Name

sandhoff disease, infantile, juvenile, and adult forms Gene Set

From OMIM Gene-Disease Associations

genes associated with the sandhoff disease, infantile, juvenile, and adult forms phenotype from the curated OMIM Gene-Disease Associations dataset.

Sandhoff disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, juvenile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

adult-onset still disease; still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Sandhoff disease, chronic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sandhoff Disease from the curated CTD Gene-Disease Associations dataset.

sandhoff disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease sandhoff disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

sandhoff disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sandhoff disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sandhoff disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sandhoff disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Sandhoff Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Sandhoff Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

longer forms of a repetitive sequence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease longer forms of a repetitive sequence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

formselective Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term formselective in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

forms Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term forms in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

gm2-gangliosidosis, several forms Gene Set

From OMIM Gene-Disease Associations

genes associated with the gm2-gangliosidosis, several forms phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia-lymphoma, adult t-cell; t-cell leukemia, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia-lymphoma, adult t-cell; t-cell leukemia, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma 3a, primary open angle, congenital, juvenile, or adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3a, primary open angle, congenital, juvenile, or adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

juvenile polyposis syndrome, infantile form Gene Set

From OMIM Gene-Disease Associations

genes associated with the juvenile polyposis syndrome, infantile form phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sandhoff Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term sandhoff in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

critical illness; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease critical illness; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth height growth to adolescence and adult stature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth height growth to adolescence and adult stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Refsum disease, adult, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Refsum disease, adult, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

adult-onset still's disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult-onset still's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sporadic adult-onset lower motor neuron disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sporadic adult-onset lower motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset of esrf in pkd1 adult polycystic kidney disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of esrf in pkd1 adult polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Still's Disease, Adult-Onset Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Still's Disease, Adult-Onset phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

polycystic kidney disease, adult type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney disease, adult type i phenotype from the curated OMIM Gene-Disease Associations dataset.

polyglucosan body disease, adult form Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyglucosan body disease, adult form phenotype from the curated OMIM Gene-Disease Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

familial hemiplegic migraine and benign familial infantile convulsions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hemiplegic migraine and benign familial infantile convulsions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea and glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile macular degeneration and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, Juvenile, With Microcornea And Glucosuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.

Juvenile macular degeneration and hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset.

cataract, juvenile, with microcornea and glucosuria Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract, juvenile, with microcornea and glucosuria phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Glycogen storage disease type II, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sialic acid storage disease, severe infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, multisystem, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Refsum Disease, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset.

infantile refsum disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease infantile refsum disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

polycystic kidney disease, infantile severe, with tuberous sclerosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune disease, multisystem, infantile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune disease, multisystem, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

Parkinson disease 19, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-sachs disease, juvenile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-sachs disease, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PAGET DISEASE, JUVENILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PAGET DISEASE, JUVENILE from the curated CTD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; rheumatoid arthritis; cholangitis, sclerosing; celiac disease; juvenile arthrit in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimers disease; juvenile arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimers disease; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

paget disease, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the paget disease, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 19, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 19, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease, juvenile, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease, juvenile, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Crohn's disease and celiac disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

coronary artery disease; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis; crohn disease; crohn's disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; graft vs host disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Gm2-gangliosidosis, adult-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gm2-gangliosidosis, adult-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Metachromatic leukodystrophy, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Metachromatic leukodystrophy, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ADULT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ADULT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult junctional epidermolysis bullosa Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult junctional epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gm2-gangliosidosis, adult Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gm2-gangliosidosis, adult phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, familial adult myoclonic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, familial adult myoclonic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult onset ataxia with oculomotor apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult onset ataxia with oculomotor apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Lactose Intolerance, Adult Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lactose Intolerance, Adult Type from the curated CTD Gene-Disease Associations dataset.

Pancreatic cancer, adult Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pancreatic cancer, adult from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Familial Adult Myoclonic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Familial Adult Myoclonic, 3 from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2 from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Nonimmune Chronic Idiopathic, Adult Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Nonimmune Chronic Idiopathic, Adult from the curated CTD Gene-Disease Associations dataset.

Adult-onset citrullinemia type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adult-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.

