Thiamine-responsive megaloblastic anemia syndrome

Clear Filter

Results for "Thiamine-responsive megaloblastic anemia syndrome": 1003 gene sets

Name
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.
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.
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.
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.
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.
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.
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.
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.
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.
MEGALOBLASTIC ANEMIA 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MEGALOBLASTIC ANEMIA 1 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.
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.
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.
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.
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.
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.
megaloblastic anemia-1, finnish type Gene Set From OMIM Gene-Disease Associations genes associated with the megaloblastic anemia-1, finnish type phenotype from the curated OMIM Gene-Disease Associations dataset.
homocystinuria-megaloblastic anemia, cbl e type Gene Set From OMIM Gene-Disease Associations genes associated with the homocystinuria-megaloblastic anemia, cbl e type phenotype from the curated OMIM Gene-Disease Associations dataset.
homocystinuria-megaloblastic anemia, cblg complementation type Gene Set From OMIM Gene-Disease Associations genes associated with the homocystinuria-megaloblastic anemia, cblg complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Constitutional megaloblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Constitutional megaloblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thiamine metabolism dysfunction syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine metabolism dysfunction syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thiamine Metabolism Dysfunction Syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine Metabolism Dysfunction Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
megaloblastic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term megaloblastic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
megaloblastic bone marrow Gene Set From HPO Gene-Disease Associations genes associated with the megaloblastic bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
megaloblastic erythroid hyperplasia Gene Set From HPO Gene-Disease Associations genes associated with the megaloblastic erythroid hyperplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Megaloblastic Erythroid Hyperplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Megaloblastic Erythroid Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bone Marrow Megaloblastic (Finding) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bone Marrow Megaloblastic (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thiamine-2894 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the thiamine-2894 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
thiamine-1744 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the thiamine-1744 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
thiamine-7479 Gene Set From CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the thiamine-7479 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
Thiamine Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Thiamine from the curated CTD Gene-Chemical Interactions dataset.
Thiamine Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thiamine Deficiency from the curated CTD Gene-Disease Associations dataset.
Thiamine Gene Set From DrugBank Drug Targets interacting proteins for the Thiamine drug from the curated DrugBank Drug Targets dataset.
thiamine Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term thiamine in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
thiamine transport Gene Set From GO Biological Process Annotations 2015 genes participating in the thiamine transport biological process from the curated GO Biological Process Annotations 2015 dataset.
thiamine diphosphate metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the thiamine diphosphate metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
thiamine-containing compound metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the thiamine-containing compound metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
thiamine transmembrane transport Gene Set From GO Biological Process Annotations 2015 genes participating in the thiamine transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset.
thiamine diphosphate biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the thiamine diphosphate biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
thiamine metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the thiamine metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
thiamine phosphate phosphatase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the thiamine phosphate phosphatase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
thiamine pyrophosphate binding Gene Set From GO Molecular Function Annotations 2015 genes performing the thiamine pyrophosphate binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
thiamine uptake transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the thiamine uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
thiamine binding Gene Set From GO Molecular Function Annotations 2015 genes performing the thiamine binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
thiamine transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the thiamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
thiamine diphosphokinase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the thiamine diphosphokinase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
[³H]thiamine Gene Set From Guide to Pharmacology Chemical Ligands of Receptors receptors of the [³H]thiamine ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.
Thiamine Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Thiamine metabolite from the curated HMDB Metabolites of Enzymes dataset.
Thiamine pyrophosphate Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Thiamine pyrophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.
Thiamine monophosphate Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Thiamine monophosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.
2-(a-Hydroxyethyl)thiamine diphosphate Gene Set From HMDB Metabolites of Enzymes interacting proteins for the 2-(a-Hydroxyethyl)thiamine diphosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.
Thiamine triphosphate Gene Set From HMDB Metabolites of Enzymes interacting proteins for the Thiamine triphosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.
Thiamine pyrophosphate enzyme, C-terminal TPP-binding Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, C-terminal TPP-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamine transporter 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine transporter 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamine transporter 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamine pyrophosphate enzyme, central domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamine triphosphatase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine triphosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Thiamine pyrophosphate enzyme, N-terminal TPP-binding domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Thiamine pyrophosphate enzyme, N-terminal TPP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
thiamine metabolism Gene Set From KEGG Pathways proteins participating in the thiamine metabolism pathway from the KEGG Pathways dataset.
Thiamine metabolism Gene Set From PANTHER Pathways proteins participating in the Thiamine metabolism pathway from the PANTHER Pathways dataset.
Thiamine Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
thiamine transmembrane transport Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine transport Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine transport biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine-containing compound metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine-containing compound metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine pyrophosphate transmembrane transport Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine pyrophosphate transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine diphosphate metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine diphosphate metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine diphosphate biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine diphosphate biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine-containing compound biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the thiamine-containing compound biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
thiamine transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the thiamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
thiamine phosphate phosphatase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the thiamine phosphate phosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
thiamine pyrophosphate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the thiamine pyrophosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
thiamine triphosphate phosphatase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the thiamine triphosphate phosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
thiamine diphosphokinase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the thiamine diphosphokinase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
Thiamine Gene Set From MW Enzyme Metabolite Associations interacting proteins for Thiamine metabolite from the MW Gene Metabolite Associations dataset.
Thiamine monophosphate Gene Set From MW Enzyme Metabolite Associations interacting proteins for Thiamine monophosphate metabolite from the MW Gene Metabolite Associations dataset.
Thiamine diphosphate Gene Set From MW Enzyme Metabolite Associations interacting proteins for Thiamine diphosphate metabolite from the MW Gene Metabolite Associations dataset.
thiamine Gene Set From LINCS L1000 CMAP Chemical Perturbation Consensus Signatures genes differentially expressed following the thiamine small molecule perturbation from the LINCS L1000 CMAP Chemical Perturbation Consensus Signatures dataset.
Thiamine metabolic pathways Gene Set From WikiPathways Pathways 2024 proteins participating in the Thiamine metabolic pathways pathway from the WikiPathways Pathways 2024 dataset.
