Name

Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.

Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis phenotype from the curated OMIM Gene-Disease Associations dataset.

low-molecular-weight proteinuria Gene Set

From HPO Gene-Disease Associations

genes associated with the low-molecular-weight proteinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Protein-tyrosine phosphatase, low molecular weight Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, low molecular weight protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein-tyrosine phosphatase, low molecular weight, mammalian Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein-tyrosine phosphatase, low molecular weight, mammalian protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ache, low back; low back pain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; low back pain; scoliosis; spinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; low back pain; scoliosis; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; arthritis, psoriatic; inflammatory bowel disease, nos; inflammatory bowel diseases; low back pain; psoriatic arthropathy; rheumatoid spondylitis; spondylarthropathies; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; arthritis, psoriatic; inflammatory bowel disease, nos; inflammatory bowel diseases; low back pain; psoriatic arthropathy; rheumatoid spondylitis; spondylarthropathies; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; acute disease; low back pain; pain; sciatica Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; acute disease; low back pain; pain; sciatica in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; intervertebral disk displacement; low back pain; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; intervertebral disk displacement; low back pain; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; intervertebral disk displacement; low back pain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; intervertebral disk displacement; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ache, low back; intervertebral disk degeneration; low back pain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; intervertebral disk degeneration; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

DJ-1-SNCA complex, high molecular weight complex Gene Set

From CORUM Protein Complexes

proteins in the DJ-1-SNCA complex, high molecular weight complex protein complex from the CORUM Protein Complexes dataset.

ultra-high molecular weight polyethylene Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ultra-high molecular weight polyethylene from the curated CTD Gene-Chemical Interactions dataset.

high molecular weight b cell growth factor receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the high molecular weight b cell growth factor receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

[high molecular weight kininogen deficiency] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high molecular weight kininogen deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset.

Nephrocalcinosis Gene Set

From CTD Gene-Disease Associations

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

nephrocalcinosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypercalciuric nephrocalcinosis Gene Set

From GAD Gene-Disease Associations

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

nephrocalcinosis Gene Set

From GeneRIF Biological Term Annotations

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

nephrocalcinosis Gene Set

From HPO Gene-Disease Associations

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

Nephrocalcinosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

nephrocalcinosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nephrocalcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

proteinuria and cardiovascular disease Gene Set

From GAD Gene-Disease Associations

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

Hypercalciuria, childhood, self-limiting Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercalciuria, childhood, self-limiting phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercalciuria, Absorptive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypercalciuria, Absorptive, 2 from the curated CTD Gene-Disease Associations dataset.

Hypophosphatemic Rickets with Hypercalciuria, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatemic Rickets with Hypercalciuria, Hereditary from the curated CTD Gene-Disease Associations dataset.

Hypercalciuria Gene Set

From CTD Gene-Disease Associations

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

Hypercalciuria, Absorptive, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypercalciuria, Absorptive, 1 from the curated CTD Gene-Disease Associations dataset.

hypercalciuria; kidney calculi; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypercalciuria; kidney calculi; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypercalcemia; hypercalciuria Gene Set

From GAD Gene-Disease Associations

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

hypercalciuria; kidney calculi Gene Set

From GAD Gene-Disease Associations

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

hypercalciuria; nephrolithiasis Gene Set

From GAD Gene-Disease Associations

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

hypercalciuria Gene Set

From GeneRIF Biological Term Annotations

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

hypercalciuria Gene Set

From HPO Gene-Disease Associations

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

Hypercalciuria Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

hypercalciuria, absorptive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercalciuria, absorptive phenotype from the curated OMIM Gene-Disease Associations dataset.

hypophosphatemic rickets with hypercalciuria Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypophosphatemic rickets with hypercalciuria phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercalciuria, absorptive, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypercalciuria, absorptive, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertension; overweight; weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; overweight; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; weight gain 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.

obesity; weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; weight gain; weight loss 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.

birth weight; weight gain Gene Set

From GAD Gene-Disease Associations

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

body weight; weight loss Gene Set

From GAD Gene-Disease Associations

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

body weight; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; obesity; weight loss 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.

weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease weight gain; weight loss 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.

birth weight; body weight Gene Set

From GAD Gene-Disease Associations

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

body weight; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; fatty liver; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; fatty liver; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; placental weight Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; weight loss; weight gain Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low mpa exposure and acute rejection in mmf/tacrolimus-treated kidney transplant patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low insulin and cholesterol levels Gene Set

From GAD Gene-Disease Associations

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

high neuroticism and low agreeableness Gene Set

From GAD Gene-Disease Associations

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

plasma apob and low density lipoprotein (ldl) cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma apob and low density lipoprotein (ldl) cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

oxidized low-density lipoprotein and cardiolipin autoantibodies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease oxidized low-density lipoprotein and cardiolipin autoantibodies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low bone-mineral density and rapid postmenopausal bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total and low-density lipoprotein cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total and low-density lipoprotein cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high and low levels of cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high and low levels of cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease and serum very low density lipopro Gene Set

From GAD Gene-Disease Associations

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

Proteinuria Gene Set

From CTD Gene-Disease Associations

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

proteinuria Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

orthostatic proteinuria Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

glomerulonephritis, iga; iga glomerulonephritides; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; pre-eclampsia; pregnancy complications; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; pre-eclampsia; pregnancy complications; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

proteinuria; recurrence Gene Set

From GAD Gene-Disease Associations

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

glomerulonephritis membranous; glomerulonephritis, membranous; haematuria; hematuria; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glomerulonephritis membranous; glomerulonephritis, membranous; haematuria; hematuria; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glomerulonephritis, iga; proteinuria Gene Set

From GAD Gene-Disease Associations

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

pre-eclampsia; proteinuria Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; proteinuria; rheumatoid arthritis; rheumatoid nodule; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria in GWAS and other genetic association datasets from the GAD 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.

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

From GAD Gene-Disease Associations

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

nephrotic syndrome; proteinuria Gene Set

From GAD Gene-Disease Associations

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

kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glomerulonephritis, iga; iga glomerulonephritides; nephrotic syndrome; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; nephrotic syndrome; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; lupus erythematosus, systemic; proteinuria Gene Set

From GAD Gene-Disease Associations

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

nephropathy, diabetic; blood pressure, arterial; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephropathy, diabetic; blood pressure, arterial; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

proteinuria Gene Set

From GAD Gene-Disease Associations

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

chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

edema; inflammation; pre-eclampsia; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease edema; inflammation; pre-eclampsia; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

proteinuria; purpura, schoenlein-henoch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney diseases; proteinuria Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nephropathy, diabetic; proteinuria Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

proteinuria Gene Set

From GeneRIF Biological Term Annotations

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

proteinuria Gene Set

From HPO Gene-Disease Associations

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

mild proteinuria Gene Set

From HPO Gene-Disease Associations

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

Proteinuria Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Copula pyramidis, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Copula pyramidis, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Crus 2, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Crus 2, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Uvula (IX), molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Uvula (IX), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pyramus (VIII), molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pyramus (VIII), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

molecular layer of CbVCx Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in molecular layer of CbVCx relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Nucleus of the lateral olfactory tract, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Nucleus of the lateral olfactory tract, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Piriform-amygdalar area, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Piriform-amygdalar area, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Paraflocculus, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Paraflocculus, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Subiculum, ventral part, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Subiculum, ventral part, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Simple lobule, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Simple lobule, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

molecular layer of S Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in molecular layer of S relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lobule III, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lobule III, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lingula (I), molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lingula (I), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

molecular layer of CbHCx Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in molecular layer of CbHCx relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Nodulus (X), molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Nodulus (X), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Folium-tuber vermis (VII), molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Folium-tuber vermis (VII), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lobules IV-V, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lobules IV-V, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Piriform area, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Piriform area, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lobule II, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lobule II, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Flocculus, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Flocculus, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Olfactory tubercle, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Olfactory tubercle, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Paramedian lobule, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Paramedian lobule, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Subiculum, dorsal part, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Subiculum, dorsal part, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Declive (VI), molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Declive (VI), molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Dentate gyrus, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Dentate gyrus, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Crus 1, molecular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Crus 1, molecular layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

molecular layer of the DG Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in molecular layer of the DG relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

molecular layer of rostral subiculum Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in molecular layer of rostral subiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

molecular layer of caudal subiculum Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in molecular layer of caudal subiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

molecular Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of molecular function Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of molecular function biological process from the curated GO Biological Process Annotations dataset.

