anemia; thrombocytopenic purpura, idiopathic

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Results for "anemia; thrombocytopenic purpura, idiopathic": 1001 gene sets

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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.
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.
Purpura, Thrombocytopenic, Idiopathic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purpura, Thrombocytopenic, Idiopathic from the curated CTD Gene-Disease Associations dataset.
multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic thrombotic thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic thrombotic thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
h. pylori infection; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, idiopathic thrombocytopenic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, idiopathic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood idiopathic thrombocytopenic purpura. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood idiopathic thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, thrombocytopenic, idiopathic; werlhof's disease Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, thrombocytopenic, idiopathic; werlhof's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cytomegalovirus infections; gastrointestinal diseases; hepatitis; pneumonia; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease cytomegalovirus infections; gastrointestinal diseases; hepatitis; pneumonia; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
helicobacter infections; purpura, thrombocytopenic, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease helicobacter infections; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Purpura, Thrombocytopenic, Idiopathic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Purpura, Thrombocytopenic, Idiopathic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chronic Idiopathic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Purpura, Thrombotic Thrombocytopenic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purpura, Thrombotic Thrombocytopenic from the curated CTD Gene-Disease Associations dataset.
thrombotic thrombocytopenic purpura Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease thrombotic thrombocytopenic purpura from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
thrombotic thrombocytopenic purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thrombotic thrombocytopenic purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autoimmune thrombocytopenic purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune thrombocytopenic purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic immune thrombocytopenic purpura. Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic immune thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital thrombotic thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital thrombotic thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, thrombotic thrombocytopenic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, thrombotic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy complications, hematologic; purpura, thrombotic thrombocytopenic Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; purpura, thrombotic thrombocytopenic 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.
Purpura, Thrombocytopenic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Purpura, Thrombocytopenic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Purpura, Thrombotic Thrombocytopenic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Purpura, Thrombotic Thrombocytopenic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
thrombocytopenic purpura, autoimmune Gene Set From OMIM Gene-Disease Associations genes associated with the thrombocytopenic purpura, autoimmune phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombotic thrombocytopenic purpura, familial Gene Set From OMIM Gene-Disease Associations genes associated with the thrombotic thrombocytopenic purpura, familial phenotype from the curated OMIM Gene-Disease Associations dataset.
Congenital Thrombotic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Thrombotic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Purpura, Thrombotic Thrombocytopenic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Purpura, Thrombotic Thrombocytopenic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Immune Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Immune Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Thrombotic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Thrombotic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Thrombotic Thrombocytopenic Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Thrombotic Thrombocytopenic Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thrombotic Thrombocytopenic Purpura, Acquired Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thrombotic Thrombocytopenic Purpura, Acquired in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thrombotic thrombocytopenic purpura Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Thrombotic thrombocytopenic purpura from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autoimmune thrombocytopenic purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune thrombocytopenic purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombotic thrombocytopenic purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombotic thrombocytopenic purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombotic thrombocytopenic purpura Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombotic thrombocytopenic purpura phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glomerulonephritis, iga; henoch-schoenlein purpura; iga glomerulonephritides; nephritis; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease glomerulonephritis, iga; henoch-schoenlein purpura; iga glomerulonephritides; nephritis; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastrointestinal hemorrhage; henoch-schoenlein purpura; kidney diseases; purpura, schoenlein-henoch; vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal hemorrhage; henoch-schoenlein purpura; kidney diseases; purpura, schoenlein-henoch; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schoenlein purpura; hypersensitivity vasculitis; purpura, schoenlein-henoch; vasculitis, hypersensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schoenlein purpura; hypersensitivity vasculitis; purpura, schoenlein-henoch; vasculitis, hypersensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schoenlein purpura; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schoenlein purpura; nephritis; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schoenlein purpura; nephritis; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schoenlein purpura; purpura, schoenlein-henoch; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schoenlein purpura; purpura, schoenlein-henoch; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Idiopathic Autoimmune Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Autoimmune Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET 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.
thrombocytopenic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term thrombocytopenic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Hereditary Thrombocytopenic Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Thrombocytopenic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Purpura Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purpura from the curated CTD Gene-Disease Associations dataset.
Purpura, Schoenlein-Henoch Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purpura, Schoenlein-Henoch from the curated CTD Gene-Disease Associations dataset.
Purpura Fulminans Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purpura Fulminans from the curated CTD Gene-Disease Associations dataset.
purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
henoch-schoenlein purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease henoch-schoenlein purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hyperglobulinemic purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hyperglobulinemic purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
edema; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, henoch-schonlein Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, henoch-schonlein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schonlein purpura. Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schonlein purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nephritis; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease nephritis; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sjogren's syndrome; purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease sjogren's syndrome; purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; beta-glucuronidase; anaphylactoid purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; beta-glucuronidase; anaphylactoid purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anaphylactoid purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease anaphylactoid purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura, allergic Gene Set From GAD Gene-Disease Associations genes associated with the disease purpura, allergic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
henoch-schonlein purpura; nephritis, henoch-schonlein Gene Set From GAD Gene-Disease Associations genes associated with the disease henoch-schonlein purpura; nephritis, henoch-schonlein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
proteinuria; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
purpura Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term purpura in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
purpura Gene Set From HPO Gene-Disease Associations genes associated with the purpura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anaphylactoid purpura Gene Set From HPO Gene-Disease Associations genes associated with the anaphylactoid purpura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Purpura, Schoenlein-Henoch Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Purpura, Schoenlein-Henoch phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
purpura Gene Set From MPO Gene-Phenotype Associations gene mutations causing the purpura phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
purpura, posttransfusion Gene Set From OMIM Gene-Disease Associations genes associated with the purpura, posttransfusion phenotype from the curated OMIM Gene-Disease Associations dataset.
Henoch-Schoenlein Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Henoch-Schoenlein Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Henoch-Schonlein Purpura Nephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Henoch-Schonlein Purpura Nephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Purpura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Purpura Fulminans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Purpura Fulminans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Purpura Hemorrhagica Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Purpura Hemorrhagica in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Purpura, Nonthrombocytopenic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Purpura, Nonthrombocytopenic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rheumatoid Purpura Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rheumatoid Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posttransfusion Purpura Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posttransfusion Purpura in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acquired Purpura Fulminans Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Purpura Fulminans in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
