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corneal disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease corneal disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
corneal disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease corneal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
corneal disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease corneal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
Corneal disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Corneal disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Corneal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene SetFrom 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. |
corneal dystrophies, hereditary; hereditary corneal dystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; coronary disease; coronary heart disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene SetFrom Biocarta Pathways proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset. |
MACULAR CORNEAL DYSTROPHY, TYPE II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cutis laxa-corneal clouding-oligophrenia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa-corneal clouding-oligophrenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fleck corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Macular corneal dystrophy Type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lattice corneal dystrophy Type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thiel-Behnke corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thiel-Behnke corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reis-Bucklers' corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Reis-Bucklers' corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy, fuchs endothelial, 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy, fuchs endothelial, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy, fuchs endothelial, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy, fuchs endothelial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy Fuchs endothelial 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal dystrophy Fuchs endothelial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Schnyder crystalline corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Schnyder crystalline corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lattice corneal dystrophy type 3A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy type 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal endothelial dystrophy type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal endothelial dystrophy type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lattice corneal dystrophy Type III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Groenouw corneal dystrophy type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Groenouw corneal dystrophy type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal epithelial dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal epithelial dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital Stromal Corneal Dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal dystrophy, gelatinous drop-like Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, gelatinous drop-like from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Juvenile Epithelial of Meesmann Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Juvenile Epithelial of Meesmann from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy Avellino type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy Avellino type from the curated CTD Gene-Disease Associations dataset. |
Corneal Neovascularization Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Neovascularization from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Fuchs Endothelial, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 6 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Fuchs Endothelial, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 3 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Endothelial, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Endothelial, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Lattice corneal dystrophy type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy, Fuchs' endothelial, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 2 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Crystalline, of Schnyder Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Crystalline, of Schnyder from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy, Fuchs' endothelial, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 1 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Lisch Epithelial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lisch Epithelial from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy, epithelial basement membrane Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, epithelial basement membrane from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy and perceptive deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset. |
Corneal endothelial dystrophy type 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal endothelial dystrophy type 2 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Fleck Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fleck from the curated CTD Gene-Disease Associations dataset. |
Corneal Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Diseases from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Posterior Polymorphous, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 2 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Fuchs Endothelial, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 7 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Posterior Polymorphous, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 1 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Posterior Polymorphous, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 3 from the curated CTD Gene-Disease Associations dataset. |
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Congenital Stromal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset. |
Corneal Opacity Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Opacity from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy, Thiel-Behnke type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy, Thiel-Behnke type from the curated CTD Gene-Disease Associations dataset. |
Groenouw type I corneal dystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Groenouw type I corneal dystrophy from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Lattice Type IIIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Fuchs Endothelial, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 5 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Fuchs Endothelial, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 4 from the curated CTD Gene-Disease Associations dataset. |
Corneal dystrophy of Bowman layer, type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal dystrophy of Bowman layer, type 1 from the curated CTD Gene-Disease Associations dataset. |
Macular dystrophy, corneal type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Macular dystrophy, corneal type 1 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophies, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophies, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Corneal Ulcer Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Ulcer from the curated CTD Gene-Disease Associations dataset. |
Corneal Topography Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Corneal Topography in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
lattice corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lattice corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal staphyloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal staphyloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal edema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
recurrent corneal erosion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal granular dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal granular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal ectasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal ectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal neovascularization Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal neovascularization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal abscess Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal abscess in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
perforated corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease perforated corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal degeneration Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
macular corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
idiopathic corneal edema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
corneal dystrophies, hereditary; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
granular corneal dystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease granular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gelatinous droplike corneal dystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gelatinous droplike corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macular corneal dystrophy. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal topography Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal topography in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; corneal diseases; dry eye syndromes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; corneal diseases; dry eye syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lattice corneal dystrophy type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lattice corneal dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blind vision; blindness; corneal diseases; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; corneal diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macular corneal dystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macular corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal ulcer; eye infections, bacterial; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal ulcer; eye infections, bacterial; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term corneal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
compound eye corneal lens development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the compound eye corneal lens development biological process from the curated GO Biological Process Annotations 2015 dataset. |
Central corneal thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Corneal curvature Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Corneal curvature phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Fuchs's corneal dystrophy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Fuchs's corneal dystrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Corneal astigmatism Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Corneal astigmatism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Corneal structure Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Corneal structure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
corneal dystrophy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease corneal dystrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
decreased corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the decreased corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
increased corneal curvature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the increased corneal curvature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
polymorphous posterior corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the polymorphous posterior corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lattice corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the lattice corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
herpetiform corneal ulceration Gene SetFrom HPO Gene-Disease Associations genes associated with the herpetiform corneal ulceration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
granular corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the granular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal scarring Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal scarring phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal crystals Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal crystals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
map-dot-fingerprint corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the map-dot-fingerprint corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased corneal reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased corneal reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
speckled corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the speckled corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
