Acquired Von Willebrand'S Disease

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Results for "Acquired Von Willebrand'S Disease": 1001 gene sets

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Acquired Von Willebrand'S Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Von Willebrand'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
von willebrand disease; von willebrand diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease von willebrand disease; von willebrand diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Acquired von Willebrand syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired von Willebrand syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pseudo von Willebrand disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Willebrand disease, platelet type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Von Willebrand disease, platelet type from the curated CTD Gene-Disease Associations dataset.
von Willebrand Disease, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease von Willebrand Disease, Type 3 from the curated CTD Gene-Disease Associations dataset.
von Willebrand Disease, Type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease von Willebrand Disease, Type 2 from the curated CTD Gene-Disease Associations dataset.
von Willebrand Disease, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease von Willebrand Disease, Type 1 from the curated CTD Gene-Disease Associations dataset.
von willebrand's disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease von willebrand's disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
von willebrand's disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease von willebrand's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dominant type 1 von willebrand's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant type 1 von willebrand's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; thrombosis; von willebrand disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; thrombosis; von willebrand disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von willebrand disease type 2n Gene Set From GAD Gene-Disease Associations genes associated with the disease von willebrand disease type 2n in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von willebrand disease Gene Set From GAD Gene-Disease Associations genes associated with the disease von willebrand disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von willebrand's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease von willebrand's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
type 1 von willebrand disease Gene Set From GAD Gene-Disease Associations genes associated with the disease type 1 von willebrand disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von willebrand's disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease von willebrand's disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
von Willebrand Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the von Willebrand Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
von Willebrand Disease, Type 1 Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the von Willebrand Disease, Type 1 phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
von willebrand disease, types 2a, 2b, 2m, and 2n Gene Set From OMIM Gene-Disease Associations genes associated with the von willebrand disease, types 2a, 2b, 2m, and 2n phenotype from the curated OMIM Gene-Disease Associations dataset.
von willebrand disease, platelet-type Gene Set From OMIM Gene-Disease Associations genes associated with the von willebrand disease, platelet-type phenotype from the curated OMIM Gene-Disease Associations dataset.
von willebrand disease, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the von willebrand disease, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
Von Willebrand Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Von Willebrand Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Von Willebrand Disease, Platelet Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Von Willebrand Disease, Platelet Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Von Willebrand'S Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Von Willebrand'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Von Willebrand Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Von Willebrand Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Von Willebrand's disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Von Willebrand's disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Von Willebrand's disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Von Willebrand's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Von Willebrand's disease 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Von Willebrand's disease 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Von Willebrand's disease 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Von Willebrand's disease 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Von Willebrand's disease 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Von Willebrand's disease 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Von Willebrand disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary von Willebrand disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pseudo von Willebrand disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
von hippel-lindau disease; von hippel-lindau syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease von hippel-lindau disease; von hippel-lindau syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von Willebrand Factor Gene Set From dbGAP Gene-Trait Associations genes associated with the trait von Willebrand Factor in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
von willebrand diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease von willebrand diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von willebrand factor levels Gene Set From GAD Gene-Disease Associations genes associated with the disease von willebrand factor levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von willebrand factor Gene Set From GAD Gene-Disease Associations genes associated with the disease von willebrand factor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
reduced levels of von willebrand factor messenger rna Gene Set From GAD Gene-Disease Associations genes associated with the disease reduced levels of von willebrand factor messenger rna in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemorrhage; von willebrand diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hemorrhage; von willebrand diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormality of von willebrand factor Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of von willebrand factor Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced von willebrand factor activity Gene Set From HPO Gene-Disease Associations genes associated with the reduced von willebrand factor activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced quantity of von willebrand factor Gene Set From HPO Gene-Disease Associations genes associated with the reduced quantity of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
von Willebrand Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the von Willebrand Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
von Willebrand factor, type D domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Willebrand factor, type D domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Mediator complex, subunit Med25, von Willebrand factor type A Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Mediator complex, subunit Med25, von Willebrand factor type A protein domain from the InterPro Predicted Protein Domain Annotations dataset.
von Willebrand factor Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Willebrand factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.
von Willebrand factor C and EGF domain-containing protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Willebrand factor C and EGF domain-containing protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
von Willebrand factor, type A Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Willebrand factor, type A protein domain from the InterPro Predicted Protein Domain Annotations dataset.
von Willebrand factor, type C Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Willebrand factor, type C protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Von Willebrand Factor, Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Von Willebrand Factor, Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reduced Quantity Of Von Willebrand Factor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Quantity Of Von Willebrand Factor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Reduced Von Willebrand Factor Activity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Von Willebrand Factor Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Von Willebrand Factor Vicenza Phenotype Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Von Willebrand Factor Vicenza Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
increased circulating von Willebrand factor level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating von Willebrand factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased circulating von Willebrand factor level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating von Willebrand factor level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Defective F8 binding to von Willebrand factor Gene Set From Reactome Pathways 2024 proteins participating in the Defective F8 binding to von Willebrand factor pathway from the Reactome Pathways 2024 dataset.
Von Willebrand disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Von Willebrand disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Von Willebrand factor Vicenza Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Von Willebrand factor Vicenza phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Reduced quantity of Von Willebrand factor Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced quantity of Von Willebrand factor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Reduced von Willebrand factor activity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced von Willebrand factor activity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
VON WILLEBRAND FACTOR HUMAN Gene Set From DGIdb Drug Targets 2026 interacting proteins for the VON WILLEBRAND FACTOR HUMAN drug from theDGIdb Drug Targets 2026 dataset.
addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von Hippel-Lindau Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease von Hippel-Lindau Disease from the curated CTD Gene-Disease Associations dataset.
von hippel-lindau disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease von hippel-lindau disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
von hippel-lindau disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease von hippel-lindau disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
von economo's disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease von economo's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
facies; neurofibromatosis 1; von recklinghausen disease Gene Set From GAD Gene-Disease Associations genes associated with the disease facies; neurofibromatosis 1; von recklinghausen disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurofibromatosis 1; von recklinghausen disease Gene Set From GAD Gene-Disease Associations genes associated with the disease neurofibromatosis 1; von recklinghausen disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease 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.
von Hippel-Lindau Disease Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the von Hippel-Lindau Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
von Hippel-Lindau disease tumour suppressor, beta/alpha domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Hippel-Lindau disease tumour suppressor, beta/alpha domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
von Hippel-Lindau disease tumour suppressor, alpha domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Hippel-Lindau disease tumour suppressor, alpha domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
von Hippel-Lindau disease tumour suppressor, beta domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Hippel-Lindau disease tumour suppressor, beta domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
