Name

dyserythropoietic anemia, congenital, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyserythropoietic anemia, congenital, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

Congenital dyserythropoietic anemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

dyserythropoietic anemia, congenital, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyserythropoietic anemia, congenital, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

dyserythropoietic anemia, congenital, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyserythropoietic anemia, congenital, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

dyserythropoietic anemia, congenital, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyserythropoietic anemia, congenital, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

dyserythropoietic anemia, congenital, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyserythropoietic anemia, congenital, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

Anemia, Dyserythropoietic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Dyserythropoietic, Congenital from the curated CTD Gene-Disease Associations dataset.

congenital dyserythropoietic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital dyserythropoietic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

macrocytic dyserythropoietic anemia Gene Set

From HPO Gene-Disease Associations

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

exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; glycogen storage disease type i; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; glycogen storage disease type i; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

dyserythropoietic Gene Set

From GeneRIF Biological Term Annotations

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

DNA ligase III-XRCC1-PNK-DNA-pol III multiprotein complex Gene Set

From CORUM Protein Complexes

proteins in the DNA ligase III-XRCC1-PNK-DNA-pol III multiprotein complex protein complex from the CORUM Protein Complexes dataset.

anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; infarction; ischemia; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; infarction; ischemia; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; apoplexy; sickle cell anemia; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; apoplexy; sickle cell anemia; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; pain; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; pain; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; sickle cell anemia; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; sickle cell anemia; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; bone diseases; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bone diseases; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; inflammation; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; inflammation; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron deficiency; anemia of chronic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron deficiency; anemia of chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fanconi anemia; fanconi's anemia; kidney neoplasms; nephroblastoma; wilms tumor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fanconi anemia; fanconi's anemia; kidney neoplasms; nephroblastoma; wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; genetic diseases, inborn; graft vs host disease; hematologic neoplasms; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; genetic diseases, inborn; graft vs host disease; hematologic neoplasms; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; bacterial infections; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bacterial infections; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fanconi anemia; fanconi's anemia; hematologic diseases Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; sickle cell anemia; trachoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; sickle cell anemia; trachoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; glucosephosphate dehydrogenase deficiency; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; glucosephosphate dehydrogenase deficiency; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; hemochromatosis; iron overload; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; hemochromatosis; iron overload; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, diamond-blackfan; diamond-blackfan anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, diamond-blackfan; diamond-blackfan anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; disease susceptibility Gene Set

From GAD Gene-Disease Associations

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

anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia Gene Set

From GAD Gene-Disease Associations

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

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; peripheral vascular diseases; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; peripheral vascular diseases; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

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

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

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

Anemia, Hemolytic, Congenital Nonspherocytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital Nonspherocytic from the curated CTD Gene-Disease Associations dataset.

Anemia, Hypoplastic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hypoplastic, Congenital from the curated CTD Gene-Disease Associations dataset.

Anemia, Hemolytic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital from the curated CTD Gene-Disease Associations dataset.

congenital hemolytic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital hypoplastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital hypoplastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital nonspherocytic hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital hemolytic anemia Gene Set

From GWASdb SNP-Disease Associations

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

congenital hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

congenital hypoplastic anemia Gene Set

From HPO Gene-Disease Associations

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

Anemia, Hemolytic, Congenital Nonspherocytic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Hemolytic, Congenital Nonspherocytic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Anemia, Hemolytic, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

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

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity 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.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Hyperammonemia, type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperammonemia, type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LEUKOCYTE ADHESION DEFICIENCY, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LEUKOCYTE ADHESION DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial complex III deficiency, nuclear type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PROPERDIN DEFICIENCY, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PROPERDIN DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary hyperoxaluria, type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary hyperoxaluria, type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type III Gene Set

From ClinVar Gene-Phenotype Associations

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

Osteogenesis imperfecta type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

HYPERALDOSTERONISM, FAMILIAL, TYPE III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the HYPERALDOSTERONISM, FAMILIAL, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

collagen type iii trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type iii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

type iii intermediate filament Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the type iii intermediate filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

type iii protein secretion system complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the type iii protein secretion system complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type iii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type iii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class iii, type ii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class iii, type ii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

type iii polyketide synthase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the type iii polyketide synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class iii, type i Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class iii, type i cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

type iii intermediate filament Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the type iii intermediate filament cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Prolyl 4-hydroxylase (alpha(III)-type) Gene Set

From CORUM Protein Complexes

proteins in the Prolyl 4-hydroxylase (alpha(III)-type) protein complex from the CORUM Protein Complexes dataset.

Leukocyte Adhesion Deficiency, Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukocyte Adhesion Deficiency, Type III from the curated CTD Gene-Disease Associations dataset.

Amelogenesis Imperfecta, Type III Gene Set

From CTD Gene-Disease Associations

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

USHER SYNDROME, TYPE IIIA Gene Set

From CTD Gene-Disease Associations

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

ATELOSTEOGENESIS, TYPE III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATELOSTEOGENESIS, TYPE III from the curated CTD Gene-Disease Associations dataset.

Hereditary Angioedema Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Angioedema Type III from the curated CTD Gene-Disease Associations dataset.

Hyperlipoproteinemia Type III Gene Set

From CTD Gene-Disease Associations

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

Glycogen Storage Disease Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type III from the curated CTD Gene-Disease Associations dataset.

Exostoses, Multiple, Type III Gene Set

From CTD Gene-Disease Associations

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

Trichorhinophalangeal Syndrome, Type III Gene Set

From CTD Gene-Disease Associations

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

Gaucher Disease, Type Iiic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Type Iiic from the curated CTD Gene-Disease Associations dataset.

HYPEROXALURIA, PRIMARY, TYPE III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPEROXALURIA, PRIMARY, TYPE III from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Lattice Type IIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset.

hyperlipoproteinemia type iii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypersensitivity reaction type iii disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tyrosinemia type iii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

severe type iii hyperlipoproteinemia Gene Set

From GAD Gene-Disease Associations

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

glycogen storage disease type iii Gene Set

From GAD Gene-Disease Associations

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

glycogen storage disease type iiia Gene Set

From GAD Gene-Disease Associations

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

hyperlipoproteinemia type iii; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

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

type iii hyperlipoproteinemia Gene Set

From GAD Gene-Disease Associations

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

regulation of type iii interferon production Gene Set

From GO Biological Process Annotations

genes participating in the regulation of type iii interferon production biological process from the curated GO Biological Process Annotations dataset.

positive regulation of type iii interferon production Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of type iii interferon production biological process from the curated GO Biological Process Annotations dataset.

positive regulation of type iii hypersensitivity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of type iii hypersensitivity biological process from the curated GO Biological Process Annotations dataset.

response to type iii interferon Gene Set

From GO Biological Process Annotations

genes participating in the response to type iii interferon biological process from the curated GO Biological Process Annotations dataset.