modulation of molecular function in other organism Gene Set

From GO Biological Process Annotations

genes participating in the modulation of molecular function in other organism biological process from the curated GO Biological Process Annotations dataset.

regulation of molecular function Gene Set

From GO Biological Process Annotations

genes participating in the regulation of molecular function biological process from the curated GO Biological Process Annotations dataset.

positive regulation of molecular function Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of molecular function biological process from the curated GO Biological Process Annotations dataset.

cerebellar molecular layer development Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar molecular layer development biological process from the curated GO Biological Process Annotations dataset.

regulation of molecular function, epigenetic Gene Set

From GO Biological Process Annotations

genes participating in the regulation of molecular function, epigenetic biological process from the curated GO Biological Process Annotations dataset.

negative regulation of production of molecular mediator of immune response Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of production of molecular mediator of immune response biological process from the curated GO Biological Process Annotations dataset.

regulation of production of molecular mediator of immune response Gene Set

From GO Biological Process Annotations

genes participating in the regulation of production of molecular mediator of immune response biological process from the curated GO Biological Process Annotations dataset.

production of molecular mediator of immune response Gene Set

From GO Biological Process Annotations

genes participating in the production of molecular mediator of immune response biological process from the curated GO Biological Process Annotations dataset.

modification by host of symbiont molecular function Gene Set

From GO Biological Process Annotations

genes participating in the modification by host of symbiont molecular function biological process from the curated GO Biological Process Annotations dataset.

molecular hydrogen transport Gene Set

From GO Biological Process Annotations

genes participating in the molecular hydrogen transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation by host of symbiont molecular function Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation by host of symbiont molecular function biological process from the curated GO Biological Process Annotations dataset.

modulation by host of viral molecular function Gene Set

From GO Biological Process Annotations

genes participating in the modulation by host of viral molecular function biological process from the curated GO Biological Process Annotations dataset.

modulation of molecular function in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the modulation of molecular function in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

positive regulation of production of molecular mediator of immune response Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of production of molecular mediator of immune response biological process from the curated GO Biological Process Annotations dataset.

negative regulation of molecular function in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of molecular function in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

production of molecular mediator involved in inflammatory response Gene Set

From GO Biological Process Annotations

genes participating in the production of molecular mediator involved in inflammatory response biological process from the curated GO Biological Process Annotations dataset.

negative regulation of molecular function in other organism Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of molecular function in other organism biological process from the curated GO Biological Process Annotations dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen molecular function from the curated GO Molecular Function Annotations dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations dataset.

molecular function regulator Gene Set

From GO Molecular Function Annotations

genes performing the molecular function regulator molecular function from the curated GO Molecular Function Annotations dataset.

molecular transducer activity Gene Set

From GO Molecular Function Annotations

genes performing the molecular transducer activity molecular function from the curated GO Molecular Function Annotations dataset.

Molecular chaperone regulator BAG-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molecular chaperone regulator BAG-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

thin cerebellar molecular layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar molecular layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

molecular layer Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

birth weight and serum triglyceride concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight and serum triglyceride concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From Reactome Pathways

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

low-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the low-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

very-low-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the very-low-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

low-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the low-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

very-low-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the very-low-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

very low density lipoprotein triglyceride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical very low density lipoprotein triglyceride from the curated CTD Gene-Chemical Interactions dataset.

Low Back Pain Gene Set

From CTD Gene-Disease Associations

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

Cardiac Output, Low Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Output, Low from the curated CTD Gene-Disease Associations dataset.