von willibrand disease, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the von willibrand disease, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
Von Hippel-Lindau disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Von Hippel-Lindau disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Von Hippel-Lindau disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Von Hippel-Lindau disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Von Economo's disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Von Economo's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
acquired metabolic disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease acquired metabolic disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
acquired metabolic disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease acquired metabolic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
acquired metabolic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired metabolic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired metabolic disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease acquired metabolic disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Acquired Cystic Kidney Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cystic Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Cystic Disease Associated Renal Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cystic Disease Associated Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Renal Cystic Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Renal Cystic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Prion Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Prion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Factor X Deficiency Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Factor X Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired metabolic disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Acquired metabolic disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Acquired metabolic disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Acquired metabolic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired metabolic disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired metabolic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired hemoglobin H disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired hemoglobin H disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
willebrand Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term willebrand in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Paramyotonia congenita of von Eulenburg Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Paramyotonia congenita of von Eulenburg phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Hippel-Lindau syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Paramyotonia congenita of Von Eulenburg Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Paramyotonia congenita of Von Eulenburg from the curated CTD Gene-Disease Associations dataset.
von hippel-lindau syndrome (vhl). Gene Set From GAD Gene-Disease Associations genes associated with the disease von hippel-lindau syndrome (vhl). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
krebs von den lungen-6 levels Gene Set From GAD Gene-Disease Associations genes associated with the disease krebs von den lungen-6 levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von hippel-lindau type 2a Gene Set From GAD Gene-Disease Associations genes associated with the disease von hippel-lindau type 2a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von hippel-lindau tumour Gene Set From GAD Gene-Disease Associations genes associated with the disease von hippel-lindau tumour in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
von Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term von in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
von Ebner's gland protein/ Bos/Can allergen Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the von Ebner's gland protein/ Bos/Can allergen protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Von Hippel-Lindau tumour suppressor protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Von Hippel-Lindau tumour suppressor protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
{von hippel-lindau syndrome, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {von hippel-lindau syndrome, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
von hippel-lindau syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the von hippel-lindau syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Von Hippel-Lindau Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Von Hippel-Lindau Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Von Hippel-Lindau Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Von Hippel-Lindau Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
von Economo neuron(VEN)_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the von Economo neuron(VEN)_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Paramyotonia congenita of Von Eulenburg Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Paramyotonia congenita of Von Eulenburg from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Paramyotonia congenita of Von Eulenburg Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Paramyotonia congenita of Von Eulenburg in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Von Hippel-Lindau syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Von Hippel-Lindau syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Paramyotonia congenita of Von Eulenburg Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Paramyotonia congenita of Von Eulenburg phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
VON HIPPEL-LINDAU SYNDR Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the VON HIPPEL-LINDAU SYNDR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
coronary artery disease; coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; graves disease; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; disease susceptibility Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease; hashimoto disease; hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis; crohn disease; crohn's disease; disease models, animal Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; graft vs host disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; graft vs host disease 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.
Acquired long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, Partial, Acquired Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Partial, Acquired from the curated CTD Gene-Disease Associations dataset.
Factor 8 deficiency, acquired Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor 8 deficiency, acquired from the curated CTD Gene-Disease Associations dataset.
Acquired angioedema Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acquired angioedema from the curated CTD Gene-Disease Associations dataset.
Acquired Immunodeficiency Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acquired Immunodeficiency Syndrome from the curated CTD Gene-Disease Associations dataset.
Acquired Immunodeficiency Syndrome Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
acquired immunodeficiency syndrome Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease acquired immunodeficiency syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
acquired thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acquired polycythemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acquired immunodeficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acquired immunodeficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
community-acquired infections; pneumonia, bacterial; pneumonia, viral Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; pneumonia, viral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; cardiovascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
community-acquired infections; pneumonia, bacterial; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
community-acquired pneumonia (cap) Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired pneumonia (cap) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
articulation disorders; dyslexia, acquired; language disorders; noonan syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease articulation disorders; dyslexia, acquired; language disorders; noonan syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aplastic anemia, acquired Gene Set From GAD Gene-Disease Associations genes associated with the disease aplastic anemia, acquired in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; hiv infections Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; substance abuse, intravenous Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; substance abuse, intravenous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
community-acquired infections; pneumonia; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
community-acquired infections; pneumonia, bacterial; pneumonia, pneumococcal Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia, bacterial; pneumonia, pneumococcal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
community-acquired infections; pneumonia; septic shock; shock, septic Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; hiv seropositivity Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv seropositivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
community-acquired infections; pneumonia; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; kaposi sarcoma; lymphoma, aids-related; sarcoma, kaposi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
community-acquired infections; pneumonia Gene Set From GAD Gene-Disease Associations genes associated with the disease community-acquired infections; pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute-phase reaction; community-acquired infections; pneumonia Gene Set From GAD Gene-Disease Associations genes associated with the disease acute-phase reaction; community-acquired infections; pneumonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis Gene Set From GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acquired Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term acquired in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Simian Acquired Immune Deficiency Syndrome_T lymphocyte_GSE4785 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Nephrotic syndrome (acquired) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Nephrotic syndrome (acquired) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
acquired immunodeficiency syndrome Gene Set From GWASdb SNP-Disease Associations genes associated with the disease acquired immunodeficiency syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
acquired abnormal hair pattern Gene Set From GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
acquired abnormal hair pattern Gene Set From HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Community-Acquired Infections Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Community-Acquired Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Simian Acquired Immunodeficiency Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Simian Acquired Immunodeficiency Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dyslexia, Acquired Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dyslexia, Acquired phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Acquired Hyperostosis Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Acquired Hyperostosis Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Acquired Immunodeficiency Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Acquired Immunodeficiency Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
{long qt syndrome 1, acquired, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {long qt syndrome 1, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{long qt syndrome 2, acquired, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {long qt syndrome 2, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{long qt syndrome, acquired, reduced susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {long qt syndrome, acquired, reduced susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{lipodystrophy, partial, acquired, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {lipodystrophy, partial, acquired, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Community Acquired Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Community Acquired Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Long Qt Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Long Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Camptodactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Camptodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hospital Acquired Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hospital Acquired Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dental Fluorosis, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dental Fluorosis, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Angioedema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Aplastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Pectus Carinatum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Pectus Carinatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Kyphoscoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Kyphoscoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Hypogammaglobulinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypogammaglobulinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Hallux Valgus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hallux Valgus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Acquired Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Acquired Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thrombotic Thrombocytopenic Purpura, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thrombotic Thrombocytopenic Purpura, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Porencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Porencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Acquired Lymphedema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Acquired Lymphedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Partial Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Partial Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Hypoparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Flat Foot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Flat Foot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metabolic Disorder, Central Nervous System, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Disorder, Central Nervous System, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Nephrogenic Diabetes Insipidus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Nephrogenic Diabetes Insipidus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Phimosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Phimosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Hypofibrinogenemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypofibrinogenemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Cubitus Valgus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cubitus Valgus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Acquired Melanosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Melanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypocalciuric Hypercalcemia, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypocalciuric Hypercalcemia, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Thrombophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Thrombophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Atrophy Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Atrophy Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Obstructive Azoospermia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Obstructive Azoospermia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Acquired Toxoplasmosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Acquired Toxoplasmosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Neuromyotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Neuromyotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Haemophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Haemophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Factor 8 Deficiency, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Factor 8 Deficiency, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Immunodeficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Clubfoot Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Clubfoot in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Polyneuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Polyneuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Protein S Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Protein S Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Anomaly Of Tongue Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Anomaly Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Hypophosphatemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypophosphatemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Methemoglobinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Methemoglobinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Deformity Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Deformity Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Platelet Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Platelet Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Sensorineural Hearing Loss Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hospital Acquired Bacterial Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hospital Acquired Bacterial Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Immunodeficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Factor Xiii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Factor Xiii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Trigger Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Trigger Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Acquired Nasolacrimal Duct Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Acquired Nasolacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Cjd Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Cjd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Protein C Deficiency, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Protein C Deficiency, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Fanconi Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Fanconi Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Antithrombin Iii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Antithrombin Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired C1 Inhibitor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired C1 Inhibitor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Communicating Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Communicating Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Immunodeficiency Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Immunodeficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acquired Meningomyelocele Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Meningomyelocele in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acquired Genu Recurvatum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Genu Recurvatum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acquired Amegakaryocytic Thrombocytopenia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Amegakaryocytic Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acquired Hearing Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acquired Purpura Fulminans Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Purpura Fulminans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acquired partial lipodystrophy Barraquer Simons syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the Acquired partial lipodystrophy Barraquer Simons syndrome pathway from the WikiPathways Pathways 2024 dataset.
Acquired immunodeficiency syndrome Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Acquired immunodeficiency syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired immunodeficiency syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired immunodeficiency syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired thrombocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired angioedema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired angioedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired hyperkeratosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired hyperkeratosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired night blindness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired polycythemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired gastric outlet stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired gastric outlet stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired laryngomalacia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired laryngomalacia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired tear duct stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired tear duct stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired color blindness Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired color blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leukodystrophy and acquired microcephaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leukodystrophy and acquired microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acquired partial lipodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired partial lipodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acquired polycythemia vera Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acquired polycythemia vera phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Genetic non-acquired premature ovarian failure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Genetic non-acquired premature ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-acquired combined pituitary hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-acquired combined pituitary hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nephrotic syndrome (acquired) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nephrotic syndrome (acquired) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
crohn disease; crohn's disease; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart disease, ischemic; peripheral arterial disease Gene Set From GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; hashimoto disease; hyperthyroidism; hypothyroidism Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; hyperthyroidism; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; granuloma Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; familial mediterranean fever Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
liver disease; wilson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease liver disease; wilson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; dna damage; genomic instability Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; dna damage; genomic instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hemochromatosis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinson's disease ; alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinson's disease ; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart disease, ischemic; cerebrovascular disease, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; sarcoidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison's disease; graves' disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison's disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
kidney disease; vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease kidney disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves ophthalmopathy; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; autoimmune diseases; graves disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; colitis, ulcerative; crohn disease Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult-onset still disease; still's disease, adult-onset Gene Set From GAD Gene-Disease Associations genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amnesia Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amnesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; coronary disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease; cerebrovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gaucher disease; nervous system diseases; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; metabolic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves' disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; coronary restenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graft-versus-host disease; psoriasis; celiac disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graft-versus-host disease; psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease parkinson's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cardiovascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart disease, ischemic; peripheral vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; spondylitis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; gastrointestinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gaucher disease; legg-perthes disease; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn's disease; ulcerative colitis; inflammatory bowel disease Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease; ulcerative colitis; inflammatory bowel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; postoperative complications; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; inflammation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease; periodontal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; heart failure; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; dyslipidemias Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; osteoporosis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; disease susceptibility Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; disease susceptibility; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hypertriglyceridemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; addison's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; hemochromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; ileal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parkinsons disease; alzheimers disease Gene Set From GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; coronary artery disease; hyperlipidemias Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; coronary artery disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; hyperplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cadaver; coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cadaver; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease Gene Set From GAD Gene-Disease Associations genes associated with the disease rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
common variable immunodeficiency; crohn disease; crohn's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease common variable immunodeficiency; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; arteriosclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; intestinal obstruction Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetic angiopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; dilatation, pathologic Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lewy body disease; parkinson disease Gene Set From GAD Gene-Disease Associations genes associated with the disease lewy body disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyloidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperlipidemias Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sanhoff disease; tay-sachs disease Gene Set From GAD Gene-Disease Associations genes associated with the disease sanhoff disease; tay-sachs disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set From GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; postoperative complications; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hemochromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; delirium; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; delirium; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease/coronary artery disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; hallucinations Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; growth disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; lewy body disease Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves disease; hashimoto disease Gene Set From GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
addison disease; addison's disease; autoimmune diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression 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.
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set From GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
celiac disease; colitis, ulcerative; crohn disease; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroid disease; thyroid disease, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroid disease; thyroid disease, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; genetic predisposition to disease Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; neural tube defects Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; cutaneous fistula; rectal fistula Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; cutaneous fistula; rectal fistula in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; spondylarthropathies Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylarthropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Crohn's disease and celiac disease Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Cardiovascular Disease+Pulmonary Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiovascular Disease+Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Parkinson's disease or first degree relation to individual with Parkinson's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease or first degree relation to individual with Parkinson's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
Alzheimer's disease or family history of Alzheimer's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease or family history of Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Crohn's disease and celiac disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes 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.
Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors Gene Set From Biocarta Pathways proteins participating in the inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors pathway from the Biocarta Pathways dataset.
deregulation of cdk5 in alzheimers disease Gene Set From Biocarta Pathways proteins participating in the deregulation of cdk5 in alzheimers disease pathway from the Biocarta Pathways dataset.
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set From Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.
Parkinson disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Premature coronary artery disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Premature coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jakob-Creutzfeldt disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jakob-Creutzfeldt disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Maple syrup urine disease type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaucher's disease, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaucher's disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stargardt Disease 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stargardt Disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Norum disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Norum disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Salla disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Salla disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Worth disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Worth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ménière's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ménière's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Maple syrup urine disease, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acute neuronopathic Gaucher's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IVF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type IXa1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type IXa1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypophosphatemic bone disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory bowel disease 25, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory bowel disease 25, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Moyamoya disease 6 with achalasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Moyamoya disease 6 with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IV, congenital neuromuscular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 4B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brain small vessel disease with hemorrhage Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
RRM2B-related mitochondrial disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Phytanic acid storage disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaucher disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 20, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasemia with bone disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasemia with bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pigmented nodular adrenocortical disease, primary, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pigmented nodular adrenocortical disease, primary, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pigmented nodular adrenocortical disease, primary, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chylomicron retention disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chylomicron retention disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Basal ganglia disease, biotin-responsive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Basal ganglia disease, biotin-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coronary artery disease, autosomal dominant 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coronary artery disease, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hepatic venoocclusive disease with immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hepatic venoocclusive disease with immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Triglyceride storage disease with ichthyosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cowden disease 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cowden disease 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type II, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2A1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type ID Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IC Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IB Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type IA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alzheimer's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alzheimer's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schindler disease, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schindler disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schindler disease, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schindler disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Niemann-pick disease, intermediate, protracted neurovisceral Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Niemann-pick disease, intermediate, protracted neurovisceral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 6, autosomal recessive early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sandhoff disease, juvenile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Darier disease, segmental Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Darier disease, segmental phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Naxos disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Naxos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2r Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, axonal, type 2q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leiner disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leiner disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic kidney disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dowling-degos disease 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dowling-degos disease 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaucher disease, atypical, due to saposin C deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary factor II deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease 0, muscle Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease 0, muscle phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Subacute neuronopathic Gaucher's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Subacute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Testicular anomalies with or without congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lafora disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lafora disease 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.