5s class rrna transcription from rna polymerase iii type 1 promoter Gene Set

From GO Biological Process Annotations

genes participating in the 5s class rrna transcription from rna polymerase iii type 1 promoter biological process from the curated GO Biological Process Annotations dataset.

regulation of type iii hypersensitivity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of type iii hypersensitivity biological process from the curated GO Biological Process Annotations dataset.

collagen type iii trimer Gene Set

From GO Cellular Component Annotations

proteins localized to the collagen type iii trimer cellular component from the curated GO Cellular Component Annotations dataset.

phosphatidylinositol 3-kinase complex, class iii, type i Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class iii, type i cellular component from the curated GO Cellular Component Annotations dataset.

phosphatidylinositol 3-kinase complex, class iii, type ii Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class iii, type ii cellular component from the curated GO Cellular Component Annotations dataset.

type iii intermediate filament Gene Set

From GO Cellular Component Annotations

proteins localized to the type iii intermediate filament cellular component from the curated GO Cellular Component Annotations dataset.

rna polymerase iii type 3 promoter dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii type 3 promoter dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase iii type 1 promoter dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii type 1 promoter dna binding molecular function from the curated GO Molecular Function Annotations dataset.

transforming growth factor beta receptor activity, type iii Gene Set

From GO Molecular Function Annotations

genes performing the transforming growth factor beta receptor activity, type iii molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase iii type 2 promoter dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii type 2 promoter dna binding molecular function from the curated GO Molecular Function Annotations dataset.

type iii transforming growth factor beta receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the type iii transforming growth factor beta receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

Hyperlipoproteinemia Type III Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Glycogen Storage Disease Type III Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Leucine-rich repeat and fibronectin type-III domain-containing protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Leucine-rich repeat and fibronectin type-III domain-containing protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Annexin, type III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Annexin, type III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fibronectin type III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fibronectin type III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Antifreeze, type III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Antifreeze, type III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased susceptibility to type iii hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to type iii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to type iii hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to type iii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal type iii hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal type iii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal type iii spiral ligament fibrocytes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal type iii spiral ligament fibrocytes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

type iii spiral ligament fibrocyte degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the type iii spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hyperoxaluria, primary, type iii Gene Set

From OMIM Gene-Disease Associations

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

mody, type iii Gene Set

From OMIM Gene-Disease Associations

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

hyperlipoproteinemia, type iii Gene Set

From OMIM Gene-Disease Associations

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

gm1-gangliosidosis, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the gm1-gangliosidosis, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

angioedema, hereditary, type iii Gene Set

From OMIM Gene-Disease Associations

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

amelogenesis imperfecta, type iii Gene Set

From OMIM Gene-Disease Associations

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

gaucher disease, type iii Gene Set

From OMIM Gene-Disease Associations

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

gaucher disease, type iiic Gene Set

From OMIM Gene-Disease Associations

genes associated with the gaucher disease, type iiic phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, lattice type iiia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lattice type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.

oi type iii Gene Set

From OMIM Gene-Disease Associations

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

stickler syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

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

hyperaldosteronism, familial, type iii Gene Set

From OMIM Gene-Disease Associations

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

mucopolysaccharidisis type iiia (sanfilippo a) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mucopolysaccharidisis type iiia (sanfilippo a) phenotype from the curated OMIM Gene-Disease Associations dataset.

leukocyte adhesion deficiency, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukocyte adhesion deficiency, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune lymphoproliferative syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

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

granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

trichorhinophalangeal syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

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

ehlers-danlos syndrome, type iii Gene Set

From OMIM Gene-Disease Associations

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

cutis laxa, autosomal recessive, type iiia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, autosomal recessive, type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, autosomal recessive, type iiib Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, autosomal recessive, type iiib phenotype from the curated OMIM Gene-Disease Associations dataset.

{spinal muscular atrophy, type iii, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

dentinogenesis imperfecta, shields type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the dentinogenesis imperfecta, shields type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

mucopolysaccharidosis type iiib (sanfilippo b) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mucopolysaccharidosis type iiib (sanfilippo b) phenotype from the curated OMIM Gene-Disease Associations dataset.

osteogenesis imperfecta, type iii Gene Set

From OMIM Gene-Disease Associations

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

tyrosinemia, type iii Gene Set

From OMIM Gene-Disease Associations

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

?mitochondrial complex iii deficiency, nuclear type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex iii deficiency, nuclear type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex iii deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

atelosteogenesis, type iii Gene Set

From OMIM Gene-Disease Associations

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

mucopolysaccharidosis type iiid Gene Set

From OMIM Gene-Disease Associations

genes associated with the mucopolysaccharidosis type iiid phenotype from the curated OMIM Gene-Disease Associations dataset.

syndactyly, type iii Gene Set

From OMIM Gene-Disease Associations

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

schindler disease, type iii Gene Set

From OMIM Gene-Disease Associations

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

hypocalciuric hypercalcemia, familial, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypocalciuric hypercalcemia, familial, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex iii deficiency, nuclear type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex iii deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

3-methylglutaconic aciduria, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the 3-methylglutaconic aciduria, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

mucopolysaccharidosis type iiic (sanfilippo c) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mucopolysaccharidosis type iiic (sanfilippo c) phenotype from the curated OMIM Gene-Disease Associations dataset.

albinism, oculocutaneous, type iii Gene Set

From OMIM Gene-Disease Associations

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

nitric-oxide-synthase-type-iii Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term nitric-oxide-synthase-type-iii in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

RNA Polymerase III Transcription Initiation From Type 3 Promoter Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Transcription Initiation From Type 3 Promoter pathway from the Reactome Pathways dataset.

RNA Polymerase III Transcription Initiation From Type 1 Promoter Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Transcription Initiation From Type 1 Promoter pathway from the Reactome Pathways dataset.

RNA Polymerase III Transcription Initiation From Type 2 Promoter Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Transcription Initiation From Type 2 Promoter pathway from the Reactome Pathways dataset.

Type III interferon signaling(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Type III interferon signaling(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

megaloblastic anemia-1, finnish type Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia-1, finnish type phenotype from the curated OMIM Gene-Disease Associations dataset.

homocystinuria-megaloblastic anemia, cbl e type Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria-megaloblastic anemia, cbl e type phenotype from the curated OMIM Gene-Disease Associations dataset.

homocystinuria-megaloblastic anemia, cblg complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the homocystinuria-megaloblastic anemia, cblg complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, rh-null, regulator type Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, rh-null, regulator type phenotype from the curated OMIM Gene-Disease Associations dataset.

megaloblastic anemia-1, norwegian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia-1, norwegian type phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia disease specific cell type Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue fanconi anemia disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

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

Congenital generalized lipodystrophy type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, congenital generalized, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, congenital generalized, type 3 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.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital secretory diarrhea, chloride type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital secretory diarrhea, chloride type 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.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw 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.

Congenital disorder of glycosylation type 2k Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1P 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.

Congenital disorder of glycosylation type 1H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1v Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type Ix Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital order of glycosylation type 1r Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1K Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1y Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1u Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1t Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital hyperammonemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myopathy with fiber type disproportion Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract congenital Volkmann type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIF Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.

MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder of Glycosylation, Type Io Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type Im Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type In Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.

Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

Adrenal hyperplasia, congenital, type 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adrenal hyperplasia, congenital, type 5 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIH from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 3 from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 4 from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIB from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A from the curated CTD Gene-Disease Associations dataset.

congenital disorder of glycosylation type ii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital disorder of glycosylation type i Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

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

From GAD Gene-Disease Associations

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

chuvash-type congenital polycythemia Gene Set

From GAD Gene-Disease Associations

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

congenital fibrosis of extraocular muscles type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital fibrosis of extraocular muscles type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ih Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ih phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ij Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ij phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ik Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ik phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type il Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type il phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type im Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type im phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type id Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type id phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ie Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ie phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type if Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type if phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ig Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ig phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iq Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iq phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type it Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type it phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iu Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iu phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, megaconial type Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

?congenital disorder of glycosylation, type iw Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?congenital disorder of glycosylation, type iw phenotype from the curated OMIM Gene-Disease Associations dataset.

?congenital disorder of glycosylation, type ix Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?congenital disorder of glycosylation, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.

?congenital disorder of glycosylation, type iy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?congenital disorder of glycosylation, type iy phenotype from the curated OMIM Gene-Disease Associations dataset.

?congenital disorder of glycosylation, type ir Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?congenital disorder of glycosylation, type ir phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type in Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type in phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type io Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type io phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type ip Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type ip phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type is Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type is phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, congenital, with fiber-type disproportion, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, congenital, with fiber-type disproportion, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

?lipodystrophy, congenital generalized, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?lipodystrophy, congenital generalized, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, congenital generalized, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, congenital generalized, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, congenital, with fiber-type disproportion 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, congenital, with fiber-type disproportion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iil Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iil phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iij Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iij phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iik Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iik phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iih Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iih phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iim Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iim phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iic Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iia Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iif Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iif phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iig Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iig phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iid Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iid phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital disorder of glycosylation, type iie Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital disorder of glycosylation, type iie phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, congenital, with fiber-type disproportion Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, congenital, with fiber-type disproportion phenotype from the curated OMIM Gene-Disease Associations dataset.

oculomotor apraxia, congenital, cogan-type Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculomotor apraxia, congenital, cogan-type phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, congenital generalized, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, congenital generalized, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

lipodystrophy, congenital generalized, type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipodystrophy, congenital generalized, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuromuscular disease, congenital, with uniform type 1 fiber Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuromuscular disease, congenital, with uniform type 1 fiber phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

III, right, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in III, right, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

III, left, paravermis Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in III, left, paravermis relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

III Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

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

III, left, lateral hemisphere Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in III, left, lateral hemisphere relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Lobule III Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lobule III 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.

Lobule III, granular layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

layer IIIa of caudal entorhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

layer III of area 35c Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer III of area 35c relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer IIIb of caudal entorhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

layer IIIu of area 35c Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer IIIu of area 35c relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer IIIu of area 35r Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in layer IIIu of area 35r relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

layer III of piriform cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

layer III of rostral entorhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

layer III of caudal entorhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

rna polymerase iii transcription Gene Set

From Biocarta Pathways

proteins participating in the rna polymerase iii transcription pathway from the Biocarta Pathways dataset.

Mitochondrial complex III deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial complex III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antithrombin III deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antithrombin III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIa Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mucolipidosis III Gamma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mucolipidosis III Gamma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIc Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIb Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mucopolysaccharidosis, MPS-III-A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mucopolysaccharidosis, MPS-III-A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mucopolysaccharidosis, MPS-III-C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mucopolysaccharidosis, MPS-III-C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mucopolysaccharidosis, MPS-III-B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mucopolysaccharidosis, MPS-III-B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mucopolysaccharidosis, MPS-III-D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mucopolysaccharidosis, MPS-III-D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

phosphatidylinositol 3-kinase complex, class iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the phosphatidylinositol 3-kinase complex, class iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

rna polymerase iii transcription factor complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the rna polymerase iii transcription factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

respiratory chain complex iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the respiratory chain complex iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

dna-directed rna polymerase iii complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the dna-directed rna polymerase iii complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

dna polymerase iii complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the dna polymerase iii complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

escrt iii complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the escrt iii complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

recq helicase-topo iii complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the recq helicase-topo iii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

phosphatidylinositol 3-kinase complex, class iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the phosphatidylinositol 3-kinase complex, class iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

escrt iii complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the escrt iii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

dna polymerase iii complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the dna polymerase iii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ribonuclease iii complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ribonuclease iii complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

respiratory chain complex iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the respiratory chain complex iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

dna ligase iii-xrcc1 complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the dna ligase iii-xrcc1 complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial respiratory chain complex iii Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial respiratory chain complex iii cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

TRF2-Rap1 complex III Gene Set

From CORUM Protein Complexes

proteins in the TRF2-Rap1 complex III protein complex from the CORUM Protein Complexes dataset.

BLM complex III Gene Set

From CORUM Protein Complexes

proteins in the BLM complex III protein complex from the CORUM Protein Complexes dataset.

BRCA1-BARD1-BRCA2-DNA damage complex III Gene Set

From CORUM Protein Complexes

proteins in the BRCA1-BARD1-BRCA2-DNA damage complex III protein complex from the CORUM Protein Complexes dataset.

ESCRT-III complex Gene Set

From CORUM Protein Complexes

proteins in the ESCRT-III complex protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

DNA ligase III-XRCC1 complex Gene Set

From CORUM Protein Complexes

proteins in the DNA ligase III-XRCC1 complex protein complex from the CORUM Protein Complexes dataset.

SKG-IIIA Gene Set

From COSMIC Cell Line Gene CNV Profiles

genes with high or low copy number in SKG-IIIA relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.

