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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. |
aland island eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aland island eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aland island eye disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the aland island eye disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
Aland Island eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aland Island eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aland island eye disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aland island eye disease phenotype from the curated ClinVar Gene-Phenotype Associations 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. |
eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye infections, fungal; fungal eye infections; histoplasmosis; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye neoplasms; melanoma; tumour of eye Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye neoplasms; melanoma; tumour of eye in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Eye-eye photoreceptor cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-eye photoreceptor cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
island of Calleja major Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in island of Calleja major relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Major island of Calleja Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Major island of Calleja relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
flinders island spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease flinders island spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
5' cpg island hypermethylation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease 5' cpg island hypermethylation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
island Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term island in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
hypomethylation of cpg island Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hypomethylation of cpg island biological process from the curated GO Biological Process Annotations 2015 dataset. |
hypermethylation of cpg island Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hypermethylation of cpg island biological process from the curated GO Biological Process Annotations 2015 dataset. |
abnormal visceral yolk sac blood island morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visceral yolk sac blood island morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Bone Island Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bone Island in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Central Topographic Island Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Central Topographic Island in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
negative regulation of gene expression via CpG island methylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of gene expression via CpG island methylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of gene expression via CpG island demethylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of gene expression via CpG island demethylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal visceral yolk sac blood island morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal visceral yolk sac blood island morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Erythroblastic island macrophage_Undefined_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Erythroblastic island macrophage_Undefined_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
positive regulation of gene expression via chromosomal CpG island demethylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of gene expression via chromosomal CpG island demethylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of gene expression via chromosomal CpG island methylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of gene expression via chromosomal CpG island methylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Flinders Island spotted fever Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Flinders Island spotted fever in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Heterochromatin island Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Heterochromatin island cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 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. |
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. |
eye disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease eye and adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
eye disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eye and adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye degenerative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye accommodation disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye accommodation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye and adnexa disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye and adnexa disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fish eye disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fish eye disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease eye disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
eye and adnexa disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease eye and adnexa disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
fish-eye disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the fish-eye disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
bornholm eye disease Gene SetFrom OMIM Gene-Disease Associations genes associated with the bornholm eye disease phenotype from the curated OMIM Gene-Disease Associations dataset. |
Bornholm Eye Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bornholm Eye Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscle Eye Brain Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Muscle Eye Brain Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fish-Eye Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fish-Eye Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eye disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Eye disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Eye degenerative disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Eye degenerative disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Eye disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Eye disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye degenerative disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Eye degenerative disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye degenerative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye accommodation disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye accommodation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fish-eye disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Muscle eye brain disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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. |
Skin/hair/eye pigmentation, variation in, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Eye Diseases, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Eye Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Eye Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset. |
Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation And Eye Coloboma from the curated CTD Gene-Disease Associations dataset. |
Dry Eye Syndromes Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dry Eye Syndromes from the curated CTD Gene-Disease Associations dataset. |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset. |
Eye Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Pain from the curated CTD Gene-Disease Associations dataset. |
Eye Infections, Bacterial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Infections, Bacterial from the curated CTD Gene-Disease Associations dataset. |
Eye Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Eye in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Eye Color Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Eye Color in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
eye lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eye carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
shipyard eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease shipyard eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dry eye syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dry eye syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
eye color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; retinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; sarcoidosis; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; sarcoidosis; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; hypersensitivity; respiratory tract diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; hypersensitivity; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; macular degeneration; retinal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anophthalmos; coloboma; eye abnormalities; microphthalmos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anophthalmos; coloboma; eye abnormalities; microphthalmos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aphakia; eye abnormalities; microphthalmos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aphakia; eye abnormalities; microphthalmos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye movement disturbances Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye movement disturbances in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dry eye syndromes; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dry eye syndromes; 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. |
eye Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; pseudoxanthoma elasticum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; pseudoxanthoma elasticum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye abnormalities; glaucoma, angle-closure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye abnormalities; glaucoma, angle-closure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; glomerulosclerosis, focal segmental; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; eye diseases; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; eye diseases; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases; stevens-johnson syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases; stevens-johnson syndrome 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. |
eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term eye in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye photoreceptor cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye photoreceptor cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigment granule organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigment granule organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
eyelid development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eyelid development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye photoreceptor cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye photoreceptor cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2015 dataset. |
optic cup morphogenesis involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigmentation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigmentation biological process from the curated GO Biological Process Annotations 2015 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. |
cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigment metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigment metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye pigment biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye pigment biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina vasculature development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
camera-type eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the camera-type eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
lens development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lens development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic camera-type eye formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic camera-type eye formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of retina development in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of retina development in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina vasculature morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina vasculature morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
lens morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lens morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
optic cup formation involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the optic cup formation involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
eye photoreceptor cell development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the eye photoreceptor cell development biological process from the curated GO Biological Process Annotations 2015 dataset. |
optic placode formation involved in camera-type eye formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the optic placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
compound eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the compound eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
lens induction in camera-type eye Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lens induction in camera-type eye biological process from the curated GO Biological Process Annotations 2015 dataset. |
post-embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the post-embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset. |
structural constituent of eye lens Gene SetFrom GO Molecular Function Annotations 2015 genes performing the structural constituent of eye lens molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Eye color traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Eye color traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Eye color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Eye color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aplasia/hypoplasia affecting the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of saccadic eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slow saccadic eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the slow saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deeply set eye Gene SetFrom HPO Gene-Disease Associations genes associated with the deeply set eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
eye of the tiger anomaly of globus pallidus Gene SetFrom HPO Gene-Disease Associations genes associated with the eye of the tiger anomaly of globus pallidus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bull's eye maculopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the bull's eye maculopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hemorrhage of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the hemorrhage of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
uncontrolled eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the uncontrolled eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
poor hand-eye coordination Gene SetFrom HPO Gene-Disease Associations genes associated with the poor hand-eye coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior segment of eye aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior segment of eye aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal conjugate eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hamartoma of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the hamartoma of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
paroxysmal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the paroxysmal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
eye poking Gene SetFrom HPO Gene-Disease Associations genes associated with the eye poking phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vasculature of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
poor eye contact Gene SetFrom HPO Gene-Disease Associations genes associated with the poor eye contact phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rapid eye movement (rem) sleep Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent anterior eye chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the absent anterior eye chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Eye Hemorrhage Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Hemorrhage phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Neoplasms Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Infections, Fungal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Infections, Fungal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Infections, Viral Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Infections, Viral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Eye Infections, Bacterial Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Eye Infections, Bacterial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Cat eye syndrome critical region protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cat eye syndrome critical region protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cat eye syndrome critical region protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cat eye syndrome critical region protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cat eye syndrome critical region protein 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cat eye syndrome critical region protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal eye morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hydropic eye lens fibers Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hydropic eye lens fibers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal non-rapid eye movement sleep pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye hemorrhage Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye posterior chamber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye posterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye pigment epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye pigment epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent eye pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent eye pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye electrophysiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye electrophysiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye distance/ position Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye opacity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye opacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vision/eye phenotype Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye anterior chamber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye anterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged eye anterior chamber Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged eye anterior chamber phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye bleb Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye bleb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye muscle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye anterior chamber depth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye anterior chamber depth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
narrow eye opening Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the narrow eye opening phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye movement Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anterior eye segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior eye segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye blink conditioning behavior Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye blink conditioning behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
eye inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the eye inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased eye pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased eye pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[skin/hair/eye pigmentation 6, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 3, blue/green eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation, variation in, 8] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 9, dark/light hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, dark/light hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 10, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 10, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 6, blue/green eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, black/nonblack hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, black/nonblack hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 1, blue/nonblue eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blue/nonblue eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 2, red hair/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 7, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 7, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, blond hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, dark/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset. |
microtia with nasolacrimal duct imperforation and eye coloboma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microtia with nasolacrimal duct imperforation and eye coloboma phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 4, fair/dark skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 4, fair/dark skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cat eye syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the cat eye syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, dark/light eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/light eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 9, brown/nonbrown eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, brown/nonbrown eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 1, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
eye Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue eye from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
eye cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue eye cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
eye Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue eye in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
anterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue anterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
vitreous chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue vitreous chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
compound eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue compound eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
eye cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue eye cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Eye-adipocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-adipocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-b cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-b cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-cd4-positive, alpha-beta t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-cd4-positive, alpha-beta t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-cd8-positive, alpha-beta t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-cd8-positive, alpha-beta t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-ciliary body Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-ciliary body relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-conjunctival epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-conjunctival epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations 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. |
