Name

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.

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.

Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, with normal red cell morphology Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, autosomal recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal tubular acidosis, distal, autosomal recessive from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset.

familial distal renal tubular acidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

distal renal tubular acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the distal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal tubular acidosis, distal, ar Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular acidosis, distal, ar phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular acidosis, distal, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular acidosis, distal, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular acidosis, distal, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular acidosis, distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

generalized distal tubular acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Osteopetrosis with renal tubular acidosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis with renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis with progressive nerve deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis with progressive nerve deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acidosis, Renal Tubular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acidosis, Renal Tubular from the curated CTD Gene-Disease Associations dataset.

Osteopetrosis with renal tubular acidosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteopetrosis with renal tubular acidosis from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

renal tubular acidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

proximal renal tubular acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the proximal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal tubular acidosis Gene Set

From HPO Gene-Disease Associations

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

bicarbonate-wasting renal tubular acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the bicarbonate-wasting renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Acidosis, Renal Tubular Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

renal tubular acidosis Gene Set

From MPO Gene-Phenotype Associations

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

osteopetrosis, autosomal recessive 3, with renal tubular acidosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, autosomal recessive 3, with renal tubular acidosis phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular acidosis, proximal, with ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular acidosis, proximal, with ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular acidosis with deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular acidosis with deafness 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.

distal tubular epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

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.

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.

myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated OMIM Gene-Disease 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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, 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.

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.

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.

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, 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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, 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, 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.

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.

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.

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.

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.

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.

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.

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.

coombs-positive hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

autoimmune hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

microangiopathic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

chronic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

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

episodic hemolytic anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the episodic hemolytic 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 Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Hemolytic 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.

Anemia, Hemolytic, Autoimmune Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

decreased susceptibility to autoimmune hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to autoimmune hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hemolytic anemia due to phosphofructokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione peroxidase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hemolytic, due to umph1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, neonatal hemolytic, fatal and near-fatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, neonatal hemolytic, fatal and near-fatal phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to g6pd deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione synthetase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione synthetase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to adenylate kinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to adenylate kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to glutathione reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to glutathione reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

{systemic lupus erythematosus with hemolytic anemia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {systemic lupus erythematosus with hemolytic anemia} 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.

hemolytic anemia due to triosephosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to triosephosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia due to hexokinase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia due to hexokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set

From Reactome Pathways

proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.

RENAL TUBULAR DYSGENESIS Gene Set

From CTD Gene-Disease Associations

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

renal tubular transport disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

mucinous tubular and spindle renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mucinous tubular and spindle renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

renal tubular transport disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal tubular damage Gene Set

From GAD Gene-Disease Associations

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

renal tubular secretion Gene Set

From GO Biological Process Annotations

genes participating in the renal tubular secretion biological process from the curated GO Biological Process Annotations dataset.

increased renal tubular phosphate reabsorption Gene Set

From HPO Gene-Disease Associations

genes associated with the increased renal tubular phosphate reabsorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased renal tubular phosphate excretion Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased renal tubular phosphate excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

parathormone-independent increased renal tubular calcium reabsorption Gene Set

From HPO Gene-Disease Associations

genes associated with the parathormone-independent increased renal tubular calcium reabsorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal tubular dysfunction Gene Set

From HPO Gene-Disease Associations

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

Renal Tubular Transport, Inborn Errors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Renal Tubular Transport, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

renal tubular necrosis Gene Set

From MPO Gene-Phenotype Associations

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

renal tubular dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene Set

From GAD Gene-Disease Associations

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

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.

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.

renal distal tubule Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Myopathy with lactic acidosis, hereditary Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy with lactic acidosis, hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acidosis, Lactic Gene Set

From CTD Gene-Disease Associations

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

Acidosis Gene Set

From CTD Gene-Disease Associations

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

Myopathy with Lactic Acidosis, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy with Lactic Acidosis, Hereditary from the curated CTD Gene-Disease Associations dataset.

Acidosis, Respiratory Gene Set

From CTD Gene-Disease Associations

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

lactic acidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

metabolic acidosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acidosis, lactic Gene Set

From GAD Gene-Disease Associations

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

acidosis Gene Set

From GAD Gene-Disease Associations

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

acidosis Gene Set

From GeneRIF Biological Term Annotations

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

MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

chronic lactic acidosis Gene Set

From HPO Gene-Disease Associations

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

respiratory acidosis Gene Set

From HPO Gene-Disease Associations

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

congenital lactic acidosis Gene Set

From HPO Gene-Disease Associations

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

severe lactic acidosis Gene Set

From HPO Gene-Disease Associations

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

mixed respiratory and metabolic acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the mixed respiratory and metabolic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hyperkalemic metabolic acidosis Gene Set

From HPO Gene-Disease Associations

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

chronic metabolic acidosis Gene Set

From HPO Gene-Disease Associations

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

acidosis Gene Set

From HPO Gene-Disease Associations

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

metabolic acidosis Gene Set

From HPO Gene-Disease Associations

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

chronic acidosis Gene Set

From HPO Gene-Disease Associations

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

stress/infection-induced lactic acidosis Gene Set

From HPO Gene-Disease Associations

genes associated with the stress/infection-induced lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hyperchloremic acidosis Gene Set

From HPO Gene-Disease Associations

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

episodic metabolic acidosis Gene Set

From HPO Gene-Disease Associations

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

hyperchloremic metabolic acidosis Gene Set

From HPO Gene-Disease Associations

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

lactic acidosis Gene Set

From HPO Gene-Disease Associations

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

Acidosis, Lactic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Acidosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

acidosis Gene Set

From MPO Gene-Phenotype Associations

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

myopathy with lactic acidosis, hereditary Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy with lactic acidosis, hereditary phenotype from the curated OMIM Gene-Disease Associations dataset.

Myopathy, tubular aggregate, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, tubular aggregate, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenia, limb-girdle, with tubular aggregates Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenia, limb-girdle, with tubular aggregates phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy with tubular aggregates Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy with tubular aggregates phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

endoplasmic reticulum tubular network Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the endoplasmic reticulum tubular network cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet dense tubular network membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet dense tubular network membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

platelet dense tubular network Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the platelet dense tubular network cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

endoplasmic reticulum tubular network Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the endoplasmic reticulum tubular network cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

tubular endosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Kidney Tubular Necrosis, Acute Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Kidney Tubular Necrosis, Acute from the curated CTD Gene-Disease Associations dataset.

gastric tubular adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute kidney tubular necrosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tubular adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tubular Gene Set

From GeneRIF Biological Term Annotations

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

positive regulation of endoplasmic reticulum tubular network organization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of endoplasmic reticulum tubular network organization biological process from the curated GO Biological Process Annotations dataset.

regulation of endoplasmic reticulum tubular network organization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of endoplasmic reticulum tubular network organization biological process from the curated GO Biological Process Annotations dataset.

endoplasmic reticulum tubular network organization Gene Set

From GO Biological Process Annotations

genes participating in the endoplasmic reticulum tubular network organization biological process from the curated GO Biological Process Annotations dataset.

protein localization to endoplasmic reticulum tubular network Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to endoplasmic reticulum tubular network biological process from the curated GO Biological Process Annotations dataset.

endoplasmic reticulum tubular network Gene Set

From GO Cellular Component Annotations

proteins localized to the endoplasmic reticulum tubular network cellular component from the curated GO Cellular Component Annotations dataset.

platelet dense tubular network membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet dense tubular network membrane cellular component from the curated GO Cellular Component Annotations dataset.

platelet dense tubular network Gene Set

From GO Cellular Component Annotations

proteins localized to the platelet dense tubular network cellular component from the curated GO Cellular Component Annotations dataset.

tubular endosome Gene Set

From GO Cellular Component Annotations

proteins localized to the tubular endosome cellular component from the curated GO Cellular Component Annotations dataset.

cortically dense long tubular bones Gene Set

From HPO Gene-Disease Associations

genes associated with the cortically dense long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tubular atrophy Gene Set

