell bile duct carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intrahepatic bile duct adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct mucinous adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct mucinous adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct mucoepidermoid carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct mucoepidermoid carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct signet ring cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct signet ring cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Wolffian duct adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Wolffian duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Wolffian duct adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Wolffian duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Breast duct papilloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast duct papilloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Common bile duct neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Common bile duct neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Extrahepatic bile duct adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrahepatic bile duct adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intrahepatic bile duct cystadenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic bile duct cystadenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct cystadenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct cystadenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Extrahepatic bile duct adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrahepatic bile duct adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acquired tear duct stenosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired tear duct stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct rhabdomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Subareolar duct papillomatosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subareolar duct papillomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Perforation of bile duct Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Perforation of bile duct in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bile duct carcinoma in situ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bile duct carcinoma in situ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Cochlear duct Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cochlear duct from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cochlear duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cochlear duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Bile duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner medullary collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Bile duct epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cortical collecting duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cortical collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Collecting duct cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Collecting duct cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Mesonephric duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Mesonephric duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Pronephric duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Pronephric duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Pancreatic duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Pancreatic duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cortical collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cortical collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Salivary duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Salivary duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Mammary duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Mammary duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Medullary collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ejaculatory duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ejaculatory duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Venom duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Venom duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Submandibular gland duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Submandibular gland duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ejaculatory duct epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ejaculatory duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Parotid gland duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Parotid gland duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Sublingual gland duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Sublingual gland duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Bile duct cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Bile duct cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Salivary duct cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Salivary duct cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Parotid gland duct epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Parotid gland duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
M-1 collecting duct cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue M-1 collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Papillary duct Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Papillary duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Submandibular gland duct epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Submandibular gland duct epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Persistent mullerian duct syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Persistent mullerian duct syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infiltrating duct carcinoma of breast Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infiltrating duct carcinoma of breast phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bile duct cancer Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bile duct cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal intrahepatic bile duct morphology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal intrahepatic bile duct morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial congenital nasolacrimal duct obstruction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial congenital nasolacrimal duct obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Collecting duct acid secretion Gene SetFrom KEGG Pathways 2026 proteins participating in the Collecting duct acid secretion pathway from the KEGG Pathways 2026 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. |
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. |
congenital nervous system abnormality Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of glucagon secretion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrin secretion abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
torsion abnormality; vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormality Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of vitamin metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endometrium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forearm bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the integument Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin d metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stomach Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of connective tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cellular immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hearing abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of oral mucosa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urethra Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of brain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endocrine system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cerebral artery Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the breast Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the autonomic nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
eeg abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femur Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin a metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the calf Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the carotid arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of retinal arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the kidney Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circle of willis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hand Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pituitary gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the myocardium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cell cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of von willebrand factor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thrombocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of neutrophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hip bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the iris Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
mesangial abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin b metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the adrenal glands Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the respiratory system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the musculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral white matter Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the duodenum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the astrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of basophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the male genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of facial skeleton Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gingiva Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lung Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating hormone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the placenta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ankles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the heart valves Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of aromatic amino acid family metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the prostate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of digit Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the testis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental eruption Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the clavicle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of homocysteine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the knees Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coronary arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin adnexa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pleura Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of interleukin secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of tryptophan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of head or neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mandible Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of humoral immunity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neurodevelopmental abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of taste sensation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skeletal system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thorax Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thyroid gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdomen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrospinal fluid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
behavioral abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the oral cavity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cholesterol metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of granulocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the fundus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forebrain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the tongue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebrae Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the spinal cord Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vascular skin abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of refraction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood volume homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dna repair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nose Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of erythrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of liposaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating protein level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
prenatal maternal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humeral diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
phenotypic abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uterus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the metaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the common coagulation pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fatty-acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genitourinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cytokine secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
growth abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the choroid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the globe Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of radial diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear ossicles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the monocyte/macrophage lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb joint Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uvea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdominal organs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the esophagus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retina Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the penis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood circulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the radius Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of urine homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the costochondral junction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral cortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone marrow cell morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the liver Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fluid regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pylorus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of adipose tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior pituitary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nasopharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intervertebral disk Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stapes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gallbladder Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
generalized abnormality of skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glial cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ulna Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lymphocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mouth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vitamin b12 metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genital system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humerus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of complement system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
chorioretinal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sulfur amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating cortisol level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prothrombin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of coagulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cervical spine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carboxylic acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skeletal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lens Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body weight Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of temperature regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the systemic arterial tree Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the rib cage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin e metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retinal vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of ion homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of macrophages Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of calcium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body height Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of polysaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intrinsic pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eosinophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the macula Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of epidermal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of higher mental function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ribs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nucleobase metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the forearm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of purine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of serum cytokine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating leptin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nephron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nephron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating glucocorticoid level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the falx cerebri Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of gastrointestinal vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choanae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choanae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the immune system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reticulocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of von willebrand factor Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebellar peduncle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the gingiva Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the gingiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lung Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lung phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vena cava Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of sharpey fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metacarpophalangeal joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fluid regulation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of secondary sexual hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pineal gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the crus of the helix Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acetabulum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acetabulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sense of smell Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of permanent molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the achilles tendon Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the myocardium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of complement system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of blood glucose concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal tubule Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the shoulder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the shoulder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chromosome condensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prostaglandin metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neurodevelopmental abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of connective tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thumb phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alanine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atlantoaxial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the atlantoaxial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lower limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thrombocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thrombocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior pituitary Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vestibulocochlear nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of binocular vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thyroid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forebrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forebrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cerebral artery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choroid plexus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choroid plexus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating protein level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the seventh cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the labia minora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the lymphoid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized abnormality of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the glial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aryepiglottic fold Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prothrombin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the subungual region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal collecting system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acoustic reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubulointerstitial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dental pulp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cysteine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of ganglioside metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of ganglioside metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of humoral immunity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of humoral immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sixth cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of calvarial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of calvarial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hip joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humeral metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humeral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine bicarbonate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine bicarbonate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the genitourinary system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the genitourinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lymphatic vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fascia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ear Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the liver Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dental color Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alkaline phosphatase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alkaline phosphatase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the larynx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the larynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating hormone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the salivary glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of primary molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of copper homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sacroiliac joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the diaphragm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal tibial epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic valve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corticospinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corticospinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the endocrine system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the endocrine system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the tarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the soft palate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the adrenal glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the adrenal glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the periorbital region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the periorbital region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the respiratory system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fontanelles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the septum pellucidum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the septum pellucidum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of renal excretion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of renal excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |