Arthrogryposis, renal dysfunction, and cholestasis 2

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Results for "Arthrogryposis, renal dysfunction, and cholestasis 2": 1003 gene sets

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Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis renal dysfunction cholestasis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis renal dysfunction cholestasis syndrome from the curated CTD Gene-Disease Associations dataset.
cholestasis, intrahepatic; intrahepatic cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; intrahepatic cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis, intrahepatic; intrahepatic cholestasis; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; intrahepatic cholestasis; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis, mental retardation, and seizures Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
?arthrogryposis, mental retardation, and seizures Gene Set From OMIM Gene-Disease Associations genes associated with the ?arthrogryposis, mental retardation, and seizures phenotype from the curated OMIM Gene-Disease Associations dataset.
Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) pathway from the Reactome Pathways 2024 dataset.
Ventriculomegaly and arthrogryposis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ventriculomegaly and arthrogryposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Sensorineural deafness with mild renal dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; renal dysfunction, posttransplantation Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; renal dysfunction, posttransplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allograft dysfunction, renal Gene Set From GAD Gene-Disease Associations genes associated with the disease allograft dysfunction, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal tubular dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the renal tubular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensorineural deafness with mild renal dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the sensorineural deafness with mild renal dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
Sensorineural Deafness With Mild Renal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Deafness With Mild Renal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
renal involvement and renal sequelae Gene Set From GAD Gene-Disease Associations genes associated with the disease renal involvement and renal sequelae in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset.
delayed graft function acute rejection episodes and long-term graft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sepsis-related organ dysfunction and shock after burn injury Gene Set From GAD Gene-Disease Associations genes associated with the disease sepsis-related organ dysfunction and shock after burn injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Erectile dysfunction and prostate cancer treatment Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set From OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal dystrophy, early-onset, and pituitary dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
sinoatrial node dysfunction and deafness Gene Set From OMIM Gene-Disease Associations genes associated with the sinoatrial node dysfunction and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
Sinoatrial Node Dysfunction And Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sinoatrial Node Dysfunction And Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence Gene Set From WikiPathways Pathways 2024 proteins participating in the NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence pathway from the WikiPathways Pathways 2024 dataset.
SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction Gene Set From WikiPathways Pathways 2024 proteins participating in the SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset.
Metabolic dysfunction and alcohol associated liver disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction and alcohol associated liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sinoatrial node dysfunction and deafness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Erectile dysfunction and prostate cancer treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.
Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lethal arthrogryposis with anterior horn cell disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal arthrogryposis type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal arthrogryposis type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, distal, type 5d Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, distal, type 5d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis multiplex congenita neurogenic type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis multiplex congenita neurogenic type from the curated CTD Gene-Disease Associations dataset.
Arthrogryposis, Distal, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis, Distal, Type 4 from the curated CTD Gene-Disease Associations dataset.
ARTHROGRYPOSIS, DISTAL, TYPE 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, DISTAL, TYPE 1A from the curated CTD Gene-Disease Associations dataset.
ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED from the curated CTD Gene-Disease Associations dataset.
Arthrogryposis multiplex congenita, distal, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset.
Arthrogryposis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis from the curated CTD Gene-Disease Associations dataset.
Distal arthrogryposis type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Distal arthrogryposis type 2B from the curated CTD Gene-Disease Associations dataset.
Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease from the curated CTD Gene-Disease Associations dataset.
distal arthrogryposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
arthrogryposis; clubfoot; Gene Set From GAD Gene-Disease Associations genes associated with the disease arthrogryposis; clubfoot; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthrogryposis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term arthrogryposis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
arthrogryposis multiplex congenita Gene Set From HPO Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal arthrogryposis Gene Set From HPO Gene-Disease Associations genes associated with the distal arthrogryposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Arthrogryposis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Arthrogryposis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
arthrogryposis, distal, type 5 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, lethal, with anterior horn cell disease Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, lethal, with anterior horn cell disease phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 2a Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis multiplex congenita, neurogenic Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, neurogenic phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis multiplex congenita, distal, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis multiplex congenita, distal, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 1b Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 5d Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5d phenotype from the curated OMIM Gene-Disease Associations dataset.
Arthrogryposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arthrogryposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Arthrogryposis Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Arthrogryposis Type 5D Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Type 5D in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Myogenic Arthrogryposis Multiplex Congenita Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Myogenic Arthrogryposis Multiplex Congenita in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arthrogryposis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Arthrogryposis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal arthrogryposis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal arthrogryposis type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 2B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal arthrogryposis type 5D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis multiplex congenita Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arthrogryposis multiplex congenita in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
neurogenic-type arthrogryposis multiplex congenita-2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease neurogenic-type arthrogryposis multiplex congenita-2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis multiplex congenita-6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arthrogryposis multiplex congenita-6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis multiplex congenita-4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arthrogryposis multiplex congenita-4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis multiplex congenita-5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arthrogryposis multiplex congenita-5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis multiplex congenita-3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arthrogryposis multiplex congenita-3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis multiplex congenita-1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arthrogryposis multiplex congenita-1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arthrogryposis multiplex congenita Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis multiplex congenita phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal arthrogryposis-anterior horn cell disease syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal arthrogryposis-anterior horn cell disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal arthrogryposis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal arthrogryposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis multiplex congenita distal Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis multiplex congenita distal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorder - epilepsy - arthrogryposis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autism spectrum disorder - epilepsy - arthrogryposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis-like hand anomaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis-like hand anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive myogenic arthrogryposis multiplex congenita Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive myogenic arthrogryposis multiplex congenita phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neonatal intrahepatic cholestasis caused by citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cholestasis, intrahepatic, of pregnancy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cholestasis, intrahepatic, of pregnancy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cholestasis of pregnancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cholestasis of pregnancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign recurrent intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, Intrahepatic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, Intrahepatic from the curated CTD Gene-Disease Associations dataset.
Intrahepatic Cholestasis of Pregnancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intrahepatic Cholestasis of Pregnancy from the curated CTD Gene-Disease Associations dataset.
Cholestasis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis from the curated CTD Gene-Disease Associations dataset.
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease intrahepatic cholestasis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cholestasis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cholestasis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cholestasis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
extrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cholestasis, intrahepatic; fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis, intrahepatic; pregnancy complications; pruritus Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; pregnancy complications; pruritus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis; biliary atresia Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis; biliary atresia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis, intrahepatic; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis, intrahepatic Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis; Gene Set From GAD Gene-Disease Associations genes associated with the disease cholestasis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstetric cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease obstetric cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
greenland familial cholestasis Gene Set From GAD Gene-Disease Associations genes associated with the disease greenland familial cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholestasis Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cholestasis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cholestasis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cholestasis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
cholestasis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cholestasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cholestasis Gene Set From HPO Gene-Disease Associations genes associated with the cholestasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intrahepatic cholestasis Gene Set From HPO Gene-Disease Associations genes associated with the intrahepatic cholestasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intrahepatic cholestasis with episodic jaundice Gene Set From HPO Gene-Disease Associations genes associated with the intrahepatic cholestasis with episodic jaundice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cholestasis, Intrahepatic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cholestasis, Intrahepatic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cholestasis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cholestasis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
intrahepatic cholestasis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intrahepatic cholestasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cholestasis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cholestasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cholestasis, progressive canalicular Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive canalicular phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis-lymphedema syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis-lymphedema syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, intrahepatic, of pregnancy, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, intrahepatic, of pregnancy, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, intrahepatic, of pregnancy, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, intrahepatic, of pregnancy, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, benign recurrent intrahepatic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Cholestasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Intrahepatic Cholestasis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Intrahepatic Cholestasis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Recurrent Intrahepatic Cholestasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Recurrent Intrahepatic Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrahepatic Cholestasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrahepatic Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Intrahepatic Cholestasis Of Pregnancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Intrahepatic Cholestasis Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrahepatic Cholestasis With Episodic Jaundice Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrahepatic Cholestasis With Episodic Jaundice in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