Niemann-Pick disease, type B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Niemann-Pick disease, type A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease, type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type X Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type X phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tangier disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tangier disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cole disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cole disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 8, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 8, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXa2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXa2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Refsum disease, adult, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Refsum disease, adult, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital heart disease, multiple types, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Werdnig-Hoffmann disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Werdnig-Hoffmann disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chronic granulomatous disease, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease 19, juvenile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Niemann-Pick disease type C2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Niemann-Pick disease type C1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cholestanol storage disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cholestanol storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cowden disease 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tay-sachs disease, juvenile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tay-sachs disease, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IIIa Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stargardt disease 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stargardt disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary factor IX deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sandhoff disease, adult type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaucher disease, perinatal lethal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alexander's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alexander's disease phenotype from the curated ClinVar Gene-Phenotype 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.
Glycogen storage disease type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dowling-Degos disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dowling-Degos disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tay-Sachs disease, B1 variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease, B1 variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mast cell disease, systemic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mast cell disease, systemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic kidney disease, adult type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease dominant intermediate 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutral lipid storage disease with myopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sandhoff disease, infantile Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary factor XI deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Maple syrup urine disease type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease XV Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease XV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemoglobin H disease, nondeletional Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemoglobin H disease, nondeletional phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe combined immunodeficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXb Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXc Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscle eye brain disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Addison's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Addison's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital cystic disease of liver Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pancreatic agenesis and congenital heart disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lhermitte-Duclos disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lhermitte-Duclos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kugelberg-Welander disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kugelberg-Welander disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Darier disease, acral hemorrhagic type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Darier disease, acral hemorrhagic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wilson's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wilson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate d Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate c Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate c phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, recessive intermediate A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IIIc Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IIIb Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hirschsprung disease ganglioneuroblastoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease ganglioneuroblastoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oguchi's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oguchi's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kanzaki disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kanzaki disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic valve disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intermediate maple syrup urine disease type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intermediate maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fish-eye disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sandhoff disease, chronic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polycystic kidney disease, infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Central core disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary factor VIII deficiency disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tay-Sachs disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease, type 2M Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tay-Sachs disease, variant AB Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease, variant AB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sialic acid storage disease, severe infantile type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
I cell disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the I cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune disease, multisystem, infantile-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene Set From ClinVar Gene-Phenotype Associations genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease type III Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Medullary cystic kidney disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Medullary cystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Danon disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Danon disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dent disease 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dent disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dent disease 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dent disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease IXd Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXd phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycogen storage disease, type V Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune disease, syndromic multisystem Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, syndromic multisystem phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Charcot-Marie-Tooth disease type 2P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dent Disease 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dent Disease 2 from the curated CTD Gene-Disease Associations dataset.
Pick Disease of the Brain Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pick Disease of the Brain from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 10 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 12 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 13 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 14 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 15 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 18 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 18 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 19 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 19 from the curated CTD Gene-Disease Associations dataset.
Huntington Disease-Like 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset.
Parkinson disease 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson disease 9 from the curated CTD Gene-Disease Associations dataset.
Oguchi disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset.
Gaucher Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease from the curated CTD Gene-Disease Associations dataset.
Tay-Sachs Disease, AB Variant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tay-Sachs Disease, AB Variant from the curated CTD Gene-Disease Associations dataset.
Naxos disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Naxos disease from the curated CTD Gene-Disease Associations dataset.
Huntington Disease-Like 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2K Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2K from the curated CTD Gene-Disease Associations dataset.
Carbamoyl-Phosphate Synthase I Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carbamoyl-Phosphate Synthase I Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Chylomicron retention disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chylomicron retention disease from the curated CTD Gene-Disease Associations dataset.
Cholesterol Ester Storage Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholesterol Ester Storage Disease from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 6 from the curated CTD Gene-Disease Associations dataset.
Addison Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Addison Disease from the curated CTD Gene-Disease Associations dataset.
Alexander Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alexander Disease from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 16 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 16 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 17 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 17 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 7 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 4 from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease 0, Liver Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease 0, Liver from the curated CTD Gene-Disease Associations dataset.
Tangier Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tangier Disease from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1C from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 26 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 26 from the curated CTD Gene-Disease Associations dataset.
Pigmented Nodular Adrenocortical Disease, Primary, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 1 from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate D from the curated CTD Gene-Disease Associations dataset.
Hartnup Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hartnup Disease from the curated CTD Gene-Disease Associations dataset.
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 1D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1D from the curated CTD Gene-Disease Associations dataset.
Intervertebral disc disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intervertebral disc disease from the curated CTD Gene-Disease Associations dataset.
Coronary Artery Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease from the curated CTD Gene-Disease Associations dataset.
Machado-Joseph Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Machado-Joseph Disease from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease from the curated CTD Gene-Disease Associations dataset.
Papillon-Lefevre Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Papillon-Lefevre Disease from the curated CTD Gene-Disease Associations dataset.