SKG-IIIA Gene Set

From COSMIC Cell Line Gene Mutation Profiles

genes mutated in the SKG-IIIA cell line from the COSMIC Cell Line Gene Mutation Profiles dataset.

hexacyanoferrate III Gene Set

From CTD Gene-Chemical Interactions

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

manganese(III) acetate dihydrate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical manganese(III) acetate dihydrate from the curated CTD Gene-Chemical Interactions dataset.

tetrakis(N-methyl-4-pyridiniumyl)porphine manganese(III) complex Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical tetrakis(N-methyl-4-pyridiniumyl)porphine manganese(III) complex from the curated CTD Gene-Chemical Interactions dataset.

sudan III Gene Set

From CTD Gene-Chemical Interactions

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

coproporphyrinogen III Gene Set

From CTD Gene-Chemical Interactions

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

iron(III)-ascorbic acid complex Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical iron(III)-ascorbic acid complex from the curated CTD Gene-Chemical Interactions dataset.

curcumin III Gene Set

From CTD Gene-Chemical Interactions

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

manganese(III)-tetrakis(4-benzoic acid)porphyrin Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical manganese(III)-tetrakis(4-benzoic acid)porphyrin from the curated CTD Gene-Chemical Interactions dataset.

5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato iron(III) chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato iron(III) chloride from the curated CTD Gene-Chemical Interactions dataset.

Mn(III) meso-tetrakis(N-n-butoxyethylpyridinium-2-yl)porphyrin Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Mn(III) meso-tetrakis(N-n-butoxyethylpyridinium-2-yl)porphyrin from the curated CTD Gene-Chemical Interactions dataset.

thallium(III) hydroxide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical thallium(III) hydroxide from the curated CTD Gene-Chemical Interactions dataset.

imidazolium-bis(imidazole)dimethylsulfoxideimidazotetrachlororuthenate(III) Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical imidazolium-bis(imidazole)dimethylsulfoxideimidazotetrachlororuthenate(III) from the curated CTD Gene-Chemical Interactions dataset.

(dichloro)tetraammineruthenium(III) Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical (dichloro)tetraammineruthenium(III) from the curated CTD Gene-Chemical Interactions dataset.

angiotensin III, Ile(7)- Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical angiotensin III, Ile(7)- from the curated CTD Gene-Chemical Interactions dataset.

difructose anhydride III Gene Set

From CTD Gene-Chemical Interactions

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

Mn(III) 5,10,15,20-tetrakis(N-methylpyridinium-2-yl)porphyrin Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Mn(III) 5,10,15,20-tetrakis(N-methylpyridinium-2-yl)porphyrin from the curated CTD Gene-Chemical Interactions dataset.

tris(1,10-phenanthroline)chromium(III) chloride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical tris(1,10-phenanthroline)chromium(III) chloride from the curated CTD Gene-Chemical Interactions dataset.

juvenile hormone III Gene Set

From CTD Gene-Chemical Interactions

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

manganese (III) meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical manganese (III) meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin from the curated CTD Gene-Chemical Interactions dataset.

calpain inhibitor III Gene Set

From CTD Gene-Chemical Interactions

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

XLF-III-43 Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical XLF-III-43 from the curated CTD Gene-Chemical Interactions dataset.

5,10,15,20-tetrakis(N-methyl-4'-pyridyl)porphyrinato-iron(III) Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 5,10,15,20-tetrakis(N-methyl-4'-pyridyl)porphyrinato-iron(III) from the curated CTD Gene-Chemical Interactions dataset.

Mitochondrial Complex III Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial Complex III Deficiency from the curated CTD Gene-Disease Associations dataset.

Antithrombin III Deficiency Gene Set

From CTD Gene-Disease Associations

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

Mucopolysaccharidosis III Gene Set

From CTD Gene-Disease Associations

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

MUCOLIPIDOSIS III ALPHA/BETA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUCOLIPIDOSIS III ALPHA/BETA from the curated CTD Gene-Disease Associations dataset.

Mucolipidosis III Gamma Gene Set

From CTD Gene-Disease Associations

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

mucopolysaccharidosis iii Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

antithrombin iii deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

antithrombin iii deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

glycogen storage disease iii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mucopolysaccharidosis iii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Heparin Disaccharide Iii-S Gene Set

From DrugBank Drug Targets

interacting proteins for the Heparin Disaccharide Iii-S drug from the curated DrugBank Drug Targets dataset.

Porphyrin Fe(Iii) Gene Set

From DrugBank Drug Targets

interacting proteins for the Porphyrin Fe(Iii) drug from the curated DrugBank Drug Targets dataset.

Coproporphyrin Iii Gene Set

From DrugBank Drug Targets

interacting proteins for the Coproporphyrin Iii drug from the curated DrugBank Drug Targets dataset.

antithrombin iii deficiency; cerebral infarction; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; cerebral infarction; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; apob; apoc-iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; apob; apoc-iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; coronary thrombosis; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; coronary thrombosis; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; insulin; lipoproteins; apob; apoc-iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; insulin; lipoproteins; apob; apoc-iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

methionine adenosyltransferase i/iii deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease methionine adenosyltransferase i/iii deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

SKG-IIIa Gene Set

From GDSC Cell Line Gene Expression Profiles

genes with high or low expression in SKG-IIIa relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.

iiinducible Gene Set

From GeneRIF Biological Term Annotations

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

iiibetaglycan Gene Set

From GeneRIF Biological Term Annotations

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

iiicatalyzed Gene Set

From GeneRIF Biological Term Annotations

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

iiiinduced Gene Set

From GeneRIF Biological Term Annotations

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

iiialpharmi1rmi2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term iiialpharmi1rmi2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

iii Gene Set

From GeneRIF Biological Term Annotations

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

iiilike Gene Set

From GeneRIF Biological Term Annotations

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

iiidependent Gene Set

From GeneRIF Biological Term Annotations

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

iiiv Gene Set

From GeneRIF Biological Term Annotations

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

iiii Gene Set

From GeneRIF Biological Term Annotations

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

iiia Gene Set

From GeneRIF Biological Term Annotations

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

iiic Gene Set

From GeneRIF Biological Term Annotations

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

iiib Gene Set

From GeneRIF Biological Term Annotations

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

iiid Gene Set

From GeneRIF Biological Term Annotations

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

iii1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term iii1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

iiibetatubulin Gene Set

From GeneRIF Biological Term Annotations

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

iiialpha Gene Set

From GeneRIF Biological Term Annotations

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

iiibeta Gene Set

From GeneRIF Biological Term Annotations

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

iiiiv Gene Set

From GeneRIF Biological Term Annotations

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

iiiii Gene Set

From GeneRIF Biological Term Annotations

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

iiiia Gene Set

From GeneRIF Biological Term Annotations

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

iiialphaxrcc1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term iiialphaxrcc1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

iiindependent Gene Set

From GeneRIF Biological Term Annotations

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

iiiiii Gene Set

From GeneRIF Biological Term Annotations

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

iiiiia Gene Set

From GeneRIF Biological Term Annotations

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

iiirelated Gene Set

From GeneRIF Biological Term Annotations

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

iiinduced Gene Set

From GeneRIF Biological Term Annotations

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

uroporphyrinogen iii metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the uroporphyrinogen iii metabolic process biological process from the curated GO Biological Process Annotations dataset.

