Name

Peeling skin syndrome, acral type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peeling skin syndrome, acral type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peeling skin syndrome, acral type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peeling skin syndrome, acral type from the curated CTD Gene-Disease Associations dataset.

Peeling Skin Syndrome Gene Set

From CTD Gene-Disease Associations

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

peeling skin syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the peeling skin syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

peeling skin syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the peeling skin syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Darier disease, acral hemorrhagic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Darier disease, acral hemorrhagic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

peeling Gene Set

From GeneRIF Biological Term Annotations

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

acral lentiginous melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acral Gene Set

From GeneRIF Biological Term Annotations

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

acral ulceration and osteomyelitis leading to autoamputation of digits Gene Set

From HPO Gene-Disease Associations

genes associated with the acral ulceration and osteomyelitis leading to autoamputation of digits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acral ulceration leading to autoamputation of digits Gene Set

From HPO Gene-Disease Associations

genes associated with the acral ulceration leading to autoamputation of digits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acral ulceration and osteomyelitis leading to autoamputation of the digits (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the acral ulceration and osteomyelitis leading to autoamputation of the digits (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 2, red hair/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 2, blond hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 5, dark/fair skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 5, dark/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

[skin/hair/eye pigmentation 4, fair/dark skin] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [skin/hair/eye pigmentation 4, fair/dark skin] phenotype from the curated OMIM Gene-Disease Associations dataset.

albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to 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.

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.

diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders 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.

insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cutaneous melanoma which is largely independent of skin type and hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cutaneous melanoma which is largely independent of skin type and hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Stiff skin syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Skin fragility woolly hair syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin fragility woolly hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia skin fragility syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tight skin contracture syndrome, lethal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tight skin contracture syndrome, lethal from the curated CTD Gene-Disease Associations dataset.

Wrinkly skin syndrome Gene Set

From CTD Gene-Disease Associations

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

Skin Fragility-Woolly Hair Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skin Fragility-Woolly Hair Syndrome from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia/ skin fragility syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia/ skin fragility syndrome from the curated CTD Gene-Disease Associations dataset.

Stiff Skin Syndrome Gene Set

From CTD Gene-Disease Associations

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

behcet syndrome; disease susceptibility; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; disease susceptibility; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dysplastic nevus syndrome; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dysplastic nevus syndrome; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stiff skin syndrome Gene Set

From OMIM Gene-Disease Associations

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

ectodermal dysplasia/skin fragility syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia/skin fragility syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

wrinkly skin syndrome Gene Set

From OMIM Gene-Disease Associations

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

skin fragility-woolly hair syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the skin fragility-woolly hair syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic 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.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance 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.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; edema Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

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

deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2 ; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2 ; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy 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.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension 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.

diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy 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.

adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

arteriosclerosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance 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.

diabetes mellitus type ii; diabetes mellitus, type 2; Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

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

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure; kidney; failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary stenosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary stenosis; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary artery disease; coronary restenosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary artery disease; coronary restenosis; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; pancreatitis, alcoholic; pancreatitis, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; pancreatitis, alcoholic; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases; diabetes mellitus type ii; diabetes mellitus, type 2; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery diseases; diabetes mellitus type ii; diabetes mellitus, type 2; disease models, animal 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.

cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity 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.

diabetes mellitus type ii; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus (disorder) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; diabetes, type 1; albuminuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; diabetes, type 1; albuminuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus ; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; intermittent claudication Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; intermittent claudication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diseases in twins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diseases in twins 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.

diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 1 and type 2 muscle fiber minicore regions Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 and type 2 muscle fiber minicore regions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

type 1 fibers relatively smaller than type 2 fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 fibers relatively smaller than type 2 fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

P-type ATPase, subfamily IIA, PMR1-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P-type ATPase, subfamily IIA, PMR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

P-type ATPase, subfamily IIA, SERCA-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the P-type ATPase, subfamily IIA, SERCA-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, receptor type R/non-receptor type 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ephrin receptor type-A /type-B Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ephrin receptor type-A /type-B protein domain from the InterPro Predicted Protein Domain Annotations dataset.

K/Cl co-transporter, type 1/type 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the K/Cl co-transporter, type 1/type 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ocular albinism, type i, nettleship-falls type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ocular albinism, type i, nettleship-falls type phenotype from the curated OMIM Gene-Disease Associations dataset.

