Infection Due To Mycobacterium Kansasii

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Results for "Infection Due To Mycobacterium Kansasii": 8 genes, 1001 gene sets

Name
SM2 Gene Hepatic fibrosis susceptibility due to Schistosoma mansoni infection
MTBS1 Gene mycobacterium tuberculosis, susceptibility to infection by, 1
MTBSX Gene Mycobacterium tuberculosis, susceptibility to infection by
OPHLC Gene Omphalocele due* to duplication of 1p31.3*
PSHK2 Gene Pseudohyperkalemia, familial, 2, due* to red cell leak*
MTBS3 Gene Mycobacterium tuberculosis, susceptibility to, 3
MTBS2 Gene Mycobacterium tuberculosis, susceptibility to, 2
PFBI Gene Plasmodium falciparum blood infection* levels*
Infection Due To Mycobacterium Kansasii Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Mycobacterium Kansasii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disseminated Mycobacterium Kansasii Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Mycobacterium Kansasii Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; mycobacterium avium-intracellulare infection Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; mycobacterium avium-intracellulare infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mycobacterium avium-intracellulare infection; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease mycobacterium avium-intracellulare infection; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aids-related opportunistic infections; cytomegalovirus retinitis; encephalomyelitis; hiv infections; hypersensitivity; mycobacterium avium-intracellulare infection; [x]human immunodeficiency virus disease Gene Set From GAD Gene-Disease Associations genes associated with the disease aids-related opportunistic infections; cytomegalovirus retinitis; encephalomyelitis; hiv infections; hypersensitivity; mycobacterium avium-intracellulare infection; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Mycobacterium avium-intracellulare Infection Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mycobacterium avium-intracellulare Infection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
{mycobacterium tuberculosis, susceptibility to infection by} Gene Set From OMIM Gene-Disease Associations genes associated with the {mycobacterium tuberculosis, susceptibility to infection by} phenotype from the curated OMIM Gene-Disease Associations dataset.
Latent infection of Homo sapiens with Mycobacterium tuberculosis Gene Set From Reactome Pathways 2014 proteins participating in the Latent infection of Homo sapiens with Mycobacterium tuberculosis pathway from the Reactome Pathways dataset.
Mycobacterium Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mycobacterium Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pulmonary Mycobacterium Avium Complex Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Mycobacterium Avium Complex Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disseminated Mycobacterium Avium Complex Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Mycobacterium Avium Complex Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mycobacterium Tuberculosis, Susceptibility To Infection By Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mycobacterium Tuberculosis, Susceptibility To Infection By in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Infection with Mycobacterium tuberculosis Gene Set From Reactome Pathways 2024 proteins participating in the Infection with Mycobacterium tuberculosis pathway from the Reactome Pathways 2024 dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset.
chronic hepatitis due to cryptospridium infection Gene Set From HPO Gene-Disease Associations genes associated with the chronic hepatitis due to cryptospridium infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set From OMIM Gene-Disease Associations genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset.
Chronic Hepatitis Due To Cryptosporidium Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Hepatitis Due To Cryptosporidium Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Due To Brucella Suis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Brucella Suis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Due To Vancomycin Resistant Staphylococcus Aureus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Vancomycin Resistant Staphylococcus Aureus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Due To Clostridium Chauvoei Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Due To Clostridium Chauvoei in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
infection; multiple myeloma; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
h. pylori infection; helicobacter pylori infection Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection; helicobacter pylori infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infection; hepatitis c infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infection; hepatitis c infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cross infection; pneumonia, ventilator-associated; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease cross infection; pneumonia, ventilator-associated; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Mycobacterium Infections Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mycobacterium Infections from the curated CTD Gene-Disease Associations dataset.
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED from the curated CTD Gene-Disease Associations dataset.
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.
MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.
Mycobacterium Infections, Nontuberculous Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mycobacterium Infections, Nontuberculous from the curated CTD Gene-Disease Associations dataset.
mycobacterium avium complex disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mycobacterium avium complex disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cryptosporidiosis; mycobacterium avium complex; pneumocystis carinii pneumonia; toxoplasmosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cryptosporidiosis; mycobacterium avium complex; pneumocystis carinii pneumonia; toxoplasmosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary disease, mycobacterium malmoense Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary disease, mycobacterium malmoense in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphadenitis; mycobacterium infections; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphadenitis; mycobacterium infections; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; mycobacterium infections, atypical Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; mycobacterium infections, atypical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mycobacterium infections, atypical; skin ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease mycobacterium infections, atypical; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mycobacterium Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mycobacterium in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
recurrent mycobacterium avium complex infections Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent mycobacterium avium complex infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent mycobacterium avium complex infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent mycobacterium avium complex infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Mycobacterium Infections Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mycobacterium Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mycobacterium Infections, Atypical Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mycobacterium Infections, Atypical phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
{mycobacterium tuberculosis, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {mycobacterium tuberculosis, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{mycobacterium tuberculosis, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {mycobacterium tuberculosis, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
{mycobacterium tuberculosis, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {mycobacterium tuberculosis, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
{mycobacterium tuberculosis, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {mycobacterium tuberculosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Mycobacterium Tuberculosis, Susceptibility To (Finding) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mycobacterium Tuberculosis, Susceptibility To (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mycobacterium Tuberculosis Meningitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mycobacterium Tuberculosis Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mycobacterium; Ulcerans (Disease) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mycobacterium; Ulcerans (Disease) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Mycobacterium Avium Complex Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mycobacterium Avium Complex Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mycobacterium avium complex disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mycobacterium avium complex disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mycobacterium tuberculosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mycobacterium tuberculosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (continuous) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (continuous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (dichotomous) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (dichotomous) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
SCID due to ADA deficiency, delayed onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia due to protein S deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive 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.