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.
Moyamoya Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Moyamoya Disease from the curated CTD Gene-Disease Associations dataset.
Gilbert Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gilbert Disease from the curated CTD Gene-Disease Associations dataset.
Congenital thrombotic disease, due to Protein C deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
Pulmonary Disease, Chronic Obstructive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Disease, Chronic Obstructive from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 14 from the curated CTD Gene-Disease Associations dataset.
Coronary Artery Disease, Autosomal Dominant 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 9 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 11 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 16 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 16 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 12 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 10 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, X-linked, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2a1 from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease 0, Muscle Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease 0, Muscle from the curated CTD Gene-Disease Associations dataset.
Basal ganglia disease, biotin-responsive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Basal ganglia disease, biotin-responsive from the curated CTD Gene-Disease Associations dataset.
Non-alcoholic Fatty Liver Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Non-alcoholic Fatty Liver Disease from the curated CTD Gene-Disease Associations dataset.
Graves Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Graves Disease from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2A2 from the curated CTD Gene-Disease Associations dataset.
Hepatic Veno-Occlusive Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset.
Hepatic venoocclusive disease with immunodeficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic venoocclusive disease with immunodeficiency from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 25, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 25, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative from the curated CTD Gene-Disease Associations dataset.
Stargardt disease 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stargardt disease 3 from the curated CTD Gene-Disease Associations dataset.
Stargardt disease 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stargardt disease 4 from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type IV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type IV from the curated CTD Gene-Disease Associations dataset.
Refsum Disease, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset.
Polycystic liver disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic liver disease from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 8, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Celiac Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Celiac Disease from the curated CTD Gene-Disease Associations dataset.
Genetic Predisposition to Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Genetic Predisposition to Disease from the curated CTD Gene-Disease Associations dataset.
Dimauro disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dimauro disease from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IXB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IXB from the curated CTD Gene-Disease Associations dataset.
Coronary Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Disease from the curated CTD Gene-Disease Associations dataset.
AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease, Secondary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease, Secondary from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Demyelinating, Type 1e from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Type 4j Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4j from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate A from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
GALLBLADDER DISEASE 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GALLBLADDER DISEASE 1 from the curated CTD Gene-Disease Associations dataset.
Acute Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Acute Disease from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 3, Autosomal Dominant Lewy Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 3, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset.
Brain Small Vessel Disease with Hemorrhage Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.
Ornithine Carbamoyltransferase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ornithine Carbamoyltransferase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease, Type IXD Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease, Type IXD from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 5, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 5, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
GLYCOGEN STORAGE DISEASE IXa1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE IXa1 from the curated CTD Gene-Disease Associations dataset.
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease XII Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease XII from the curated CTD Gene-Disease Associations dataset.
Legionnaires' Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Legionnaires' Disease from the curated CTD Gene-Disease Associations dataset.
Hepatorenal form of glycogen storage disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatorenal form of glycogen storage disease from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.
Schindler Disease, Type I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Schindler Disease, Type I from the curated CTD Gene-Disease Associations dataset.
Pulmonary Veno-Occlusive Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset.
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4A from the curated CTD Gene-Disease Associations dataset.
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.
Huntington Disease-Like 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 3 from the curated CTD Gene-Disease Associations dataset.
Refsum Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Refsum Disease from the curated CTD Gene-Disease Associations dataset.
Aland Island Eye Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aland Island Eye Disease from the curated CTD Gene-Disease Associations dataset.
Bowen's Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bowen's Disease from the curated CTD Gene-Disease Associations dataset.
Hodgkin Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hodgkin Disease from the curated CTD Gene-Disease Associations dataset.
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II from the curated CTD Gene-Disease Associations dataset.
Niemann-Pick Disease, Type C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick Disease, Type C from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate C from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 2 from the curated CTD Gene-Disease Associations dataset.
Pyruvate Dehydrogenase Complex Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase Complex Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 13 from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L from the curated CTD Gene-Disease Associations dataset.
Medullary Cystic Kidney Disease 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Medullary Cystic Kidney Disease 2 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4C from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4E from the curated CTD Gene-Disease Associations dataset.
Huntington Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease from the curated CTD Gene-Disease Associations dataset.
PAGET DISEASE, JUVENILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PAGET DISEASE, JUVENILE from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE, LATE-ONSET Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE, LATE-ONSET from the curated CTD Gene-Disease Associations dataset.
Neutral Lipid Storage Disease with Myopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type III Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type III from the curated CTD Gene-Disease Associations dataset.
End Stage Liver Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease End Stage Liver Disease from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type II from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 5 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Recessive Intermediate A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Recessive Intermediate A from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 6 from the curated CTD Gene-Disease Associations dataset.
Hashimoto Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hashimoto Disease from the curated CTD Gene-Disease Associations dataset.
Canavan Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Canavan Disease from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 1F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1F from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2G from the curated CTD Gene-Disease Associations dataset.
Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.
Stargardt disease 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stargardt disease 1 from the curated CTD Gene-Disease Associations dataset.
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease XIII Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease XIII from the curated CTD Gene-Disease Associations dataset.
Lafora Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lafora Disease from the curated CTD Gene-Disease Associations dataset.
Van Buchem disease type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Van Buchem disease type 2 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Disease Models, Animal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disease Models, Animal from the curated CTD Gene-Disease Associations dataset.
Fabry Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fabry Disease from the curated CTD Gene-Disease Associations dataset.
Motor Neuron Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Motor Neuron Disease from the curated CTD Gene-Disease Associations dataset.
Niemann-Pick Disease, Type A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick Disease, Type A from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type VII Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type VII from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 3 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 5 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 8 from the curated CTD Gene-Disease Associations dataset.
dowling-degos disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease dowling-degos disease from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 6, Autosomal Recessive Early-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 6, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.
Darier Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Darier Disease from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease from the curated CTD Gene-Disease Associations dataset.
Paget Disease Of Bone 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Paget Disease Of Bone 4 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2D from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2E from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2I from the curated CTD Gene-Disease Associations dataset.
Disease Progression Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disease Progression from the curated CTD Gene-Disease Associations dataset.
Disease Susceptibility Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Disease Susceptibility from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B from the curated CTD Gene-Disease Associations dataset.
Dent Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dent Disease from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2F from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2J from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2H from the curated CTD Gene-Disease Associations dataset.