Vision, Low Gene Set

From CTD Gene-Disease Associations

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

low tension glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

low compliance bladder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ache, low back; intervertebral disk displacement; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ache, low back; intervertebral disk displacement; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low plasma levels of factor viic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low plasma levels of factor viic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; low tension glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; low tension glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high triglyceride/ low hdl cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high triglyceride/ low hdl cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac output, low Gene Set

From GAD Gene-Disease Associations

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

low tension glaucoma Gene Set

From GAD Gene-Disease Associations

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

low amplitude p300 waves Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low amplitude p300 waves in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low high-density lipoprotein cholesterol concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low high-density lipoprotein cholesterol concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum low-density lipoprotein metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum low-density lipoprotein metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular degeneration; vision, low Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macular degeneration; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

longer telomeres at low folate nutritional status Gene Set

From GAD Gene-Disease Associations

genes associated with the disease longer telomeres at low folate nutritional status in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low back pain Gene Set

From GAD Gene-Disease Associations

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

low hepatic lipase activity Gene Set

From GAD Gene-Disease Associations

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

low cetp activity Gene Set

From GAD Gene-Disease Associations

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

very low bone mass Gene Set

From GAD Gene-Disease Associations

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

apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low 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.

high or low factor xiii specific activity. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high or low factor xiii specific activity. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low-level lead exposure Gene Set

From GAD Gene-Disease Associations

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

glaucoma, open-angle; low tension glaucoma; ocular hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; low tension glaucoma; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low-density lipoprotein cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low-density lipoprotein cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced low-density lipoprotein particle size Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced low-density lipoprotein particle size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

resistance in vitro to low-dose aspirin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease resistance in vitro to low-dose aspirin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low birthweight Gene Set

From GAD Gene-Disease Associations

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

low expression of nb1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low expression of nb1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac output, low; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac output, low; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low Gene Set

From GeneRIF Biological Term Annotations

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

AIRE_KO_GDS2274_245_mouse_Medullary thymic epithelial cells (with low CD80 expression) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the AIRE_KO_GDS2274_245_mouse_Medullary thymic epithelial cells (with low CD80 expression) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

low-density lipoprotein receptor particle metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein receptor particle metabolic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

regulation of very-low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of very-low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

response to low light intensity stimulus Gene Set

From GO Biological Process Annotations

genes participating in the response to low light intensity stimulus biological process from the curated GO Biological Process Annotations dataset.

very-low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the very-low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

positive regulation of low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

response to low-density lipoprotein particle Gene Set

From GO Biological Process Annotations

genes participating in the response to low-density lipoprotein particle biological process from the curated GO Biological Process Annotations dataset.

positive regulation of low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

receptor-mediated endocytosis of low-density lipoprotein particle involved in cholesterol transport Gene Set

From GO Biological Process Annotations

genes participating in the receptor-mediated endocytosis of low-density lipoprotein particle involved in cholesterol transport biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle mediated signaling Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle mediated signaling biological process from the curated GO Biological Process Annotations dataset.

cellular response to low-density lipoprotein particle stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to low-density lipoprotein particle stimulus biological process from the curated GO Biological Process Annotations dataset.

regulation of low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

very-low-density lipoprotein particle assembly Gene Set

From GO Biological Process Annotations

genes participating in the very-low-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of very-low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of very-low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

negative regulation of low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the low-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

very-low-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the very-low-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

low-affinity sodium:dicarboxylate symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity sodium:dicarboxylate symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

low-density lipoprotein particle binding Gene Set

From GO Molecular Function Annotations

genes performing the low-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations dataset.

very-low-density lipoprotein particle binding Gene Set

From GO Molecular Function Annotations

genes performing the very-low-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations dataset.

low voltage-gated calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the low voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

very-low-density lipoprotein particle receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the very-low-density lipoprotein particle receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

low-density lipoprotein particle receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the low-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity l-arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity l-arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity glucose:sodium symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity basic amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

very-low-density lipoprotein particle receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the very-low-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

low-density lipoprotein receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the low-density lipoprotein receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