Severe combined immunodeficiency due to ADA deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency due to ADA deficiency 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.
HNSHA due to aldolase A deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaucher disease, atypical, due to saposin C deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megaloblastic anemia due to inborn errors of metabolism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Leigh syndrome due to mitochondrial complex I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Homocysteinemia due to MTHFR deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency due to ficolin 3 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia due to activated protein C resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermethioninemia due to adenosine kinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia due to thrombomodulin defect Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency due to defect in cd3-zeta Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Homocystinuria due to MTHFR deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria due to MTHFR deficiency 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.
Leigh syndrome due to mitochondrial complex II deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor 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.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency 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.
Obesity, severe, due to leptin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adenylate kinase deficiency, hemolytic anemia due to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect 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.
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.
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.
Congenital thrombotic disease, due to Protein C deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.
Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.
Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Severe combined immunodeficiency due to adenosine deaminase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency 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.
METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset.
Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency 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.
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.
Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset.
Thrombophilia due to Activated Protein C Resistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia due to Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset.
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Immunodeficiency due to Defect in CD3-Zeta Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Metachromatic Leukodystrophy due to Saposin B Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset.
Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein 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.
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.
thrombocytopenia due to platelet alloimmunization Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pneumoconiosis due to talc Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pneumoconiosis due to talc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary spastic paraparesis due to a frame shift mutat Gene Set From GAD Gene-Disease Associations genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressed suicide; suicide due to depression Gene Set From GAD Gene-Disease Associations genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
due Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term due in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations 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.
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set From HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles 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.
restricted neck movement due to contractures Gene Set From HPO Gene-Disease Associations genes associated with the restricted neck movement due to contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chronic rhinitis due to narrow nasal airway Gene Set From HPO Gene-Disease Associations genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteomyelitis due to immunodeficiency Gene Set From HPO Gene-Disease Associations genes associated with the osteomyelitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set From HPO Gene-Disease Associations genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bowing of limbs due to multiple fractures Gene Set From HPO Gene-Disease Associations genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
respiratory insufficiency due to muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteomyelitis leading to amputation due to slow healing fractures Gene Set From HPO Gene-Disease Associations genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
weakness due to upper motor neuron dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
self-mutilation of tongue and lips due to involuntary movements Gene Set From HPO Gene-Disease Associations genes associated with the self-mutilation of tongue and lips due to involuntary movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
respiratory insufficiency due to defective ciliary clearance Gene Set From HPO Gene-Disease Associations genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent infections due to aspiration Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypotonia due to defect at the neuromuscular junction Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subperiosteal erosions due to secondary hyperparathyroidism Gene Set From HPO Gene-Disease Associations genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
painless fractures due to injury Gene Set From HPO Gene-Disease Associations genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hepatic abscesses due to immunodeficiency Gene Set From HPO Gene-Disease Associations genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cellulitis due to immunodeficiency Gene Set From HPO Gene-Disease Associations genes associated with the cellulitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sweating due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intermittent episodes of respiratory insufficiency due to muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
orthostatic hypotension due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
{chronic infections, due to mbl deficiency} Gene Set From OMIM Gene-Disease Associations genes associated with the {chronic infections, due to mbl deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to hrg deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to hrg deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to thrombomodulin defect Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.
severe combined immunodeficiency due to il2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to protein s deficiency, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
bleeding disorder due to p2rx1 defect Gene Set From OMIM Gene-Disease Associations genes associated with the bleeding disorder due to p2rx1 defect 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.
nephropathy due to cfhr5 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.
megaloblastic anemia due to dihydrofolate reductase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to protein s deficiency, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
chronic granulomatous disease, autosomal, due to deficiency of cyba Gene Set From OMIM Gene-Disease Associations genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset.
?isolated growth hormone deficiency due to defect in ghrf Gene Set From OMIM Gene-Disease Associations genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to heparin cofactor ii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, morbid, due to leptin receptor deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hypercholesterolemia, due to ligand-defective apo b Gene Set From OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, due to ligand-defective apo b phenotype from the curated OMIM Gene-Disease Associations dataset.
glucocorticoid deficiency, due to acth unresponsiveness Gene Set From OMIM Gene-Disease Associations genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset.
disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene Set From OMIM Gene-Disease Associations genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase 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.
muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene Set From OMIM Gene-Disease Associations genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency due to purine nucleoside phosphorylase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hemolytic anemia due to glutathione peroxidase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to protein c deficiency, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
lacticacidemia due to pdx1 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the lacticacidemia due to pdx1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome, autosomal recessive, due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
omphalocele due to duplication of 1p31.3 Gene Set From OMIM Gene-Disease Associations genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset.
muscular dystrophy, congenital, due to itga7 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
anemia, hemolytic, due to umph1 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the anemia, hemolytic, due to umph1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
homocystinuria due to mthfr deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the homocystinuria due to mthfr deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
severe combined immunodeficiency due to ada deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to mitochondrial complex i deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial complex i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to protein c deficiency, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein c deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
cirrhosis due to liver phosphorylase kinase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the cirrhosis due to liver phosphorylase kinase deficiency 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.
metachromatic leukodystrophy due to sap-b deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the metachromatic leukodystrophy due to sap-b deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
gigantism due to ghrf hypersecretion Gene Set From OMIM Gene-Disease Associations genes associated with the gigantism due to ghrf hypersecretion phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, morbid, due to leptin deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, morbid, due to leptin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
pseudohyperkalemia, familial, 2, due to red cell leak Gene Set From OMIM Gene-Disease Associations genes associated with the pseudohyperkalemia, familial, 2, due to red cell leak phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia, familial, due to decreased release of plat Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia, familial, due to decreased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome, due to cox deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome, due to cox deficiency 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.
growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperammonemia due to carbonic anhydrase va deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hemolytic anemia due to g6pd deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to g6pd deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} 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.
hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase i/iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
{drug-induced liver injury due to flucloxacillin} Gene Set From OMIM Gene-Disease Associations genes associated with the {drug-induced liver injury due to flucloxacillin} phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to activated protein c resistance Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to activated protein c resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
?male pseudohermaphroditism due to defective lh Gene Set From OMIM Gene-Disease Associations genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset.
hydrocephalus due to aqueductal stenosis Gene Set From OMIM Gene-Disease Associations genes associated with the hydrocephalus due to aqueductal stenosis phenotype from the curated OMIM Gene-Disease Associations dataset.
bare lymphocyte syndrome, type i, due to tap2 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the bare lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to elevated hrg Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to elevated hrg 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.
emphysema due to aat deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the emphysema due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to antithrombin iii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to antithrombin iii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
erythrocytosis due to bisphosphoglycerate mutase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the erythrocytosis due to bisphosphoglycerate mutase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
thalassemia due to hb lepore Gene Set From OMIM Gene-Disease Associations genes associated with the thalassemia due to hb lepore phenotype from the curated OMIM Gene-Disease Associations dataset.
rickets due to defect in vitamin d 25-hydroxylation Gene Set From OMIM Gene-Disease Associations genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.
aica-ribosiduria due to atic deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the aica-ribosiduria due to atic deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoaldosteronism, congenital, due to cmo i deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hypoaldosteronism, congenital, due to cmo i deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to mitochondrial cox4 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial cox4 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
methylmalonic aciduria due to transcobalamin receptor defect Gene Set From OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.
chronic granulomatous disease due to deficiency of ncf-2 Gene Set From OMIM Gene-Disease Associations genes associated with the chronic granulomatous disease due to deficiency of ncf-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
chronic granulomatous disease due to deficiency of ncf-1 Gene Set From OMIM Gene-Disease Associations genes associated with the chronic granulomatous disease due to deficiency of ncf-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia, x-linked, due to factor ix defect Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.
hypermethioninemia due to adenosine kinase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hypermethioninemia due to adenosine kinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
{thrombophilia, susceptibility to, due to factor v leiden} Gene Set From OMIM Gene-Disease Associations genes associated with the {thrombophilia, susceptibility to, due to factor v leiden} phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency due to defect in mapbp-interacting protein Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to cytochrome c oxidase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to cytochrome c oxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
neurodegeneration due to cerebral folate transport deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the neurodegeneration due to cerebral folate transport deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
goiter, familial, due to ttf-1 defect Gene Set From OMIM Gene-Disease Associations genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.
thrombophilia due to thrombin defect Gene Set From OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency due to ficolin 3 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency due to ficolin 3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperfibrinolysis, familial, due to increased release of plat Gene Set From OMIM Gene-Disease Associations genes associated with the hyperfibrinolysis, familial, due to increased release of plat phenotype from the curated OMIM Gene-Disease Associations dataset.
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leigh syndrome due to mitochondrial complex 1 deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the leigh syndrome due to mitochondrial complex 1 deficiency 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.
{resistance to malaria due to g6pd deficiency} Gene Set From OMIM Gene-Disease Associations genes associated with the {resistance to malaria due to g6pd 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.
hemosiderosis, systemic, due to aceruloplasminemia Gene Set From OMIM Gene-Disease Associations genes associated with the hemosiderosis, systemic, due to aceruloplasminemia phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy due to cpt ii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy due to cpt ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
emphysema-cirrhosis, due to aat deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the emphysema-cirrhosis, due to aat deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
hypoaldosteronism, congenital, due to cmo ii deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set From OMIM Gene-Disease Associations genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.
?male infertility due to acrosin deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy due to myoadenylate deaminase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy due to myoadenylate deaminase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) Gene Set From Reactome Pathways 2014 proteins participating in the Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD) pathway from the Reactome Pathways dataset.
Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Apoptosis-related network due to altered Notch3 in ovarian cancer(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Malignant Hyperpyrexia Due To Anesthesia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Hyperpyrexia Due To Anesthesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudohyperkalemia, Familial, 2, Due To Red Cell Leak in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Functional Diarrhoea (Due To Spastic Colon) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Functional Diarrhoea (Due To Spastic Colon) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Neuropathy Due To And Following Chemotherapy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy Due To And Following Chemotherapy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemolytic Disease Of Fetus Or Newborn Due To Abo Immunization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemolytic Disease Of Fetus Or Newborn Due To Abo Immunization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Viral Gastroenteritis Due To Rotavirus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Viral Gastroenteritis Due To Rotavirus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dementia Due To Alzheimer'S Disease (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dementia Due To Alzheimer'S Disease (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Whooping Cough Due To Unspecified Organism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Whooping Cough Due To Unspecified Organism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteopenia Due To Disuse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteopenia Due To Disuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scid Due To Ada Deficiency, Early-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scid Due To Ada Deficiency, Early-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypermethioninemia Due To Adenosine Kinase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypermethioninemia Due To Adenosine Kinase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disease Due To Parvoviridae Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disease Due To Parvoviridae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Respiratory Disease Due To Mycoplasma Gallisepticum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Respiratory Disease Due To Mycoplasma Gallisepticum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Differentiation Syndrome Due To And Following Chemotherapy Co-Occurrent With Acute Promyelocytic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Differentiation Syndrome Due To And Following Chemotherapy Co-Occurrent With Acute Promyelocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Adenocarcinoma Of Lower Third Of Esophagus Due To Barrett Esophagus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Adenocarcinoma Of Lower Third Of Esophagus Due To Barrett Esophagus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Addison'S Disease Due To Autoimmunity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Addison'S Disease Due To Autoimmunity 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.