transcription elongation from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the transcription elongation from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

trna transcription from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the trna transcription from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

transcription initiation from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the transcription initiation from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

positive regulation of transcription from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of transcription from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

uroporphyrinogen iii biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the uroporphyrinogen iii biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

snrna transcription from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the snrna transcription from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

termination of rna polymerase iii transcription Gene Set

From GO Biological Process Annotations

genes participating in the termination of rna polymerase iii transcription biological process from the curated GO Biological Process Annotations dataset.

transcription from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the transcription from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

negative regulation of transcription from rna polymerase iii promoter Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transcription from rna polymerase iii promoter biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii assembly biological process from the curated GO Biological Process Annotations dataset.

response to iron(iii) ion Gene Set

From GO Biological Process Annotations

genes participating in the response to iron(iii) ion biological process from the curated GO Biological Process Annotations dataset.

cellular response to iron(iii) ion Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to iron(iii) ion biological process from the curated GO Biological Process Annotations dataset.

mitochondrial respiratory chain complex iii biogenesis Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial respiratory chain complex iii biogenesis biological process from the curated GO Biological Process Annotations dataset.

respiratory chain complex iii assembly Gene Set

From GO Biological Process Annotations

genes participating in the respiratory chain complex iii assembly biological process from the curated GO Biological Process Annotations dataset.

phosphatidylinositol 3-kinase complex, class iii Gene Set

From GO Cellular Component Annotations

proteins localized to the phosphatidylinositol 3-kinase complex, class iii cellular component from the curated GO Cellular Component Annotations dataset.

rna polymerase iii transcription factor complex Gene Set

From GO Cellular Component Annotations

proteins localized to the rna polymerase iii transcription factor complex cellular component from the curated GO Cellular Component Annotations dataset.

ribonuclease iii complex Gene Set

From GO Cellular Component Annotations

proteins localized to the ribonuclease iii complex cellular component from the curated GO Cellular Component Annotations dataset.

respiratory chain complex iii Gene Set

From GO Cellular Component Annotations

proteins localized to the respiratory chain complex iii cellular component from the curated GO Cellular Component Annotations dataset.

dna-directed rna polymerase iii complex Gene Set

From GO Cellular Component Annotations

proteins localized to the dna-directed rna polymerase iii complex cellular component from the curated GO Cellular Component Annotations dataset.

escrt iii complex Gene Set

From GO Cellular Component Annotations

proteins localized to the escrt iii complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial respiratory chain complex iii Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial respiratory chain complex iii cellular component from the curated GO Cellular Component Annotations dataset.

dna polymerase iii complex Gene Set

From GO Cellular Component Annotations

proteins localized to the dna polymerase iii complex cellular component from the curated GO Cellular Component Annotations dataset.

rna polymerase iii regulatory region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii regulatory region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase iii activity Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii activity molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase iii core binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii core binding molecular function from the curated GO Molecular Function Annotations dataset.

glyoxalase iii activity Gene Set

From GO Molecular Function Annotations

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

ribonuclease iii activity Gene Set

From GO Molecular Function Annotations

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

rna polymerase iii transcription factor binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii transcription factor binding molecular function from the curated GO Molecular Function Annotations dataset.

uroporphyrinogen-iii synthase activity Gene Set

From GO Molecular Function Annotations

genes performing the uroporphyrinogen-iii synthase activity molecular function from the curated GO Molecular Function Annotations dataset.

exodeoxyribonuclease iii activity Gene Set

From GO Molecular Function Annotations

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

group iii metabotropic glutamate receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the group iii metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

ω-agatoxin IIIA Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ω-agatoxin IIIA ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Bc-III Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the Bc-III ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

vMIP-III Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the vMIP-III ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

GnRH III Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the GnRH III ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

peptide III-BTD Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the peptide III-BTD ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

jingzhaotoxin-III Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the jingzhaotoxin-III ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Hexacarboxylporphyrin III Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Hexacarboxylporphyrin III metabolite from the curated HMDB Metabolites of Enzymes dataset.

Angiotensin III Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Angiotensin III metabolite from the curated HMDB Metabolites of Enzymes dataset.

Coproporphyrinogen III Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Coproporphyrinogen III metabolite from the curated HMDB Metabolites of Enzymes dataset.

Heptacarboxylporphyrin III Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Heptacarboxylporphyrin III metabolite from the curated HMDB Metabolites of Enzymes dataset.

adenosylcob(III)yrinic acid a,c-diamide Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the adenosylcob(III)yrinic acid a,c-diamide metabolite from the curated HMDB Metabolites of Enzymes dataset.

Coproporphyrin III Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Coproporphyrin III metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uroporphyrinogen III Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uroporphyrinogen III metabolite from the curated HMDB Metabolites of Enzymes dataset.

decreased mitochondrial complex iii activity in liver tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased mitochondrial complex iii activity in liver tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased activity of mitochondrial complex iii Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial complex iii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced antithrombin iii activity Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced antithrombin iii activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased platelet glycoprotein iib-iiia Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased platelet glycoprotein iib-iiia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Antithrombin III Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

methylglyoxal degradation III Gene Set

From HumanCyc Pathways

proteins participating in the methylglyoxal degradation III pathway from the HumanCyc Pathways dataset.

putrescine degradation III Gene Set

From HumanCyc Pathways

proteins participating in the putrescine degradation III pathway from the HumanCyc Pathways dataset.

lactose degradation III Gene Set

From HumanCyc Pathways

proteins participating in the lactose degradation III pathway from the HumanCyc Pathways dataset.

thiamin salvage III Gene Set

From HumanCyc Pathways

proteins participating in the thiamin salvage III pathway from the HumanCyc Pathways dataset.

adenine and adenosine salvage III Gene Set

From HumanCyc Pathways

proteins participating in the adenine and adenosine salvage III pathway from the HumanCyc Pathways dataset.

heme biosynthesis from uroporphyrinogen-III I Gene Set

From HumanCyc Pathways

proteins participating in the heme biosynthesis from uroporphyrinogen-III I pathway from the HumanCyc Pathways dataset.

cholesterol biosynthesis III (via desmosterol) Gene Set

From HumanCyc Pathways

proteins participating in the cholesterol biosynthesis III (via desmosterol) pathway from the HumanCyc Pathways dataset.

fatty acid α-oxidation III Gene Set

From HumanCyc Pathways

proteins participating in the fatty acid α-oxidation III pathway from the HumanCyc Pathways dataset.

oxidative ethanol degradation III Gene Set

From HumanCyc Pathways

proteins participating in the oxidative ethanol degradation III pathway from the HumanCyc Pathways dataset.

thiosulfate disproportionation III (rhodanese) Gene Set

From HumanCyc Pathways

proteins participating in the thiosulfate disproportionation III (rhodanese) pathway from the HumanCyc Pathways dataset.