From HPO Gene-Disease Associations

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

periosteal thickening of long tubular bones Gene Set

From HPO Gene-Disease Associations

genes associated with the periosteal thickening of long tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

epiphyseal deformities of tubular bones Gene Set

From HPO Gene-Disease Associations

genes associated with the epiphyseal deformities of tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tubular basement membrane disintegration Gene Set

From HPO Gene-Disease Associations

genes associated with the tubular basement membrane disintegration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short tubular bones (hand) Gene Set

From HPO Gene-Disease Associations

genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

flattened, squared-off epiphyses of tubular bones Gene Set

From HPO Gene-Disease Associations

genes associated with the flattened, squared-off epiphyses of tubular bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aorta tubular hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

tubular nephritis Gene Set

From MPO Gene-Phenotype Associations

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

myasthenia, congenital, with tubular aggregates 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenia, congenital, with tubular aggregates 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, tubular aggregate Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, tubular aggregate phenotype from the curated OMIM Gene-Disease Associations dataset.

?myopathy, tubular aggregate, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?myopathy, tubular aggregate, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

proximale tubular epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

proximale tubular epithelium cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Atypical hemolytic-uremic syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atypical hemolytic-uremic syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atypical hemolytic-uremic syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atypical hemolytic-uremic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

atypical hemolytic-uremic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the atypical hemolytic-uremic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atypical Hemolytic Uremic Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atypical Hemolytic Uremic Syndrome from the curated CTD Gene-Disease Associations dataset.

Hemolytic-Uremic Syndrome Gene Set

From CTD Gene-Disease Associations

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

hemolytic-uremic syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hemolytic-uremic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemolytic disease of the newborn Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

hemolytic-uremic syndrome; kidney failure, acute Gene Set

From GAD Gene-Disease Associations

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

escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

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

haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

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

hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

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

hemolytic uremic syndrome Gene Set

From GAD Gene-Disease Associations

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

hemolytic disease Gene Set

From GAD Gene-Disease Associations

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

hemolytic-uremic syndrome; purpura, thrombotic thrombocytopenic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemolytic-uremic syndrome; purpura, thrombotic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atypical hemolytic uremic syndrome Gene Set

From GAD Gene-Disease Associations

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

haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set

From GAD Gene-Disease Associations

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

hemolytic Gene Set

From GeneRIF Biological Term Annotations

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

hemolytic-uremic syndrome Gene Set

From HPO Gene-Disease Associations

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

macrocytic hemolytic disease Gene Set

From HPO Gene-Disease Associations

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

spontaneous hemolytic crises Gene Set

From HPO Gene-Disease Associations

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

Hemolytic-Uremic Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

{hemolytic uremic syndrome, atypical, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hemolytic uremic syndrome, atypical, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hemolytic uremic syndrome, atypical, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

diabetes, post-renal transplant; post-renal transplant diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, post-renal transplant; post-renal transplant diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, renal cell; kidney neoplasms; renal cell carcinoma; von hippel-lindau disease; von hippel-lindau syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, renal cell; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, renal cell; diabetes mellitus; hypertension; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, renal cell; colonic neoplasms; kidney neoplasms; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, renal cell; kidney neoplasms; neoplasm recurrence, local; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, renal cell; gilbert disease; hyperbilirubinemia; kidney neoplasms; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

carcinoma, papillary; carcinoma, renal cell; kidney neoplasms; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

renal involvement and renal sequelae Gene Set

From GAD Gene-Disease Associations

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

Distal hereditary motor neuronopathy 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, X-linked 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal myopathy Markesbery-Griggs type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, distal, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 5B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal arthrogryposis type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal arthrogryposis type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 7B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal hereditary motor neuronopathy type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal arthrogryposis type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal arthrogryposis type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, distal, type 5d Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, distal, type 5d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, distal, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, distal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, autosomal recessive 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, Distal, with Anterior Tibial Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.

Welander distal myopathy, Swedish type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Distal Hereditary Motor, Type IIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset.

Neuronopathy, Distal Hereditary Motor, Type V Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset.