Eye Disorder Due To Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Eye Disorder Due To Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ketoacidosis Due To Acute Alcohol Intoxication Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ketoacidosis Due To Acute Alcohol Intoxication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Human Anaplasmosis Due To Anaplasma Phagocytophilum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Human Anaplasmosis Due To Anaplasma Phagocytophilum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia, Familial, Due To Ligand-Defective Apolipoprotein B in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
End Stage Renal Disease Due To Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease End Stage Renal Disease Due To Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Male Infertility With Teratozoospermia Due To Single Gene Mutation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Teratozoospermia Due To Single Gene Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hydrops Fetalis Due To Alpha Thalassemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hydrops Fetalis Due To Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leigh Syndrome Due To Mitochondrial Complex I Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leigh Syndrome Due To Mitochondrial Complex I Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disease Due To Acanthocephala Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disease Due To Acanthocephala in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fast Acetylator Due To N-Acetyltransferase Enzyme Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fast Acetylator Due To N-Acetyltransferase Enzyme Variant 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.
Antibody Deficiency Due To Defect In Cd19 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Due To Defect In Cd19 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disease Due To Neisseria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disease Due To Neisseria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteomyelitis Due To Staphylococcus Aureus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteomyelitis Due To Staphylococcus Aureus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardioencephalomyopathy, Fatal Infantile, Due To Cytochrome C Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemosiderosis, Systemic, Due To Aceruloplasminemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemosiderosis, Systemic, Due To Aceruloplasminemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuronal Ceroid Lipofuscinosis Due To Cathepsin D Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuronal Ceroid Lipofuscinosis Due To Cathepsin D Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inherited Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slow Acetylator Due To N-Acetyltransferase Enzyme Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slow Acetylator Due To N-Acetyltransferase Enzyme Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercholesterolemia Due To Cholesterol 7Alpha-Hydroxylase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercholesterolemia Due To Cholesterol 7Alpha-Hydroxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Body Skin Hyperlaxity Due To Vitamin K Dependent Coagulation Factor Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Body Skin Hyperlaxity Due To Vitamin K Dependent Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Infections Due To Aspiration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Due To Aspiration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Duodenal Obstruction Due To Malrotation Of Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duodenal Obstruction Due To Malrotation Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Krabbe Disease, Atypical, Due To Saposin A Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Krabbe Disease, Atypical, Due To Saposin A Deficiency 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.
Hydronephrosis Due To Pujo Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hydronephrosis Due To Pujo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyrotoxicosis Due To Pituitary Thyroid Hormone Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyrotoxicosis Due To Pituitary Thyroid Hormone Resistance 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.
Disseminated Due To Other Mycobacteria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Due To Other Mycobacteria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diabetes (Mellitus) Due To Autoimmune Process Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diabetes (Mellitus) Due To Autoimmune Process in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diabetes (Mellitus) Due To Immune Mediated Pancreatic Islet Beta-Cell Destruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diabetes (Mellitus) Due To Immune Mediated Pancreatic Islet Beta-Cell Destruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Syndromic Multisystem Autoimmune Disease Due To Itch Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Syndromic Multisystem Autoimmune Disease Due To Itch Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Immunodeficiency Syndrome Due To P14 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Immunodeficiency Syndrome Due To P14 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Scoliosis Due To Bony Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Scoliosis Due To Bony Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Neonatal Lactic Acidosis Due To Nfs1-Isd11 Complex Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Renal Failure Due To Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Renal Failure Due To Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dementia Due To Parkinson'S Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dementia Due To Parkinson'S Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urticaria Due To Cold And Heat Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urticaria Due To Cold And Heat in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urticaria Due To Cold Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urticaria Due To Cold in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance 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.