Blood pressure measurement (low sodium intervention) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (low sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

low alkaline phosphatase Gene Set

From HPO Gene-Disease Associations

genes associated with the low alkaline phosphatase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low gonadotropins (secondary hypogonadism) Gene Set

From HPO Gene-Disease Associations

genes associated with the low gonadotropins (secondary hypogonadism) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low cholesterol esterification rates Gene Set

From HPO Gene-Disease Associations

genes associated with the low cholesterol esterification rates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased circulating very-low-density lipoprotein cholesterol Gene Set

From HPO Gene-Disease Associations

genes associated with the increased circulating very-low-density lipoprotein cholesterol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-to-normal blood pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the low-to-normal blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-frequency hearing loss Gene Set

From HPO Gene-Disease Associations

genes associated with the low-frequency hearing loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-frequency sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

low-set, posteriorly rotated ears Gene Set

From HPO Gene-Disease Associations

genes associated with the low-set, posteriorly rotated ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low anterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the low anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low plasma citrulline Gene Set

From HPO Gene-Disease Associations

genes associated with the low plasma citrulline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low posterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the low posterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormally low-pitched voice Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormally low-pitched voice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low maternal serum estriol Gene Set

From HPO Gene-Disease Associations

genes associated with the low maternal serum estriol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low urinary cyclic amp response to pth administration Gene Set

From HPO Gene-Disease Associations

genes associated with the low urinary cyclic amp response to pth administration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low back pain Gene Set

From HPO Gene-Disease Associations

genes associated with the low back pain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-set ears Gene Set

From HPO Gene-Disease Associations

genes associated with the low-set ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low frustration tolerance Gene Set

From HPO Gene-Disease Associations

genes associated with the low frustration tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low hanging columella Gene Set

From HPO Gene-Disease Associations

genes associated with the low hanging columella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low-set nipples Gene Set

From HPO Gene-Disease Associations

genes associated with the low-set nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Low Back Pain Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Low Back Pain phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cardiac Output, Low Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Low Tension Glaucoma Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Low Tension Glaucoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Vision, Low Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Low temperature viability protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low temperature viability protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Low-density lipoprotein (LDL) receptor class A, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low-density lipoprotein (LDL) receptor class A, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Low density lipoprotein receptor-related protein, 5/6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low density lipoprotein receptor-related protein, 5/6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Low-density lipoprotein (LDL) receptor class A repeat Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low-density lipoprotein (LDL) receptor class A repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased ly6c low monocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased ly6c low monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ly6c low monocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ly6c low monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

low mean erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the low mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

low sweet preference Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the low sweet preference phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

plasma triglyceride level qtl, low Gene Set

From OMIM Gene-Disease Associations

genes associated with the plasma triglyceride level qtl, low phenotype from the curated OMIM Gene-Disease Associations dataset.

{low renin hypertension, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {low renin hypertension, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{high density lipoprotein cholesterol, low serum, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {high density lipoprotein cholesterol, low serum, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{low density lipoprotein cholesterol level qtl 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {low density lipoprotein cholesterol level qtl 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

[low density lipoprotein cholesterol level qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [low density lipoprotein cholesterol level qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

[low density lipoprotein cholesterol level qtl6] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [low density lipoprotein cholesterol level qtl6] phenotype from the curated OMIM Gene-Disease Associations dataset.

{bone mineral density, low, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bone mineral density, low, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

Birth Weight Gene Set

From CTD Gene-Disease Associations

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

Weight Gain Gene Set

From CTD Gene-Disease Associations

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

Fetal Weight Gene Set

From CTD Gene-Disease Associations

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

Body Weight Changes Gene Set

From CTD Gene-Disease Associations

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

Body Weight Gene Set

From CTD Gene-Disease Associations

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

Weight Loss Gene Set

From CTD Gene-Disease Associations

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

Body Weight Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Body Weight in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Birth Weight Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Birth Weight in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Body Weight Changes Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Body Weight Changes in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

metabolic syndrome x; obesity; overweight; thinness; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome x; obesity; overweight; thinness; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

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

body weight; insulin resistance; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; growth disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; disorders Gene Set