Jacobsen Distal 11q Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Jacobsen Distal 11q Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

Neuronopathy, Distal Hereditary Motor, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset.

Arthrogryposis, Distal, Type 4 Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.

ARTHROGRYPOSIS, DISTAL, TYPE 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ARTHROGRYPOSIS, DISTAL, TYPE 1A from the curated CTD Gene-Disease Associations dataset.

Distal myopathy, Nonaka type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset.

NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset.

Arthrogryposis multiplex congenita, distal, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset.

Distal Myopathies Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.

Neuronopathy, Distal Hereditary Motor, Type Viib Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

Distal arthrogryposis type 2B Gene Set

From CTD Gene-Disease Associations

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

distal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

distal hereditary motor neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

distal arthrogryposis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

proximal chromosome 9p to q and distal chromosome 9q Gene Set

From GAD Gene-Disease Associations

genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

distal myopathies; myositis, inclusion body Gene Set

From GAD Gene-Disease Associations

genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

distal Gene Set

From GeneRIF Biological Term Annotations

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

proximal/distal pattern formation involved in nephron development Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations dataset.

metanephric distal convoluted tubule development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation involved in metanephric nephron development Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations dataset.

metanephric distal tubule development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations dataset.

metanephric distal tubule morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations dataset.

distal tubule morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations dataset.

distal tubule development Gene Set

From GO Biological Process Annotations

genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations dataset.

lung proximal/distal axis specification Gene Set

From GO Biological Process Annotations

genes participating in the lung proximal/distal axis specification biological process from the curated GO Biological Process Annotations dataset.

polarity specification of proximal/distal axis Gene Set

From GO Biological Process Annotations

genes participating in the polarity specification of proximal/distal axis biological process from the curated GO Biological Process Annotations dataset.

proximal/distal axis specification Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations dataset.

distal convoluted tubule development Gene Set

From GO Biological Process Annotations

genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations dataset.

rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii distal enhancer sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii distal enhancer sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations dataset.

wide tufts of distal phalanges Gene Set

From HPO Gene-Disease Associations

genes associated with the wide tufts of distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tapering pointed ends of distal finger phalanges Gene Set

From HPO Gene-Disease Associations

genes associated with the tapering pointed ends of distal finger phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal upper limb muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the distal upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal widening of metacarpals Gene Set

From HPO Gene-Disease Associations

genes associated with the distal widening of metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late-onset distal muscle weakness Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired distal vibration sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired distal vibration sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the broad distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

duplication of distal phalanx of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the duplication of distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

partial duplication of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the partial duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired distal tactile sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired distal tactile sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

duplication of the distal phalanx of hand Gene Set

From HPO Gene-Disease Associations

genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal phalanges of all fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the broad distal phalanges of all fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

duplication of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerosis of distal finger phalanx Gene Set

From HPO Gene-Disease Associations

genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

trapezoidal distal femoral condyles Gene Set

From HPO Gene-Disease Associations

genes associated with the trapezoidal distal femoral condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

partial duplication of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dysplastic distal thumb phalanges with a central hole Gene Set

From HPO Gene-Disease Associations

genes associated with the dysplastic distal thumb phalanges with a central hole phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

widened distal phalanges Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal femoral epiphysis Gene Set

From HPO Gene-Disease Associations

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

small distal femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the small distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

partial duplication of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal hallux Gene Set

From HPO Gene-Disease Associations

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

absent distal interphalangeal creases Gene Set

From HPO Gene-Disease Associations

genes associated with the absent distal interphalangeal creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

slender distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the slender distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the broad distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal ulnar hypoplasia Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive distal muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

distal upper limb amyotrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the distal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bifid distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the bifid distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal lower limb amyotrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the distal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal lower limb muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the distal lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

decreased distal sensory nerve action potential Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased distal sensory nerve action potential phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal femoral metaphyseal abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the distal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal tapering of metatarsals Gene Set

From HPO Gene-Disease Associations

genes associated with the distal tapering of metatarsals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal ileal atresia Gene Set