purpura Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the purpura phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Henoch-Schoenlein purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Henoch-Schoenlein purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Purpura fulminans Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Purpura fulminans in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperglobulinemic purpura Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperglobulinemic purpura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Short stature, idiopathic, autosomal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutropenia, nonimmune chronic idiopathic, of adults Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutropenia, nonimmune chronic idiopathic, of adults phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Basal ganglia calcification, idiopathic, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Basal ganglia calcification, idiopathic, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic hypercalcemia of infancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic hypercalcemia of infancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, idiopathic, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic fibrosing alveolitis, chronic form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic fibrosing alveolitis, chronic form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, idiopathic, steroid-resistant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic basal ganglia calcification 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic basal ganglia calcification 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Idiopathic basal ganglia calcification 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Idiopathic basal ganglia calcification 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital idiopathic intestinal pseudoobstruction Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Idiopathic Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Idiopathic Generalized from the curated CTD Gene-Disease Associations dataset.
Idiopathic dilation cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic dilation cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephrotic syndrome, idiopathic, steroid-resistant from the curated CTD Gene-Disease Associations dataset.
Short Stature, Idiopathic, Autosomal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, Autosomal from the curated CTD Gene-Disease Associations dataset.
Idiopathic basal ganglia calcification 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic basal ganglia calcification 1 from the curated CTD Gene-Disease Associations dataset.
Neutropenia, Nonimmune Chronic Idiopathic, Adult Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Nonimmune Chronic Idiopathic, Adult from the curated CTD Gene-Disease Associations dataset.
Jaundice, Chronic Idiopathic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Chronic Idiopathic from the curated CTD Gene-Disease Associations dataset.
Short Stature, Idiopathic, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset.
Idiopathic Hypogonadotropic Hypogonadism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Hypogonadotropic Hypogonadism from the curated CTD Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic Pulmonary Fibrosis from the curated CTD Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
idiopathic interstitial pneumonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic interstitial pneumonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic pulmonary fibrosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic juvenile osteoporosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease idiopathic juvenile osteoporosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
idiopathic pulmonary fibrosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic pulmonary fibrosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic cd4-positive t-lymphocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic cd4-positive t-lymphocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic interstitial pneumonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic interstitial pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diffuse idiopathic skeletal hyperostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diffuse idiopathic skeletal hyperostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic juvenile osteoporosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
systemic juvenile idiopathic arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease systemic juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic recurrent miscarriage. Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic osteoarthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic premature ovarian failure Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic recurrent miscarriages Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic infertility Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic deep venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic deep venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonfamilial idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease nonfamilial idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic short stature Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic short stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic atrial fibrillation Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic atrial fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic environmental intolerance Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic environmental intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypersomnolence, idiopathic; narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypersomnolence, idiopathic; narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, idiopathic dilated Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, idiopathic dilated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic idiopathic neutropenia Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic idiopathic neutropenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis (juvenile idiopathic) Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis (juvenile idiopathic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic chronic pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic chronic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic orthostatic intolerance Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic orthostatic intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent or chronic idiopathic pancreatitis Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent or chronic idiopathic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic torsion dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic torsion dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
juvenile idiopathic arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease juvenile idiopathic arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, idiopathic generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, idiopathic generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema Gene Set From GAD Gene-Disease Associations genes associated with the disease graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic azoospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic azoospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myopathy, idiopathic inflammatory Gene Set From GAD Gene-Disease Associations genes associated with the disease myopathy, idiopathic inflammatory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term idiopathic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Idiopathic fibrosing alveolitis_Lung Tissue_GSE21369 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Idiopathic fibrosing alveolitis_Lung Tissue_GSE21369 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Arthritis (juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Arthritis (juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Nephropathy (idiopathic membranous) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Nephropathy (idiopathic membranous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to methotrexate in juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to methotrexate in juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
idiopathic interstitial pneumonia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease idiopathic interstitial pneumonia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From GWASdb SNP-Disease Associations genes associated with the disease idiopathic pulmonary fibrosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Hypersomnolence, Idiopathic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hypersomnolence, Idiopathic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Pulmonary Fibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Idiopathic Interstitial Pneumonias Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Idiopathic Interstitial Pneumonias phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hyperostosis, Diffuse Idiopathic Skeletal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperostosis, Diffuse Idiopathic Skeletal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
{scoliosis, idiopathic, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {scoliosis, idiopathic, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
neutropenia, nonimmune chronic idiopathic, of adults Gene Set From OMIM Gene-Disease Associations genes associated with the neutropenia, nonimmune chronic idiopathic, of adults phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
pulmonary fibrosis, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the pulmonary fibrosis, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, idiopathic generalized, susceptibility to 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
hypereosinophilic syndrome, idiopathic, resistant to imatinib Gene Set From OMIM Gene-Disease Associations genes associated with the hypereosinophilic syndrome, idiopathic, resistant to imatinib phenotype from the curated OMIM Gene-Disease Associations dataset.
ventricular tachycardia, idiopathic Gene Set From OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, idiopathic phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
scoliosis, idiopathic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
scoliosis, idiopathic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the scoliosis, idiopathic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{pulmonary fibrosis, idiopathic, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {pulmonary fibrosis, idiopathic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
basal ganglia calcification, idiopathic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the basal ganglia calcification, idiopathic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
hydrocephalus with congenital idiopathic intestinal pseudoobstruction Gene Set From OMIM Gene-Disease Associations genes associated with the hydrocephalus with congenital idiopathic intestinal pseudoobstruction phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, idiopathic familial Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.
{pancreatitis, idiopathic} Gene Set From OMIM Gene-Disease Associations genes associated with the {pancreatitis, idiopathic} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{scoliosis, idiopathic 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {scoliosis, idiopathic 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.
idiopathic pulmonary fibrosis Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease idiopathic pulmonary fibrosis from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Adolescent Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adolescent Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Achalasia Of Esophagus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Achalasia Of Esophagus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Inflammatory Myopathies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Inflammatory Myopathies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Arterial Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Nephrotic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Bronchiectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Bronchiectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Arterial Calcification Of Infancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Arterial Calcification Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypereosinophilic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypereosinophilic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypogonadotropic Hypogonadism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypogonadotropic Hypogonadism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Crescentic Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Crescentic Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pulmonary Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Urticaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Urticaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Normal Pressure Hydrocephalus (Inph) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Normal Pressure Hydrocephalus (Inph) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypercalciuria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypercalciuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exacerbation Of Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exacerbation Of Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Premature Ovarian Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Premature Ovarian Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Membranous Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Membranous Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Pneumonia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Pneumonia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trigeminal Neuralgia, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trigeminal Neuralgia, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypoparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatitis Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatitis Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Chronic Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Chronic Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Idiopathic Focal Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Idiopathic Focal Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Idiopathic Torsion Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Idiopathic Torsion Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Central Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Central Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Interstitial Pneumonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Interstitial Pneumonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