Bartter syndrome, type 3, with hypocalciuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome, type 3, with hypocalciuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib-polydactyly syndrome, Majewski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Duane syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Duane syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Waardenburg syndrome type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Waardenburg syndrome type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome antenatal type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome antenatal type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome antenatal type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome antenatal type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome, type 4b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome, type 4b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Waardenburg syndrome type 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Waardenburg syndrome type 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune lymphoproliferative syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune lymphoproliferative syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bartter syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bartter syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome progeroid type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome progeroid type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Larsen syndrome, dominant type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Larsen syndrome, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, musculocontractural type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, musculocontractural type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Popliteal pterygium syndrome lethal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple pterygium syndrome Escobar type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schwartz Jampel syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schwartz Jampel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acrocallosal syndrome, Schinzel type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrocallosal syndrome, Schinzel type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome, type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 7B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, musculocontractural type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, musculocontractural type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Carbohydrate-deficient glycoprotein syndrome type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbohydrate-deficient glycoprotein syndrome type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune polyglandular syndrome type 1, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune polyglandular syndrome type 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Loeys-Dietz syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Loeys-Dietz syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglandular autoimmune syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglandular autoimmune syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome, type A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome, type A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Griscelli syndrome type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Griscelli syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Griscelli syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Griscelli syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cockayne syndrome type A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cockayne syndrome type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leigh syndrome, French Canadian type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leigh syndrome, French Canadian type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Loeys-Dietz syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Loeys-Dietz syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oto-palato-digital syndrome, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oto-palato-digital syndrome, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cockayne syndrome, type B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cockayne syndrome, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stickler syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stickler syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Axenfeld-Rieger syndrome type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Axenfeld-Rieger syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Axenfeld-Rieger syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Axenfeld-Rieger syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trichorhinophalangeal syndrome type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trichorhinophalangeal syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose transporter type 1 deficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bare lymphocyte syndrome type 2, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bare lymphocyte syndrome type 2, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Meckel syndrome, type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Meckel syndrome, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oto-palato-digital syndrome, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oto-palato-digital syndrome, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Loeys-Dietz syndrome, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Loeys-Dietz syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Usher syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Usher syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune lymphoproliferative syndrome, type 1a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune lymphoproliferative syndrome, type 1a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bernard-Soulier syndrome type C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bernard-Soulier syndrome type C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pena-Shokeir syndrome type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pena-Shokeir syndrome type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

USHER SYNDROME, TYPE IJ Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease USHER SYNDROME, TYPE IJ from the curated CTD Gene-Disease Associations dataset.

Bartter syndrome, antenatal type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter syndrome, antenatal type 1 from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome, type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome, type 4 from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1C from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1F from the curated CTD Gene-Disease Associations dataset.

Griscelli syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Griscelli syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Griscelli syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Griscelli syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE) from the curated CTD Gene-Disease Associations dataset.

Griscelli syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Griscelli syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

Usher Syndrome, Type IG Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher Syndrome, Type IG from the curated CTD Gene-Disease Associations dataset.

USHER SYNDROME, TYPE IIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease USHER SYNDROME, TYPE IIIA from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 2A from the curated CTD Gene-Disease Associations dataset.

USHER SYNDROME, TYPE IID Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease USHER SYNDROME, TYPE IID from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 2C from the curated CTD Gene-Disease Associations dataset.

Heart-hand syndrome, Slovenian type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart-hand syndrome, Slovenian type from the curated CTD Gene-Disease Associations dataset.

Blepharophimosis syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blepharophimosis syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

AXENFELD-RIEGER SYNDROME, TYPE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AXENFELD-RIEGER SYNDROME, TYPE 1 from the curated CTD Gene-Disease Associations dataset.

AXENFELD-RIEGER SYNDROME, TYPE 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AXENFELD-RIEGER SYNDROME, TYPE 3 from the curated CTD Gene-Disease Associations dataset.

AXENFELD-RIEGER SYNDROME, TYPE 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AXENFELD-RIEGER SYNDROME, TYPE 2 from the curated CTD Gene-Disease Associations dataset.

Usher Syndrome, Type IH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher Syndrome, Type IH from the curated CTD Gene-Disease Associations dataset.