thiamine transmembrane transport Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine transport Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine transport biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine-containing compound metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine-containing compound metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine pyrophosphate transmembrane transport Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine pyrophosphate transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine diphosphate metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine diphosphate metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine diphosphate biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine diphosphate biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine-containing compound biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the thiamine-containing compound biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
thiamine transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the thiamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
thiamine phosphate phosphatase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the thiamine phosphate phosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
thiamine pyrophosphate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the thiamine pyrophosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
thiamine triphosphate phosphatase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the thiamine triphosphate phosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
thiamine diphosphokinase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the thiamine diphosphokinase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
UTP thiamine diphosphokinase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the UTP thiamine diphosphokinase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Thiamine deficiency disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thiamine deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood encephalopathy due to thiamine pyrophosphokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thiamine metabolism Gene Set From KEGG Pathways 2026 proteins participating in the Thiamine metabolism pathway from the KEGG Pathways 2026 dataset.
THIAMINE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the THIAMINE drug from theDGIdb Drug Targets 2026 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.
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, 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.
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.
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.
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.
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.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
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.
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.
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.
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.
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.
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, 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.
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.
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.
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; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hereditary nonspherocytic hemolytic anemia (hnsha). Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary nonspherocytic hemolytic anemia (hnsha). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
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; 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.
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.
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.
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.
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.
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.
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, 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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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, 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to erythrocyte adenosine deaminase overproduction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hemolytic anemia due to adenylate kinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to adenylate kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hemolytic anemia due to glutathione reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hemolytic anemia due to glutathione reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant sideroblastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Inherited aplastic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Inherited aplastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Normochromic microcytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Normochromic microcytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrocytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrocytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic congenital hemolytic and dyserythropoietic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic congenital hemolytic and dyserythropoietic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autoimmune hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoimmune hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diamond-Blackfan anemia-like Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diamond-Blackfan anemia-like phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked congenital hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked congenital hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vaso-occlusive pain in sickle-cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vaso-occlusive pain in sickle-cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Red blood cell density in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red blood cell density in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe aplastic anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe aplastic anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hemoglobin A2 levels in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hemoglobin A2 levels in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fetal hemoglobin levels in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fetal hemoglobin levels in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Alloimmunization response to red blood cell transfusion in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alloimmunization response to red blood cell transfusion in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Systolic blood pressure in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sickle cell anemia (haemolysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sickle cell anemia (haemolysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cholelithiasis-related traits in sickle cell anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cholelithiasis-related traits in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ribavirin-induced anemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ribavirin-induced anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fanconi anemia pathway Gene Set From KEGG Pathways 2026 proteins participating in the Fanconi anemia pathway pathway from the KEGG Pathways 2026 dataset.
Lynch syndrome:Turcot syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marfan's syndrome:Marfan's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome:Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
IFAP syndrome with or without BRESHECK syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome I:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset.
Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset.
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cornelia de lange syndrome; de lange syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set From GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; uveomeningoencephalitic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; uveomeningoencephalitic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melas syndrome; merrf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease melas syndrome; merrf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angelman syndrome; rett syndrome; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolic syndrome ; metabolic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolic syndrome ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; ehlers-danlos syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; felty's syndrome; large granular lymphocyte syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart-hand syndrome, holt-oram syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
digeorge syndrome/velocardiofacial syndrome complex-2 Gene Set From OMIM Gene-Disease Associations genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ifap syndrome with or without bresheck syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Crouzon syndrome-acanthosis nigricans syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Crouzon syndrome-acanthosis nigricans syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Crouzon syndrome-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
Branchiootic syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Branchiootic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome, type 3, with hypocalciuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome, type 3, with hypocalciuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple synostoses syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sjögren-Larsson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sjögren-Larsson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hennekam lymphangiectasia-lymphedema syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hennekam lymphangiectasia-lymphedema syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
UV-sensitive syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the UV-sensitive syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib-polydactyly syndrome, Majewski type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Char syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Char syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fragile X syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fragile X syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Shwachman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Shwachman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Greig cephalopolysyndactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Greig cephalopolysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Melnick-Fraser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Melnick-Fraser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marfan's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Melnick-Needles syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Melnick-Needles syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Branchiootorenal syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Branchiootorenal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PTEN hamartoma tumor syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PTEN hamartoma tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lesch-Nyhan syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lesch-Nyhan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculofaciocardiodental syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculofaciocardiodental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow Sorauf syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow Sorauf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