opacification of the corneal epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the opacification of the corneal epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal opacity Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal opacity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
crystalline corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the crystalline corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
marginal corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the marginal corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal ulceration Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal ulceration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal erosion Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal erosion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal perforation Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal perforation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal guttata Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal guttata phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased corneal thickness Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased corneal thickness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of corneal epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of corneal epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased corneal thickness Gene SetFrom HPO Gene-Disease Associations genes associated with the increased corneal thickness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nodular corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the nodular corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
juvenile epithelial corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the juvenile epithelial corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mosaic corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the mosaic corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal arcus Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal arcus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
punctate corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the punctate corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent corneal erosions Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent corneal erosions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
opacification of the corneal stroma Gene SetFrom HPO Gene-Disease Associations genes associated with the opacification of the corneal stroma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased corneal curvature Gene SetFrom HPO Gene-Disease Associations genes associated with the increased corneal curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of corneal endothelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
reduced number of corneal endothelial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the reduced number of corneal endothelial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal neovascularization Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal neovascularization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of corneal stroma Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of corneal stroma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal degeneration Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of corneal thickness Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of corneal thickness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal migration of corneal endothelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corneal stromal edema Gene SetFrom HPO Gene-Disease Associations genes associated with the corneal stromal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of corneal size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of corneal size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Corneal Ulcer Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Corneal Ulcer phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Corneal Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Corneal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Corneal Opacity Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Corneal Opacity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Corneal Dystrophies, Hereditary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Corneal Dystrophies, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal corneal stroma development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneal stroma development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased corneal stroma thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased corneal stroma thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal scarring Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the corneal scarring phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal opacity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the corneal opacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased corneal stroma thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased corneal stroma thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneal epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneal epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased corneal light-scattering Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased corneal light-scattering phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneal endothelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneal endothelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal abrasion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the corneal abrasion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal vascularization Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the corneal vascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal deposits Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the corneal deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased incidence of corneal inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased incidence of corneal inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent corneal endothelium Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent corneal endothelium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal-lenticular stalk Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the corneal-lenticular stalk phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneal stroma morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneal stroma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
?corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, schnyder type Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, schnyder type phenotype from the curated OMIM Gene-Disease Associations dataset. |
cataract with late-onset corneal dystrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, congenital stromal Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, congenital stromal phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, lattice type iiia Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type iiia phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, gelatinous drop-like Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, gelatinous drop-like phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, posterior polymorphous, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, posterior polymorphous, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, fuchs endothelial, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, fuchs endothelial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, epithelial basement membrane Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, epithelial basement membrane phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal endothelial dystrophy and perceptive deafness Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy and perceptive deafness phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal endothelial dystrophy 1, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, reis-bucklers type Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, reis-bucklers type phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, thiel-behnke type Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, thiel-behnke type phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, endothelial, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal endothelial dystrophy 2, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal endothelial dystrophy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, lattice type i Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lattice type i phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal opacification and other ocular anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal opacification and other ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, posterior polymorphous 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, groenouw type i Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal clouding, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal clouding, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
meesmann corneal dystrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the meesmann corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal fleck dystrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal fleck dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
macular corneal dystrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the macular corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, avellino type Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, avellino type phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, lisch epithelial Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, lisch epithelial phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue corneal cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
corneal epithelium Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue corneal epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
corneal fibroblast cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue corneal fibroblast cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
corneal epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue corneal epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
corneal fibroblast cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue corneal fibroblast cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
corneal cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue corneal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
corneal epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue corneal epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Eye-corneal epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-corneal epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-corneal keratocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-corneal keratocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Corneal Erosion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Erosion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fleck Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fleck Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Avellino Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Avellino Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Graft Rejection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Graft Rejection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thiel-Behnke Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thiel-Behnke Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Regular Astigmatism - Corneal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Regular Astigmatism - Corneal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lattice Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lattice Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Pannus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Pannus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Neovascularization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Allograft Rejection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Allograft Rejection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Ulcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Schnyder Crystalline Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Schnyder Crystalline Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Irido-Corneal Dysgenesis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irido-Corneal Dysgenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polymorphous Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polymorphous Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Fibrosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Thinning Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Thinning in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mosaic Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mosaic Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Hypoesthesia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Hypoesthesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Macular Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Macular