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 4b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 4b from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 4c Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 4c from the curated CTD Gene-Disease Associations dataset.

Bartter syndrome, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter syndrome, type 3 from the curated CTD Gene-Disease Associations dataset.

Bare Lymphocyte Syndrome, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bare Lymphocyte Syndrome, Type I from the curated CTD Gene-Disease Associations dataset.

Meckel syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos Syndrome, Type VIII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VIII from the curated CTD Gene-Disease Associations dataset.

Simpson-Golabi-Behmel Syndrome, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Simpson-Golabi-Behmel Syndrome, Type 2 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos syndrome type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos syndrome type 6 from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1B from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1D from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Kenny-Caffey syndrome, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Kenny-Caffey syndrome, Type 1 from the curated CTD Gene-Disease Associations dataset.

Meckel syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Meckel syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type from the curated CTD Gene-Disease Associations dataset.

Laron syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Laron syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Pena Shokeir syndrome, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pena Shokeir syndrome, type 1 from the curated CTD Gene-Disease Associations dataset.

Crigler Najjar syndrome, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Crigler Najjar syndrome, type 2 from the curated CTD Gene-Disease Associations dataset.

Long QT syndrome type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Long QT syndrome type 3 from the curated CTD Gene-Disease Associations dataset.

Alport syndrome, recessive type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport syndrome, recessive type from the curated CTD Gene-Disease Associations dataset.

Meckel Syndrome, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel Syndrome, Type 4 from the curated CTD Gene-Disease Associations dataset.

Usher syndrome, type 1E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Usher syndrome, type 1E from the curated CTD Gene-Disease Associations dataset.

WAARDENBURG SYNDROME, TYPE 4A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease WAARDENBURG SYNDROME, TYPE 4A from the curated CTD Gene-Disease Associations dataset.

Bartter Syndrome, Type 4A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter Syndrome, Type 4A from the curated CTD Gene-Disease Associations dataset.

Bartter Syndrome, Type 4b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter Syndrome, Type 4b from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) from the curated CTD Gene-Disease Associations dataset.

BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Hyper-IgM Immunodeficiency Syndrome, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyper-IgM Immunodeficiency Syndrome, Type 1 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

Bartter syndrome, antenatal , type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bartter syndrome, antenatal , type 2 from the curated CTD Gene-Disease Associations dataset.

Meckel Syndrome, Type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel Syndrome, Type 6 from the curated CTD Gene-Disease Associations dataset.

Meckel Syndrome, Type 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Meckel Syndrome, Type 5 from the curated CTD Gene-Disease Associations dataset.

Waardenburg Syndrome, Type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg Syndrome, Type 2D from the curated CTD Gene-Disease Associations dataset.

Autoimmune polyendocrinopathy syndrome, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Autoimmune polyendocrinopathy syndrome, type 1 from the curated CTD Gene-Disease Associations dataset.

Trichorhinophalangeal Syndrome, Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichorhinophalangeal Syndrome, Type III from the curated CTD Gene-Disease Associations dataset.

EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) from the curated CTD Gene-Disease Associations dataset.

Oto-palato-digital syndrome, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oto-palato-digital syndrome, type 2 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) from the curated CTD Gene-Disease Associations dataset.

Leigh syndrome , French Canadian type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leigh syndrome , French Canadian type from the curated CTD Gene-Disease Associations dataset.

Stickler syndrome, type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler syndrome, type 3 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

Stickler syndrome, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler syndrome, type 2 from the curated CTD Gene-Disease Associations dataset.

Orofaciodigital syndrome type1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Orofaciodigital syndrome type1 from the curated CTD Gene-Disease Associations dataset.

Klippel Feil syndrome dominant type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Klippel Feil syndrome dominant type from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome type 2B from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome type 2A from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

Waardenburg syndrome type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Waardenburg syndrome type 2 from the curated CTD Gene-Disease Associations dataset.

Scapuloperoneal Syndrome, Neurogenic, Kaeser Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scapuloperoneal Syndrome, Neurogenic, Kaeser Type from the curated CTD Gene-Disease Associations dataset.

NEPHROTIC SYNDROME, TYPE 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEPHROTIC SYNDROME, TYPE 3 from the curated CTD Gene-Disease Associations dataset.