intrahepatic cholestasis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intrahepatic cholestasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cholestasis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cholestasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
extrahepatic cholestasis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the extrahepatic cholestasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Cholestasis Gene Set From WikiPathways Pathways 2024 proteins participating in the Cholestasis pathway from the WikiPathways Pathways 2024 dataset.
Intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign recurrent intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Intrahepatic cholestasis of pregnancy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Intrahepatic cholestasis of pregnancy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrahepatic cholestasis of pregnancy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic cholestasis of pregnancy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrahepatic cholestasis of pregnancy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic cholestasis of pregnancy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign recurrent intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrahepatic cholestasis of pregnancy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic cholestasis of pregnancy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal intrahepatic cholestasis due to citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal intrahepatic cholestasis due to citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Benign recurrent intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign recurrent intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cholestasis-pigmentary retinopathy-cleft palate syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cholestasis-pigmentary retinopathy-cleft palate syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ABCB4-Related Intrahepatic Cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ABCB4-Related Intrahepatic Cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2014 proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
diabetes, post-renal transplant; post-renal transplant diabetes Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, post-renal transplant; post-renal transplant diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; colonic neoplasms; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; colonic neoplasms; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; gilbert disease; hyperbilirubinemia; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; gilbert disease; hyperbilirubinemia; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, papillary; carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, papillary; carcinoma, renal cell; kidney neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Surfactant metabolism dysfunction, pulmonary, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Surfactant metabolism dysfunction, pulmonary, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ventricular Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction from the curated CTD Gene-Disease Associations dataset.
Phagocyte Bactericidal Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phagocyte Bactericidal Dysfunction from the curated CTD Gene-Disease Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Temporomandibular Joint Dysfunction Syndrome from the curated CTD Gene-Disease Associations dataset.
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Left Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Left from the curated CTD Gene-Disease Associations dataset.
Sexual Dysfunction, Physiological Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sexual Dysfunction, Physiological from the curated CTD Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erectile Dysfunction from the curated CTD Gene-Disease Associations dataset.
Ventricular Dysfunction, Right Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Right from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 1 from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 2 from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 4 from the curated CTD Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction, Pulmonary, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 3 from the curated CTD Gene-Disease Associations dataset.
Sphincter of Oddi Dysfunction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sphincter of Oddi Dysfunction from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Erectile Dysfunction in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
phagocyte bactericidal dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sexual dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
labyrinthine dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
phagocyte bactericidal dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bowel dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ovarian dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sexual dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular diseases; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; erectile dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ovarian dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease ovarian dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
physiological sexual disorders; sexual dysfunction, physiological Gene Set From GAD Gene-Disease Associations genes associated with the disease physiological sexual disorders; sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sexual dysfunction, physiological Gene Set From GAD Gene-Disease Associations genes associated with the disease sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
allograft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease allograft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; inflammation; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; inflammation; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
biliary atresia; liver diseases; primary graft dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease biliary atresia; liver diseases; primary graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
beta thalassemia; beta-thalassemia; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes complications; erectile dysfunction; hypogonadism Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; erectile dysfunction; hypogonadism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erectile dysfunction; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease erectile dysfunction; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endothelial dysfunction in normal humans. Gene Set From GAD Gene-Disease Associations genes associated with the disease endothelial dysfunction in normal humans. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
left ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease left ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; autonomic nervous system dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; autonomic nervous system dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erectile dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarction; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporomandibular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease temporomandibular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; coronary vascular endothelial dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary vascular endothelial dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; coronary endothelial vasomotor dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; coronary endothelial vasomotor dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; ventricular dysfunction, left; ventricular remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercholesterolemia; myocardial infarction; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, coronary; myocardial dysfunction, non-ischaemic Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; myocardial dysfunction, non-ischaemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart diseases; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease heart diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dysfunction Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dysfunction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Sexual dysfunction (SSRI/SNRI-related) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Erectile dysfunction Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sexual dysfunction (female) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
sexual dysfunction Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sexual dysfunction in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
muscle abnormality related to mitochondrial dysfunction Gene Set From 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.
autonomic bladder dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the autonomic bladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle abnormality related to mitochondrial dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
beta-cell dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the beta-cell dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vestibular dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the vestibular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
gallbladder dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the gallbladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness due to upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autonomic erectile dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the autonomic erectile dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
urinary bladder sphincter dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the urinary bladder sphincter dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sweating due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
orthostatic hypotension due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Ventricular Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Posterior Tibial Tendon Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Posterior Tibial Tendon Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Dysfunction, Left Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Left phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Primary Graft Dysfunction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Primary Graft Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Sexual Dysfunction, Physiological Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Sexual Dysfunction, Physiological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ventricular Dysfunction, Right Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Right phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
multisystemic smooth muscle dysfunction syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the multisystemic smooth muscle dysfunction syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
autonomic nervous system dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the autonomic nervous system dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
surfactant metabolism dysfunction, pulmonary, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
Surfactant Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Surfactant Metabolism Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Metabolism Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erectile Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysfunction Adrenal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysfunction Adrenal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Testicular Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Testicular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Microvascular Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Microvascular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Memory Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Memory Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculogenic Erectile Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculogenic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Diastolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Placental Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Placental Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bowel Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bowel Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychosexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychosexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Minimal Brain Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Minimal Brain Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sleep Initiation Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurogenic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organ Dysfunction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organ Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leptin Deficiency Or Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leptin Deficiency Or Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sinus Node Dysfunction (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sinus Node Dysfunction (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Executive Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Executive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic-Pituitary-Adrenal Axis Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic-Pituitary-Adrenal Axis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meibomian Gland Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meibomian Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neutrophil Actin Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neutrophil Actin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypothalamic Dysfunction Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Dysfunction Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symphysis Pubis Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symphysis Pubis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autonomic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autonomic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Female Sexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Female Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporomandibular Joint Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pangastrointestinal System Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pangastrointestinal System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Colonic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Colonic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Emotional Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Emotional Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Phagocyte