(Idiopathic) Normal Pressure Hydrocephalus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease (Idiopathic) Normal Pressure Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unspecified Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unspecified Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Transverse Myelitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Transverse Myelitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile And Adolescent Idiopathic Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile And Adolescent Idiopathic Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Polypoidal Choroidal Vasculopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Polypoidal Choroidal Vasculopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Urethral Stricture Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Urethral Stricture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
T-Lymphocytopenia, Idiopathic Cd4-Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease T-Lymphocytopenia, Idiopathic Cd4-Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Osteoporosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Copper Toxicosis, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Copper Toxicosis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilic Myositis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilic Myositis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Pulmonary Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Pulmonary Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Retroperitoneal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Retroperitoneal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Uveitis Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Uveitis Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypercatabolic Hypoproteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypercatabolic Hypoproteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersomnolence, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersomnolence, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Thrombocytopenia (Itp) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Thrombocytopenia (Itp) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Partial Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Partial Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Idiopathic Arthritis, Enthesitis Related Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Idiopathic Arthritis, Enthesitis Related Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Gynecomastia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Gynecomastia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Juxtafoveal Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Juxtafoveal Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Granulomatous Mastitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Granulomatous Mastitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Idiopathic Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Idiopathic Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Growth Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Growth Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Infantile Hypercalcemia - Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Infantile Hypercalcemia - Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymyositis, Idiopathic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymyositis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Basal Ganglia Calcification 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Basal Ganglia Calcification 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Atrophoderma Of Pasini And Pierini Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Atrophoderma Of Pasini And Pierini in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Neutropenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Neutropenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Idiopathic Intestinal Pseudoobstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Idiopathic Intestinal Pseudoobstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Stature, Idiopathic, Autosomal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Stature, Idiopathic, Autosomal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Parathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Parathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Extrahepatic Biliary Atresia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Extrahepatic Biliary Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypopituitarism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypopituitarism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Cirrhotic Portal Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Cirrhotic Portal Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Diabetes (Mellitus) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Diabetes (Mellitus) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Extended Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Extended Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Persistent Oligoarticular Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Oligoarticular Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Recurrent Pericarditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Recurrent Pericarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Acute Pancreatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Acute Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Cd4 Lymphocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Cd4 Lymphocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Anaphylaxis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Anaphylaxis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Angioedema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Angioedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Cardiac Hypertrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Cardiac Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary And Idiopathic Neuropathy, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary And Idiopathic Neuropathy, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psoriatic Juvenile Idiopathic Arthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psoriatic Juvenile Idiopathic Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Guttate Hypomelanosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Guttate Hypomelanosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Multicentric Osteolyses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Multicentric Osteolyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hypertrophic Subaortic Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hypertrophic Subaortic Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Eosinophilic Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Eosinophilic Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Hyperprolactinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Hyperprolactinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Parkinsonism Or Parkinson'S Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Parkinsonism Or Parkinson'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Membranous Glomerulopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Membranous Glomerulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scoliosis, Idiopathic, Susceptibility To, 1 (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scoliosis, Idiopathic, Susceptibility To, 1 (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Idiopathic Hirsutism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Idiopathic Hirsutism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chronic Idiopathic Constipation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Idiopathic Constipation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypereosinophilic Syndrome, Idiopathic, Resistant To Imatinib Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypereosinophilic Syndrome, Idiopathic, Resistant To Imatinib in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Idiopathic pulmonary fibrosis cell_Lung_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Idiopathic pulmonary fibrosis myofibroblast_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1) pathway from the Reactome Pathways 2024 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic generalized epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic juvenile osteoporosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic juvenile osteoporosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic generalized epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic scoliosis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic scoliosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Diffuse idiopathic skeletal hyperostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diffuse idiopathic skeletal hyperostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic interstitial pneumonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic interstitial pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic scoliosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic scoliosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic juvenile osteoporosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic juvenile osteoporosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic peripheral autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic peripheral autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic progressive polyneuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic progressive polyneuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked chronic idiopathic intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic CD4-positive T-lymphocytopenia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic CD4-positive T-lymphocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic pulmonary fibrosis disease specific cell type Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Idiopathic pulmonary fibrosis disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic steroid-resistant nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic steroid-resistant nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic and/or familial pulmonary arterial hypertension Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic and/or familial pulmonary arterial hypertension phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic Pulmonary Fibrosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic Pulmonary Fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic basal ganglia calcification Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic basal ganglia calcification phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic growth hormone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic hypereosinophilic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic hypereosinophilic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic camptocormia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic camptocormia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic CD4 lymphocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic CD4 lymphocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonimmune chronic idiopathic neutropenia of adults Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonimmune chronic idiopathic neutropenia of adults phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic hypercalciuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic hypercalciuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic scoliosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Idiopathic environmental intolerance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic environmental intolerance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial idiopathic inflammatory myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial idiopathic inflammatory myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Systemic juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systemic juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Arthritis (juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arthritis (juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adolescent idiopathic scoliosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adolescent idiopathic scoliosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Juvenile idiopathic arthritis (oligoarticular or rheumatoid factor-negative polyarticular) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Juvenile idiopathic arthritis (oligoarticular or rheumatoid factor-negative polyarticular) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic osteonecrosis of the femoral head Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic osteonecrosis of the femoral head phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic downbeat nystagmus Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic downbeat nystagmus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic pulmonary fibrosis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic pulmonary fibrosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic inflammatory myopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic inflammatory myopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to methotrexate in juvenile idiopathic arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to methotrexate in juvenile idiopathic arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic dilated cardiomyopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic dilated cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic membranous nephropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic membranous nephropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adolescent idiopathic scoliosis (severe) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adolescent idiopathic scoliosis (severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic intracranial hypertension Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic intracranial hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Arthritis (oligoarticular juvenile idiopathic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arthritis (oligoarticular juvenile idiopathic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diamond-Blackfan anemia 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diamond-Blackfan anemia 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diamond-Blackfan anemia 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diamond-Blackfan anemia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sideroblastic anemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Anemia sideroblastic and spinocerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diamond-Blackfan anemia 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diamond-Blackfan anemia 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diamond-Blackfan anemia 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diamond-Blackfan anemia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diamond-Blackfan anemia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diamond-Blackfan anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diamond-Blackfan anemia 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diamond-Blackfan anemia 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group M Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Hemolytic anemia due to hexokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypochromic microcytic anemia with iron overload Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypochromic microcytic anemia with iron overload phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aplastic anemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aplastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Renal tubular acidosis, distal, with hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi anemia, complementation group D2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group D2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adenylate kinase deficiency, hemolytic anemia due to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ANEMIA, 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.
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.
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.
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.
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.
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.
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.
FANCONI ANEMIA, COMPLEMENTATION GROUP E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP E from the curated CTD Gene-Disease Associations dataset.
FANCONI ANEMIA, COMPLEMENTATION GROUP F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP F from the curated CTD Gene-Disease Associations dataset.
Anemia, Diamond-Blackfan, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Diamond-Blackfan, 2 from the curated CTD Gene-Disease Associations dataset.
Fanconi Anemia, Complementation Group J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group J from the curated CTD Gene-Disease Associations dataset.
Anemia, sideroblastic spinocerebellar ataxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, sideroblastic spinocerebellar ataxia from the curated CTD Gene-Disease Associations dataset.
Fanconi Anemia, Complementation Group B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group B from the curated CTD Gene-Disease Associations dataset.
Fanconi Anemia, Complementation Group N Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group N from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset.
MEGALOBLASTIC ANEMIA 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MEGALOBLASTIC ANEMIA 1 from the curated CTD Gene-Disease Associations dataset.
Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.
Myopathy with lactic acidosis and sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with lactic acidosis and sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Fanconi Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia from the curated CTD Gene-Disease Associations dataset.
Anemia, Hemolytic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic from the curated CTD Gene-Disease Associations dataset.
Anemia, 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, 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.
Anemia, Sideroblastic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Sideroblastic from the curated CTD Gene-Disease Associations dataset.
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.
Anemia, Sickle Cell Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Sickle Cell from the curated CTD Gene-Disease Associations dataset.
SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP D2 from the curated CTD Gene-Disease Associations dataset.
Thiamine responsive megaloblastic anemia syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thiamine responsive megaloblastic anemia syndrome from the curated CTD Gene-Disease Associations dataset.
Anemia, Macrocytic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Macrocytic from the curated CTD Gene-Disease Associations dataset.
X-linked sideroblastic anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease X-linked sideroblastic anemia from the curated CTD Gene-Disease Associations dataset.
Fanconi Anemia, Complementation Group I Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group I from the curated CTD Gene-Disease Associations dataset.
FANCONI ANEMIA, COMPLEMENTATION GROUP O Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP O from the curated CTD Gene-Disease Associations dataset.
Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Iron-Refractory Iron Deficiency Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iron-Refractory Iron Deficiency Anemia from the curated CTD Gene-Disease Associations dataset.
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.
Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia from the curated CTD Gene-Disease Associations dataset.
Fanconi Anemia, Complementation Group D1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group D1 from the curated CTD Gene-Disease Associations dataset.
DIAMOND-BLACKFAN ANEMIA 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DIAMOND-BLACKFAN ANEMIA 6 from the curated CTD Gene-Disease Associations dataset.
Anemia, Diamond-Blackfan, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Diamond-Blackfan, 3 from the curated CTD Gene-Disease Associations dataset.
Diamond-Blackfan Anemia 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diamond-Blackfan Anemia 9 from the curated CTD Gene-Disease Associations dataset.
Diamond-Blackfan Anemia 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diamond-Blackfan Anemia 8 from the curated CTD Gene-Disease Associations dataset.
Diamond-Blackfan Anemia 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diamond-Blackfan Anemia 5 from the curated CTD Gene-Disease Associations dataset.
Diamond-Blackfan Anemia 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diamond-Blackfan Anemia 7 from the curated CTD Gene-Disease Associations dataset.
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, Hemolytic, Autoimmune Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Hemolytic, Autoimmune from the curated CTD Gene-Disease Associations dataset.
Anemia, Neonatal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Neonatal from the curated CTD Gene-Disease Associations dataset.
Diamond-Blackfan Anemia 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diamond-Blackfan Anemia 10 from the curated CTD Gene-Disease Associations dataset.
Anemia, hypochromic microcytic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, hypochromic microcytic from the curated CTD Gene-Disease Associations dataset.
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Anemia, 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 Association 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 Association 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 Association 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 Association Evidence Scores genes involed in the disease sideroblastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
hemolytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hemolytic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
normocytic anemia Gene Set From DISEASES Curated Gene-Disease Association 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 Association 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 Association 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 Association Evidence Scores genes involed in the disease aplastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital hemolytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital hemolytic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital hypoplastic anemia Gene Set From DISEASES Curated Gene-Disease Association 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 Association 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 Association 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 Association Evidence Scores genes associated with the disease anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
hemolytic anemia Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease hemolytic anemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
microcytic anemia Gene Set From DISEASES Experimental Gene-Disease Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association Evidence Scores genes co-occuring with the disease myelophthisic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autoimmune hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune hemolytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