Hypophosphatasia, Adult Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatasia, Adult from the curated CTD Gene-Disease Associations dataset.

Leukemia-Lymphoma, Adult T-Cell Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukemia-Lymphoma, Adult T-Cell from the curated CTD Gene-Disease Associations dataset.

Primary Lateral Sclerosis, Adult, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Primary Lateral Sclerosis, Adult, 1 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Myoclonic, Benign Adult Familial, Type 1 from the curated CTD Gene-Disease Associations dataset.

Respiratory Distress Syndrome, Adult Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Respiratory Distress Syndrome, Adult from the curated CTD Gene-Disease Associations dataset.

adolescence-adult electroclinical syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease adolescence-adult electroclinical syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

adult t-cell leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult t-cell leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult mesoblastic nephroma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult mesoblastic nephroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult acute lymphocytic leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult acute lymphocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult respiratory distress syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult respiratory distress syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult astrocytic tumour Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult astrocytic tumour in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult fibrosarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult pleomorphic rhabdomyosarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult pleomorphic rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

t-cell adult acute lymphocytic leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease t-cell adult acute lymphocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult xanthogranuloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult xanthogranuloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult medulloblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult malignant schwannoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult oligodendroglioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult dermatomyositis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult teratoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult teratoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adolescence-adult electroclinical syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adolescence-adult electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adult onset multi/minicore myopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult onset multi/minicore myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased development of adult t-cell leukemia/lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased development of adult t-cell leukemia/lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult male height Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult male height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; respiratory distress syndrome, adult; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; respiratory distress syndrome, adult; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, adult acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, adult acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult separation anxiety Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult separation anxiety in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory distress syndrome, adult; respiratory insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory distress syndrome, adult; respiratory insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney diseases; lead poisoning, nervous system, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney diseases; lead poisoning, nervous system, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, adult acute lymphocytic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, adult acute lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute t cell leukemia; burkitt lymphoma; burkitt; acute lymphoblastic leukemia (type); leukemia, lymphocytic, acute, l1; leukemia-lymphoma, adult t-cell; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute t cell leukemia; burkitt lymphoma; burkitt; acute lymphoblastic leukemia (type); leukemia, lymphocytic, acute, l1; leukemia-lymphoma, adult t-cell; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchial asthma (childhood & adult) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchial asthma (childhood & adult) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

citrullinemia, adult-onset type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease citrullinemia, adult-onset type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult brain tumors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult brain tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult t-cell leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult t-cell leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

community-acquired infections; pneumonia; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease community-acquired infections; pneumonia; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lung injury; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lung injury; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypolactasia, adult-type Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypolactasia, adult-type in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute t cell leukemia; leukemia-lymphoma, adult t-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute t cell leukemia; leukemia-lymphoma, adult t-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult-type hypolactasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult-type hypolactasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult adhd ; attention deficit hyperactivity disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult adhd ; attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lead poisoning, nervous system, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lead poisoning, nervous system, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult height urinary pyridinoline excretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult height urinary pyridinoline excretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult atopic dermatitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult atopic dermatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term adult in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Leukemia, Adult T Cell_Blood monocyte_GSE10789 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Leukemia, Adult T Cell_Blood monocyte_GSE10789 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

MIR122_Antisense Inhibition_GDS1729_759_mouse_Livers (from C57BL/6 adult males) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the MIR122_Antisense Inhibition_GDS1729_759_mouse_Livers (from C57BL/6 adult males) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

adult heart development Gene Set

From GO Biological Process Annotations

genes participating in the adult heart development biological process from the curated GO Biological Process Annotations dataset.

determination of adult lifespan Gene Set

From GO Biological Process Annotations

genes participating in the determination of adult lifespan biological process from the curated GO Biological Process Annotations dataset.

adult locomotory behavior Gene Set

From GO Biological Process Annotations

genes participating in the adult locomotory behavior biological process from the curated GO Biological Process Annotations dataset.

adult walking behavior Gene Set

From GO Biological Process Annotations

genes participating in the adult walking behavior biological process from the curated GO Biological Process Annotations dataset.