Eye-dendritic cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-dendritic cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-endothelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-epithelial cell of lacrimal sac Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-epithelial cell of lacrimal sac relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-erythroid lineage cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-erythroid lineage cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-fibroblast Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-fibroblast relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-lacrimal gland functional unit cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-lacrimal gland functional unit cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-limbal stem cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-limbal stem cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-limbal stromal cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-limbal stromal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-macrophage Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-macrophage relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-mast cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-mast cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-melanocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-melanocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-microglial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-microglial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-monocyte Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-monocyte relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-muller cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-muller cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-ocular surface cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-ocular surface cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-plasma cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-plasma cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-radial glial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-radial glial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retina horizontal cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retina horizontal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal bipolar neuron Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal bipolar neuron relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal blood vessel endothelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal blood vessel endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal ganglion cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal ganglion cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-retinal pigment epithelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal pigment epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Eye-t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Dry Eye Syndromes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dry Eye Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inflammatory Abnormality Of The Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Abnormality Of The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pterygium Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pterygium Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cat Eye Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cat Eye Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rieger Eye Malformation Sequence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rieger Eye Malformation Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eye Disorder Due To Diabetes Mellitus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Eye Disorder Due To Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Anomaly Of Anterior Segment Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomaly Of Anterior Segment Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Congenital Malformations Of Anterior Segment Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Congenital Malformations Of Anterior Segment Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Involuntary Eye Movements Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Involuntary Eye Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skin/Hair/Eye Pigmentation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skin/Hair/Eye Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Saccadic Eye Movement Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Saccadic Eye Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Infection Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Infection Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Eye Disorders (Excl Glaucoma) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Eye Disorders (Excl Glaucoma) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Rapid Eye Movement Parasomnia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Rapid Eye Movement Parasomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Eye Poking Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Eye Poking in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dermoid Choristoma Of Eye Proper Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dermoid Choristoma Of Eye Proper in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bull'S Eye Macular Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bull'S Eye Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dryness Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dryness Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Paroxysmal Involuntary Eye Movements Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paroxysmal Involuntary Eye Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Depth Of Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Depth Of Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Eye Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Eye Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Coloboma (In Some Patients) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Coloboma (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Poor Eye Contact Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Eye Contact in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shallow Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shallow Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Color Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Color in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skin/Hair/Eye Pigmentation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skin/Hair/Eye Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Injected Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Injected Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Manifestations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Manifestations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Uncontrolled Eye Movements Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uncontrolled Eye Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Redness Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Redness Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deep Anterior Chamber Of Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deep Anterior Chamber Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Of The Tiger Anomaly Of Globus Pallidus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Of The Tiger Anomaly Of Globus Pallidus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Rapid Eye Movement Sleep Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Rapid Eye Movement Sleep in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Conjugate Eye Movement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Conjugate Eye Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Affecting The Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Affecting The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Segment Of Eye Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Segment Of Eye Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Eye Problem Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eye Problem in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Poor Hand-Eye Coordination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Poor Hand-Eye Coordination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain Around Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain Around Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Eye Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Eye Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye photoreceptor cell development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye photoreceptor cell development biological process from the curated GO Biological Process Annotations 2023 dataset. |
camera-type eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the camera-type eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of vasculature development involved in avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of vasculature development involved in avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
vertebrate eye-specific patterning Gene SetFrom GO Biological Process Annotations 2023 genes participating in the vertebrate eye-specific patterning biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
retina vasculature development in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
camera-type eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the camera-type eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye pigment biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye pigment biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
post-embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the post-embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
optic cup morphogenesis involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye pigment granule organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye pigment granule organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
lens placode formation involved in camera-type eye formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lens placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset. |
avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2023 genes participating in the avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2023 dataset. |
eye pigment metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the eye pigment metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal eye development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye muscle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye muscle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye muscle development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye muscle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal anterior eye segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal anterior eye segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye anterior chamber morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye anterior chamber morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent eye anterior chamber Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye anterior chamber phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye distance/ position Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye distance/ position phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased eye pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased eye pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