Tetrapyrrole biosynthesis, uroporphyrinogen III synthase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tetrapyrrole biosynthesis, uroporphyrinogen III synthase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C2, calpain, large subunit, domain III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C2, calpain, large subunit, domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine-protein kinase, receptor class III, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine-protein kinase, receptor class III, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription factor IIIB subunit Brf1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription factor IIIB subunit Brf1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome c oxidase subunit III domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome c oxidase subunit III domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coproporphyrinogen III oxidase, oxygen-independent related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coproporphyrinogen III oxidase, oxygen-independent related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Endonuclease III-like, conserved site-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Endonuclease III-like, conserved site-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tissue factor/coagulation factor III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tissue factor/coagulation factor III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CoA-transferase family III domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CoA-transferase family III domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription factor IIIC, subunit 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription factor IIIC, subunit 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed RNA polymerase III, subunit Rpc31 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed RNA polymerase III, subunit Rpc31 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed RNA polymerase III subunit Rpc5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed RNA polymerase III subunit Rpc5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA polymerase III, clamp loader complex, gamma/delta/delta subunit, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA polymerase III, clamp loader complex, gamma/delta/delta subunit, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome c oxidase, subunit III, 4-helical bundle Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome c oxidase, subunit III, 4-helical bundle protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed RNA polymerase III subunit RPC1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed RNA polymerase III subunit RPC1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA-directed RNA polymerase III subunit RPC4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA-directed RNA polymerase III subunit RPC4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alcohol dehydrogenase class III/S-(hydroxymethyl)glutathione dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coproporphyrinogen III oxidase, aerobic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coproporphyrinogen III oxidase, aerobic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peptidase C2, calpain, domain III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peptidase C2, calpain, domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase,subfamily IIIA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase,subfamily IIIA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome c oxidase subunit III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome c oxidase subunit III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription factor IIIC, putative zinc-finger Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription factor IIIC, putative zinc-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Elongation factor G, III-V domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Elongation factor G, III-V domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Repressor of RNA polymerase III transcription Maf1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Repressor of RNA polymerase III transcription Maf1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-D-phosphohexomutase, alpha/beta/alpha domain III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-D-phosphohexomutase, alpha/beta/alpha domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Endonuclease III, iron-sulphur binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Endonuclease III, iron-sulphur binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aminotransferase class-III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aminotransferase class-III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Iodothyronine deiodinase I/III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Iodothyronine deiodinase I/III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

AdipoR/Haemolysin-III-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the AdipoR/Haemolysin-III-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RNA polymerase III subunit RPC82-related, helix-turn-helix Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RNA polymerase III subunit RPC82-related, helix-turn-helix protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribonuclease III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribonuclease III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribonuclease III domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribonuclease III domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Urocortin II/III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Urocortin II/III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription factor IIIC, 90kDa subunit, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription factor IIIC, 90kDa subunit, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vitamin D binding protein, domain III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vitamin D binding protein, domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TRAPP III complex, Trs85 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TRAPP III complex, Trs85 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RNA polymerase III, subunit Rpc25 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RNA polymerase III, subunit Rpc25 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Secretogranin III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Secretogranin III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sirtuin, class III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sirtuin, class III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coproporphyrinogen III oxidase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coproporphyrinogen III oxidase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Endonuclease III-like, iron-sulphur cluster loop motif Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Endonuclease III-like, iron-sulphur cluster loop motif protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Antithrombin-III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Antithrombin-III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RNA polymerase III Rpc82, C -terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RNA polymerase III Rpc82, C -terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-D-phosphohexomutase, alpha/beta/alpha I/II/III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-D-phosphohexomutase, alpha/beta/alpha I/II/III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hly-III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hly-III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily hydrolase, subfamily IIID Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily hydrolase, subfamily IIID protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CoA-transferase family III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CoA-transferase family III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

HAD-superfamily phosphatase, subfamily IIIC Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the HAD-superfamily phosphatase, subfamily IIIC protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Exonuclease, RNase T/DNA polymerase III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Exonuclease, RNase T/DNA polymerase III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

KATO III Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles

genes with high or low copy number in KATO III relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.

KATO III Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles

genes with high or low expression in KATO III relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset.

KATO III Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles

genes mutated in the KATO III cell line from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_A549_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_A549_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_H1299_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_H1299_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_NCIH2073_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_NCIH2073_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-A84189516_BACCATIN III_VCAP_24.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-A84189516_BACCATIN III_VCAP_24.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_SW620_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_SW620_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_HCC515_24.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_HCC515_24.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_SKLU1_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_SKLU1_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_HA1E_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_HA1E_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_HA1E_24.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_HA1E_24.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-A84189516_BACCATIN III_PC3_24.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-A84189516_BACCATIN III_PC3_24.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_A375_24.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_A375_24.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_HCC515_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_HCC515_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K23875128_Rho kinase inhibitor III [rockout]_OV7_6.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K23875128_Rho kinase inhibitor III [rockout]_OV7_6.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

abnormal cerebellum vermis lobule iii morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellum vermis lobule iii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

glycogen storage disease iiia Gene Set

From OMIM Gene-Disease Associations

genes associated with the glycogen storage disease iiia phenotype from the curated OMIM Gene-Disease Associations dataset.

glycogen storage disease iiib Gene Set

From OMIM Gene-Disease Associations

genes associated with the glycogen storage disease iiib phenotype from the curated OMIM Gene-Disease Associations dataset.

[glutaric aciduria iii] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [glutaric aciduria iii] phenotype from the curated OMIM Gene-Disease Associations dataset.

keratosis palmoplantaris striata iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the keratosis palmoplantaris striata iii phenotype from the curated OMIM Gene-Disease Associations dataset.

mucolipidosis iii gamma Gene Set

From OMIM Gene-Disease Associations

genes associated with the mucolipidosis iii gamma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to antithrombin iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

apoa-i and apoc-iii deficiency, combined Gene Set

From OMIM Gene-Disease Associations

genes associated with the apoa-i and apoc-iii deficiency, combined phenotype from the curated OMIM Gene-Disease Associations dataset.

apolipoprotein c-iii deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the apolipoprotein c-iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

mucolipidosis iii alpha/beta Gene Set

From OMIM Gene-Disease Associations

genes associated with the mucolipidosis iii alpha/beta phenotype from the curated OMIM Gene-Disease Associations dataset.