17q2131 microdeletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 17q2131 microdeletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Desbuquois syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Desbuquois syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly/autism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly/autism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mohr-Tranebjaerg syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mohr-Tranebjaerg syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteopenic nonfracture syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteopenic nonfracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Barakat syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Barakat syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Raine syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Raine syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digitorenocerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digitorenocerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alport syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alstrom syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alstrom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinism-hyperammonemia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinism-hyperammonemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal multiple pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MORM syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MORM syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Upshaw-Schulman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Upshaw-Schulman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Martsolf syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Martsolf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome 2q32-q33 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Blepharophimosis-ptosis-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Borrone Di Rocco Crovato syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Borrone Di Rocco Crovato syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hurler syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hurler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angelman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angelman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lig4 syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lig4 syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rubinstein-Taybi syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rubinstein-Taybi syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hajdu-Cheney syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hajdu-Cheney syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperferritinemia cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Temtamy preaxial brachydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Temtamy preaxial brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperimmunoglobulin E syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bannayan-Riley-Ruvalcaba syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bannayan-Riley-Ruvalcaba syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chudley-McCullough syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chudley-McCullough syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poretti-boltshauser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poretti-boltshauser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bosch-boonstra-schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frank Ter Haar syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frank Ter Haar syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Androgen resistance syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Androgen resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoparathyroidism retardation dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoparathyroidism retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holt-Oram syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holt-Oram syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duane syndrome type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duane syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Young Simpson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Young Simpson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frasier syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frasier syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
C-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the C-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meier-Gorlin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meier-Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pili torti-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pili torti-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gorlin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marshall syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marshall syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carpenter syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carpenter syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duane-radial ray syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duane-radial ray syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
22q133 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 22q133 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa-corneal clouding-oligophrenia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa-corneal clouding-oligophrenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TNF receptor-associated periodic fever syndrome (TRAPS) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the TNF receptor-associated periodic fever syndrome (TRAPS) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Waardenburg syndrome type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Waardenburg syndrome type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Steel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Steel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome 1q43-q44 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 1q43-q44 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Roberts-SC phocomelia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Roberts-SC phocomelia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bloom syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bloom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
McLeod neuroacanthocytosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the McLeod neuroacanthocytosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebrooculofacioskeletal syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebrooculofacioskeletal syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nicolaides-Baraitser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nicolaides-Baraitser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nager syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nager syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chédiak-Higashi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chédiak-Higashi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kindler's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kindler's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnevale syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnevale syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kenny syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kenny syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rienhoff syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rienhoff syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Weaver syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Weaver syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia/short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Siderius X-linked mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lymphoproliferative syndrome, ebv-associated, autosomal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lymphoproliferative syndrome, ebv-associated, autosomal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kohlschutter's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kohlschutter's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with marfanoid habitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebro-oculo-facio-skeletal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebro-oculo-facio-skeletal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis-lymphedema-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis-lymphedema-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LEOPARD syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LEOPARD syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Treacher collins syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Treacher collins syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wiskott-Aldrich syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wiskott-Aldrich syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyper-IgE syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyper-IgE syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tourette Syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tourette Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, macrosomia, facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, macrosomia, facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome antenatal type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome antenatal type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gamstorp-Wohlfart syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gamstorp-Wohlfart syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Turcot syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sick sinus syndrome 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyaline fibromatosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyaline fibromatosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