Hypercoagulability Syndrome Due To Glycosylphosphatidylinositol Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercoagulability Syndrome Due To Glycosylphosphatidylinositol Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Bronchitis Due To Respiratory Syncytial Virus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Bronchitis Due To Respiratory Syncytial Virus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Irritant Contact Dermatitis Due To Incontinence Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Irritant Contact Dermatitis Due To Incontinence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Thrombotic Disease, Due To Protein C Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Thrombotic Disease, Due To Protein C Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metachromatic Leukodystrophy Due To Saposin B Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metachromatic Leukodystrophy Due To Saposin B Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hemolytic Disease Of Fetus Or Newborn Due To Rhd Isoimmunization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hemolytic Disease Of Fetus Or Newborn Due To Rhd Isoimmunization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Extraoral Halitosis Due To Methanethiol Oxidase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Extraoral Halitosis Due To Methanethiol Oxidase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complement Component 4, Partial Deficiency Of, Due To Dysfunctional C1 Inhibitor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complement Component 4, Partial Deficiency Of, Due To Dysfunctional C1 Inhibitor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dermatophilosis Due To Dermatophilus Congolensis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dermatophilosis Due To Dermatophilus Congolensis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Perinatal Jaundice Due To Inspissated Bile Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Perinatal Jaundice Due To Inspissated Bile Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Developmental And Speech Delay Due To Sox5 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Developmental And Speech Delay Due To Sox5 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Rhinitis Due To Narrow Nasal Airway Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Rhinitis Due To Narrow Nasal Airway in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteomalacia Due To Vitamin D Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteomalacia Due To Vitamin D Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycythemia Due To Erythropoietin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Erythropoietin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycythemia Due To Excess Erythopoetin Production Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Excess Erythopoetin Production in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycythemia Due To Fall In Plasma Volume Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Fall In Plasma Volume in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycythemia Due To High Altitude Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To High Altitude in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polycythemia Due To Stress Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polycythemia Due To Stress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Muscle Atrophy Due To Neurologic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Respiratory Insufficiency Due To Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Psychomotor Retardation Due To S-Adenosylhomocysteine Hydrolase Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Psychomotor Retardation Due To S-Adenosylhomocysteine Hydrolase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Respiratory Insufficiency Due To Defective Ciliary Clearance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Respiratory Insufficiency Due To Defective Ciliary Clearance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Orthostatic Hypotension Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Orthostatic Hypotension Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Osteomyelitis Leading To Amputation Due To Slow Healing Fractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteomyelitis Leading To Amputation Due To Slow Healing Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosomal Mosaicism Due To Mitotic Instability Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosomal Mosaicism Due To Mitotic Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Weakness Due To Upper Motor Neuron Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cephalhematoma Due To Birth Trauma Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cephalhematoma Due To Birth Trauma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bowing Of Limbs Due To Multiple Fractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bowing Of Limbs Due To Multiple Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Restricted Neck Movement Due To Contractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Restricted Neck Movement Due To Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Painless Fractures Due To Injury Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Painless Fractures Due To Injury in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Sweating Due To Autonomic Dysfunction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Sweating Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acanthocytosis Due To Band 3 Ht Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acanthocytosis Due To Band 3 Ht in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Self-Mutilation Of Tongue And Lips Due To Involuntary Movements Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Self-Mutilation Of Tongue And Lips Due To Involuntary Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Apoptosis related network due to altered Notch3 in ovarian cancer Gene Set From WikiPathways Pathways 2024 proteins participating in the Apoptosis related network due to altered Notch3 in ovarian cancer pathway from the WikiPathways Pathways 2024 dataset.
Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects Gene Set From Reactome Pathways 2024 proteins participating in the Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects pathway from the Reactome Pathways 2024 dataset.
Aberrant regulation of mitotic cell cycle due to RB1 defects Gene Set From Reactome Pathways 2024 proteins participating in the Aberrant regulation of mitotic cell cycle due to RB1 defects pathway from the Reactome Pathways 2024 dataset.
Aberrant regulation of mitotic exit in cancer due to RB1 defects Gene Set From Reactome Pathways 2024 proteins participating in the Aberrant regulation of mitotic exit in cancer due to RB1 defects pathway from the Reactome Pathways 2024 dataset.
Defective DNA double strand break response due to BARD1 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective DNA double strand break response due to BARD1 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective DNA double strand break response due to BRCA1 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective DNA double strand break response due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function Gene Set From Reactome Pathways 2024 proteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function pathway from the Reactome Pathways 2024 dataset.
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function Gene Set From Reactome Pathways 2024 proteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function pathway from the Reactome Pathways 2024 dataset.
Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations Gene Set From Reactome Pathways 2024 proteins participating in the Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations pathway from the Reactome Pathways 2024 dataset.
Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations Gene Set From Reactome Pathways 2024 proteins participating in the Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations pathway from the Reactome Pathways 2024 dataset.
Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function Gene Set From Reactome Pathways 2024 proteins participating in the Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function pathway from the Reactome Pathways 2024 dataset.
Defective homologous recombination repair (HRR) due to BRCA1 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective homologous recombination repair (HRR) due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective homologous recombination repair (HRR) due to BRCA2 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective homologous recombination repair (HRR) due to BRCA2 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective homologous recombination repair (HRR) due to PALB2 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective homologous recombination repair (HRR) due to PALB2 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to ABCA4 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to ABCA4 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to LRAT loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to LRAT loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1LW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1LW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1MW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1MW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to OPN1SW loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to OPN1SW loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to RDH12 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to RDH12 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to RDH5 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to RDH5 loss of function pathway from the Reactome Pathways 2024 dataset.
Defective visual phototransduction due to STRA6 loss of function Gene Set From Reactome Pathways 2024 proteins participating in the Defective visual phototransduction due to STRA6 loss of function pathway from the Reactome Pathways 2024 dataset.
Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 pathway from the Reactome Pathways 2024 dataset.
Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 pathway from the Reactome Pathways 2024 dataset.
Evasion of Oncogene Induced Senescence Due to p14ARF Defects Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oncogene Induced Senescence Due to p14ARF Defects pathway from the Reactome Pathways 2024 dataset.
Evasion of Oncogene Induced Senescence Due to p16INK4A Defects Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oncogene Induced Senescence Due to p16INK4A Defects pathway from the Reactome Pathways 2024 dataset.
Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 pathway from the Reactome Pathways 2024 dataset.
Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 pathway from the Reactome Pathways 2024 dataset.
Evasion of Oxidative Stress Induced Senescence Due to p14ARF Defects Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oxidative Stress Induced Senescence Due to p14ARF Defects pathway from the Reactome Pathways 2024 dataset.
Evasion of Oxidative Stress Induced Senescence Due to p16INK4A Defects Gene Set From Reactome Pathways 2024 proteins participating in the Evasion of Oxidative Stress Induced Senescence Due to p16INK4A Defects pathway from the Reactome Pathways 2024 dataset.
Loss of function of TP53 in cancer due to loss of tetramerization ability Gene Set From Reactome Pathways 2024 proteins participating in the Loss of function of TP53 in cancer due to loss of tetramerization ability pathway from the Reactome Pathways 2024 dataset.