adult behavior Gene Set

From GO Biological Process Annotations

genes participating in the adult behavior biological process from the curated GO Biological Process Annotations dataset.

adult feeding behavior Gene Set

From GO Biological Process Annotations

genes participating in the adult feeding behavior biological process from the curated GO Biological Process Annotations dataset.

adult somatic muscle development Gene Set

From GO Biological Process Annotations

genes participating in the adult somatic muscle development biological process from the curated GO Biological Process Annotations dataset.

adult syndrome Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease adult syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

adult testis Gene Set

From HPM Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in adult testis relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset.

adult retina Gene Set

From HPM Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in adult retina relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset.

adult ovary Gene Set

From HPM Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in adult ovary relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset.

young adult onset Gene Set

From HPO Gene-Disease Associations

genes associated with the young adult onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adult onset Gene Set

From HPO Gene-Disease Associations

genes associated with the adult onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adult-onset night blindness Gene Set

From HPO Gene-Disease Associations

genes associated with the adult-onset night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adult onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the adult onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prominent supraorbital arches in adult Gene Set

From HPO Gene-Disease Associations

genes associated with the prominent supraorbital arches in adult phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Leukemia-Lymphoma, Adult T-Cell Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia-Lymphoma, Adult T-Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Distress Syndrome, Adult Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Respiratory Distress Syndrome, Adult phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lead Poisoning, Nervous System, Adult Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lead Poisoning, Nervous System, Adult phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

glaucoma 1b, primary open angle, adult onset, Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1b, primary open angle, adult onset, phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenomyeloneuropathy, adult Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenomyeloneuropathy, adult phenotype from the curated OMIM Gene-Disease Associations dataset.

adult syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the adult syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?epilepsy, familial adult myoclonic, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epilepsy, familial adult myoclonic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, kufs type, adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, kufs type, adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, adult-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, adult-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

citrullinemia, adult-onset type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the citrullinemia, adult-onset type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

primary lateral sclerosis, adult, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the primary lateral sclerosis, adult, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, familial adult myoclonic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, familial adult myoclonic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

adult i phenotype without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

hypophosphatasia, adult Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypophosphatasia, adult phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, myoclonic, familial adult, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, myoclonic, familial adult, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 13 with adult i phenotype Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 13 with adult i phenotype phenotype from the curated OMIM Gene-Disease Associations dataset.

adult Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term adult in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

adult stem cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue adult stem cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

adult stem cell Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue adult stem cell in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

adult Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue adult in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

adult t-cell lymphoma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue adult t-cell lymphoma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

gravid adult Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue gravid adult in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

adult stem cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue adult stem cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

adult t-cell lymphoma cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue adult t-cell lymphoma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

adult liver stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue adult liver stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

alate adult Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue alate adult in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

adult liver stem cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue adult liver stem cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

adult stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue adult stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Benign familial neonatal-infantile seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign familial neonatal-infantile seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation with infantile enterocolitis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation with infantile enterocolitis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Galactosialidosis, late infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Galactosialidosis, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carnitine palmitoyltransferase II deficiency, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked infantile nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked infantile nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile myofibromatosis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile myofibromatosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amish infantile epilepsy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile liver failure syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile liver failure syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile liver failure syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile liver failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile nephronophthisis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile nephronophthisis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Galactosialidosis, early infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Galactosialidosis, early infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyloric stenosis, infantile hypertrophic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile hypophosphatasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile GM1 gangliosidosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile GM1 gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile neuroaxonal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile-onset ascending hereditary spastic paralysis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Metachromatic leukodystrophy, late infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Metachromatic leukodystrophy, late infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile neuroaxonal neurodegeneration with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile neuroaxonal neurodegeneration with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial infantile myasthenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial infantile myasthenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Liver failure acute infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Liver failure acute infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile Parkinsonism-dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sting-associated vasculopathy, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sting-associated vasculopathy, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonic epilepsy, familial infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoclonic epilepsy, familial infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile cortical hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile cortical hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinsonism-Dystonia, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.

Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.