Bactericidal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Phagocyte Bactericidal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Male Sexual Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Male Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Segmental Autonomic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Segmental Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pineal Gland Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pineal Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Tibial Tendon Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Tibial Tendon Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyramidal Tract Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Tract Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonneurogenic Neurogenic Bladder Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonneurogenic Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroxisomal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leptin Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leptin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Immune Dysfunction With T-Cell Inactivation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Immune Dysfunction With T-Cell Inactivation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Right Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Right Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Dysfunction, Postpartum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Dysfunction, Postpartum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischemic Myocardial Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Myocardial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Endothelial Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endothelial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Liver Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Liver Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Beta-Cell Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Beta-Cell Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Urinary Bladder Sphincter Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Urinary Bladder Sphincter Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ventricular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Postoperative Cognitive Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postoperative Cognitive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dysfunction Of Lateral Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysfunction Of Lateral Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurologic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurologic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Orthostatic Hypotension Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Orthostatic Hypotension Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Vestibular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vestibular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Gastrointestinal Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gastrointestinal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Velopharyngeal Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Due To Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Uterine Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uterine Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autonomic Erectile Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Right Ventricular Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autonomic Nervous System Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Nervous System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Abnormality Related To Mitochondrial Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Abnormality Related To Mitochondrial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Speech Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Speech Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Primary Graft Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Primary Graft Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Sweating Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Sweating Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diastolic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Left Ventricular Systolic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
ROS in COVID 19 endothelial dysfunction Gene Set From WikiPathways Pathways 2024 proteins participating in the ROS in COVID 19 endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset.
Phagocyte bactericidal dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Metabolic dysfunction-associated steatotic liver disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ovarian dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Metabolic dysfunction-associated steatotic liver disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ovarian dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Sexual dysfunction Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Ovarian dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatotic liver disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatotic liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Metabolic dysfunction-associated steatohepatitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatohepatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sexual dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Phagocyte bactericidal dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bowel dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Labyrinthine dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thiamine metabolism dysfunction syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine metabolism dysfunction syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Surfactant metabolism dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Surfactant metabolism dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multisystemic smooth muscle dysfunction syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multisystemic smooth muscle dysfunction syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pulmonary Surfactant Metabolism Dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary Surfactant Metabolism Dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diastolic dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diastolic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thiamine Metabolism Dysfunction Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine Metabolism Dysfunction Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (responsive search score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (responsive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exploratory eye movement dysfunction in schizophrenia (cognitive search score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (cognitive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Memory dysfunction in frontotemporal lobe dementia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Memory dysfunction in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sexual dysfunction (SSRI/SNRI-related) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sexual dysfunction (female) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erectile dysfunction in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary leiomyomatosis and renal cell cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.
Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
Renal cysts and diabetes syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset.
mucinous tubular and spindle renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mucinous tubular and spindle renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal function and chronic kidney disease Gene Set From GAD Gene-Disease Associations genes associated with the disease renal function and chronic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increasing risk and a poor prognosis of renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease increasing risk and a poor prognosis of renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Renal function and chronic kidney disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal function and chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
lymphedema-distichiasis syndrome with renal disease and diabetes mellitus Gene Set From OMIM Gene-Disease Associations genes associated with the lymphedema-distichiasis syndrome with renal disease and diabetes mellitus phenotype from the curated OMIM Gene-Disease Associations dataset.
renal cysts and diabetes syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the renal cysts and diabetes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set From OMIM Gene-Disease Associations genes associated with the hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoparathyroidism, sensorineural deafness, and renal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the hypoparathyroidism, sensorineural deafness, and renal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
renal cell carcinoma, papillary, 1, familial and somatic Gene Set From OMIM Gene-Disease Associations genes associated with the renal cell carcinoma, papillary, 1, familial and somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
leiomyomatosis and renal cell cancer Gene Set From OMIM Gene-Disease Associations genes associated with the leiomyomatosis and renal cell cancer phenotype from the curated OMIM Gene-Disease Associations dataset.
bifid nose with or without anorectal and renal anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the bifid nose with or without anorectal and renal anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Hereditary Leiomyomatosis And Renal Cell Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Leiomyomatosis And Renal Cell Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Dysplasia And Retinal Aplasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Dysplasia And Retinal Aplasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Carcinoma Of The Renal Pelvis And Ureter Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Carcinoma Of The Renal Pelvis And Ureter in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Pelvis And Ureter Urothelial Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Pelvis And Ureter Urothelial Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Cysts And Diabetes Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Cysts And Diabetes Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lymphedema-Distichiasis Syndrome With Renal Disease And Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lymphedema-Distichiasis Syndrome With Renal Disease And Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vertebral, Cardiac, Renal, And Limb Defects Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vertebral, Cardiac, Renal, And Limb Defects Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Structural Heart Defects And Renal Anomalies Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Structural Heart Defects And Renal Anomalies Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary leiomyomatosis and renal cell carcinoma pathway Gene Set From WikiPathways Pathways 2024 proteins participating in the Hereditary leiomyomatosis and renal cell carcinoma pathway pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) pathway from the Reactome Pathways 2024 dataset.
Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) pathway from the Reactome Pathways 2024 dataset.
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mucinous tubular and spindle renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mucinous tubular and spindle renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
syndactyly-telecanthus-anogenital and renal malformations syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease syndactyly-telecanthus-anogenital and renal malformations syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal dysplasia and retinal aplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal dysplasia and retinal aplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndactyly-telecanthus-anogenital and renal malformations syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndactyly-telecanthus-anogenital and renal malformations syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal cysts and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal cysts and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary leiomyomatosis and renal cell cancer Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Structural heart defects and renal anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Structural heart defects and renal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Renal function and chronic kidney disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Renal function and chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set From Biocarta Pathways proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety and hostility and depression Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set From GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
vitamins and metabolites in pregnant women and neonates Gene Set From GAD Gene-Disease Associations genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
racemase and epimerase activity, acting on amino acids and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2015 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2014 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2014 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2014 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2014 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2014 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2014 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.
Synthesis and interconversion of nucleotide di- and triphosphates Gene Set From Reactome Pathways 2014 proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease High-Grade B-Cell Lymphoma, With Myc And Bcl2 And/Or Bcl6 Rearrangements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Contractures Of The Limbs And Face, Hypotonia, And Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Intraepithelial Neoplasia I And Ii (Ain I And Ii) (Histologically Confirmed) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pierre Robin Sequence With Pectus Excavatum And Rib And Scapular Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2023 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.
SRF and miRs in smooth muscle differentiation and proliferation Gene Set From WikiPathways Pathways 2024 proteins participating in the SRF and miRs in smooth muscle differentiation and proliferation pathway from the WikiPathways Pathways 2024 dataset.
SREBF and miR33 in cholesterol and lipid homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.
RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis Gene Set From WikiPathways Pathways 2024 proteins participating in the RIOK1 and RIOK2 in EGFR and PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.
ApoE and miR 146 in inflammation and atherosclerosis Gene Set From WikiPathways Pathways 2024 proteins participating in the ApoE and miR 146 in inflammation and atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.
Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine Gene Set From WikiPathways Pathways 2024 proteins participating in the Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.
Somatroph axis GH and its relationship to dietary restriction and aging Gene Set From WikiPathways Pathways 2024 proteins participating in the Somatroph axis GH and its relationship to dietary restriction and aging pathway from the WikiPathways Pathways 2024 dataset.
Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms Gene Set From WikiPathways Pathways 2024 proteins participating in the Mechanoregulation and pathology of YAP TAZ via Hippo and non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene Set From WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.
Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set From Reactome Pathways 2024 proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways 2024 dataset.
Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) Gene Set From Reactome Pathways 2024 proteins participating in the Biosynthesis of protectin and resolvin conjugates in tissue regeneration (PCTR and RCTR) pathway from the Reactome Pathways 2024 dataset.
Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set From Reactome Pathways 2024 proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways 2024 dataset.
FGFR1c and Klotho ligand binding and activation Gene Set From Reactome Pathways 2024 proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways 2024 dataset.
MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis Gene Set From Reactome Pathways 2024 proteins participating in the MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis pathway from the Reactome Pathways 2024 dataset.
Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set From Reactome Pathways 2024 proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways 2024 dataset.
PI and PC transport between ER and Golgi membranes Gene Set From Reactome Pathways 2024 proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways 2024 dataset.
PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 Gene Set From Reactome Pathways 2024 proteins participating in the PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 pathway from the Reactome Pathways 2024 dataset.
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Gene Set From Reactome Pathways 2024 proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.
Synthesis and processing of ENV and VPU Gene Set From Reactome Pathways 2024 proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways 2024 dataset.
Transcriptional and post-translational regulation of MITF-M expression and activity Gene Set From Reactome Pathways 2024 proteins participating in the Transcriptional and post-translational regulation of MITF-M expression and activity pathway from the Reactome Pathways 2024 dataset.
Transport of bile salts and organic acids, metal ions and amine compounds Gene Set From Reactome Pathways 2024 proteins participating in the Transport of bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways 2024 dataset.
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set From Reactome Pathways 2024 proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways 2024 dataset.
racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set From GO Molecular Function Annotations 2025 genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Regulation of gene expression and signal transduction in immune and stress responses Gene Set From CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of gene expression and signal transduction in immune and stress responses assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Renal hypodysplasia/aplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hypodysplasia/aplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal-hepatic-pancreatic dysplasia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal-hepatic-pancreatic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteopetrosis with renal tubular acidosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteopetrosis with renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomagnesemia 6, renal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomagnesemia 6, renal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromophobe renal cell carcinoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromophobe renal cell carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Enamel-renal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Enamel-renal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomagnesemia 4, renal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomagnesemia 4, renal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, with normal red cell morphology Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal cell carcinoma, papillary, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal cell carcinoma, papillary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomagnesemia 5, renal, with ocular involvement Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomagnesemia 5, renal, with ocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal carnitine transport defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal hypouricemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal hypouricemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, with hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal coloboma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal coloboma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis with progressive nerve deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis with progressive nerve deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal adysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal adysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial renal hypouricemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary renal agenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary renal agenesis from the curated CTD Gene-Disease Associations dataset.
Renal Hypodysplasia, Nonsyndromic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Hypodysplasia, Nonsyndromic, 1 from the curated CTD Gene-Disease Associations dataset.
Multicystic renal dysplasia, bilateral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multicystic renal dysplasia, bilateral from the curated CTD Gene-Disease Associations dataset.
Acidosis, Renal Tubular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acidosis, Renal Tubular from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset.
Osteopetrosis with renal tubular acidosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteopetrosis with renal tubular acidosis from the curated CTD Gene-Disease Associations dataset.
Renal Artery Obstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Artery Obstruction from the curated CTD Gene-Disease Associations dataset.
Renal tubular acidosis, distal, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal tubular acidosis, distal, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Renal hypouricemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal hypouricemia from the curated CTD Gene-Disease Associations dataset.
Hypomagnesemia 5, Renal, with Ocular Involvement Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypomagnesemia 5, Renal, with Ocular Involvement from the curated CTD Gene-Disease Associations dataset.
Renal Insufficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Insufficiency from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.
Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia from the curated CTD Gene-Disease Associations dataset.
Hypomagnesemia 2, renal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypomagnesemia 2, renal from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset.
Hypouricemia, Renal, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypouricemia, Renal, 2 from the curated CTD Gene-Disease Associations dataset.
Hypomagnesemia 4, Renal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypomagnesemia 4, Renal from the curated CTD Gene-Disease Associations dataset.
MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) from the curated CTD Gene-Disease Associations dataset.
RENAL TUBULAR DYSGENESIS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease RENAL TUBULAR DYSGENESIS from the curated CTD Gene-Disease Associations dataset.
Carcinoma, Renal Cell Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Renal Cell from the curated CTD Gene-Disease Associations dataset.
Torticollis keloids cryptorchidism renal dysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Torticollis keloids cryptorchidism renal dysplasia from the curated CTD Gene-Disease Associations dataset.
Oncocytoma, renal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oncocytoma, renal from the curated CTD Gene-Disease Associations dataset.
Hypertension, Renal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Renal from the curated CTD Gene-Disease Associations dataset.
Branchio-Oto-Renal Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Branchio-Oto-Renal Syndrome from the curated CTD Gene-Disease Associations dataset.
Nephrolithiasis, X-Linked Recessive, with Renal Failure Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephrolithiasis, X-Linked Recessive, with Renal Failure from the curated CTD Gene-Disease Associations dataset.
Renal Insufficiency, Chronic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Insufficiency, Chronic from the curated CTD Gene-Disease Associations dataset.
Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset.
Renal Failure, Progressive, with Hypertension Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Failure, Progressive, with Hypertension from the curated CTD Gene-Disease Associations dataset.
Glycosuria, Renal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycosuria, Renal from the curated CTD Gene-Disease Associations dataset.
Renal Osteodystrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Osteodystrophy from the curated CTD Gene-Disease Associations dataset.
BETA-AMINO ACIDS, RENAL TRANSPORT OF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BETA-AMINO ACIDS, RENAL TRANSPORT OF from the curated CTD Gene-Disease Associations dataset.
Carcinoma, Renal Cell Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Carcinoma, Renal Cell in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
impaired renal function disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease impaired renal function disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
renal tubular transport disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease renal tubular transport disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
renal carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal oncocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal tubular acidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal tubular acidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
impaired renal function disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease impaired renal function disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal agenesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal agenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal clear cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal clear cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
end stage renal failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease end stage renal failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal oncocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal oncocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sarcomatoid renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sarcomatoid renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal tuberculosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal tuberculosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal artery atheroma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal artery atheroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary conventional renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary conventional renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal tubular transport disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal tubular transport disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multilocular clear cell renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multilocular clear cell renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eosinophilic variant of chromophobe renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eosinophilic variant of chromophobe renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal osteodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal osteodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
papillary renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease papillary renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal wilms' tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal artery obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal artery obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal pelvis transitional cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal pelvis transitional cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal artery disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal artery disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal glycosuria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal glycosuria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
nonpapillary renal cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease nonpapillary renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial renal papillary carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease familial renal papillary carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal pelvis carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal pelvis carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
renal pelvis adenocarcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease renal pelvis adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hemorrhagic fever with renal syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hemorrhagic fever with renal syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic renal failure; diabetes mellitus; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal amyloidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease renal amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
paediatric renal allograft Gene Set From GAD Gene-Disease Associations genes associated with the disease paediatric renal allograft in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hypertension, renovascular; renal artery obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension, renovascular; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal clearance of metformin Gene Set From GAD Gene-Disease Associations genes associated with the disease renal clearance of metformin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic kidney insufficiency; hypertension; nephrosclerosis; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension; nephrosclerosis; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; nephritis, interstitial Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; nephritis, interstitial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