thiamine-responsive megaloblastic anemia syndrome Gene Set

thiamine-responsive megaloblastic anemia syndrome Gene Set

thiamine-responsive megaloblastic anemia syndrome Gene Set

Cystic fibrosis-gastritis-megaloblastic anemia syndrome 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

Megaloblastic anemia due to inborn errors of metabolism Gene Set

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

Megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

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

MEGALOBLASTIC ANEMIA 1 Gene Set

Anemia, Megaloblastic Gene Set

megaloblastic anemia Gene Set

megaloblastic anemia Gene Set

folate-unresponsive megaloblastic anemia Gene Set

Anemia, Megaloblastic Gene Set

megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set

megaloblastic anemia-1, finnish type Gene Set

homocystinuria-megaloblastic anemia, cbl e type Gene Set

homocystinuria-megaloblastic anemia, cblg complementation type Gene Set

megaloblastic anemia-1, norwegian type Gene Set

Defective AMN causes hereditary megaloblastic anemia 1 Gene Set

Defective CUBN causes hereditary megaloblastic anemia 1 Gene Set

Defective TCN2 causes hereditary megaloblastic anemia Gene Set

Megaloblastic Anemia Gene Set

Combined Immunodeficiency And Megaloblastic Anemia With Or Without Hyperhomocysteinemia Gene Set

Folate-Unresponsive Megaloblastic Anemia Gene Set

Megaloblastic anemia Gene Set

Megaloblastic anemia Gene Set

homocystinuria-megaloblastic anemia cblG type Gene Set

homocystinuria-megaloblastic anemia cblE type Gene Set

Homocystinuria-megaloblastic anemia cblD Gene Set

Megaloblastic anemia Gene Set

Combined immunodeficiency and megaloblastic anemia Gene Set

Constitutional megaloblastic anemia Gene Set

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

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

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

Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene Set

Thiamine metabolism dysfunction syndrome 2 Gene Set

Thiamine Metabolism Dysfunction Syndrome 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

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

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

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

anemia, aplastic; aplastic anemia Gene Set

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

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

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

megaloblastic Gene Set

megaloblastic bone marrow Gene Set

megaloblastic erythroid hyperplasia Gene Set

Megaloblastic Erythroid Hyperplasia Gene Set

[³H]thiamine Gene Set