Myasthenia, Familial Infantile, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenia, Familial Infantile, 1 from the curated CTD Gene-Disease Associations dataset.

Hereditary spastic paralysis, infantile onset ascending Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.

Ceroid lipofuscinosis, neuronal 1, infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceroid lipofuscinosis, neuronal 1, infantile from the curated CTD Gene-Disease Associations dataset.

Infantile polyarteritis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Infantile polyarteritis from the curated CTD Gene-Disease Associations dataset.

LIVER FAILURE, INFANTILE, TRANSIENT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LIVER FAILURE, INFANTILE, TRANSIENT from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.

Glaucoma 3, primary infantile, B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 3, primary infantile, B from the curated CTD Gene-Disease Associations dataset.

SEIZURES, BENIGN FAMILIAL INFANTILE, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SEIZURES, BENIGN FAMILIAL INFANTILE, 2 from the curated CTD Gene-Disease Associations dataset.

Amish Infantile Epilepsy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amish Infantile Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.

Pyloric Stenosis, Infantile Hypertrophic, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.

Pyloric Stenosis, Infantile Hypertrophic, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.

Hemangioma, capillary infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemangioma, capillary infantile from the curated CTD Gene-Disease Associations dataset.

Striatonigral degeneration infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Striatonigral degeneration infantile from the curated CTD Gene-Disease Associations dataset.

Pyloric Stenosis, Infantile Hypertrophic, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 5 from the curated CTD Gene-Disease Associations dataset.

Spasms, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spasms, Infantile from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 from the curated CTD Gene-Disease Associations dataset.

Convulsions, Benign Familial Infantile, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Convulsions, Benign Familial Infantile, 4 from the curated CTD Gene-Disease Associations dataset.

Pyloric Stenosis, Infantile Hypertrophic 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic 1 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.

Carnitine Palmitoyltransferase II Deficiency, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Infantile from the curated CTD Gene-Disease Associations dataset.

Pyloric Stenosis, Infantile Hypertrophic, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyloric Stenosis, Infantile Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.

Polycystic kidneys, severe infantile with tuberous sclerosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.

Hypophosphatasia, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatasia, Infantile from the curated CTD Gene-Disease Associations dataset.

MYOCLONIC EPILEPSY, FAMILIAL INFANTILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOCLONIC EPILEPSY, FAMILIAL INFANTILE from the curated CTD Gene-Disease Associations dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease infantile onset spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

benign familial infantile epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease benign familial infantile epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

fatal infantile encephalocardiomyopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease fatal infantile encephalocardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

seborrheic infantile dermatitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease seborrheic infantile dermatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

neurofibromatosis 1; spasms, infantile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neurofibromatosis 1; spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infantile hypophosphatasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile hypophosphatasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infantile hypertrophic pyloric stenosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile hypertrophic pyloric stenosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variant late infantile neuronal ceroid lipofuscinosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variant late infantile neuronal ceroid lipofuscinosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infantile-onset ascending hereditary spastic paralysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infantile hypertrophic pyloric stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile hypertrophic pyloric stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diarrhea, infantile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diarrhea, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spasms, infantile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spasms, infantile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infantile Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term infantile in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Infantile neuronal ceroid lipofuscinosis_Brain_GSE6678 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Infantile hypertrophic pyloric stenosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Infantile hypertrophic pyloric stenosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

calcific stippling of infantile cartilaginous skeleton Gene Set

From HPO Gene-Disease Associations

genes associated with the calcific stippling of infantile cartilaginous skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile onset Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile hypercalcemia Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile hypercalcemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile muscular hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile muscular hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile encephalopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile spasms Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile spasms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile axial hypotonia Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile axial hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Spasms, Infantile Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spasms, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Infantile Apparent Life-Threatening Event Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infantile Apparent Life-Threatening Event phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Diarrhea, Infantile Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Diarrhea, Infantile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

pyloric stenosis, infantile hypertrophic, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyloric stenosis, infantile hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

pyloric stenosis, infantile hypertrophic, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyloric stenosis, infantile hypertrophic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

pyloric stenosis, infantile hypertrophic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyloric stenosis, infantile hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

pyloric stenosis, infantile hypertrophic, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pyloric stenosis, infantile hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, x-linked 2, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

seizures, benign familial infantile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the seizures, benign familial infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

amish infantile epilepsy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the amish infantile epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertriglyceridemia, transient infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertriglyceridemia, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

liver failure, transient infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the liver failure, transient infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