NEPHROTIC SYNDROME, TYPE 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEPHROTIC SYNDROME, TYPE 4 from the curated CTD Gene-Disease Associations dataset.

Autoimmune Lymphoproliferative Syndrome, Type IIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Autoimmune Lymphoproliferative Syndrome, Type IIA from the curated CTD Gene-Disease Associations dataset.

Larsen syndrome, dominant type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Larsen syndrome, dominant type from the curated CTD Gene-Disease Associations dataset.

Stickler Syndrome, Type I, Nonsyndromic Ocular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler Syndrome, Type I, Nonsyndromic Ocular from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) from the curated CTD Gene-Disease Associations dataset.

Stickler syndrome, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stickler syndrome, type 1 from the curated CTD Gene-Disease Associations dataset.

Oto-Palato-digital syndrome type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oto-Palato-digital syndrome type 1 from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE) from the curated CTD Gene-Disease Associations dataset.

TRICHORHINOPHALANGEAL SYNDROME, TYPE I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHORHINOPHALANGEAL SYNDROME, TYPE I from the curated CTD Gene-Disease Associations dataset.

Orofaciodigital syndrome, Shashi type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Orofaciodigital syndrome, Shashi type from the curated CTD Gene-Disease Associations dataset.

trichorhinophalangeal syndrome type ii Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease trichorhinophalangeal syndrome type ii from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autoimmune polyendocrine syndrome type 2 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune polyendocrine syndrome type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune polyendocrine syndrome type 1 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune polyendocrine syndrome type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

trichorhinophalangeal syndrome type ii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

type i ehlers-danlos syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

type vi ehlers-danlos syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

trichorhinophalangeal syndrome type i Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; diabetic angiopathies; long qt syndrome; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus; rheumatoid arthritis; sjogren's syndrome; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; rheumatoid arthritis; sjogren's syndrome; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ehlers-danlos syndrome type iv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ehlers-danlos syndrome type iv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; fatty liver; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; fatty liver; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; polycystic ovarian syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; polycystic ovarian syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic ketoacidosis; disease susceptibility; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic ketoacidosis; disease susceptibility; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2 ; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2 ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; lupus erythematosus, systemic; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; lupus erythematosus, systemic; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mild ehlers-danlos syndrome type iv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mild ehlers-danlos syndrome type iv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; hypertension; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; hypertension; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; polymetabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; polymetabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Usher syndrome type-1C protein-binding protein 1, PDZ domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Usher syndrome type-1C protein-binding protein 1, PDZ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

{retinal disease in usher syndrome type iia, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {retinal disease in usher syndrome type iia, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal syndrome, neurogenic, kaeser type Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal syndrome, neurogenic, kaeser type phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, progeroid type, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, progeroid type, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, progeroid type, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, progeroid type, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

opitz gbbb syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the opitz gbbb syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, musculocontractural type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, musculocontractural type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, siderius type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, siderius type phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 4a (alpers type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 4a (alpers type) phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2e, with or without neurologic involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2e, with or without neurologic involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

popliteal pterygium syndrome 2, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the popliteal pterygium syndrome 2, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 6 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 6 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple pterygium syndrome, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1f Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1g Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

crigler-najjar syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the crigler-najjar syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type ij Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type ij phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type ik Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type ik phenotype from the curated OMIM Gene-Disease Associations dataset.

leigh syndrome, french-canadian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the leigh syndrome, french-canadian type phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type vi Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viii Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viii phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viic Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viic phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viib Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type viia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type viia phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

?ehlers-danlos syndrome, musculocontractural type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?ehlers-danlos syndrome, musculocontractural type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 4b Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 4b phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 4c Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 4c phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 4a Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, autosomal dominant, hypermobility type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, autosomal dominant, hypermobility type phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 12 (cardiomyopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 12 (cardiomyopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1d/f digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1d/f digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

griscelli syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the griscelli syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

griscelli syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the griscelli syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

griscelli syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the griscelli syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

knobloch syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the knobloch syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

heart-hand syndrome, slovenian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the heart-hand syndrome, slovenian type phenotype from the curated OMIM Gene-Disease Associations dataset.