x-linked sideroblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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 Association 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 Association 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.
congenital nonspherocytic hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association 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.
macrocytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association Evidence Scores genes co-occuring with the disease normocytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hemolytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diamond-blackfan anemia Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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 Association 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 Association 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.
congenital hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association 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.
sideroblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association 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 Association 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 Association 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 Association 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 Association 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, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary nonspherocytic hemolytic anemia (hnsha). Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary nonspherocytic hemolytic anemia (hnsha). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, aplastic; fanconi syndrome; Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, aplastic; fanconi syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sickle cell anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, malaria related; malaria, cerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; pain Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bloom syndrome; fanconi's anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease bloom syndrome; fanconi's anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia in pregnancy Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia in pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, aplastic; Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, aplastic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sickle cell anemia; g6pd deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease sickle cell anemia; g6pd deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; ischemia; recurrence; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; ischemia; recurrence; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary hemolytic anemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary hemolytic anemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, aplastic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, aplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholelithiasis; sickle cell anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cholelithiasis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; lung diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; lung diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; brain death Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; brain death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; kidney diseases; red-cell aplasia, pure Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; osteomyelitis Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; osteomyelitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; anemia; chronic disease Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; anemia; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diamond-blackfan anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease diamond-blackfan anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; gallbladder diseases; hyperbilirubinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; gallbladder diseases; hyperbilirubinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; sickle cell anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fanconi anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fanconi anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; gastritis, atrophic; nervous system diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aplastic anemia, acquired Gene Set From GAD Gene-Disease Associations genes associated with the disease aplastic anemia, acquired in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebrovascular disease; sickle cell anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebrovascular disease; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia, sickle cell; cholelithiasis Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia, sickle cell; cholelithiasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malarial anemia and cerebral malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease malarial anemia and cerebral malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; hepatitis c Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, hemolytic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, hemolytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malarial anemia in ghanaian children Gene Set From GAD Gene-Disease Associations genes associated with the disease malarial anemia in ghanaian children in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, hemolytic; hepatitis c, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, hemolytic; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; beta-thalassemia; hemoglobinopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; beta-thalassemia; hemoglobinopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; hepatitis c, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria; malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic nonspherocytic anemia. Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic nonspherocytic anemia. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aplastic anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease aplastic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; inflammation; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; inflammation; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia, hypochromic Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia, hypochromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; drug toxicity; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; thrombocytopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary hemolytic anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary hemolytic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; arterial occlusive diseases; constriction, pathologic; ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; arterial occlusive diseases; constriction, pathologic; ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; polycythemia vera Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; polycythemia vera in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; anemia, hypochromic Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, hypochromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic hemolytic anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic hemolytic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macrothrombocytopenia and anemia Gene Set From GAD Gene-Disease Associations genes associated with the disease macrothrombocytopenia and anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; chronic renal failure; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; hemoglobinopathies; iron overload; thalassemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; hemoglobinopathies; iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; bacteremia; Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; bacteremia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sickle cell anemia; thalassemia; gilbert syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease sickle cell anemia; thalassemia; gilbert syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; avitaminosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; avitaminosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term anemia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Systolic blood pressure in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Sickle cell anemia (haemolysis) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Sickle cell anemia (haemolysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Ribavirin-induced anemia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Ribavirin-induced anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
iron deficiency anemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease iron deficiency anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
anemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
hemolytic anemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease hemolytic anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
microcytic anemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease microcytic anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
sickle cell anemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sickle cell anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
normocytic anemia Gene Set From GWASdb SNP-Disease Associations genes associated with the disease normocytic anemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
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.
anemia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the anemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
anemia due to reduced life span of red cells Gene Set From GWASdb SNP-Phenotype Associations genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
hemolytic anemia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the hemolytic anemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
iron deficiency anemia Gene Set From HPO Gene-Disease Associations genes associated with the iron deficiency anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
microcytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the microcytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonspherocytic hemolytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the nonspherocytic hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
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.
fava bean-induced hemolytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the fava bean-induced hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thiamine-responsive megaloblastic anemia Gene Set From HPO Gene-Disease Associations genes associated with the thiamine-responsive megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
refractory anemia Gene Set From HPO Gene-Disease Associations genes associated with the refractory anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anemia due to reduced life span of red cells Gene Set From HPO Gene-Disease Associations genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplastic anemia Gene Set From HPO Gene-Disease Associations genes associated with the hypoplastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypochromic anemia Gene Set From HPO Gene-Disease Associations genes associated with the hypochromic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
refractory macrocytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the refractory macrocytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
heinz body anemia Gene Set From HPO Gene-Disease Associations genes associated with the heinz body anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
compensated hemolytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the compensated hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
anemia of inadequate production Gene Set From HPO Gene-Disease Associations genes associated with the anemia of inadequate production phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypochromic microcytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the hypochromic microcytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
folate-responsive megaloblastic anemia Gene Set From HPO Gene-Disease Associations genes associated with the folate-responsive megaloblastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
normocytic hypoplastic anemia Gene Set From HPO Gene-Disease Associations genes associated with the normocytic hypoplastic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macrocytic anemia Gene Set From HPO Gene-Disease Associations genes associated with the macrocytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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, 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.