From GAD Gene-Disease Associations

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

body weight; hypertension; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; coronary disease Gene Set

From GAD Gene-Disease Associations

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

insulin resistance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; seasonal affective disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hyperbilirubinemia, neonatal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperbilirubinemia, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

body weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; growth disorders; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; growth disorders; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

antipsychotic response ; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antipsychotic response ; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; overweight; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; obesity; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; obesity; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, gestational; gestational diabetes mellitus ; weight gain Gene Set

From GAD Gene-Disease Associations

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

body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; glucose intolerance; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; glucose intolerance; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; infant, newborn, diseases; infection; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; infant, newborn, diseases; infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscle testing; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscle testing; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

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

birth weight preterm delivery Gene Set

From GAD Gene-Disease Associations

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

body weight; thromboembolism Gene Set

From GAD Gene-Disease Associations

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

birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; sudden infant death 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.

body weight; hiv infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; puberty, delayed Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; puberty, delayed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chorioamnionitis; infection; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chorioamnionitis; infection; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus, type 1 Gene Set

From GAD Gene-Disease Associations

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

zinc; lead toxicity; height; weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease zinc; lead toxicity; height; weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; Gene Set

From GAD Gene-Disease Associations

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

body weight; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; insulin resistance 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.

body weight; cardiovascular diseases; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; cardiovascular diseases; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight gain (antipsychotic-drug induced) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease weight gain (antipsychotic-drug induced) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; height; weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; height; weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hyperglycemia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperglycemia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; body weight Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antipsychotic agent-induced weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antipsychotic agent-induced weight gain 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.

birth weight; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

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

coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight loss Gene Set

From GAD Gene-Disease Associations

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

body weight; insulin resistance; obesity; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; insulin resistance; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; birth weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

body weight; hypertension; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

acromegaly; body weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic 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.

body weight; gastrointestinal stromal tumors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; gastrointestinal stromal tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus; postoperative complications 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.

body weight; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

birth weight; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus, type 1; Gene Set

From GAD Gene-Disease Associations

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

body weight; familial mediterranean fever; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight changes Gene Set

From GAD Gene-Disease Associations

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

hypertension; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; thinness Gene Set

From GAD Gene-Disease Associations

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

body weight; cystic fibrosis; growth disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; retinopathy of prematurity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; retinopathy of prematurity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; overweight Gene Set

From GAD Gene-Disease Associations

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

body weight; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

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

obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications; weight gain 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.

birth weight; fetal growth retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

birth weight; cord blood igf-ii levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cord blood igf-ii levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

birth weight Gene Set

From GAD Gene-Disease Associations

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

adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; birth weight; height Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; birth weight; height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; obesity; osteoarthritis, knee; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; obesity; osteoarthritis, knee; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight regulation Gene Set

From GAD Gene-Disease Associations

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

birth weight; preterm delivery Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; preterm delivery 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.

schizophrenia; schizoaffective disorder; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; schizoaffective disorder; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; body fat; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; body fat; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

insulin resistance; overweight; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; obesity Gene Set

From GAD Gene-Disease Associations

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

birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cardiovascular diseases; metabolic syndrome x; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; bulimia; starvation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; bulimia; starvation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; cystic fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c; liver cirrhosis; recurrence; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; liver cirrhosis; recurrence; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass (bwt, weight gain, bmi); fertility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass (bwt, weight gain, bmi); fertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatty liver; insulin resistance; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatty liver; insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; critical illness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; critical illness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight maintenance Gene Set

From GAD Gene-Disease Associations

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

body weight; hypertension Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; weight gain Gene Set

From GAD Gene-Disease Associations

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

alcoholism; body weight Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; cardiovascular disease; birth weight Gene Set

From GAD Gene-Disease Associations

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

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; spinal osteophytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

birth weight; premature birth Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; obesity; birth weight Gene Set

From GAD Gene-Disease Associations

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

body weight; puberty, precocious; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; puberty, precocious; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus, type 2; obesity; overweight Gene Set