From HPO Gene-Disease Associations

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

distal tapering femur Gene Set

From HPO Gene-Disease Associations

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

ivory epiphyses of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the ivory epiphyses of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

duplication of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the duplication of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic distal humeri Gene Set

From HPO Gene-Disease Associations

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

complete duplication of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the complete duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal phalanx of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the broad distal phalanx of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal amyotrophy Gene Set

From HPO Gene-Disease Associations

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

broad distal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the broad distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

wide distal femoral metaphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the wide distal femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal shortening of limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the distal shortening of limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteolytic defects of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal sensory impairment of all modalities Gene Set

From HPO Gene-Disease Associations

genes associated with the distal sensory impairment of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fifth finger distal phalanx clinodactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the fifth finger distal phalanx clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

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

duplication of the distal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

club-shaped distal femur Gene Set

From HPO Gene-Disease Associations

genes associated with the club-shaped distal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

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

shortening of all distal phalanges of the fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the shortening of all distal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal/middle symphalangism of 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the distal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

distal femoral bowing Gene Set

From HPO Gene-Disease Associations

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

long distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal muscle weakness Gene Set

From HPO Gene-Disease Associations

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

absent distal phalanges Gene Set

From HPO Gene-Disease Associations

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

distal symphalangism Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

partial duplication of the distal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the partial duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bifid distal phalanx of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the bifid distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypermobility of distal interphalangeal joints Gene Set

From HPO Gene-Disease Associations

genes associated with the hypermobility of distal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular distal femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal sensory impairment Gene Set

From HPO Gene-Disease Associations

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

duplication of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive distal muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tapered distal phalanges of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the tapered distal phalanges of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal peripheral sensory neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

complete duplication of distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the complete duplication of distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

acroosteolysis of distal phalanges (feet) Gene Set

From HPO Gene-Disease Associations

genes associated with the acroosteolysis of distal phalanges (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal tibial bowing Gene Set

From HPO Gene-Disease Associations

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

distal urethral duplication Gene Set

From HPO Gene-Disease Associations

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

distal sensory loss of all modalities Gene Set

From HPO Gene-Disease Associations

genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

enlargement of the distal femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the enlargement of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal arthrogryposis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal symphalangism (hands) Gene Set

From HPO Gene-Disease Associations

genes associated with the distal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired distal proprioception Gene Set

From HPO Gene-Disease Associations

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

absent fourth finger distal interphalangeal crease Gene Set

From HPO Gene-Disease Associations

genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Distal-less-like homeobox protein, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Distal-less-like homeobox protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

dilated distal convoluted tubules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dilated distal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal distal convoluted tubule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal distal visceral endoderm morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal proximal-distal axis patterning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent distal visceral endoderm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset.

neuronopathy, distal hereditary motor, type vi Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuronopathy, distal hereditary motor, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, distal, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuronopathy, distal hereditary motor, type vb Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuronopathy, distal hereditary motor, type vb phenotype from the curated OMIM Gene-Disease Associations dataset.

neuronopathy, distal hereditary motor, type viia Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuronopathy, distal hereditary motor, type viia phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis, distal, type 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthrogryposis, distal, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis, distal, type 3 Gene Set

From OMIM Gene-Disease Associations

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

spinal muscular atrophy, chronic distal, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

neuronopathy, distal hereditary motor, type iid Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset.

arthyrgryposis, distal, type 2b Gene Set

From OMIM Gene-Disease Associations

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

chromosome 22q11.2 deletion syndrome, distal Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, jerash type Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis, distal, type 2b Gene Set

From OMIM Gene-Disease Associations

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

arthrogryposis, distal, type 2a Gene Set

From OMIM Gene-Disease Associations

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

welander distal myopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, distal 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

laing distal myopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

?neuronopathy, distal hereditary motor, type iic Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?neuronopathy, distal hereditary motor, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type va Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis multiplex congenita, distal, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthrogryposis multiplex congenita, distal, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis multiplex congenita, distal, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthrogryposis multiplex congenita, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, distal, with anterior tibial onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, x-linked 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type viib Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis, distal, type 1b Gene Set

From OMIM Gene-Disease Associations

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

spinal muscular atrophy, distal, congenital nonprogressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis, distal, type 5d Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthrogryposis, distal, type 5d phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, distal, tateyama type Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.

neuropathy, distal hereditary motor, type iia Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.

distal tip Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

distal tip cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue distal tip 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.