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.
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, 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, 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.
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.
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.
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.
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.
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.
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.
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.
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.
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, 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.
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.
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.
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.
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.
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.
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.
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.
?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.
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.
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.
{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.
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.
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.
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.
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.
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.
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.
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 2014 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 2014 proteins participating in the Defective AMN causes hereditary megaloblastic anemia 1 pathway from the Reactome Pathways dataset.
Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set From Reactome Pathways 2014 proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.
Defective CUBN causes hereditary megaloblastic anemia 1 Gene Set From Reactome Pathways 2014 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 2014 proteins participating in the Defective TCN2 causes hereditary megaloblastic anemia pathway from the Reactome Pathways dataset.
Fanconi Anemia pathway Gene Set From Reactome Pathways 2014 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.
Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stomatocytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stomatocytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, Sideroblastic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Sideroblastic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcytic Hypochromic Anemia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcytic Hypochromic Anemia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Anemia With Excess Blasts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Anemia With Excess Blasts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fanconi Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fanconi Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Normocytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Normocytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Aplastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iron-Refractory Iron Deficiency Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iron-Refractory Iron Deficiency Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cooley'S Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cooley'S Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonspherocytic Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonspherocytic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypoplastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Acquired Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Acquired Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diamond-Blackfan Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diamond-Blackfan Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microangiopathic Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microangiopathic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenintal Dyserythropoeitic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenintal Dyserythropoeitic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macrocytic Dyserythropoietic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macrocytic Dyserythropoietic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyridoxine-Responsive Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyridoxine-Responsive Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia Hemoglobin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia Hemoglobin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine-Responsive Megaloblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine-Responsive Megaloblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Megaloblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Megaloblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Aplastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypochromic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypochromic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, Congenital Dyserythropoietic, Type Ib Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Congenital Dyserythropoietic, Type Ib in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fava Bean-Induced Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fava Bean-Induced Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coombs Positive Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coombs Positive Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Compensated Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Compensated Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcytic Normochromic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcytic Normochromic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Drug-Induced Immune Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Drug-Induced Immune Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erythropoietin-Resistant Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erythropoietin-Resistant Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Normocytic Normochromic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Normocytic Normochromic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Treatment-Induced Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Treatment-Induced Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uremic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uremic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Estren-Dameshek Variant Of Fanconi Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Estren-Dameshek Variant Of Fanconi Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Regenerative Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Regenerative Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Immune Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Immune Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Non-Spherocytic Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Non-Spherocytic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Drug-Induced Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Drug-Induced Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, X-Linked, With Or Without Neutropenia And/Or Platelet Abnormalities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, X-Linked, With Or Without Neutropenia And/Or Platelet Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dyserythropoietic Anemia With Thrombocytopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dyserythropoietic Anemia With Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due To Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asiderotic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asiderotic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glutathione Peroxidase Deficiency, Hemolytic Anemia Possibly Due To Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glutathione Peroxidase Deficiency, Hemolytic Anemia Possibly Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glutathione Synthetase Deficiency Of Erythrocytes, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemolytic Anemia Due To Hexokinase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemolytic Anemia Due To Hexokinase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Constitutional Aplastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Constitutional Aplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aplastic Anemia, Susceptibility To (Finding) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aplastic Anemia, Susceptibility To (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Iron Loading Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Iron Loading Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine Responsive Megaloblastic Anemia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Responsive Megaloblastic Anemia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leukoerythroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leukoerythroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hydrops, Lactic Acidosis, And Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hydrops, Lactic Acidosis, And Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Normocytic Hypoplastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Normocytic Hypoplastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Macrocytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Macrocytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Warm Autoimmune Hemolytic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Warm Autoimmune Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, Hypochromic Microcytic, With Iron Overload 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Hypochromic Microcytic, With Iron Overload 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, Perinatal Hemolytic, Fatal Or Near-Fatal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Perinatal Hemolytic, Fatal Or Near-Fatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anemia, Hypochromic Microcytic, With Iron Overload 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anemia, Hypochromic Microcytic, With Iron Overload 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Folate-Unresponsive Megaloblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Folate-Unresponsive Megaloblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyrimidine-Responsive Megaloblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyrimidine-Responsive Megaloblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Hemolytic Anemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Hemolytic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Normochromic Anemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Normochromic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Secondary Anemia Nos Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Secondary Anemia Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Folate-Responsive Megaloblastic Anemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Folate-Responsive Megaloblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
macrocytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the macrocytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hypochromic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hypochromic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hemolytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hemolytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased susceptibility to autoimmune hemolytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
microcytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the microcytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hypochromic microcytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hypochromic microcytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptibility to autoimmune hemolytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hypochromic macrocytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hypochromic macrocytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hyperchromic macrocytic anemia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hyperchromic macrocytic anemia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN) Gene Set From Reactome Pathways 2024 proteins participating in the Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN) pathway from the Reactome Pathways 2024 dataset.
Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1) pathway from the Reactome Pathways 2024 dataset.
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) pathway from the Reactome Pathways 2024 dataset.
Fanconi Anemia Pathway Gene Set From Reactome Pathways 2024 proteins participating in the Fanconi Anemia Pathway pathway from the Reactome Pathways 2024 dataset.
Fanconi anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Fanconi anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Normocytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Normocytic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital hypoplastic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital hypoplastic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Aplastic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Aplastic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Diamond-Blackfan anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Diamond-Blackfan anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital dyserythropoietic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital hemolytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital hemolytic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hemolytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hemolytic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Microcytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Microcytic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sideroblastic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sideroblastic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked sideroblastic anemia with ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sideroblastic anemia 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sideroblastic anemia 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
thiamine-responsive megaloblastic anemia syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease thiamine-responsive megaloblastic anemia syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital nonspherocytic hemolytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital nonspherocytic hemolytic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Macrocytic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Macrocytic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Megaloblastic anemia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Megaloblastic anemia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital hemolytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Microcytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Microcytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hemolytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Normocytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Normocytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital hypoplastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital hypoplastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Aplastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aplastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypochromic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypochromic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sickle cell anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sickle cell anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Iron deficiency anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Iron deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sideroblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sideroblastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
thiamine-responsive megaloblastic anemia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease thiamine-responsive megaloblastic anemia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune hemolytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pernicious anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pernicious anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macrocytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macrocytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-blackfan anemia 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-blackfan anemia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myelophthisic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myelophthisic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked dyserythropoietic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked dyserythropoietic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Megaloblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Megaloblastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypochromic microcytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypochromic microcytic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neonatal anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group D1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group D1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group U Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group U in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked sideroblastic anemia with ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Sideroblastic anemia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sideroblastic anemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type Ia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type Ia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group J Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group J in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group N Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group N in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group D2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group D2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type III Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type III in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group L Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group L in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Heinz body anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Heinz body anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital nonspherocytic hemolytic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Fanconi anemia complementation group T Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group T in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group Q Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group Q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type I Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital dyserythropoietic anemia type IV Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type IV in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease myopathy, lactic acidosis, and sideroblastic anemia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
homocystinuria-megaloblastic anemia cblG type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease homocystinuria-megaloblastic anemia cblG type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Folic acid deficiency anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Diamond-Blackfan anemia 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anemia of prematurity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anemia of prematurity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group G Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group V Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group V in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
pyridoxine-responsive sideroblastic anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 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 2025 dataset.
Congenital dyserythropoietic anemia type Ib Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital dyserythropoietic anemia type Ib in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 14 with mandibulofacial dysostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 14 with mandibulofacial dysostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia complementation group O Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group O in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pyridoxine deficiency anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pyridoxine deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
protein-deficiency anemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease protein-deficiency anemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 15 with mandibulofacial dysostosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 15 with mandibulofacial dysostosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
homocystinuria-megaloblastic anemia cblE type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease homocystinuria-megaloblastic anemia cblE type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diamond-Blackfan anemia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diamond-Blackfan anemia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fanconi anemia lymphoid cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 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 2025 dataset.
Homocystinuria-megaloblastic anemia cblD Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Homocystinuria-megaloblastic anemia cblD phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fanconi anemia complementation group Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fanconi anemia complementation group phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fanconi anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fanconi anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sideroblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital dyserythropoietic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital dyserythropoietic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iron-refractory iron deficiency anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iron-refractory iron deficiency anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pancreatic insufficiency-anemia-hyperostosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancreatic insufficiency-anemia-hyperostosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aplastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diamond-Blackfan anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diamond-Blackfan anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Megaloblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Megaloblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD deficient hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD deficient hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital nonspherocytic hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital nonspherocytic hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked dyserythropoetic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked dyserythropoetic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked sideroblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Iron deficiency anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Iron deficiency anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Prenatal anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Prenatal anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency and megaloblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency and megaloblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hemolytic anemia due to glucophosphate isomerase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to glucophosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Heinz body anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Heinz body anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cystic fibrosis-gastritis-megaloblastic anemia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cystic fibrosis-gastritis-megaloblastic anemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thiamine-responsive megaloblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine-responsive megaloblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sideroblastic Anemia and Ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sideroblastic Anemia and Ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary Sideroblastic Anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary Sideroblastic Anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hemolytic anemia due to hexokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Refractory anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Refractory anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Harmonizome 3.0