xeroderma pigmentosum, type f/cockayne syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the xeroderma pigmentosum, type f/cockayne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

trichorhinophalangeal syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichorhinophalangeal syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

amelogenesis imperfecta, type ig (enamel-renal syndrome) Gene Set

From OMIM Gene-Disease Associations

genes associated with the amelogenesis imperfecta, type ig (enamel-renal syndrome) phenotype from the curated OMIM Gene-Disease Associations dataset.

axenfeld-rieger syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the axenfeld-rieger syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

axenfeld-rieger syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the axenfeld-rieger syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type a2 (dominant) Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type a2 (dominant) phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group d Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group d phenotype from the curated OMIM Gene-Disease Associations dataset.

simpson-golabi-behmel syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the simpson-golabi-behmel syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

simpson-golabi-behmel syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the simpson-golabi-behmel syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 2 (myopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 2 (myopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 3a Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 3a phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1c Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1c phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 1h Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.

meckel syndrome, type 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the meckel syndrome, type 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?stickler syndrome, type v Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?stickler syndrome, type v phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 4b (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 4b (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type a1 (recessive) Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type a1 (recessive) phenotype from the curated OMIM Gene-Disease Associations dataset.

?autoimmune lymphoproliferative syndrome, type iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?autoimmune lymphoproliferative syndrome, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type c Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type c phenotype from the curated OMIM Gene-Disease Associations dataset.

bernard-soulier syndrome, type b Gene Set

From OMIM Gene-Disease Associations

genes associated with the bernard-soulier syndrome, type b phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 4a Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent mullerian duct syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent mullerian duct syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 13 (encephalomyopathic type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 13 (encephalomyopathic type) phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type v Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome, type v phenotype from the curated OMIM Gene-Disease Associations dataset.

schwartz-jampel syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the schwartz-jampel syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

loeys-dietz syndrome, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the loeys-dietz syndrome, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

otopalatodigital syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the otopalatodigital syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2c, gpr98/pdzd7 digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2c, gpr98/pdzd7 digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

scapuloperoneal syndrome, myopathic type Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal syndrome, myopathic type phenotype from the curated OMIM Gene-Disease Associations dataset.

opitz gbbb syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the opitz gbbb syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

persistent mullerian duct syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the persistent mullerian duct syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune lymphoproliferative syndrome type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

stickler syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the stickler syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome type 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome type 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

otopalatodigital syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the otopalatodigital syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 1 (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 1 (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-thalassemia/mental retardation syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia/mental retardation syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bartter syndrome, type 4b, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the bartter syndrome, type 4b, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

kenny-caffey syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the kenny-caffey syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 3 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 3 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 7 (hepatocerebral type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 7 (hepatocerebral type) phenotype from the curated OMIM Gene-Disease Associations dataset.

cockayne syndrome, type b Gene Set

From OMIM Gene-Disease Associations

genes associated with the cockayne syndrome, type b phenotype from the curated OMIM Gene-Disease Associations dataset.

cockayne syndrome, type a Gene Set

From OMIM Gene-Disease Associations

genes associated with the cockayne syndrome, type a phenotype from the curated OMIM Gene-Disease Associations dataset.

rieger syndrome, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the rieger syndrome, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.

bare lymphocyte syndrome, type ii, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the bare lymphocyte syndrome, type ii, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 8b (mngie type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 8b (mngie type) phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type iic, gpr98/pdzd7 digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type iic, gpr98/pdzd7 digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

trichorhinophalangeal syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichorhinophalangeal syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 8a (encephalomyopathic type with renal tubulopathy) phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

usher syndrome, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the usher syndrome, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

crigler-najjar syndrome, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the crigler-najjar syndrome, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

Waardenburg syndrome type 2 Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Waardenburg syndrome type 2 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Lynch syndrome:Turcot syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Marfan's syndrome:Marfan's syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Marfan's syndrome:Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IFAP syndrome with or without BRESHECK syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome I:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome I:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset.

Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset.

menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic 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.

hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome 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.

cornelia de lange syndrome; de lange syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; uveomeningoencephalitic syndrome Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melas syndrome; merrf syndrome Gene Set

From GAD Gene-Disease Associations

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

haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angelman syndrome; rett syndrome; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome 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.

digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; 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.

insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome ; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

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

obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma 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.

down syndrome; ehlers-danlos syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; felty's syndrome; large granular lymphocyte syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart-hand syndrome, holt-oram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia 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.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome/velocardiofacial syndrome complex-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ifap syndrome with or without bresheck syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Skin Gene Set

From BioGPS Human Cell Type and Tissue Gene Expression Profiles

genes with high or low expression in Skin relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.