Lewy Body Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lewy Body Disease from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 16 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 16 from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 12 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2n from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
De Vivo disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease De Vivo disease from the curated CTD Gene-Disease Associations dataset.
Alzheimer disease type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer disease type 4 from the curated CTD Gene-Disease Associations dataset.
Alzheimer disease type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer disease type 2 from the curated CTD Gene-Disease Associations dataset.
Leigh Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leigh Disease from the curated CTD Gene-Disease Associations dataset.
Pigmented Nodular Adrenocortical Disease, Primary, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 2 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 28, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 28, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Granulomatous Disease, Chronic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Dominant Intermediate B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate B from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IXC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IXC from the curated CTD Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset.
AORTIC VALVE DISEASE 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AORTIC VALVE DISEASE 1 from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type VI Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type VI from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IB from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 10 from the curated CTD Gene-Disease Associations dataset.
Niemann-Pick Disease, Type B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick Disease, Type B from the curated CTD Gene-Disease Associations dataset.
Raynaud Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Raynaud Disease from the curated CTD Gene-Disease Associations dataset.
Moyamoya disease 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Moyamoya disease 1 from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type IIb Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type IIb from the curated CTD Gene-Disease Associations dataset.
Moyamoya disease 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Moyamoya disease 3 from the curated CTD Gene-Disease Associations dataset.
Niemann-Pick disease, type C2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick disease, type C2 from the curated CTD Gene-Disease Associations dataset.
Hodgkin disease, X-linked pseudoautosomal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hodgkin disease, X-linked pseudoautosomal from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 8 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 9 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 7 from the curated CTD Gene-Disease Associations dataset.
Sialic Acid Storage Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sialic Acid Storage Disease from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 24 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 24 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease from the curated CTD Gene-Disease Associations dataset.
Gallbladder Disease 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gallbladder Disease 4 from the curated CTD Gene-Disease Associations dataset.
Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 20 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 20 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 22 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 22 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 27 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 27 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth Disease, Type 4H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 21 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 21 from the curated CTD Gene-Disease Associations dataset.
Alzheimer Disease 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 15 from the curated CTD Gene-Disease Associations dataset.
Inflammatory Bowel Disease 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 23 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset.
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.
GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.
Peripheral Arterial Occlusive Disease 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Arterial Occlusive Disease 1 from the curated CTD Gene-Disease Associations dataset.
Maple Syrup Urine Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Maple Syrup Urine Disease from the curated CTD Gene-Disease Associations dataset.
GLYCOGEN STORAGE DISEASE XV Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE XV from the curated CTD Gene-Disease Associations dataset.
Gaucher Disease, Type Iiic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Type Iiic from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2B1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 2B2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B2 from the curated CTD Gene-Disease Associations dataset.
Multiple Sulfatase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease from the curated CTD Gene-Disease Associations dataset.
Graft vs Host Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Graft vs Host Disease from the curated CTD Gene-Disease Associations dataset.
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4B1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B1 from the curated CTD Gene-Disease Associations dataset.
Pelizaeus-Merzbacher Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pelizaeus-Merzbacher Disease from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type I from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease of Heart, Lethal Congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.
Sandhoff Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sandhoff Disease from the curated CTD Gene-Disease Associations dataset.
Microvillus inclusion disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microvillus inclusion disease from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 4, Autosomal Dominant Lewy Body Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 4, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease IC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IC from the curated CTD Gene-Disease Associations dataset.
Coronary Artery Disease, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Desmoid disease, hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Desmoid disease, hereditary from the curated CTD Gene-Disease Associations dataset.
Pyruvate Carboxylase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Carboxylase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Gaucher Disease, Perinatal Lethal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Perinatal Lethal from the curated CTD Gene-Disease Associations dataset.
Gestational Trophoblastic Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gestational Trophoblastic Disease from the curated CTD Gene-Disease Associations dataset.
Crohn Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Crohn Disease 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.
PARKINSON DISEASE 11, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 11, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Gerstmann-Straussler-Scheinker Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gerstmann-Straussler-Scheinker Disease from the curated CTD Gene-Disease Associations dataset.
Dent disease 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dent disease 1 from the curated CTD Gene-Disease Associations dataset.
Norrie disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Norrie disease from the curated CTD Gene-Disease Associations dataset.
Rippling muscle disease, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Rippling muscle disease, 1 from the curated CTD Gene-Disease Associations dataset.
Tay-Sachs Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tay-Sachs Disease from the curated CTD Gene-Disease Associations dataset.
Charcot-Marie-Tooth disease, Type 4B2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B2 from the curated CTD Gene-Disease Associations dataset.
Glycogen Storage Disease Type V Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type V from the curated CTD Gene-Disease Associations dataset.
Granulomatous Disease, Chronic, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, X-Linked from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease 7, Autosomal Recessive Early-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 7, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.
Legg-Calve-Perthes Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Legg-Calve-Perthes Disease from the curated CTD Gene-Disease Associations dataset.
Medullary cystic kidney disease 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Medullary cystic kidney disease 1 from the curated CTD Gene-Disease Associations dataset.
Celiac Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Celiac Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Coronary Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Coronary Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Hirschsprung Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Hirschsprung Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Gaucher Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Gaucher Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Alzheimer Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Alzheimer Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Non-alcoholic Fatty Liver Disease [Supplementary Concept] Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Non-alcoholic Fatty Liver Disease [Supplementary Concept] in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Hodgkin Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Hodgkin Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Coronary Artery Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Coronary Artery Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Paget's disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Paget's disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Parkinson Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Parkinson Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Moyamoya Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Moyamoya Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Pulmonary Disease, Chronic Obstructive Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Pulmonary Disease, Chronic Obstructive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Crohn Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Crohn Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Nonalcoholic Fatty Liver Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Nonalcoholic Fatty Liver Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Graves Disease Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Graves Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
autoimmune disease of gastrointestinal tract Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autoimmune disease of gastrointestinal tract from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bronchial disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bronchial disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
collagen disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease collagen disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
diaphragm disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease diaphragm disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores 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.
bone remodeling disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone remodeling disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
polycystic kidney disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease polycystic kidney disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bone marrow disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone marrow disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
lafora disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lafora disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Harmonizome 3.0