?myofibromatosis, infantile 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?myofibromatosis, infantile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercalcemia, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercalcemia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

nephronophthisis 2, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephronophthisis 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

myofibromatosis, infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myofibromatosis, infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuroaxonal neurodegeneration, infantile, with facial dysmophism Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuroaxonal neurodegeneration, infantile, with facial dysmophism phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinsonism-dystonia, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

sting-associated vasculopathy, infantile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the sting-associated vasculopathy, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

?infantile liver failure syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?infantile liver failure syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?infantile liver failure syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?infantile liver failure syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenia, familial infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenia, familial infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemangioma, capillary infantile, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemangioma, capillary infantile, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

nystagmus, infantile periodic alternating, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the nystagmus, infantile periodic alternating, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

hemangioma, capillary infantile, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemangioma, capillary infantile, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

infantile neuroaxonal dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

myoclonic epilepsy, infantile, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the myoclonic epilepsy, infantile, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

?epileptic encephalopathy, early infantile, 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypophosphatasia, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypophosphatasia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, myofibrillar, fatal infantile hypertrophy, alpha-b crystallin-related phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

infantile cerebellar-retinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

sialic acid storage disorder, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the sialic acid storage disorder, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

autoinflammation with infantile enterocolitis Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoinflammation with infantile enterocolitis phenotype from the curated OMIM Gene-Disease Associations dataset.

convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.

striatonigral degeneration, infantile Gene Set

From OMIM Gene-Disease Associations

genes associated with the striatonigral degeneration, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 3, primary infantile, b Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3, primary infantile, b phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paralysis, infantile onset ascending Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP24A1 causes Hypercalcemia, infantile (HCAI) pathway from the Reactome Pathways dataset.

Glaucoma, primary open angle, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma, primary open angle, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemic nephropathy, familial juvenile, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemic nephropathy, familial juvenile, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile primary lateral sclerosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile primary lateral sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile neuronal ceroid lipofuscinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile neuronal ceroid lipofuscinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile nephropathic cystinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile nephropathic cystinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile GM>1< gangliosidosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile GM>1< gangliosidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gm2-gangliosidosis, juvenile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gm2-gangliosidosis, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile-onset dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 16, juvenile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 16, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial juvenile gout Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial juvenile gout phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Metachromatic leukodystrophy, juvenile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Metachromatic leukodystrophy, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary open angle glaucoma juvenile onset 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary open angle glaucoma juvenile onset 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

juvenile hormone III Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical juvenile hormone III from the curated CTD Gene-Chemical Interactions dataset.

Nephronophthisis, familial juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephronophthisis, familial juvenile from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Juvenile Epithelial of Meesmann Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Juvenile Epithelial of Meesmann from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.

Rheumatoid Arthritis, Systemic Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Rheumatoid Arthritis, Systemic Juvenile from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 4, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 4, Juvenile from the curated CTD Gene-Disease Associations dataset.

Arthritis, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arthritis, Juvenile from the curated CTD Gene-Disease Associations dataset.

Primary lateral sclerosis juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Primary lateral sclerosis juvenile from the curated CTD Gene-Disease Associations dataset.

Juvenile-onset dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile-onset dystonia from the curated CTD Gene-Disease Associations dataset.

Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia from the curated CTD Gene-Disease Associations dataset.

Cataract, Cortical, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Cortical, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

Hyperuricemic Nephropathy, Familial Juvenile 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperuricemic Nephropathy, Familial Juvenile 2 from the curated CTD Gene-Disease Associations dataset.

Leukemia, Myelomonocytic, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukemia, Myelomonocytic, Juvenile from the curated CTD Gene-Disease Associations dataset.

HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 from the curated CTD Gene-Disease Associations dataset.

Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type from the curated CTD Gene-Disease Associations dataset.