human renal transplantation Gene Set From GAD Gene-Disease Associations genes associated with the disease human renal transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood pressure; aldosterone; glomerular filtration rate; renal plasma flow Gene Set From GAD Gene-Disease Associations genes associated with the disease blood pressure; aldosterone; glomerular filtration rate; renal plasma flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, renal; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, renal; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal allograft outcome Gene Set From GAD Gene-Disease Associations genes associated with the disease renal allograft outcome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; inflammation; kidney failure, chronic; wasting syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; inflammation; kidney failure, chronic; wasting syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
clear cell renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease clear cell renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; chronic renal failure; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial distal renal tubular acidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney; failure; renal insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney; failure; renal insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
end-stage renal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease end-stage renal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; lipoid nephrosis; nephrosis, lipoid Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; lipoid nephrosis; nephrosis, lipoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
delayed renal graft function Gene Set From GAD Gene-Disease Associations genes associated with the disease delayed renal graft function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; hypertension; renal artery obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; calcinosis; cardiovascular diseases; chronic renal failure; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; calcinosis; cardiovascular diseases; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute renal allograft rejection Gene Set From GAD Gene-Disease Associations genes associated with the disease acute renal allograft rejection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
end- stage renal disease (esrd) Gene Set From GAD Gene-Disease Associations genes associated with the disease end- stage renal disease (esrd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fibromuscular dysplasia; hypertension; renal artery obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease fibromuscular dysplasia; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure. Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypercalcemia; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypercalcemia; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
irinotecan, renal clearance of Gene Set From GAD Gene-Disease Associations genes associated with the disease irinotecan, renal clearance of in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal disease, end stage Gene Set From GAD Gene-Disease Associations genes associated with the disease renal disease, end stage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic kidney insufficiency; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
non-papillary renal cell carcinomas Gene Set From GAD Gene-Disease Associations genes associated with the disease non-papillary renal cell carcinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; inflammation; kidney neoplasms; neoplasm metastasis Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; inflammation; kidney neoplasms; neoplasm metastasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhagic fever with renal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhagic fever with renal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; microsatellite instability Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, renal cell; kidney neoplasms; leiomyoma; leiomyomatosis; uterine neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, renal cell; kidney neoplasms; leiomyoma; leiomyomatosis; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african Gene Set From GAD Gene-Disease Associations genes associated with the disease african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conventional renal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease conventional renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease renal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hyperhomocysteinemia; kidney failure, chronic; proteinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hyperhomocysteinemia; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, renal Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal allograft function Gene Set From GAD Gene-Disease Associations genes associated with the disease renal allograft function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal tubular damage Gene Set From GAD Gene-Disease Associations genes associated with the disease renal tubular damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; inflammation; kidney failure, chronic; malnutrition Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; inflammation; kidney failure, chronic; malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease renal failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal disease, end stage; hyperhomocystinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease renal disease, end stage; hyperhomocystinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic kidney insufficiency; gout; kidney calculi; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; gout; kidney calculi; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cadaver; chronic renal failure; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease cadaver; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; uremia; vesico-ureteral reflux; vesicoureteral reflux Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; uremia; vesico-ureteral reflux; vesicoureteral reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal insufficiency; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease renal insufficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; carcinoma, renal cell; kidney neoplasms; paraganglioma; pheochromocytoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; kidney neoplasms; paraganglioma; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal transplant outcome Gene Set From GAD Gene-Disease Associations genes associated with the disease renal transplant outcome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal artery stenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease renal artery stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus; glomerulonephritis; kidney failure, chronic; nephrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus; glomerulonephritis; kidney failure, chronic; nephrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hemochromatosis; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hemochromatosis; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney diseases; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney diseases; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertension; kidney failure, chronic; nephrosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; nephrosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; inflammation; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; inflammation; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease renal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhagic fever with renal syndrome; pleural effusion Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhagic fever with renal syndrome; pleural effusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
urinary tract infections after renal transplantation Gene Set From GAD Gene-Disease Associations genes associated with the disease urinary tract infections after renal transplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; renal disease, end stage Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; renal disease, end stage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal transplant survival Gene Set From GAD Gene-Disease Associations genes associated with the disease renal transplant survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, type 1; renal transplant outcome Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; renal transplant outcome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; chronic renal failure; inflammation; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; inflammation; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
end stage renal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease end stage renal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal cancer; morphine response Gene Set From GAD Gene-Disease Associations genes associated with the disease renal cancer; morphine response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; nephritis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; nephritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; nephrotic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetic nephropathies; diabetic nephropathy; glomerulonephritis; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; glomerulonephritis; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; chronic renal failure; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease renal insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angiomyolipomas, renal Gene Set From GAD Gene-Disease Associations genes associated with the disease angiomyolipomas, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal transplant Gene Set From GAD Gene-Disease Associations genes associated with the disease renal transplant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; renal sodium handling Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; renal sodium handling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; renal disease, end stage Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; renal disease, end stage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal allograft survival Gene Set From GAD Gene-Disease Associations genes associated with the disease renal allograft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal function; uricemia Gene Set From GAD Gene-Disease Associations genes associated with the disease renal function; uricemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital anomalies; renal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital anomalies; renal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aortic valve stenosis; calcinosis; mitral valve stenosis; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; calcinosis; mitral valve stenosis; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive renal damage Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive renal damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; diabetic nephropathies; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; diabetic nephropathies; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal allograft rejection Gene Set From GAD Gene-Disease Associations genes associated with the disease renal allograft rejection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; chronic renal failure; hyperhomocysteinemia; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; hyperhomocysteinemia; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; substance withdrawal syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyslipidemias; metabolic syndrome x; obesity; renal hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease dyslipidemias; metabolic syndrome x; obesity; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arterial disease, renal Gene Set From GAD Gene-Disease Associations genes associated with the disease arterial disease, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal transplantation, rejection after Gene Set From GAD Gene-Disease Associations genes associated with the disease renal transplantation, rejection after in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney failure; kidney; failure; renal insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney failure; kidney; failure; renal insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal graft survival Gene Set From GAD Gene-Disease Associations genes associated with the disease renal graft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertension; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; chronic renal failure; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hyperparathyroidism, secondary; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hyperparathyroidism, secondary; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal function Gene Set From GAD Gene-Disease Associations genes associated with the disease renal function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hypertension; kidney failure, chronic; lupus erythematosus, systemic; lupus nephritis; nephritis sle; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; lupus erythematosus, systemic; lupus nephritis; nephritis sle; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; kidney failure, chronic; uremia Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; uremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal graft function Gene Set From GAD Gene-Disease Associations genes associated with the disease renal graft function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hyperhomocysteinemia; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hyperhomocysteinemia; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic kidney insufficiency; diabetic nephropathies; diabetic nephropathy; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; diabetic nephropathies; diabetic nephropathy; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hyperparathyroidism; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hyperparathyroidism; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
renal Gene Set From GAD High Level Gene-Disease Associations genes associated with the disease renal in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.
renal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term renal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
LHX1_KO_GDS2748_298_mouse_embryonic renal vesicles Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LHX1_KO_GDS2748_298_mouse_embryonic renal vesicles gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
renal cortex development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal cortex development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal phosphate ion absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the renal phosphate ion absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of renal water transport Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of renal water transport biological process from the curated GO Biological Process Annotations 2015 dataset.
renal tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal water homeostasis Gene Set From GO Biological Process Annotations 2015 genes participating in the renal water homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset.