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.

Microcytic anemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcytic anemia 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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, 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.

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.

Heinz Body Anemias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heinz Body Anemias 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.

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.

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.

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.

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.

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.

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.

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, 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, 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.

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.

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.

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.

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.

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, 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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, 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, 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.

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.

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; 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.

anemiabrca Gene Set

From GeneRIF Biological Term Annotations

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

anemiafagene Gene Set

From GeneRIF Biological Term Annotations

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

anemias Gene Set

From GeneRIF Biological Term Annotations

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

Sickle Cell Anemia_Endothelial cell_GSE9877 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Sickle Cell Anemia_Endothelial cell_GSE9877 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases 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.

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.

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.

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.

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.

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.

pyrimidine-responsive megaloblastic anemia Gene Set

From HPO Gene-Disease Associations

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

normochromic microcytic anemia Gene Set

From HPO Gene-Disease Associations

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

megaloblastic anemia Gene Set

From HPO Gene-Disease Associations

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

normochromic anemia Gene Set

From HPO Gene-Disease Associations

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

aplastic anemia Gene Set

From HPO Gene-Disease Associations

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

anemia Gene Set

From HPO Gene-Disease Associations

genes associated with the 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.

folate-unresponsive megaloblastic anemia Gene Set

From HPO Gene-Disease Associations

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

normocytic anemia Gene Set

From HPO Gene-Disease Associations

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

sideroblastic anemia Gene Set

From HPO Gene-Disease Associations

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

Anemia, Iron-Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Refractory, with Excess of Blasts Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anemia, Refractory, with Excess of Blasts phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Anemia, Aplastic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Fanconi Anemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Pernicious Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Diamond-Blackfan Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Megaloblastic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Sickle Cell Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Macrocytic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Hypochromic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Anemia, Refractory Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Fanconi anemia-associated protein of 24kDa Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anemia-associated protein of 24kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anemia-associated protein of 100kDa Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anemia-associated protein of 100kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anemia group I protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anemia group I protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fanconi anemia complex, subunit FancL, WD-repeat containing domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fanconi anemia complex, subunit FancL, WD-repeat containing domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

microcytic anemia Gene Set

From MPO Gene-Phenotype Associations

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

hypochromic microcytic anemia Gene Set

From MPO Gene-Phenotype Associations

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

hypochromic anemia Gene Set

From MPO Gene-Phenotype Associations

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

hyperchromic macrocytic anemia Gene Set

From MPO Gene-Phenotype Associations

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

macrocytic anemia Gene Set

From MPO Gene-Phenotype Associations

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

anemia Gene Set

From MPO Gene-Phenotype Associations

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

hypochromic macrocytic anemia Gene Set

From MPO Gene-Phenotype Associations

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

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.

fanconi anemia, complementation group p Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group p phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group q Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group q phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group i Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group i phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group j Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group j phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group l Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group l phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group m Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group m phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group n Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group n phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group o Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group o phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group b Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group b phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group f Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group f phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group g Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group g phenotype from the curated OMIM Gene-Disease Associations dataset.

heinz body anemias, alpha- Gene Set

From OMIM Gene-Disease Associations

genes associated with the heinz body anemias, alpha- phenotype from the curated OMIM Gene-Disease 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.

sickle cell anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the sickle cell anemia phenotype from the curated OMIM 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.

megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, sideroblastic, with ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, sideroblastic, with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

?diamond-blackfan anemia 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?diamond-blackfan anemia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

?diamond-blackfan anemia 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?diamond-blackfan anemia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

heinz body anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the heinz body anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

diamond-blackfan anemia 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypochromic microcytic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypochromic microcytic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group d1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group d1 phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi anemia, complementation group d2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi anemia, complementation group d2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?anemia, hypochromic microcytic, with iron overload 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?anemia, hypochromic microcytic, with iron overload 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

?anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?anemia, sideroblastic, pyridoxine-refractory, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, sideroblastic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, sideroblastic, x-linked 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.