Cataract, Pulverulent, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Pulverulent, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

CATARACT, CONGENITAL OR JUVENILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT, CONGENITAL OR JUVENILE from the curated CTD Gene-Disease Associations dataset.

Juvenile polyposis syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile polyposis syndrome from the curated CTD Gene-Disease Associations dataset.

Myoclonic Epilepsy, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myoclonic Epilepsy, Juvenile from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 2, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 2, Juvenile from the curated CTD Gene-Disease Associations dataset.

Arthritis, Juvenile Rheumatoid Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Arthritis, Juvenile Rheumatoid in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease familial juvenile hyperuricemic nephropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

juvenile rheumatoid arthritis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease juvenile rheumatoid arthritis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

juvenile myoclonic epilepsy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease juvenile myoclonic epilepsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

idiopathic juvenile osteoporosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease idiopathic juvenile osteoporosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

juvenile rheumatoid arthritis Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease juvenile rheumatoid arthritis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

juvenile absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile type testicular granulosa cell tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile type testicular granulosa cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile xanthogranuloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile xanthogranuloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile rheumatoid arthritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile rheumatoid arthritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile pilocytic astrocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

familial juvenile hyperuricemic nephropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease familial juvenile hyperuricemic nephropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile astrocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile myelomonocytic leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile myelomonocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile dermatitis herpetiformis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile dermatitis herpetiformis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

idiopathic juvenile osteoporosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

systemic juvenile idiopathic arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease systemic juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile arthritis; measles Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile arthritis; measles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory papillomatosis, juvenile-onset; recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory papillomatosis, juvenile-onset; recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thyrotoxicosis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thyrotoxicosis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myoclonic epilepsy, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polyposis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polyposis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; chronic periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; chronic periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; arthritis, juvenile rheumatoid; arthritis, rheumatoid; autoimmune diseases; lupus erythematosus, systemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; arthritis, juvenile rheumatoid; arthritis, rheumatoid; autoimmune diseases; lupus erythematosus, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

rheumatoid arthritis; arthritis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rheumatoid arthritis; arthritis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy; myoclonic epilepsy, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x linked juvenile retinoschisis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x linked juvenile retinoschisis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; juvenile arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, rheumatoid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; respiratory syncytial virus; juvenile arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; respiratory syncytial virus; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis (juvenile idiopathic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis (juvenile idiopathic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile myoclonic epilepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile myoclonic epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; familial mediterranean fever; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; familial mediterranean fever; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; chronic childhood arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; asthma; lupus erythematosus, systemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; asthma; lupus erythematosus, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile dermatomyositis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile dermatomyositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; lymphohistiocytosis, hemophagocytic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; lymphohistiocytosis, hemophagocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy, juvenile myoclonic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, juvenile myoclonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; atopy; juvenile arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; atopy; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, rheumatoid; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile idiopathic arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelomonocytic, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelomonocytic, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile endogenous attack-like psychoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile endogenous attack-like psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile polyposis syndrome; polyposis, gastric Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile polyposis syndrome; polyposis, gastric in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

rheumatoid arthritis; juvenile arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rheumatoid arthritis; juvenile arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; bone resorption; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; bone resorption; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; dental caries; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; dental caries; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, rheumatoid; autoimmune diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, rheumatoid; rheumatic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; rheumatic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; dermatomyositis; juvenile arthritis; polymyositis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; dermatomyositis; juvenile arthritis; polymyositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term juvenile in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Pauciarticular juvenile arthritis_Peripheral blood mononuclear cell_GSE1402 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Pauciarticular juvenile arthritis_Peripheral blood mononuclear cell_GSE1402 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