renal system development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal system development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal water transport Gene Set From GO Biological Process Annotations 2015 genes participating in the renal water transport biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of renal output by angiotensin Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of renal output by angiotensin biological process from the curated GO Biological Process Annotations 2015 dataset.
renal system process involved in regulation of blood volume Gene Set From GO Biological Process Annotations 2015 genes participating in the renal system process involved in regulation of blood volume biological process from the curated GO Biological Process Annotations 2015 dataset.
renal water absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the renal water absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
mesenchymal to epithelial transition involved in renal vesicle formation Gene Set From GO Biological Process Annotations 2015 genes participating in the mesenchymal to epithelial transition involved in renal vesicle formation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of renal sodium excretion Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of renal sodium excretion biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of renal system process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of renal system process biological process from the curated GO Biological Process Annotations 2015 dataset.
renal vesicle formation Gene Set From GO Biological Process Annotations 2015 genes participating in the renal vesicle formation biological process from the curated GO Biological Process Annotations 2015 dataset.
renal filtration cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the renal filtration cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
renal capsule development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal capsule development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal sodium ion transport Gene Set From GO Biological Process Annotations 2015 genes participating in the renal sodium ion transport biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of renal output by angiotensin Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of renal output by angiotensin biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of renal phosphate excretion Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of renal phosphate excretion biological process from the curated GO Biological Process Annotations 2015 dataset.
renal tubular secretion Gene Set From GO Biological Process Annotations 2015 genes participating in the renal tubular secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of blood volume by renal aldosterone Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of blood volume by renal aldosterone biological process from the curated GO Biological Process Annotations 2015 dataset.
renal inner medulla development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal inner medulla development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal vesicle morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the renal vesicle morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
renal tubule morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the renal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2015 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric renal vesicle morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric renal vesicle morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of renal phosphate excretion Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of renal phosphate excretion biological process from the curated GO Biological Process Annotations 2015 dataset.
renal sodium ion absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the renal sodium ion absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
renal absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the renal absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2015 genes participating in the renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of renal water transport Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of renal water transport biological process from the curated GO Biological Process Annotations 2015 dataset.
renal protein absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the renal protein absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
mesenchymal cell differentiation involved in renal system development Gene Set From GO Biological Process Annotations 2015 genes participating in the mesenchymal cell differentiation involved in renal system development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal vesicle progenitor cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the renal vesicle progenitor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
renal capsule specification Gene Set From GO Biological Process Annotations 2015 genes participating in the renal capsule specification biological process from the curated GO Biological Process Annotations 2015 dataset.
mesenchymal to epithelial transition involved in metanephric renal vesicle formation Gene Set From GO Biological Process Annotations 2015 genes participating in the mesenchymal to epithelial transition involved in metanephric renal vesicle formation biological process from the curated GO Biological Process Annotations 2015 dataset.
renal interstitial fibroblast development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal interstitial fibroblast development biological process from the curated GO Biological Process Annotations 2015 dataset.
renal vesicle induction Gene Set From GO Biological Process Annotations 2015 genes participating in the renal vesicle induction biological process from the curated GO Biological Process Annotations 2015 dataset.
renal artery morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the renal artery morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
epithelial cell proliferation involved in renal tubule morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the epithelial cell proliferation involved in renal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
bmp signaling pathway involved in renal system segmentation Gene Set From GO Biological Process Annotations 2015 genes participating in the bmp signaling pathway involved in renal system segmentation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of renal albumin absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of renal albumin absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of renal albumin absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of renal albumin absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
renal glucose absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the renal glucose absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of renal sodium excretion Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of renal sodium excretion biological process from the curated GO Biological Process Annotations 2015 dataset.
renal outer medulla development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal outer medulla development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of renal sodium excretion Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of renal sodium excretion biological process from the curated GO Biological Process Annotations 2015 dataset.
renal system process Gene Set From GO Biological Process Annotations 2015 genes participating in the renal system process biological process from the curated GO Biological Process Annotations 2015 dataset.
renal filtration Gene Set From GO Biological Process Annotations 2015 genes participating in the renal filtration biological process from the curated GO Biological Process Annotations 2015 dataset.
renal system process involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2015 genes participating in the renal system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset.
renal system vasculature development Gene Set From GO Biological Process Annotations 2015 genes participating in the renal system vasculature development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of renal albumin absorption Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of renal albumin absorption biological process from the curated GO Biological Process Annotations 2015 dataset.
Renal function-related traits (urea) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal function-related traits (urea) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Renal cell carcinoma Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal cell carcinoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Renal function-related traits (eGRFcrea) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal function-related traits (eGRFcrea) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Renal sinus fat Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal sinus fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Renal transplant outcome Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal transplant outcome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Renal function-related traits (sCR) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal function-related traits (sCR) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Renal function-related traits (BUN) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Renal function-related traits (BUN) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
End-stage renal disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the End-stage renal disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
renal cell carcinoma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease renal cell carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
renal artery disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease renal artery disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
renal carcinoma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease renal carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
end stage renal failure Gene Set From GWASdb SNP-Disease Associations genes associated with the disease end stage renal failure in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
renal cell carcinoma Gene Set From GWASdb SNP-Phenotype Associations genes associated with the renal cell carcinoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal renal physiology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
embryonal renal neoplasm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the embryonal renal neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
renal neoplasm Gene Set From GWASdb SNP-Phenotype Associations genes associated with the renal neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
renal insufficiency Gene Set From GWASdb SNP-Phenotype Associations genes associated with the renal insufficiency phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal renal morphology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
renal amyloidosis Gene Set From HPO Gene-Disease Associations genes associated with the renal amyloidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal salt wasting Gene Set From HPO Gene-Disease Associations genes associated with the renal salt wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal magnesium wasting Gene Set From HPO Gene-Disease Associations genes associated with the renal magnesium wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal potassium wasting Gene Set From HPO Gene-Disease Associations genes associated with the renal potassium wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal aminoaciduria Gene Set From HPO Gene-Disease Associations genes associated with the renal aminoaciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the renal tubule Gene Set From 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.
renal cell carcinoma Gene Set From HPO Gene-Disease Associations genes associated with the renal cell carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
crossed fused renal ectopia Gene Set From HPO Gene-Disease Associations genes associated with the crossed fused renal ectopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal renal corticomedullary differentiation Gene Set From HPO Gene-Disease Associations genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal fanconi syndrome Gene Set From HPO Gene-Disease Associations genes associated with the renal fanconi syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased renal tubular phosphate reabsorption Gene Set From HPO Gene-Disease Associations genes associated with the increased renal tubular phosphate reabsorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the renal collecting system Gene Set From 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.
papillary renal cell carcinoma Gene Set From HPO Gene-Disease Associations genes associated with the papillary renal cell carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal angiomyolipoma Gene Set From HPO Gene-Disease Associations genes associated with the renal angiomyolipoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dilatation of the renal pelvis Gene Set From HPO Gene-Disease Associations genes associated with the dilatation of the renal pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal agenesis Gene Set From HPO Gene-Disease Associations genes associated with the renal agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of renal excretion Gene Set From 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.
renal duplication Gene Set From HPO Gene-Disease Associations genes associated with the renal duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal renal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the proximal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the renal cortex Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the renal cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impaired renal uric acid clearance Gene Set From HPO Gene-Disease Associations genes associated with the impaired renal uric acid clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased renal tubular phosphate excretion Gene Set From HPO Gene-Disease Associations genes associated with the decreased renal tubular phosphate excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal hypoplasia/aplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced renal corticomedullary differentiation Gene Set From HPO Gene-Disease Associations genes associated with the reduced renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of renal resorption Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of renal resorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal malrotation Gene Set From HPO Gene-Disease Associations genes associated with the renal malrotation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of renal pelvis Gene Set From HPO Gene-Disease Associations genes associated with the duplication of renal pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal artery stenosis Gene Set From HPO Gene-Disease Associations genes associated with the renal artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