Skin/hair/eye pigmentation, variation in, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 9 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.

Skin/hair/eye pigmentation, variation in, 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin/hair/eye pigmentation, variation in, 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skin/hair/eye pigmentation, variation in, 11 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.

Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dominant dystrophic epidermolysis bullosa with absence of skin phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis and recurrent skin vesicles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skin Diseases Gene Set

From CTD Gene-Disease Associations

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

Skin Abnormalities Gene Set

From CTD Gene-Disease Associations

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

Hypotrichosis And Recurrent Skin Vesicles Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.

Skin Diseases, Vascular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skin Diseases, Vascular from the curated CTD Gene-Disease Associations dataset.

Skin Ulcer Gene Set

From CTD Gene-Disease Associations

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

PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset.

Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.

Skin Neoplasms Gene Set

From CTD Gene-Disease Associations

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

Skin Pigmentation Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Skin Pigmentation in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

skin disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

vascular skin disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

skin benign neoplasm Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

vesiculobullous skin disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

skin cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease skin cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

skin disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

vascular skin disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease vascular skin disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

skin melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

verruciform xanthoma of skin Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin squamous cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin sarcoidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

malignant skin fibrous histiocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sarcomatoid squamous cell skin carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sarcomatoid squamous cell skin carcinoma 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.

bullous skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin lipoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin carcinoma in situ Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vesiculobullous skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eccrine mixed tumor of skin Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin papilloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin pilomatrix carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vascular skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin sarcoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin tag Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

chronic ulcer of skin Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin hemangioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

skin benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

H3K4me3_fibroblast of skin of abdomen_hg19_1 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_fibroblast of skin of abdomen_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

H3K4me3_fibroblast of skin of abdomen_hg19_2 Gene Set

From ENCODE Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_fibroblast of skin of abdomen_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.

CTCF_fibroblast of skin of abdomen_hg19_2 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_fibroblast of skin of abdomen_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

CTCF_fibroblast of skin of abdomen_hg19_1 Gene Set

From ENCODE Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CTCF_fibroblast of skin of abdomen_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.

lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms 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.

skin cancer, nonmelanoma Gene Set

From GAD Gene-Disease Associations

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

melanoma; nevus; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases; sarcoidosis; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases; sarcoidosis; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

erythema; psoriasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease erythema; psoriasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma, amelanotic; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma, amelanotic; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, t-cell, cutaneous; parapsoriasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

skin color Gene Set

From GAD Gene-Disease Associations

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

lung cancer; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer Gene Set

From GAD Gene-Disease Associations

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

colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

melanoma; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer; squamous cell carcinoma; carcinoma, basal cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin cancer; squamous cell carcinoma; carcinoma, basal cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psoriasis; skin diseases, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease psoriasis; skin diseases, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

papillomavirus infections; skin neoplasms; sunburn; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease papillomavirus infections; skin neoplasms; sunburn; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasm invasiveness; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasm invasiveness; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

erythema; rare diseases; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease erythema; rare diseases; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin condition Gene Set

From GAD Gene-Disease Associations

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

neoplasms, basal cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, basal cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; skin basal cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; skin basal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin diseases; sunburn Gene Set

From GAD Gene-Disease Associations

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

dna damage; neoplasms; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; neoplasms; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin carcinomas Gene Set

From GAD Gene-Disease Associations

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

cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell transformation, neoplastic; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

edema; hypertension; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease edema; hypertension; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

keratosis; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease keratosis; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; skin diseases, vesiculobullous Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arsenic poisoning; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arsenic poisoning; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

keratosis; skin diseases Gene Set

From GAD Gene-Disease Associations

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

skin cancer; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin cancer; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin sensitivity to sun Gene Set

From GAD Gene-Disease Associations

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

skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

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

facial neoplasms; horse diseases; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease facial neoplasms; horse diseases; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypersensitivity; skin diseases Gene Set

From GAD Gene-Disease Associations

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

skin lesion Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; skin diseases, genetic; vitiligo Gene Set