Metabotropic glutamate receptor group III pathway Gene Set

From PANTHER Pathways

proteins participating in the Metabotropic glutamate receptor group III pathway pathway from the PANTHER Pathways dataset.

iii Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Signaling events mediated by HDAC Class III Gene Set

From PID Pathways

proteins participating in the Signaling events mediated by HDAC Class III pathway from the PID Pathways dataset.

RNA Polymerase III Transcription Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Transcription pathway from the Reactome Pathways dataset.

RNA Polymerase III Chain Elongation Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Chain Elongation pathway from the Reactome Pathways dataset.

MPS IIIA - Sanfilippo syndrome A Gene Set

From Reactome Pathways

proteins participating in the MPS IIIA - Sanfilippo syndrome A pathway from the Reactome Pathways dataset.

RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase I, RNA Polymerase III, and Mitochondrial Transcription pathway from the Reactome Pathways dataset.

MPS IIID - Sanfilippo syndrome D Gene Set

From Reactome Pathways

proteins participating in the MPS IIID - Sanfilippo syndrome D pathway from the Reactome Pathways dataset.

RNA Polymerase III Transcription Termination Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Transcription Termination pathway from the Reactome Pathways dataset.

RNA Polymerase III Abortive And Retractive Initiation Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Abortive And Retractive Initiation pathway from the Reactome Pathways dataset.

RNA Polymerase III Transcription Initiation Gene Set

From Reactome Pathways

proteins participating in the RNA Polymerase III Transcription Initiation pathway from the Reactome Pathways dataset.

MPS IIIB - Sanfilippo syndrome B Gene Set

From Reactome Pathways

proteins participating in the MPS IIIB - Sanfilippo syndrome B pathway from the Reactome Pathways dataset.

MPS IIIC - Sanfilippo syndrome C Gene Set

From Reactome Pathways

proteins participating in the MPS IIIC - Sanfilippo syndrome C pathway from the Reactome Pathways dataset.

kato-iii cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Fanconi anemia, complementation group O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcytic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcytic anemia 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.

Diamond-Blackfan anemia 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sideroblastic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia 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.

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.

Diamond-Blackfan anemia 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diamond-Blackfan anemia 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diamond-Blackfan anemia 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group G 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.

Megaloblastic anemia due to inborn errors of metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia due to hexokinase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypochromic microcytic anemia with iron overload Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypochromic microcytic anemia with iron overload phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplastic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, with hemolytic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fanconi anemia, complementation group D2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fanconi anemia, complementation group D2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adenylate kinase deficiency, hemolytic anemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adenylate kinase deficiency, hemolytic anemia due to 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.

Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

FA core complex (Fanconi anemia core complex) Gene Set

From CORUM Protein Complexes

proteins in the FA core complex (Fanconi anemia core complex) protein complex from the CORUM Protein Complexes dataset.

FA core complex 1 (Fanconi anemia core complex 1) Gene Set

From CORUM Protein Complexes

proteins in the FA core complex 1 (Fanconi anemia core complex 1) protein complex from the CORUM Protein Complexes dataset.

FA complex (Fanconi anemia complex), cytoplasmic Gene Set

From CORUM Protein Complexes

proteins in the FA complex (Fanconi anemia complex), cytoplasmic protein complex from the CORUM Protein Complexes dataset.

FA complex (Fanconi anemia complex) Gene Set

From CORUM Protein Complexes

proteins in the FA complex (Fanconi anemia complex) protein complex from the CORUM Protein Complexes dataset.

Anemia, Iron-Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Iron-Deficiency from the curated CTD Gene-Disease Associations dataset.

Anemia, Aplastic Gene Set

From CTD Gene-Disease Associations

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

FANCONI ANEMIA, COMPLEMENTATION GROUP C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP C from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 4 from the curated CTD Gene-Disease Associations dataset.

Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP E from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP F from the curated CTD Gene-Disease Associations dataset.

Anemia, Diamond-Blackfan, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Diamond-Blackfan, 2 from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group J from the curated CTD Gene-Disease Associations dataset.

Anemia, sideroblastic spinocerebellar ataxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, sideroblastic spinocerebellar ataxia from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group B from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group N Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group N from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset.

MEGALOBLASTIC ANEMIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MEGALOBLASTIC ANEMIA 1 from the curated CTD Gene-Disease Associations dataset.

Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.

Myopathy with lactic acidosis and sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia Gene Set

From CTD Gene-Disease Associations

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

Anemia, Hemolytic Gene Set

From CTD Gene-Disease Associations

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

Anemia, Diamond-Blackfan Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Diamond-Blackfan from the curated CTD Gene-Disease Associations dataset.

Anemia, Megaloblastic Gene Set

From CTD Gene-Disease Associations

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

Anemia, Sideroblastic Gene Set

From CTD Gene-Disease Associations

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

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Anemia, Sickle Cell Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Sickle Cell from the curated CTD Gene-Disease Associations dataset.

SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP D2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP D2 from the curated CTD Gene-Disease Associations dataset.

Thiamine responsive megaloblastic anemia syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thiamine responsive megaloblastic anemia syndrome from the curated CTD Gene-Disease Associations dataset.

Anemia, Macrocytic Gene Set

From CTD Gene-Disease Associations

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

X-linked sideroblastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.

Fanconi Anemia, Complementation Group I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group I from the curated CTD Gene-Disease Associations dataset.

FANCONI ANEMIA, COMPLEMENTATION GROUP O Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP O from the curated CTD Gene-Disease Associations dataset.

Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Iron-Refractory Iron Deficiency Anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iron-Refractory Iron Deficiency Anemia from the curated CTD Gene-Disease Associations dataset.

Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.

Anemia Gene Set

From CTD Gene-Disease Associations

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

Fanconi Anemia, Complementation Group D1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fanconi Anemia, Complementation Group D1 from the curated CTD Gene-Disease Associations dataset.

DIAMOND-BLACKFAN ANEMIA 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DIAMOND-BLACKFAN ANEMIA 6 from the curated CTD Gene-Disease Associations dataset.

Anemia, Diamond-Blackfan, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Diamond-Blackfan, 3 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 9 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 8 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 5 from the curated CTD Gene-Disease Associations dataset.

Diamond-Blackfan Anemia 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 7 from the curated CTD Gene-Disease Associations dataset.