parathormone-independent increased renal tubular calcium reabsorption Gene Set From HPO Gene-Disease Associations genes associated with the parathormone-independent increased renal tubular calcium reabsorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impaired renal concentrating ability Gene Set From HPO Gene-Disease Associations genes associated with the impaired renal concentrating ability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the renal pelvis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the renal pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystic renal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the cystic renal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal juxtaglomerular cell hypertrophy/hyperplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal juxtaglomerular cell hypertrophy/hyperplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal steatosis Gene Set From HPO Gene-Disease Associations genes associated with the renal steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal renal physiology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the renal artery Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the renal artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal corticomedullary cysts Gene Set From HPO Gene-Disease Associations genes associated with the renal corticomedullary cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the renal medulla Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the renal medulla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
unilateral renal agenesis Gene Set From HPO Gene-Disease Associations genes associated with the unilateral renal agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal renal morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal renal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of renal corticomedullary differentiation Gene Set From HPO Gene-Disease Associations genes associated with the absence of renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal insufficiency Gene Set From HPO Gene-Disease Associations genes associated with the renal insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical microcysts Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical microcysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of renal calyx morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of renal calyx morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal calcium wasting Gene Set From HPO Gene-Disease Associations genes associated with the renal calcium wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple small medullary renal cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple small medullary renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical adenoma Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical adenoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal phosphate wasting Gene Set From HPO Gene-Disease Associations genes associated with the renal phosphate wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal renal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the distal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
embryonal renal neoplasm Gene Set From HPO Gene-Disease Associations genes associated with the embryonal renal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the renal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal hamartoma Gene Set From HPO Gene-Disease Associations genes associated with the renal hamartoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cyst Gene Set From HPO Gene-Disease Associations genes associated with the renal cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical cysts Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal sodium wasting Gene Set From HPO Gene-Disease Associations genes associated with the renal sodium wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple renal cysts Gene Set From HPO Gene-Disease Associations genes associated with the multiple renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal neoplasm Gene Set From HPO Gene-Disease Associations genes associated with the renal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bicarbonate-wasting renal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the bicarbonate-wasting renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Acidosis, Renal Tubular Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Acidosis, Renal Tubular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Renal Insufficiency, Acute Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Renal Insufficiency, Acute phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Renal Artery Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Renal Artery Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Renal Tubular Transport, Inborn Errors Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Renal Tubular Transport, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Renal Aminoacidurias Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Renal Aminoacidurias phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Branchio-Oto-Renal Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Branchio-Oto-Renal Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hemorrhagic Fever with Renal Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hemorrhagic Fever with Renal Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Carcinoma, Renal Cell Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Renal Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hypertension, Renal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Renal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Renal Insufficiency, Chronic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Renal Insufficiency, Chronic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Renal dipeptidase family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Renal dipeptidase family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
renal cell carcinoma Gene Set From KEGG Pathways proteins participating in the renal cell carcinoma pathway from the KEGG Pathways dataset.
abnormal renal protein reabsorption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal glomerulus apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal glomerulus apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal glomerulus basement membrane thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal tubule epithelial cell primary cilium morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus lipidosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus lipidosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal tubule apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal tubule apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal glomerulus lobularity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal glomerulus lobularity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal glomerular filtration rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal glomerular filtration rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal sodium reabsorbtion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal sodium reabsorbtion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal ischemia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal ischemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal calcium reabsorbtion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal calcium reabsorbtion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased compensatory renal growth Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased compensatory renal growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerular synechia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerular synechia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal cast Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal cast phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal glucose reabsorption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glucose reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal plasma flow rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal plasma flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal/urinary system inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal/urinary system inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal tubular acidosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal tubular acidosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal sodium ion transport Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal sodium ion transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal fat pad morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal tubule atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal tubular necrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal tubular necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal/urinary system phenotype Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal/urinary system phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal filtration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal filtration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dilated renal glomerular capsule Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated renal glomerular capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal plasma flow rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal plasma flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal corpuscle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal corpuscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cortical renal glomerulopathies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cortical renal glomerulopathies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal phosphate reabsorbtion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal phosphate reabsorbtion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal filtration rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal filtration rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus cysts Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal right renal artery morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal right renal artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal carcinoma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal water transport Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal water transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal glomerular capsule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerular capsule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal glomerulus basement membrane morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus basement membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal tubule hypertrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal tubule hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal hamartoma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal hamartoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal glomerular filtration rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal glomerular filtration rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal tubule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal cystadenoma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal cystadenoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal/urinary system morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal/urinary system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal tubule apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal tubule apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal glomerular filtration rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerular filtration rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal necrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal plasma flow rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal plasma flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal water reabsorbtion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal water reabsorbtion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal artery morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal glomerular filtration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerular filtration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal vein morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal glomerulus number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal glomerulus number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal transport Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal glomerulus basement membrane thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal/urinary system physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal/urinary system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus hypertrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dilated renal tubules Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated renal tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal water homeostasis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal water homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
accumulation of giant lysosomes in kidney/renal tubule cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the accumulation of giant lysosomes in kidney/renal tubule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal glomerulus basement membrane thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal left renal vein morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal left renal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal reabsorbtion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal reabsorbtion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal interstitial fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal glomerulus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal tubule epithelium morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hypouricemia, renal Gene Set From OMIM Gene-Disease Associations genes associated with the hypouricemia, renal phenotype from the curated OMIM Gene-Disease Associations dataset.
amyloidosis, renal Gene Set From OMIM Gene-Disease Associations genes associated with the amyloidosis, renal phenotype from the curated OMIM Gene-Disease Associations dataset.
renal cell carcinoma Gene Set From OMIM Gene-Disease Associations genes associated with the renal cell carcinoma phenotype from the curated OMIM Gene-Disease Associations dataset.
renal hypodysplasia/aplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the renal hypodysplasia/aplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomagnesemia 5, renal, with ocular involvement Gene Set From OMIM Gene-Disease Associations genes associated with the hypomagnesemia 5, renal, with ocular involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
renal hypodysplasia, nonsyndromic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the renal hypodysplasia, nonsyndromic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
renal-hepatic-pancreatic dysplasia 1 Gene Set From OMIM Gene-Disease Associations genes associated with the renal-hepatic-pancreatic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
osteopetrosis, autosomal recessive 3, with renal tubular acidosis Gene Set From OMIM Gene-Disease Associations genes associated with the osteopetrosis, autosomal recessive 3, with renal tubular acidosis phenotype from the curated OMIM Gene-Disease Associations dataset.
renal cell carcinoma, papillary Gene Set From OMIM Gene-Disease Associations genes associated with the renal cell carcinoma, papillary phenotype from the curated OMIM Gene-Disease Associations dataset.
renal agenesis Gene Set From OMIM Gene-Disease Associations genes associated with the renal agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