Acquired Von Willebrand'S Disease Gene Set

von willebrand disease; von willebrand diseases Gene Set

Acquired von Willebrand syndrome Gene Set

Pseudo von Willebrand disease Gene Set

Von Willebrand disease, platelet type Gene Set

von Willebrand Disease, Type 3 Gene Set

von Willebrand Disease, Type 2 Gene Set

von Willebrand Disease, Type 1 Gene Set

von willebrand's disease Gene Set

von willebrand's disease Gene Set

dominant type 1 von willebrand's disease Gene Set

hemorrhage; thrombosis; von willebrand disease Gene Set

von willebrand disease type 2n Gene Set

von willebrand disease Gene Set

von willebrand's disease Gene Set

type 1 von willebrand disease Gene Set

von willebrand's disease Gene Set

von Willebrand Disease Gene Set

von Willebrand Disease, Type 1 Gene Set

von willebrand disease, types 2a, 2b, 2m, and 2n Gene Set

von willebrand disease, platelet-type Gene Set

von willebrand disease, type 1 Gene Set

Von Willebrand Disease Gene Set

Von Willebrand Disease, Platelet Type Gene Set

Congenital Von Willebrand'S Disease Gene Set

Von Willebrand Disease Gene Set

Von Willebrand's disease Gene Set

Von Willebrand's disease Gene Set

Von Willebrand's disease 1 Gene Set

Von Willebrand's disease 2 Gene Set

Von Willebrand's disease 3 Gene Set

Von Willebrand disease Gene Set

Hereditary von Willebrand disease Gene Set

Pseudo von Willebrand disease Gene Set

carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome Gene Set

von hippel-lindau disease; von hippel-lindau syndrome Gene Set

von Willebrand Factor Gene Set

von willebrand diseases Gene Set

von willebrand factor levels Gene Set

von willebrand factor Gene Set

reduced levels of von willebrand factor messenger rna Gene Set

hemorrhage; von willebrand diseases Gene Set

abnormality of von willebrand factor Gene Set

abnormality of von willebrand factor Gene Set

reduced von willebrand factor activity Gene Set

reduced quantity of von willebrand factor Gene Set

von Willebrand Diseases Gene Set

von Willebrand factor, type D domain Gene Set

Mediator complex, subunit Med25, von Willebrand factor type A Gene Set

von Willebrand factor Gene Set

von Willebrand factor C and EGF domain-containing protein Gene Set

von Willebrand factor, type A Gene Set

von Willebrand factor, type C Gene Set

Von Willebrand Factor, Deficiency Gene Set

Reduced Quantity Of Von Willebrand Factor Gene Set

Reduced Von Willebrand Factor Activity Gene Set

Von Willebrand Factor Vicenza Phenotype Gene Set

increased circulating von Willebrand factor level Gene Set

decreased circulating von Willebrand factor level Gene Set

Defective F8 binding to von Willebrand factor Gene Set

Von Willebrand disorder Gene Set

Von Willebrand factor Vicenza Gene Set

Reduced quantity of Von Willebrand factor Gene Set

Reduced von Willebrand factor activity Gene Set

VON WILLEBRAND FACTOR HUMAN Gene Set

addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set

von Hippel-Lindau Disease Gene Set

von hippel-lindau disease Gene Set

von hippel-lindau disease Gene Set

von economo's disease Gene Set

facies; neurofibromatosis 1; von recklinghausen disease Gene Set

head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene Set

adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease Gene Set

von hippel-lindau disease Gene Set

neurofibromatosis 1; von recklinghausen disease Gene Set

cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease Gene Set

adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set

von Hippel-Lindau Disease Gene Set

von Hippel-Lindau disease tumour suppressor, beta/alpha domain Gene Set