Corneal Dystrophy Type Ii (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Macular Corneal Dystrophy Type Ii (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pseudophakic Corneal Edema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pseudophakic Corneal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Degeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Guttata Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Guttata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fine Corneal Edema Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fine Corneal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Marginal Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Marginal Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Granular Dystrophy, Corneal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Granular Dystrophy, Corneal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Clouding Of Corneal Stroma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Clouding Of Corneal Stroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Corneal Stroma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Corneal Stroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Melt Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Melt in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Corneal Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Corneal Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Epithelial Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Epithelial Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Speckled Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Speckled Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Endotheliitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Endotheliitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Deposit Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Deposit in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pre-Descemet'S Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pre-Descemet'S Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Defect Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Corneal Opacity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Corneal Opacity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gelatinous Droplike Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gelatinous Droplike Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Herpetiform Corneal Ulceration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Herpetiform Corneal Ulceration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Groenouw Corneal Dystrophy Type I (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Groenouw Corneal Dystrophy Type I (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Punctate Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Punctate Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reis-Bucklers' Corneal Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Reis-Bucklers' Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Corneal Endothelium Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Corneal Endothelium Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Reflex, Corneal, Absent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reflex, Corneal, Absent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reflex, Corneal, Decreased Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reflex, Corneal, Decreased in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Opacity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Opacity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Stromal Opacities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Stromal Opacities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Central Corneal Thickness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Corneal Thickness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Topography Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Topography in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Ghost Vessels Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Ghost Vessels in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Scar Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Scar in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Opacification Of The Corneal Epithelium Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Opacification Of The Corneal Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Thickening Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Thickening in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Calcification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Crystalline Deposits Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Crystalline Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Striae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Striae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Stromal Edema Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Stromal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Corneal Thickness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Corneal Thickness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Sensitivity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Corneal Thickness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Corneal Thickness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Corneal Limbus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Corneal Limbus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Anesthesia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Anesthesia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nodular Corneal Dystrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nodular Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
increased corneal epithelium thickness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased corneal epithelium thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corneal epithelium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corneal epithelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent corneal endothelium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent corneal endothelium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corneal endothelium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corneal endothelium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased incidence of corneal inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased incidence of corneal inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal scarring Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal scarring phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal opacity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal opacity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corneal stroma development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corneal stroma development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased corneal stroma thickness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased corneal stroma thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corneal stroma morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corneal stroma morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal vascularization Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal vascularization phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal-lenticular stalk Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal-lenticular stalk phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased corneal epithelium thickness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased corneal epithelium thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized corneal epithelium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized corneal epithelium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased corneal stroma thickness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased corneal stroma thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal epithelium hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal epithelium hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal limbitis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal limbitis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased corneal light-scattering Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased corneal light-scattering phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corneal wound healing Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corneal wound healing phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal abrasion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal abrasion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent corneal epithelium Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent corneal epithelium phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal epithelium hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal epithelium hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corneal stroma collagen fibril morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corneal stroma collagen fibril morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal opacity Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the corneal opacity phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
corneal vascularization Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the corneal vascularization phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
corneal deposits Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the corneal deposits phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Human - Fetal Development - L1 - Corneal and conjunctival epithelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Corneal and conjunctival epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Corneal epithelial progenitor cell_Embryonic stem cell_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal epithelial progenitor cell_Embryonic stem cell_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Corneal limbal stem cell_Limbal epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal limbal stem cell_Limbal epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Corneal epithelial stem cell_Eye_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal epithelial stem cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Corneal endothelial cell_Eye_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal endothelial cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Corneal endothelial cell_Corneal endothelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal endothelial cell_Corneal endothelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Corneal cell_Cornea_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal cell_Cornea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Corneal epithelial cell_Eye_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal epithelial cell_Eye_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Corneal cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Corneal cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Gelatinous drop-like corneal dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Gelatinous drop-like corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Corneal dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Lattice corneal dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lattice corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Granular corneal dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Granular corneal dystrophy 2 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Granular corneal dystrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Meesmann corneal dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Meesmann corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Corneal endothelial dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Corneal endothelial dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Congenital stromal corneal dystrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital stromal corneal dystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Corneal staphyloma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal staphyloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal degeneration Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal edema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Macular corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal neovascularization Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal neovascularization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal endothelial dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal endothelial dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lattice corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lattice corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Schnyder corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Schnyder corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal abscess Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal abscess in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital stromal corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital stromal corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Subepithelial mucinous corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subepithelial mucinous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fleck corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fleck corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Gelatinous drop-like corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gelatinous drop-like corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Meesmann corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Meesmann corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Granular corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal ectasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal ectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thiel-Behnke corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thiel-Behnke corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Perforated corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Perforated corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal deposit Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal deposit in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent corneal erosion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Granular corneal dystrophy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lisch epithelial corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lisch epithelial corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal dystrophy-perceptive deafness syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal dystrophy-perceptive deafness syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior amorphous corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior amorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Secondary corneal edema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Granular corneal dystrophy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Granular corneal dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Reis-Bucklers corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Reis-Bucklers corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Central corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Marginal corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Marginal corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked endothelial corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked endothelial corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ring corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ring corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mycotic corneal ulcer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mycotic corneal ulcer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spondylometaphyseal dysplasia with corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondylometaphyseal dysplasia with corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal intraepithelial neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal intraepithelial neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Deep corneal vascularisation Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Deep corneal vascularisation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Idiopathic corneal edema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Corneal epithelium Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Corneal epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Corneal cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Corneal cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Corneal fibroblast cell line Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Corneal fibroblast cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Corneal epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Corneal epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Corneal epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Corneal epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Corneal cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Corneal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Corneal fibroblast cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Corneal fibroblast cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Corneal dystrophy-perceptive deafness syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Corneal dystrophy-perceptive deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Macular corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Macular corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lisch epithelial corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lisch epithelial corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Groenouw corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Groenouw corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lattice corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lattice corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thiel-Behnke corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiel-Behnke corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Avellino corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Avellino corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reis-Bucklers' corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reis-Bucklers' corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polymorphous corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polymorphous corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Schnyder crystalline corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Schnyder crystalline corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Gelatinous droplike corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Gelatinous droplike corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fleck corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital stromal corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital stromal corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Opacification of the corneal stroma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Opacification of the corneal stroma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Posterior polymorphous corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Posterior polymorphous corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Central corneal thickness Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Central corneal thickness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corneal hysteresis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal hysteresis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corneal resistance factor Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal resistance factor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corneal curvature Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal curvature phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corneal astigmatism Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal astigmatism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure and central corneal thickness (multi-trait analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure and central corneal thickness (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corneal structure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal structure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corneal endothelial cell density Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal endothelial cell density phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corneal endothelial cell shape (percentage of hexagonally shaped cells) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal endothelial cell shape (percentage of hexagonally shaped cells) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure (corneal compensated) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure (corneal compensated) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fuchs's corneal dystrophy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fuchs's corneal dystrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
crohn disease; crohn's disease; inflammation Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetic angiopathies Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alzheimer's disease or family history of Alzheimer's disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 7 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Norum disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Salla disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Salla disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Worth disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Worth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ménière's disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4B1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chylomicron retention disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 18 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden disease 6 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudo von Willebrand disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, juvenile type Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Naxos disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leiner disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leiner disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycystic kidney disease 2 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease, type B Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 15 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type 13 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle eye brain disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lhermitte-Duclos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kugelberg-Welander disease Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Darier disease, acral hemorrhagic type Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease ganglioneuroblastoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oguchi's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oguchi's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kanzaki disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, chronic Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Danon disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dent disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent disease 1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson disease 9 from the curated CTD Gene-Disease Associations dataset. |
Oguchi disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Addison Disease from the curated CTD Gene-Disease Associations dataset. |
Alexander Disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intervertebral disc disease from the curated CTD Gene-Disease Associations dataset. |
Von Willebrand disease, platelet type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Von Willebrand disease, platelet type from the curated CTD Gene-Disease Associations dataset. |
Coronary Artery Disease Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Machado-Joseph Disease from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease from the curated CTD Gene-Disease Associations dataset. |
Papillon-Lefevre Disease Gene SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
Moyamoya Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Moyamoya Disease from the curated CTD Gene-Disease Associations dataset. |
Gilbert Disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic venoocclusive disease with immunodeficiency from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 25, Autosomal Recessive Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
GALLBLADDER DISEASE 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease GALLBLADDER DISEASE 1 from the curated CTD Gene-Disease Associations dataset. |
Acute Disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease XII Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bowen's Disease from the curated CTD Gene-Disease Associations dataset. |
Hodgkin Disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Medullary Cystic Kidney Disease 2 from the curated CTD Gene-Disease Associations dataset. |
von Willebrand Disease, Type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease von Willebrand Disease, Type 3 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 4C Gene SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease from the curated CTD Gene-Disease Associations dataset. |
PAGET DISEASE, JUVENILE Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 6 from the curated CTD Gene-Disease Associations dataset. |
Hashimoto Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hashimoto Disease from the curated CTD Gene-Disease Associations dataset. |
Canavan Disease Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease XIII from the curated CTD Gene-Disease Associations dataset. |