From GAD Gene-Disease Associations

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

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperpigmentation; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperpigmentation; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

melanoma; neoplasm metastasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

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

brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

scleroderma, systemic; skin ulcer; systemic scleroderma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin pigmentation Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

scleroderma, systemic; skin ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease scleroderma, systemic; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma skin cancer Gene Set

From GAD Gene-Disease Associations

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

cocarcinogenesis; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cocarcinogenesis; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin diseases Gene Set

From GAD Gene-Disease Associations

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

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

microsatellite instability; nevus, pigmented; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease microsatellite instability; nevus, pigmented; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; nevus; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mycobacterium infections, atypical; skin ulcer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mycobacterium infections, atypical; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; cell transformation, neoplastic; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; cell transformation, neoplastic; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe photoaging of facial skin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe photoaging of facial skin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin Gene Set

From GeneRIF Biological Term Annotations

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

Get-1_Deficiency_GDS2629_161_mouse_embryonic skin Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the Get-1_Deficiency_GDS2629_161_mouse_embryonic skin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

regulation of water loss via skin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of water loss via skin biological process from the curated GO Biological Process Annotations dataset.

establishment of skin barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of skin barrier biological process from the curated GO Biological Process Annotations dataset.

skin development Gene Set

From GO Biological Process Annotations

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

skin epidermis development Gene Set

From GO Biological Process Annotations

genes participating in the skin epidermis development biological process from the curated GO Biological Process Annotations dataset.

skin morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the skin morphogenesis biological process from the curated GO Biological Process Annotations dataset.

skin Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in skin relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

Skin sensitivity to sun Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Skin sensitivity to sun phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Skin pigmentation Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Skin pigmentation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Non-melanoma skin cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-melanoma skin cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

skin melanoma Gene Set

From GWASdb SNP-Disease Associations

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

skin cancer Gene Set

From GWASdb SNP-Disease Associations

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

skin disease Gene Set

From GWASdb SNP-Disease Associations

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

bullous skin disease Gene Set

From GWASdb SNP-Disease Associations

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

skin carcinoma Gene Set

From GWASdb SNP-Disease Associations

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

inflammatory abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

neoplasm of the skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the neoplasm of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

localized skin lesion Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the localized skin lesion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin adnexa Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

vascular skin abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

atypical scarring of skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the atypical scarring of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

skin rash Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the skin rash phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

generalized abnormality of skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

skin Gene Set

From HPA Tissue Gene Expression Profiles

genes with high or low expression in skin relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.

skin Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in skin relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

dry skin Gene Set

From HPO Gene-Disease Associations

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

thin skin Gene Set

From HPO Gene-Disease Associations

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

reticulated skin pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the reticulated skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

telangiectases in sun-exposed and nonexposed skin Gene Set

From HPO Gene-Disease Associations

genes associated with the telangiectases in sun-exposed and nonexposed skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized abnormality of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypopigmentation of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the hypopigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal delayed hypersensitivity skin test Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inflammatory abnormality of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin ulcer Gene Set

From HPO Gene-Disease Associations

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

fine, reticulate skin pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the fine, reticulate skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

punctate vasculitis skin lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the punctate vasculitis skin lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

profuse pigmented skin lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the profuse pigmented skin lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital localized absence of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital localized absence of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

excessive wrinkling of palmar skin Gene Set

From HPO Gene-Disease Associations

genes associated with the excessive wrinkling of palmar skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skin adnexa Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skin adnexa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

postauricular skin tag Gene Set

From HPO Gene-Disease Associations

genes associated with the postauricular skin tag phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

blotching pigmentation of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the blotching pigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the plantar skin of foot Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the plantar skin of foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse skin atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin erosion Gene Set

From HPO Gene-Disease Associations

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

skin tags Gene Set

From HPO Gene-Disease Associations

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

vascular skin abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the vascular skin abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal elasticity of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

localized skin lesion Gene Set

From HPO Gene-Disease Associations

genes associated with the localized skin lesion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypopigmented skin patches on arms Gene Set