JRA - Juvenile rheumatoid arthritis_Peripheral blood mononuclear cell_GSE7753 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during JRA - Juvenile rheumatoid arthritis_Peripheral blood mononuclear cell_GSE7753 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Arthritis (juvenile idiopathic) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Arthritis (juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to methotrexate in juvenile idiopathic arthritis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to methotrexate in juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

juvenile rheumatoid arthritis Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease juvenile rheumatoid arthritis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

juvenile rheumatoid arthritis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the juvenile rheumatoid arthritis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

juvenile cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile colonic polyposis Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile colonic polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile aseptic necrosis Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile aseptic necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile gastrointestinal polyposis Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile gastrointestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile posterior subcapsular lenticular opacities Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile posterior subcapsular lenticular opacities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile cortical cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile epithelial corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile epithelial corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile myelomonocytic leukemia Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile myelomonocytic leukemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile zonular cataracts Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile zonular cataracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile onset Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Arthritis, Juvenile Rheumatoid Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Arthritis, Juvenile Rheumatoid phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Periodontitis, Juvenile Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Periodontitis, Juvenile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Leukemia, Myelomonocytic, Juvenile Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia, Myelomonocytic, Juvenile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Myoclonic Epilepsy, Juvenile Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Myoclonic Epilepsy, Juvenile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

polyposis, juvenile intestinal Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyposis, juvenile intestinal phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, juvenile, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, juvenile, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 2, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 2, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperuricemic nephropathy, familial juvenile 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperuricemic nephropathy, familial juvenile 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 16, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 16, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

primary lateral sclerosis, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the primary lateral sclerosis, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

{myoclonic epilepsy, juvenile, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {myoclonic epilepsy, juvenile, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

cystinosis, late-onset juvenile or adolescent nephropathic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cystinosis, late-onset juvenile or adolescent nephropathic phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

periodontitis 1, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the periodontitis 1, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperuricemic nephropathy, familial juvenile 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperuricemic nephropathy, familial juvenile 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myoclonic epilepsy, juvenile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myoclonic epilepsy, juvenile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypotrichosis, congenital, with juvenile macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypotrichosis, congenital, with juvenile macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperuricemic nephropathy, familial juvenile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperuricemic nephropathy, familial juvenile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptiblity to, 9} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptiblity to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 4, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 4, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, juvenile myelomonocytic Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, juvenile myelomonocytic phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile absence, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to, 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 5, juvenile recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 5, juvenile recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

macular degeneration, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular degeneration, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

{rheumatoid arthritis, systemic juvenile} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {rheumatoid arthritis, systemic juvenile} phenotype from the curated OMIM Gene-Disease Associations dataset.

nephronophthisis 1, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephronophthisis 1, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1k, primary open angle, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1k, primary open angle, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

{rheumatoid arthritis, systemic juvenile, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {rheumatoid arthritis, systemic juvenile, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile myoclonic, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile myoclonic, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, juvenile myoclonic 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, juvenile myoclonic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, juvenile absence, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, juvenile absence, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

juvenile Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue juvenile in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

juvenile leaf Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue juvenile leaf in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase and epimerase activity, acting on amino acids and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set

From Reactome Pathways

proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set

From Reactome Pathways

proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

From Reactome Pathways

proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.

eye and adnexa disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease eye and adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

eye and adnexa disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease eye and adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

hand, foot and mouth disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

extrapyramidal and movement disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease extrapyramidal and movement disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of skin and connective tissue Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

eye and adnexa disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation 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.

proteinuria and cardiovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease proteinuria and cardiovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acid lipase deficiency and cholesterol ester storage disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acid lipase deficiency and cholesterol ester storage disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn's disease and ibd Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn's disease and ibd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease and antioxidant enzyme defense Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular disease and antioxidant enzyme defense in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia and cardiovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia and cardiovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease and myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease and myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome and electrocardiographic coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome and electrocardiographic coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

liver disease, chronic and cirrhosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver disease, chronic and cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disease models, animal; neoplasms, germ cell and embryonal; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disease models, animal; neoplasms, germ cell and embryonal; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease and vascular dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease and vascular dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease. plasma lipoproteins. and longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease. plasma lipoproteins. and longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic stiffness and disease severity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic stiffness and disease severity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease and plasma soluble thrombomodulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease and plasma soluble thrombomodulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ulcerative colitis and crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ulcerative colitis and crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease and plasma lipid levels. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease and plasma lipid levels. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hpv infection and cervical disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hpv infection and cervical disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obstructive pulmonary disease and disseminated bronchiectasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstructive pulmonary disease and disseminated bronchiectasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn's disease and sarcoidosis (combined) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn's disease and sarcoidosis (combined) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