Harmonizome 3.0

Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set

arthrogryposis, renal dysfunction, and cholestasis 1 Gene Set

Arthrogryposis renal dysfunction cholestasis syndrome Gene Set

Arthrogryposis renal dysfunction cholestasis syndrome Gene Set

cholestasis, intrahepatic; intrahepatic cholestasis Gene Set

cholestasis, intrahepatic; intrahepatic cholestasis; pregnancy complications Gene Set

myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene Set

Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set

Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set

Arthrogryposis, mental retardation, and seizures Gene Set

?arthrogryposis, mental retardation, and seizures Gene Set

Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis Gene Set

Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS) Gene Set

Ventriculomegaly and arthrogryposis Gene Set

chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic Gene Set

chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene Set

chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene Set

Sensorineural deafness with mild renal dysfunction Gene Set

chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left Gene Set

chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene Set

hypertension; renal dysfunction, posttransplantation Gene Set

allograft dysfunction, renal Gene Set

renal tubular dysfunction Gene Set

sensorineural deafness with mild renal dysfunction Gene Set

Sensorineural Deafness With Mild Renal Dysfunction Gene Set

renal involvement and renal sequelae Gene Set

Sinoatrial node dysfunction and deafness Gene Set

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene Set

delayed graft function acute rejection episodes and long-term graft dysfunction Gene Set

sepsis-related organ dysfunction and shock after burn injury Gene Set

Erectile dysfunction and prostate cancer treatment Gene Set

hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set

retinal dystrophy, early-onset, and pituitary dysfunction Gene Set

sinoatrial node dysfunction and deafness Gene Set

?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

Sinoatrial Node Dysfunction And Deafness Gene Set

Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction Gene Set

Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction Gene Set

NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence Gene Set

SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction Gene Set

Metabolic dysfunction and alcohol associated liver disease Gene Set

Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set

Sinoatrial node dysfunction and deafness Gene Set

Erectile dysfunction and prostate cancer treatment Gene Set

Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set

Toe Syndactyly, Telecanthus, And Anogenital And Renal Malformations Gene Set

Lethal arthrogryposis with anterior horn cell disease Gene Set

Distal arthrogryposis type 1B Gene Set

Distal arthrogryposis type 2B Gene Set

Arthrogryposis, distal, type 5d Gene Set

Arthrogryposis multiplex congenita neurogenic type Gene Set

Arthrogryposis, Distal, Type 4 Gene Set

ARTHROGRYPOSIS, DISTAL, TYPE 1A Gene Set

ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set

Arthrogryposis multiplex congenita, distal, X-linked Gene Set

Arthrogryposis Gene Set

Distal arthrogryposis type 2B Gene Set

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

distal arthrogryposis Gene Set

arthrogryposis; clubfoot; Gene Set

arthrogryposis Gene Set

arthrogryposis multiplex congenita Gene Set

distal arthrogryposis Gene Set

Arthrogryposis Gene Set

arthrogryposis, distal, type 5 Gene Set

arthrogryposis, distal, type 3 Gene Set

arthrogryposis, lethal, with anterior horn cell disease Gene Set

arthrogryposis, distal, type 2b Gene Set

arthrogryposis, distal, type 2a Gene Set

arthrogryposis multiplex congenita, neurogenic Gene Set

arthrogryposis multiplex congenita, distal, type 1 Gene Set