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.

diamond-blackfan anemia 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the diamond-blackfan anemia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial myopathy and sideroblastic anemia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial myopathy and sideroblastic anemia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine-responsive megaloblastic anemia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine-responsive megaloblastic anemia syndrome 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.

aplastic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the aplastic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

{aplastic anemia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {aplastic anemia} phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, sideroblastic, pyridoxine-refractory, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, sideroblastic, pyridoxine-refractory, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, hypochromic microcytic Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, hypochromic microcytic 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.

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.

heinz body anemias, beta- Gene Set

From OMIM Gene-Disease Associations

genes associated with the heinz body anemias, beta- 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.

iron-refractory iron deficiency anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the iron-refractory iron deficiency anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

Fanconi anemia pathway Gene Set

From PID Pathways

proteins participating in the Fanconi anemia pathway pathway from the PID Pathways dataset.

Regulation of the Fanconi anemia pathway Gene Set

From Reactome Pathways

proteins participating in the Regulation of the Fanconi anemia pathway pathway from the Reactome Pathways dataset.

Defective AMN causes hereditary megaloblastic anemia 1 Gene Set

From Reactome Pathways

proteins participating in the Defective AMN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.

Defective CUBN causes hereditary megaloblastic anemia 1 Gene Set

From Reactome Pathways

proteins participating in the Defective CUBN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.

Defective TCN2 causes hereditary megaloblastic anemia Gene Set

From Reactome Pathways

proteins participating in the Defective TCN2 causes hereditary megaloblastic anemia pathway from the Reactome Pathways dataset.

Fanconi Anemia pathway Gene Set

From Reactome Pathways

proteins participating in the Fanconi Anemia pathway pathway from the Reactome Pathways 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.

fanconi anemia lymphoid cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hypodysplasia/aplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hypodysplasia/aplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal-hepatic-pancreatic dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal-hepatic-pancreatic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomagnesemia 6, renal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomagnesemia 6, renal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromophobe renal cell carcinoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromophobe renal cell carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Enamel-renal syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomagnesemia 4, renal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomagnesemia 4, renal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensorineural deafness with mild renal dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal cell carcinoma, papillary, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal cell carcinoma, papillary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomagnesemia 5, renal, with ocular involvement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomagnesemia 5, renal, with ocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal carnitine transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary leiomyomatosis and renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis renal dysfunction cholestasis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis renal dysfunction cholestasis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hypouricemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hypouricemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal coloboma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Familial renal glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial renal glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal adysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal adysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial renal hypouricemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial renal hypouricemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary renal agenesis Gene Set

From CTD Gene-Disease Associations

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

Renal Hypodysplasia, Nonsyndromic, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Hypodysplasia, Nonsyndromic, 1 from the curated CTD Gene-Disease Associations dataset.

Multicystic renal dysplasia, bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multicystic renal dysplasia, bilateral from the curated CTD Gene-Disease Associations dataset.

HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.

Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

Renal Artery Obstruction Gene Set

From CTD Gene-Disease Associations

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

Renal hypouricemia Gene Set

From CTD Gene-Disease Associations

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

Hypomagnesemia 5, Renal, with Ocular Involvement Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypomagnesemia 5, Renal, with Ocular Involvement from the curated CTD Gene-Disease Associations dataset.

Renal Insufficiency Gene Set

From CTD Gene-Disease Associations

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

EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.

RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Carcinoma, Papillary, With Papillary Renal Neoplasia from the curated CTD Gene-Disease Associations dataset.

Hypomagnesemia 2, renal Gene Set

From CTD Gene-Disease Associations

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

Hypouricemia, Renal, 2 Gene Set

From CTD Gene-Disease Associations

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

Hypomagnesemia 4, Renal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypomagnesemia 4, Renal from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Carcinoma, Renal Cell Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carcinoma, Renal Cell from the curated CTD Gene-Disease Associations dataset.