From GAD Gene-Disease Associations

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

body mass; diabetes, type 2; glucose; birth weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; cystic fibrosis; ileus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cystic fibrosis; ileus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; obesity; syndrome Gene Set

From GAD Gene-Disease Associations

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

obesity; weight gain Gene Set

From GAD Gene-Disease Associations

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

anoxia; body weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight Gene Set

From GAD Gene-Disease Associations

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

weight gain, antipsychotic drug-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease weight gain, antipsychotic drug-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, abdominal; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, abdominal; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; hellp syndrome; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; hellp syndrome; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, morbid; postoperative complications; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; postoperative complications; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; spinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; osteoarthritis, knee Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; osteoarthritis, knee in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

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

body weight; cardiovascular diseases; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

body weight; insulin resistance; overweight; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

birth weight; fetal growth retardation; intrauterine growth retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; hypertension; obesity; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; hypertension; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; insulin resistance; lipodystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; insulin resistance; lipodystrophy 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.

body weight; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperphagia; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperphagia; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight gain Gene Set

From GAD Gene-Disease Associations

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

obesity; birth weight Gene Set

From GAD Gene-Disease Associations

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

birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

growth disorders; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease growth disorders; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; weight gain Gene Set

From GAD Gene-Disease Associations

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

birth weight; hypertension Gene Set

From GAD Gene-Disease Associations

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

glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight Gene Set

From GeneRIF Biological Term Annotations

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

Weight loss (gastric bypass surgery) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Weight loss (gastric bypass surgery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Weight Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Birth weight Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Birth weight phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

weight loss Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the weight loss phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

decreased body weight Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the decreased body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased body weight Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of body weight Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

weight loss Gene Set

From HPO Gene-Disease Associations

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

decreased body weight Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of body weight Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased body weight Gene Set

From HPO Gene-Disease Associations

genes associated with the increased body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Birth Weight Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Weight Gain Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Fetal Weight Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Body Weight Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Weight Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

slow postnatal weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the slow postnatal weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left atrium weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased oviduct weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased oviduct weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased heart left atrium weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urinary bladder weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased gonadal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pancreas weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal prostate gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal prostate gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased prostate gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased prostate gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased retroperitoneal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retroperitoneal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal aortic weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal aortic weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased adrenal gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased adrenal gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased vagina weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased vagina weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased extensor digitorum longus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased epididymis weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased epididymis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal liver weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal liver weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal soleus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal soleus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal prenatal growth/weight/body size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal prenatal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal fetal growth/weight/body size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased interscapular fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased interscapular fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal testis weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal testis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal seminal vesicle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal seminal vesicle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased ovary weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal embryonic growth/weight/body size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal embryonic growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal uterus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal uterus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased tibialis anterior weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal epididymis weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal epididymis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased wet-to-dry lung weight ratio Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased wet-to-dry lung weight ratio phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased total fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased liver weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased liver weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased heart left ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased heart left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased epididymis weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased epididymis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased omental fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased omental fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal postnatal growth/weight/body size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal postnatal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spleen weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spleen weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased adrenal gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased adrenal gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thymus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal thymus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased placenta weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased placenta weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased extensor digitorum longus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal gastrocnemius weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal gastrocnemius weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased placenta weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased placenta weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased birth weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased birth weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased renal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased renal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased body weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased body weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased lung weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lung weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased omental fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased omental fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased uterine fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased uterine fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased soleus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased soleus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased thyroid gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased thyroid gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased heart weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased heart weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased gastrocnemius weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased gastrocnemius weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased testis weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased testis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased embryo weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased embryo weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased quadriceps weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased quadriceps weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased quadriceps weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased quadriceps weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal quadriceps weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal quadriceps weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased thymus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased thymus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased brain weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased brain weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased abdominal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased abdominal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased heart weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased heart weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pancreas weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased body weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased body weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased abdominal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased abdominal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal wet-to-dry lung weight ratio Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal wet-to-dry lung weight ratio phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased renal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased renal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased left ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lung weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lung weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spleen weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spleen weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal body weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal body weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal oviduct weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal oviduct weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased fetal weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased fetal weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ovary weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased liver weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased liver weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pancreas weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased total fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased uterus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased uterus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased seminal vesicle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased seminal vesicle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased gastrocnemius weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased gastrocnemius weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retroperitoneal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retroperitoneal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pituitary gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pituitary gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal birth weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal birth weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tibialis anterior weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased pituitary gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased pituitary gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mesenteric fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mesenteric fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased fetal weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased fetal weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased embryo weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased embryo weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal adrenal gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal adrenal gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased interscapular fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased interscapular fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased pituitary gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased pituitary gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mesenteric fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mesenteric fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased gonadal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased epididymal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased epididymal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased soleus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased soleus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vagina weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vagina weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased brain weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased brain weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased ovary weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased urinary bladder weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart right ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased tibialis anterior weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mammary fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mammary fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased parametrial fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased parametrial fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased kidney weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased kidney weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased femoral fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased femoral fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased inguinal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased inguinal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased birth weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased birth weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased uterus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased uterus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal total fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal total fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased kidney weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased kidney weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased testis weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased testis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased spleen weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased spleen weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased prostate gland weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased prostate gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased lung weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased lung weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal extensor digitorum longus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal placenta weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased epididymal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased epididymal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased inguinal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased inguinal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased seminal vesicle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased seminal vesicle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased heart right ventricle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased heart right ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased thymus weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased thymus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mammary fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mammary fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased parametrial fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased parametrial fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