From HPO Gene-Disease Associations

genes associated with the hypopigmented skin patches on arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

stiff skin Gene Set

From HPO Gene-Disease Associations

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

skin dimple over apex of long bone angulation Gene Set

From HPO Gene-Disease Associations

genes associated with the skin dimple over apex of long bone angulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

periauricular skin pits Gene Set

From HPO Gene-Disease Associations

genes associated with the periauricular skin pits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

redundant skin Gene Set

From HPO Gene-Disease Associations

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

atypical scarring of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the atypical scarring of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

desquamation of skin soon after birth Gene Set

From HPO Gene-Disease Associations

genes associated with the desquamation of skin soon after birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin nodule Gene Set

From HPO Gene-Disease Associations

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

excessive wrinkled skin Gene Set

From HPO Gene-Disease Associations

genes associated with the excessive wrinkled skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline skin dimples over anterior/posterior fontanelles Gene Set

From HPO Gene-Disease Associations

genes associated with the midline skin dimples over anterior/posterior fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal wrinkled skin of hands and feet Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal wrinkled skin of hands and feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vasculitis in the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the vasculitis in the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

redundant skin on fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the redundant skin on fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hyperextensible skin Gene Set

From HPO Gene-Disease Associations

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

redundant neck skin Gene Set

From HPO Gene-Disease Associations

genes associated with the redundant neck skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

preauricular skin tag Gene Set

From HPO Gene-Disease Associations

genes associated with the preauricular skin tag phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

squamous cell carcinoma of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the squamous cell carcinoma of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skin morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skin morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thickened nuchal skin fold Gene Set

From HPO Gene-Disease Associations

genes associated with the thickened nuchal skin fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature skin wrinkling Gene Set

From HPO Gene-Disease Associations

genes associated with the premature skin wrinkling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal blistering of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pigmentation anomalies of sun-exposed skin Gene Set

From HPO Gene-Disease Associations

genes associated with the pigmentation anomalies of sun-exposed skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hyperpigmentation of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the hyperpigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

preauricular skin furrow Gene Set

From HPO Gene-Disease Associations

genes associated with the preauricular skin furrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

soft skin Gene Set

From HPO Gene-Disease Associations

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

hypertrophy of skin of soles Gene Set

From HPO Gene-Disease Associations

genes associated with the hypertrophy of skin of soles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypopigmented skin patches Gene Set

From HPO Gene-Disease Associations

genes associated with the hypopigmented skin patches phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

warfarin-induced skin necrosis Gene Set

From HPO Gene-Disease Associations

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

skin vesicle Gene Set

From HPO Gene-Disease Associations

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

abnormality of skin pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent skin infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin rash Gene Set

From HPO Gene-Disease Associations

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

yellow subcutaneous tissue covered by thin, scaly skin Gene Set

From HPO Gene-Disease Associations

genes associated with the yellow subcutaneous tissue covered by thin, scaly skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lack of skin elasticity Gene Set

From HPO Gene-Disease Associations

genes associated with the lack of skin elasticity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fragile skin Gene Set

From HPO Gene-Disease Associations

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

skin dimples Gene Set

From HPO Gene-Disease Associations

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

depigmentation/hyperpigmentation of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the depigmentation/hyperpigmentation of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skin physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skin physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mixed hypo- and hyperpigmentation of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the mixed hypo- and hyperpigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

soft, doughy skin Gene Set

From HPO Gene-Disease Associations

genes associated with the soft, doughy skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

regional abnormality of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the regional abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent bacterial skin infections Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent bacterial skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin fragility with non-scarring blistering Gene Set

From HPO Gene-Disease Associations

genes associated with the skin fragility with non-scarring blistering phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

teleangiectasia of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the teleangiectasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormally lax or hyperextensible skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormally lax or hyperextensible skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

asymmetric, linear skin defects Gene Set

From HPO Gene-Disease Associations

genes associated with the asymmetric, linear skin defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thickened skin Gene Set

From HPO Gene-Disease Associations

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

absent skin pigmentation Gene Set

From HPO Gene-Disease Associations

genes associated with the absent skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skin pit Gene Set

From HPO Gene-Disease Associations

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

Skin Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Abnormalities Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Ulcer Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Diseases, Genetic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Diseases, Viral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Galvanic Skin Response Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Galvanic Skin Response phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Parasitic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Diseases, Vesiculobullous Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Diseases, Vascular Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Diseases, Bacterial Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Staphylococcal Skin Infections Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Staphylococcal Skin Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skin Diseases, Metabolic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Skin-specific protein 32 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Skin-specific protein 32 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

dry skin Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dry skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin skin Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.