Torticollis keloids cryptorchidism renal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Torticollis keloids cryptorchidism renal dysplasia from the curated CTD Gene-Disease Associations dataset.

Oncocytoma, renal Gene Set

From CTD Gene-Disease Associations

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

Hypertension, Renal Gene Set

From CTD Gene-Disease Associations

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

Branchio-Oto-Renal Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Branchio-Oto-Renal Syndrome from the curated CTD Gene-Disease Associations dataset.

Nephrolithiasis, X-Linked Recessive, with Renal Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephrolithiasis, X-Linked Recessive, with Renal Failure from the curated CTD Gene-Disease Associations dataset.

Renal Insufficiency, Chronic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Insufficiency, Chronic from the curated CTD Gene-Disease Associations dataset.

Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset.

Renal cysts and diabetes syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset.

Renal Failure, Progressive, with Hypertension Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Failure, Progressive, with Hypertension from the curated CTD Gene-Disease Associations dataset.

Glycosuria, Renal Gene Set

From CTD Gene-Disease Associations

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

Renal Osteodystrophy Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

BETA-AMINO ACIDS, RENAL TRANSPORT OF Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BETA-AMINO ACIDS, RENAL TRANSPORT OF from the curated CTD Gene-Disease Associations dataset.

Arthrogryposis renal dysfunction cholestasis syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arthrogryposis renal dysfunction cholestasis syndrome from the curated CTD Gene-Disease Associations dataset.

Carcinoma, Renal Cell Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Carcinoma, Renal Cell in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

impaired renal function disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

renal carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial renal oncocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

impaired renal function disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal agenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal clear cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

end stage renal failure Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal oncocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sarcomatoid renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal tuberculosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal artery atheroma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary conventional renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease hereditary conventional renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multilocular clear cell renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease multilocular clear cell renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

eosinophilic variant of chromophobe renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease eosinophilic variant of chromophobe renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

renal osteodystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

papillary renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal wilms' tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal artery obstruction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal pelvis transitional cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease renal pelvis transitional cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

renal hypertension Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal artery disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal glycosuria Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

nonpapillary renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial renal papillary carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal adenoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal pelvis carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

renal pelvis adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemorrhagic fever with renal syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

chronic renal failure; diabetes mellitus; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

renal amyloidosis Gene Set

From GAD Gene-Disease Associations

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

paediatric renal allograft Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; kidney failure, chronic; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; hypertension, renovascular; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; hypertension, renovascular; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

renal clearance of metformin Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

chronic renal failure; kidney failure, chronic; nephritis, interstitial Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

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

human renal transplantation Gene Set

From GAD Gene-Disease Associations

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

blood pressure; aldosterone; glomerular filtration rate; renal plasma flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; aldosterone; glomerular filtration rate; renal plasma flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, renal; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

renal allograft outcome Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; inflammation; kidney failure, chronic; wasting syndrome Gene Set

From GAD Gene-Disease Associations

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

clear cell renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; chronic renal failure; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

kidney; failure; renal insufficiency Gene Set

From GAD Gene-Disease Associations

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

end-stage renal disease Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

delayed renal graft function Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hypertension; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; calcinosis; cardiovascular diseases; chronic renal failure; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

acute renal allograft rejection Gene Set

From GAD Gene-Disease Associations

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

end- stage renal disease (esrd) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease end- stage renal disease (esrd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibromuscular dysplasia; hypertension; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibromuscular dysplasia; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

renal insufficiency, chronic Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure. Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; hypercalcemia; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

irinotecan, renal clearance of Gene Set

From GAD Gene-Disease Associations

genes associated with the disease irinotecan, renal clearance of in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, renal cell Gene Set

From GAD Gene-Disease Associations

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

renal disease, end stage Gene Set

From GAD Gene-Disease Associations

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

chronic kidney insufficiency; renal insufficiency, chronic Gene Set

From GAD Gene-Disease Associations

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