occlusive artery disease and deep vein thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease occlusive artery disease and deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute neonatal disease and hyperammonemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute neonatal disease and hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease and serum very low density lipopro Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease and serum very low density lipopro in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cigarette smoking. coronary artery disease. and diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cigarette smoking. coronary artery disease. and diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

renal function and chronic kidney disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease renal function and chronic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn's disease and ulcerative colitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn's disease and ulcerative colitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Parkinson's disease (motor and cognition) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Parkinson's disease (motor and cognition) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Crohn's disease and psoriasis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Crohn's disease and psoriasis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Celiac disease and Rheumatoid arthritis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Celiac disease and Rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Chronic kidney disease and serum creatinine levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Chronic kidney disease and serum creatinine levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Renal function and chronic kidney disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Renal function and chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

hand, foot and mouth disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease hand, foot and mouth disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

eye and adnexa disease Gene Set

From 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.

Hand, Foot and Mouth Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hand, Foot and Mouth Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the von willebrand disease, types 2a, 2b, 2m, and 2n phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphedema-distichiasis syndrome with renal disease and diabetes mellitus Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphedema-distichiasis syndrome with renal disease and diabetes mellitus phenotype from the curated OMIM Gene-Disease Associations dataset.

inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From OMIM Gene-Disease Associations

genes associated with the glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated OMIM Gene-Disease Associations dataset.

?inflammatory skin and bowel disease, neonatal, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?inflammatory skin and bowel disease, neonatal, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inflammatory skin and bowel disease, neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic kidney and hepatic disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney and hepatic disease phenotype from the curated OMIM Gene-Disease Associations dataset.

interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease, type 3, with spastic paraparesis and unusual plaques Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease, type 3, with spastic paraparesis and unusual plaques phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease, type 3, with spastic paraparesis and apraxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease, type 3, with spastic paraparesis and apraxia phenotype from the curated OMIM Gene-Disease Associations dataset.

The role of Nef in HIV-1 replication and disease pathogenesis Gene Set

From Reactome Pathways

proteins participating in the The role of Nef in HIV-1 replication and disease pathogenesis pathway from the Reactome Pathways dataset.

crohn disease; crohn's disease; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral arterial disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease; hyperthyroidism; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease; hyperthyroidism; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; granuloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

liver disease; wilson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver disease; wilson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; dna damage; genomic instability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; dna damage; genomic instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hemochromatosis; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease ; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease ; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; sarcoidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison's disease; graves' disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison's disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney disease; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; olfaction disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; colitis, ulcerative; crohn disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease celiac disease; colitis, ulcerative; crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amnesia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amnesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; coronary disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; coronary disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular disease; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gaucher disease; nervous system diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; metabolic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft-versus-host disease; psoriasis; celiac disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft-versus-host disease; psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease parkinson's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; spondylitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; spondylitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; gastrointestinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gaucher disease; legg-perthes disease; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn's disease; ulcerative colitis; inflammatory bowel disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn's disease; ulcerative colitis; inflammatory bowel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; postoperative complications; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease; periodontal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; dyslipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; addison's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; ileal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; coronary artery disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; coronary artery disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadaver; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadaver; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

common variable immunodeficiency; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease common variable immunodeficiency; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; dilatation, pathologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lewy body disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lewy body disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyloidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sanhoff disease; tay-sachs disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sanhoff disease; tay-sachs disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; postoperative complications; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; delirium; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; delirium; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease/coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; hallucinations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; growth disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; lewy body disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; lewy body disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; addison's disease; autoimmune diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; colitis, ulcerative; crohn disease; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease celiac disease; colitis, ulcerative; crohn disease; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroid disease; thyroid disease, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroid disease; thyroid disease, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; cutaneous fistula; rectal fistula Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; cutaneous fistula; rectal fistula in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; spondylarthropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; spondylarthropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From