[birth weight qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

{bulimia nervosa, age of onset of weight loss in} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset.

[birth weight qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

[birth weight qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[birth weight qtl4] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [birth weight qtl4] phenotype from the curated OMIM Gene-Disease Associations dataset.

weight Gene Set

From Phosphosite Textmining Biological Term Annotations

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

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

From Biocarta Pathways

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

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

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

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

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

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

From GO Molecular Function Annotations

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

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

From GO Molecular Function Annotations

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

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

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

From Reactome Pathways

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

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

From Reactome Pathways

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

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

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

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

From Reactome Pathways

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

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

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

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

From Reactome Pathways

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

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

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

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

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

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

From Wikipathways Pathways

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

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

From Wikipathways Pathways

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

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

From Wikipathways Pathways

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

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.

visceral fat deposits and the metabolic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

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

From Biocarta Pathways

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

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.

degradation of the rar and rxr by the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.

cadmium induces dna synthesis and proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

chrebp regulation by carbohydrates and camp Gene Set

From Biocarta Pathways

proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.

pten dependent cell cycle arrest and apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

CIITA-18437201-Raji B cells and iDC-human Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypothyroidism, central, and testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly and ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sinoatrial node dysfunction and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

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

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death 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.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mullerian aplasia and hyperandrogenism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Knuckle pads, deafness AND leukonychia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Multicentric osteolysis, nodulosis and arthropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stapes ankylosis with broad thumb and toes Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness 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.

Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

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

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract and cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract and cardiomyopathy 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.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, microphthalmia and nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone fragility with contractures, arterial rupture, and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor v and factor viii, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary Paragangliomas and Pheochromocytomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Band-like calcification with simplified gyration and polymicrogyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, epilepsy, and diabetes syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea and glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, deafness, and narcolepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile macular degeneration and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary leiomyomatosis and renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Microcephaly, hiatal hernia and nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined malonic and methylmalonic aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

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

Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis Gyrata syndrome of Beare and Stevenson Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor and sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis and dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebroretinal microangiopathy with calcifications and cysts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, normal intelligence and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Calcification of joints and arteries Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Calcification of joints and arteries 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.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pineal hyperplasia AND diabetes mellitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Morbid obesity and spermatogenic failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sensory and autonomic neuropathy type IIA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract and vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of factor V and factor VIII, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.