Anemia, Refractory Gene Set

From CTD Gene-Disease Associations

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

Anemia, Hypochromic Microcytic, With Iron Overload Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hypochromic Microcytic, With Iron Overload from the curated CTD Gene-Disease Associations dataset.

Anemia, Hemolytic, Autoimmune Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Autoimmune from the curated CTD Gene-Disease Associations dataset.

Anemia, Neonatal Gene Set

From CTD Gene-Disease Associations

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

Diamond-Blackfan Anemia 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diamond-Blackfan Anemia 10 from the curated CTD Gene-Disease Associations dataset.

Anemia, hypochromic microcytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, hypochromic microcytic from the curated CTD Gene-Disease Associations dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Anemia Gene Set

From dbGAP Gene-Trait Associations

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

Anemia, Sickle Cell Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Anemia, Sickle Cell in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

fanconi's anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease fanconi's anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

diamond-blackfan anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

sideroblastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hemolytic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

normocytic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

aplastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

iron deficiency anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease iron deficiency anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

hemolytic anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease hemolytic anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

microcytic anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease microcytic anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

normocytic anemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease normocytic anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fanconi's anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sickle cell anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

folic acid deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pernicious anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anemia of prematurity Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

iron deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

neonatal anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sideroblastic anemia with spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

microcytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myelophthisic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pyridoxine-responsive sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypochromic microcytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

macrocytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

normocytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemolytic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

diamond-blackfan anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pyridoxine deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sideroblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypochromic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

protein-deficiency anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

megaloblastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

aplastic anemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anemia; hepatitis c Gene Set

From GAD Gene-Disease Associations

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

anemia; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria, cerebral; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; thrombocytopenic purpura, idiopathic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary nonspherocytic hemolytic anemia (hnsha). Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary nonspherocytic hemolytic anemia (hnsha). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; fanconi syndrome; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; fanconi syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sickle cell anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, malaria related; malaria, cerebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria; parasitemia Gene Set

From GAD Gene-Disease Associations

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

anemia, iron deficiency Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; pain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bloom syndrome; fanconi's anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bloom syndrome; fanconi's anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia in pregnancy Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; Gene Set

From GAD Gene-Disease Associations

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

sickle cell anemia; g6pd deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sickle cell anemia; g6pd deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; ischemia; recurrence; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; ischemia; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary hemolytic anemia. Gene Set

From GAD Gene-Disease Associations

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

anemia, aplastic Gene Set

From GAD Gene-Disease Associations

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

cholelithiasis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholelithiasis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; lung diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; lung diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; brain death Gene Set

From GAD Gene-Disease Associations

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

anemia; kidney diseases; red-cell aplasia, pure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; osteomyelitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; osteomyelitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; anemia; chronic disease Gene Set

From GAD Gene-Disease Associations

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

diamond-blackfan anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; gallbladder diseases; hyperbilirubinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; gallbladder diseases; hyperbilirubinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stroke; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stroke; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria Gene Set

From GAD Gene-Disease Associations

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

fanconi anemia Gene Set

From GAD Gene-Disease Associations

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

anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aplastic anemia, acquired Gene Set

From GAD Gene-Disease Associations

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

alpha-thalassemia; anemia; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disease; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disease; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia, sickle cell; cholelithiasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; cholelithiasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malarial anemia and cerebral malaria Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; hepatitis c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, hemolytic Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malarial anemia in ghanaian children Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell Gene Set

From GAD Gene-Disease Associations

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

anemia, hemolytic; hepatitis c, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, hemolytic; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta-thalassemia; hemoglobinopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta-thalassemia; hemoglobinopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; hepatitis c, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; malaria; malaria, falciparum; parasitemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; malaria; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic nonspherocytic anemia. Gene Set

From GAD Gene-Disease Associations

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

aplastic anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; inflammation; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

alpha-thalassemia; anemia, hypochromic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, hypochromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia Gene Set

From GAD Gene-Disease Associations

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

anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary hemolytic anemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; arterial occlusive diseases; constriction, pathologic; ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; arterial occlusive diseases; constriction, pathologic; ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; polycythemia vera Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, hypochromic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, hypochromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic hemolytic anemia Gene Set

From GAD Gene-Disease Associations

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

macrothrombocytopenia and anemia Gene Set

From GAD Gene-Disease Associations

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

anemia; chronic renal failure; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

anemia; hemoglobinopathies; iron overload; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; hemoglobinopathies; iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; bacteremia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; bacteremia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency Gene Set

From GAD Gene-Disease Associations

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

sickle cell anemia; thalassemia; gilbert syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sickle cell anemia; thalassemia; gilbert syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, iron-deficiency; avitaminosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; avitaminosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia Gene Set

From GeneRIF Biological Term Annotations

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

Systolic blood pressure in sickle cell anemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Sickle cell anemia (haemolysis) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sickle cell anemia (haemolysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Ribavirin-induced anemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

iron deficiency anemia Gene Set

From GWASdb SNP-Disease Associations

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

anemia Gene Set

From GWASdb SNP-Disease Associations

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

hemolytic anemia Gene Set

From GWASdb SNP-Disease Associations

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

microcytic anemia Gene Set

From GWASdb SNP-Disease Associations

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

sickle cell anemia Gene Set

From GWASdb SNP-Disease Associations

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

normocytic anemia Gene Set

From GWASdb SNP-Disease Associations

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

anemia Gene Set

From GWASdb SNP-Phenotype Associations

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

anemia due to reduced life span of red cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

hemolytic anemia Gene Set

From GWASdb SNP-Phenotype Associations

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

iron deficiency anemia Gene Set

From HPO Gene-Disease Associations

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

microcytic anemia Gene Set

From HPO Gene-Disease Associations

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

nonspherocytic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

fava bean-induced hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the fava bean-induced hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thiamine-responsive megaloblastic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the thiamine-responsive megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

refractory anemia Gene Set

From HPO Gene-Disease Associations

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

anemia due to reduced life span of red cells Gene Set

From HPO Gene-Disease Associations

genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic anemia Gene Set

From HPO Gene-Disease Associations

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

hypochromic anemia Gene Set

From HPO Gene-Disease Associations

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

refractory macrocytic anemia Gene Set

From HPO Gene-Disease Associations

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

heinz body anemia Gene Set

From HPO Gene-Disease Associations

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

compensated hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

anemia of inadequate production Gene Set

From HPO Gene-Disease Associations

genes associated with the anemia of inadequate production phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypochromic microcytic anemia Gene Set

From HPO Gene-Disease Associations

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

folate-responsive megaloblastic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the folate-responsive megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

normocytic hypoplastic anemia Gene Set

From HPO Gene-Disease Associations

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

macrocytic anemia Gene Set

From HPO Gene-Disease Associations

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