anemia; thrombocytopenic purpura, idiopathic Gene Set

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

Purpura, Thrombocytopenic, Idiopathic Gene Set

multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set

idiopathic thrombotic thrombocytopenic purpura Gene Set

thrombocytopenic purpura, idiopathic Gene Set

purpura, thrombocytopenic, idiopathic Gene Set

myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic Gene Set

h. pylori infection; thrombocytopenic purpura, idiopathic Gene Set

purpura, idiopathic thrombocytopenic Gene Set

childhood idiopathic thrombocytopenic purpura. Gene Set

purpura, thrombocytopenic, idiopathic; werlhof's disease Gene Set

cytomegalovirus infections; gastrointestinal diseases; hepatitis; pneumonia; purpura, thrombocytopenic, idiopathic Gene Set

helicobacter infections; purpura, thrombocytopenic, idiopathic Gene Set

Purpura, Thrombocytopenic, Idiopathic Gene Set

Chronic Idiopathic Thrombocytopenic Purpura Gene Set

Purpura, Thrombotic Thrombocytopenic Gene Set

thrombotic thrombocytopenic purpura Gene Set

thrombotic thrombocytopenic purpura Gene Set

autoimmune thrombocytopenic purpura Gene Set

chronic immune thrombocytopenic purpura. Gene Set

congenital thrombotic thrombocytopenic purpura Gene Set

purpura, thrombotic thrombocytopenic Gene Set

pregnancy complications, hematologic; purpura, thrombotic thrombocytopenic Gene Set

hemolytic-uremic syndrome; purpura, thrombotic thrombocytopenic Gene Set

Purpura, Thrombocytopenic Gene Set

Purpura, Thrombotic Thrombocytopenic Gene Set

thrombocytopenic purpura, autoimmune Gene Set

thrombotic thrombocytopenic purpura, familial Gene Set

Congenital Thrombotic Thrombocytopenic Purpura Gene Set

Purpura, Thrombotic Thrombocytopenic Gene Set

Immune Thrombocytopenic Purpura Gene Set

Autoimmune Thrombotic Thrombocytopenic Purpura Gene Set

Familial Thrombotic Thrombocytopenic Purpura Gene Set

Thrombotic Thrombocytopenic Purpura, Acquired Gene Set

Thrombotic thrombocytopenic purpura Gene Set

Autoimmune thrombocytopenic purpura Gene Set

Thrombotic thrombocytopenic purpura Gene Set

Thrombotic thrombocytopenic purpura Gene Set

gastrointestinal hemorrhage; haematuria; hematuria; henoch-schoenlein purpura; purpura, schoenlein-henoch; respiratory tract infections Gene Set

glomerulonephritis, iga; henoch-schoenlein purpura; iga glomerulonephritides; nephritis; purpura, schoenlein-henoch Gene Set

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

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

familial mediterranean fever; henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set

gastrointestinal hemorrhage; henoch-schoenlein purpura; kidney diseases; purpura, schoenlein-henoch; vasculitis Gene Set

henoch-schoenlein purpura; hypersensitivity vasculitis; purpura, schoenlein-henoch; vasculitis, hypersensitivity Gene Set

henoch-schoenlein purpura; purpura, schoenlein-henoch Gene Set

henoch-schoenlein purpura; nephritis; purpura, schoenlein-henoch Gene Set

henoch-schoenlein purpura; purpura, schoenlein-henoch; thrombophilia Gene Set

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

Idiopathic Autoimmune Hemolytic Anemia Gene Set

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

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

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

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

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

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

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

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

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

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

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

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

anemia, iron deficiency; anemia of chronic disease Gene Set

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

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

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

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

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

anemia, sickle cell; sickle cell anemia Gene Set

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

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

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

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

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

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

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

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

anemia, aplastic; aplastic anemia; disease susceptibility Gene Set