narrow eye opening Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the narrow eye opening phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye electrophysiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye electrophysiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hydropic eye lens fibers Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hydropic eye lens fibers phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye blink conditioning behavior Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye blink conditioning behavior phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye opacity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye opacity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye posterior chamber morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal non-rapid eye movement sleep pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior eye segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased eye anterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased eye anterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased eye anterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased eye anterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent eye pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye hemorrhage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye movement Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye movement phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye bleb Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye bleb phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye vasculature morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye vasculature morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged eye anterior chamber Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged eye anterior chamber phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye lesions Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye lesions phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye muscle topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye muscle topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent eye muscles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent eye muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye anterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye anterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye posterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
variegated eye pigmentation pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the variegated eye pigmentation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
eye discharge Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the eye discharge phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
vision/eye phenotype Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber depth Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal eye posterior chamber depth phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal eye anterior chamber depth Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal eye anterior chamber depth phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal eye morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal eye morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
narrow eye opening Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the narrow eye opening phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
eye hemorrhage Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the eye hemorrhage phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Human - Fetal Development - L2 - Eye-Ganglion cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Ganglion cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Stromal cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Vascular endothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Astrocytes Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Microglia Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Photoreceptor cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Photoreceptor cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Skeletal muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Smooth muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Horizontal cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Horizontal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Amacrine cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Amacrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Retinal pigment cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-Bipolar cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Bipolar 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. |
Human - Fetal Development - L2 - Eye-Lens fibre cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Lens fibre cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye photoreceptor cell development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye photoreceptor cell development biological process from the curated GO Biological Process Annotations 2025 dataset. |
camera-type eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the camera-type eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of vasculature development involved in avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of vasculature development involved in avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
vertebrate eye-specific patterning Gene SetFrom GO Biological Process Annotations 2025 genes participating in the vertebrate eye-specific patterning biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic retina morphogenesis in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic retina morphogenesis in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
retina vasculature development in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the retina vasculature development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
camera-type eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the camera-type eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
camera-type eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the camera-type eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye pigment biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye pigment biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
post-embryonic eye morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the post-embryonic eye morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye photoreceptor cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic camera-type eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic camera-type eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
optic cup morphogenesis involved in camera-type eye development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye pigment granule organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye pigment granule organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
lens placode formation involved in camera-type eye formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lens placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset. |
avascular cornea development in camera-type eye Gene SetFrom GO Biological Process Annotations 2025 genes participating in the avascular cornea development in camera-type eye biological process from the curated GO Biological Process Annotations 2025 dataset. |
eye pigment metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the eye pigment metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of eye pigmentation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of eye pigmentation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Dry eye syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dry eye syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Shipyard eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Shipyard eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lateral displacement of eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lateral displacement of eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with eye movement abnormalities and ataxia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with eye movement abnormalities and ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Eye carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Blind hypotensive eye Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Blind hypotensive eye in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Eye Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Eye from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye cancer cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Eye cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Eye in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Compound eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Compound eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Vitreous chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Vitreous chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Anterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Anterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Eye cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Eye cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
SKIN/HAIR/EYE PIGMENTATION Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SKIN/HAIR/EYE PIGMENTATION phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormality of the eye Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of the eye phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormality of eye movement Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of eye movement phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Deeply set eye Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Deeply set eye phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SKIN/HAIR/EYE PIGMENTAT Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SKIN/HAIR/EYE PIGMENTAT phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PITX2-Related Eye Abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PITX2-Related Eye Abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Disorder of eye Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Disorder of eye phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Reduced eye contact Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Reduced eye contact phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Exploratory eye movement dysfunction in schizophrenia (responsive search score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (responsive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Exploratory eye movement dysfunction in schizophrenia (cognitive search score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (cognitive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color (brightness) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color (brightness) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color (saturation) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color (saturation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color (hue) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color (hue) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Skin, hair and eye pigmentation (multivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Skin, hair and eye pigmentation (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye morphology Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye length Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye length phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye color traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye color traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye movement (horizontal position gain) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye movement (horizontal position gain) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Eye movement in schizophrenia (horizontal position gain) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eye movement in schizophrenia (horizontal position gain) 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. |
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. |
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. |