Severe congenital encephalopathy due to MECP2 mutation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Severe congenital encephalopathy due to MECP2 mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Male infertility due to globozoospermia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male infertility due to globozoospermia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital muscular dystrophy due to LMNA mutation from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Male infertility due to globozoospermia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to globozoospermia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Male infertility due to acephalic spermatozoa Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to acephalic spermatozoa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombocytopenia due to platelet alloimmunization Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Polyneuropathy due to drug Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Polyneuropathy due to drug in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to LMNA mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Encephalopathy due to defective mitochondrial and peroxisomal fission 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to activated protein C resistance Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to activated protein C resistance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to thrombin defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple epiphyseal dysplasia due to collagen 9 anomaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple epiphyseal dysplasia due to collagen 9 anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy due to integrin alpha-7 deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Severe congenital encephalopathy due to MECP2 mutation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Severe congenital encephalopathy due to MECP2 mutation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to HRG deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to HRG deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked thrombophilia due to factor IX defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked thrombophilia due to factor IX defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive thrombophilia due to protein C deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive thrombophilia due to protein C deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant thrombophilia due to protein C deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant thrombophilia due to protein C deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thrombophilia due to thrombomodulin defect Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thrombophilia due to thrombomodulin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant thrombophilia due to protein S deficiency Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant thrombophilia due to protein S deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperphenylalaninemia due to tetrahydrobiopterin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperphenylalaninemia due to tetrahydrobiopterin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thrombophilia due to activated protein C resistance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thrombophilia due to protein C deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to protein C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary thrombophilia due to congenital protein C deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombophilia due to congenital protein C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Methylmalonic aciduria due to complete methylmalonyl-CoA mutase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic aciduria due to complete methylmalonyl-CoA mutase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCID due to ADA deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCID due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to glycogen branching enzyme deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to glycogen branching enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Predisposition to invasive fungal disease due to CARD9 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Predisposition to invasive fungal disease due to CARD9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Homocystinuria due to methylene tetrahydrofolate reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Homocystinuria due to methylene tetrahydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thrombophilia due to thrombin defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to thrombin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive ataxia due to ubiquinone deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive ataxia due to ubiquinone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to acid maltase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to acid maltase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hepatoencephalopathy due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hepatoencephalopathy due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic multisystem autoimmune disease due to ITCH deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic multisystem autoimmune disease due to ITCH deficiency 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.
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rubinstein-Taybi syndrome due to EP300 haploinsufficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to DCLRE1C deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to DCLRE1C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to ficolin3 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to ficolin3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Fatal mitochondrial disease due to combined oxidative phosphorylation defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Fatal mitochondrial disease due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal intrahepatic cholestasis due to citrin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal intrahepatic cholestasis due to citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial hyperthyroidism due to mutations in TSH receptor Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial hyperthyroidism due to mutations in TSH receptor phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypothyroidism due to TSH receptor mutations Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypothyroidism due to TSH receptor mutations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lissencephaly due to TUBA1A mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to TUBA1A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peroxisome biogenesis disorder due to PEX1 defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peroxisome biogenesis disorder due to PEX1 defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alagille syndrome due to a JAG1 point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alagille syndrome due to a JAG1 point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to growth hormone secretagogue receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to growth hormone secretagogue receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Interstitial lung disease due to ABCA3 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Interstitial lung disease due to ABCA3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lissencephaly due to LIS1 mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to LIS1 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to leptin receptor gene deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to leptin receptor gene deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ehlers-Danlos syndrome due to tenascin-X deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ehlers-Danlos syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to partial GHR deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to partial GHR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital lipoid adrenal hyperplasia due to STAR deficency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital lipoid adrenal hyperplasia due to STAR deficency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
T-B+ severe combined immunodeficiency due to JAK3 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the T-B+ severe combined immunodeficiency due to JAK3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rubinstein-Taybi syndrome due to CREBBP mutations Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rubinstein-Taybi syndrome due to CREBBP mutations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to phosphoglycerate kinase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hydrocephalus due to aqueductal stenosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hydrocephalus due to aqueductal stenosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked lymphoproliferative disease due to SH2D1A deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked lymphoproliferative disease due to SH2D1A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lissencephaly due to doublecortin gene mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lissencephaly due to doublecortin gene mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to glucose-6-phosphatase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to glucose-6-phosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to CD3gamma deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to CD3gamma deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leigh syndrome due to mitochondrial complex IV deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leigh syndrome due to mitochondrial complex IV deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dopa-responsive dystonia due to sepiapterin reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dopa-responsive dystonia due to sepiapterin reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to partial RAG1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to partial RAG1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to ZAP70 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to ZAP70 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thrombophilia due to protein S deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thrombophilia due to protein S deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to pro-opiomelanocortin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to pro-opiomelanocortin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Gaucher disease due to saposin C deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gaucher disease due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Krabbe disease due to saposin A deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Krabbe disease due to saposin A deficiency 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.
Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to melanocortin 4 receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to melanocortin 4 receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to LMNA mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to LMNA mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary familial polycythemia due to EPO receptor mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary familial polycythemia due to EPO receptor mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth delay due to insulin-like growth factor I resistance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth delay due to insulin-like growth factor I resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperinsulinism due to HNF1A deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperinsulinism due to HNF1A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to growth hormone qualitative anomaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to growth hormone qualitative anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disorder due to hepatic glycogen synthase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disorder due to hepatic glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy due to GLUT1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to GLUT1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperinsulinism due to glucokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperinsulinism due to glucokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to muscle beta-enolase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to muscle beta-enolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to LRBA deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to LRBA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to STK4 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to STK4 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to STIM1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to STIM1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epidermolysis bullosa simplex due to plakophilin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Epidermolysis bullosa simplex due to plakophilin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to CARD11 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CARD11 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to SLC37A4 mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to SLC37A4 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to DOCK8 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to DOCK8 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy due to integrin alpha-7 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy due to integrin alpha-7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limb-girdle muscular dystrophy due to POMK deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscular dystrophy due to POMK deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Vasculitis due to ADA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Vasculitis due to ADA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to muscle and heart glycogen synthase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to muscle and heart glycogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcephalic primordial dwarfism due to RTTN deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephalic primordial dwarfism due to RTTN deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ketoacidosis due to monocarboxylate transporter-1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ketoacidosis due to monocarboxylate transporter-1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Metabolic myopathy due to lactate transporter defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcephalic primordial dwarfism due to ZNF335 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephalic primordial dwarfism due to ZNF335 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorder due to AUTS2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autism spectrum disorder due to AUTS2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pyogenic bacterial infections due to MyD88 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pyogenic bacterial infections due to MyD88 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alagille syndrome due to a NOTCH2 point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alagille syndrome due to a NOTCH2 point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Methylmalonic acidemia due to transcobalamin receptor defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic acidemia due to transcobalamin receptor defect phenotype from the curated ClinVar Gene-Phenotype Associations 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.
Severe combined immunodeficiency due to CTPS1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CTPS1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to CSF3R deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neurofibromatosis due to NF1 mutation or intragenic deletion Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurofibromatosis due to NF1 mutation or intragenic deletion phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to ORAI1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to ORAI1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperinsulinism due to INSR deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperinsulinism due to INSR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to CD25 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to CD25 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DeSanto-Shinawi syndrome due to WAC point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the DeSanto-Shinawi syndrome due to WAC point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to SIM1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to SIM1 deficiency 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.
X-linked lymphoproliferative disease due to XIAP deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked lymphoproliferative disease due to XIAP deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to CARMIL2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CARMIL2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Growth delay due to insulin-like growth factor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Growth delay due to insulin-like growth factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to MASP-2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to MASP-2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital brain dysgenesis due to glutamine synthetase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital brain dysgenesis due to glutamine synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to prohormone convertase I deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to prohormone convertase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to congenital leptin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to congenital leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperlipidemia due to hepatic triglyceride lipase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperlipidemia due to hepatic triglyceride lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature due to primary acid-labile subunit deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to primary acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to defect in CD3-gamma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to defect in CD3-gamma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
HNSHA due to aldolase A deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to moesin deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to moesin deficiency 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.
Severe combined immunodeficiency due to DNA-PKcs deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to DNA-PKcs deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy due to defective mitochondrial and peroxisomal fission Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy due to defective mitochondrial and peroxisomal fission phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to CORO1A deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to CORO1A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to OX40 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to OX40 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to IKK2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to IKK2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Beckwith-Wiedemann syndrome due to CDKN1C mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Beckwith-Wiedemann syndrome due to CDKN1C mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy due to calsequestrin and SERCA1 protein overload Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy due to calsequestrin and SERCA1 protein overload phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant hyperinsulinism due to SUR1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant hyperinsulinism due to SUR1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperinsulinism due to HNF4A deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperinsulinism due to HNF4A 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 recessive severe congenital neutropenia due to JAGN1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to MALT1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to MALT1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SIN3A-related intellectual disability syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SIN3A-related intellectual disability syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to LCK deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to LCK deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to a late component of complement deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to a late component of complement deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lactic aciduria due to D-lactic acid Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lactic aciduria due to D-lactic acid phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent Neisseria infections due to factor D deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent Neisseria infections due to factor D deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Kleefstra syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Kleefstra syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperphenylalaninemia due to DNAJC12 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperphenylalaninemia due to DNAJC12 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Obesity due to CEP19 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Obesity due to CEP19 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pancytopenia due to IKZF1 mutations Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pancytopenia due to IKZF1 mutations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hao-Fountain syndrome due to USP7 mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hao-Fountain syndrome due to USP7 mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive retinal dystrophy due to retinol transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary immunodeficiency syndrome due to p14 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary immunodeficiency syndrome due to p14 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe combined immunodeficiency due to LAT deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe combined immunodeficiency due to LAT deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Combined immunodeficiency due to GINS1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Combined immunodeficiency due to GINS1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary thrombophilia due to congenital histidine-rich Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombophilia due to congenital histidine-rich phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile arthritis due to defect in LA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile arthritis due to defect in LA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neurometabolic disorder due to serine deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurometabolic disorder due to serine deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency due to purine nucleoside phosphorylase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary thrombophilia due to congenital protein S deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary thrombophilia due to congenital protein S deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked acrogigantism due to Xq26 microduplication Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked acrogigantism due to Xq26 microduplication phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Male infertility due to gonadal dysgenesis or sperm disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Male infertility due to gonadal dysgenesis or sperm disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Female infertility due to zona pellucida defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility due to zona pellucida defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Disseminated atypical mycobacterial infection Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Disseminated atypical mycobacterial infection phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infection Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infection from the curated CTD Gene-Disease Associations dataset.
ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.
PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL from the curated CTD Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity from the curated CTD Gene-Disease Associations dataset.
bacteriuria; urinary tract infection; urinary tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bacteriuria; urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; bacterial infections; enterobacteriaceae infections; osteomyelitis; sepsis; sickle cell anemia; staphylococcal infections; systemic infection; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiratory syncytial virus infection Gene Set From GAD Gene-Disease Associations genes associated with the disease respiratory syncytial virus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c; schistosoma mansoni infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c; schistosoma mansoni infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sepsis; systemic infection; wounds, nonpenetrating Gene Set From GAD Gene-Disease Associations genes associated with the disease sepsis; systemic infection; wounds, nonpenetrating in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cancer; hiv infection Gene Set From GAD Gene-Disease Associations genes associated with the disease cancer; hiv infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; kidney failure, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; kidney failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parasitic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease parasitic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
helicobacter pylori infection. Gene Set From GAD Gene-Disease Associations genes associated with the disease helicobacter pylori infection. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
human papillomavirus infection Gene Set From GAD Gene-Disease Associations genes associated with the disease human papillomavirus infection 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.
infection; lymphohistiocytosis, hemophagocytic Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; lymphohistiocytosis, hemophagocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria infection Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
h. pylori infection; stomach cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection; stomach cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
burns; disease susceptibility; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease burns; disease susceptibility; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv/siv infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv/siv infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pulmonary function; nitric oxide; pseudomonas aeruginosa infection Gene Set From GAD Gene-Disease Associations genes associated with the disease pulmonary function; nitric oxide; pseudomonas aeruginosa infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; infant, newborn, diseases; infection; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; infant, newborn, diseases; infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypercholesterolemia; h. pylori infection; coagulation disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; h. pylori infection; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
parvovirus b19 infection Gene Set From GAD Gene-Disease Associations genes associated with the disease parvovirus b19 infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cross infection; pneumonia, ventilator-associated; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease cross infection; pneumonia, ventilator-associated; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cross infection; hepatitis b; hepatitis c; hiv infections; hiv seropositivity; occupational diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease cross infection; hepatitis b; hepatitis c; hiv infections; hiv seropositivity; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasmodium falciparum infection Gene Set From GAD Gene-Disease Associations genes associated with the disease plasmodium falciparum infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pancreatitis; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease pancreatitis; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
h. pylori infection Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; diabetes complications; diabetes mellitus, type 1; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; diabetes complications; diabetes mellitus, type 1; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
staphylococcal infection Gene Set From GAD Gene-Disease Associations genes associated with the disease staphylococcal infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ascaris infection Gene Set From GAD Gene-Disease Associations genes associated with the disease ascaris infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; chorioamnionitis; infection; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; chorioamnionitis; infection; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; infection of amniotic sac and membranes Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bacterial infection Gene Set From GAD Gene-Disease Associations genes associated with the disease bacterial infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bacterial infections; cross infection Gene Set From GAD Gene-Disease Associations genes associated with the disease bacterial infections; cross infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
critical illness; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease critical illness; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
critical illness; pneumonia; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease critical illness; pneumonia; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cross infection; paramyxoviridae infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cross infection; paramyxoviridae infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
burns; infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease burns; infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
postoperative complications; sepsis; septic shock; shock, septic; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease postoperative complications; sepsis; septic shock; shock, septic; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infection; dementia, aids Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infection; dementia, aids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neonatal infection Gene Set From GAD Gene-Disease Associations genes associated with the disease neonatal infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
urinary tract infection; urinary tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; inflammation; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; inflammation; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epstein-barr virus infection Gene Set From GAD Gene-Disease Associations genes associated with the disease epstein-barr virus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
helicobacter pylori infection Gene Set From GAD Gene-Disease Associations genes associated with the disease helicobacter pylori infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv-1 infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv-1 infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
h. pylori infection; stomach cancer; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection; stomach cancer; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis b and c virus infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis b and c virus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hcv infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hcv infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; homocystinuria; hyperhomocysteinemia; muscle spasticity; sepsis; septic shock; shock, septic; systemic infection; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; homocystinuria; hyperhomocysteinemia; muscle spasticity; sepsis; septic shock; shock, septic; systemic infection; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sepsis; septic shock; shock, septic; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease sepsis; septic shock; shock, septic; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carotid atherosclerosis in hiv infection Gene Set From GAD Gene-Disease Associations genes associated with the disease carotid atherosclerosis in hiv infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c virus infection. Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c virus infection. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cicatrix; pyelonephritis; urinary tract infection; urinary tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cicatrix; pyelonephritis; urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; h. pylori infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; h. pylori infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection, post allograft Gene Set From GAD Gene-Disease Associations genes associated with the disease infection, post allograft in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
helicobacter pylori infection; gastritis, helicobacter pylori-induced Gene Set From GAD Gene-Disease Associations genes associated with the disease helicobacter pylori infection; gastritis, helicobacter pylori-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
papillomavirus infection Gene Set From GAD Gene-Disease Associations genes associated with the disease papillomavirus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
h. pylori infection; thrombocytopenic purpura, idiopathic Gene Set From GAD Gene-Disease Associations genes associated with the disease h. pylori infection; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
graft vs host disease; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease graft vs host disease; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cancer; hiv infection; gastrointestinal bleeding; thiopurine methyltransferase activity Gene Set From GAD Gene-Disease Associations genes associated with the disease cancer; hiv infection; gastrointestinal bleeding; thiopurine methyltransferase activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic active hepatitis c infection. Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic active hepatitis c infection. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
urinary tract infection Gene Set From GAD Gene-Disease Associations genes associated with the disease urinary tract infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gram-negative bacterial infections; gram-positive bacterial infections; leukemia, myeloid, acute; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease gram-negative bacterial infections; gram-positive bacterial infections; leukemia, myeloid, acute; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c virus infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c virus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
critical illness; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease critical illness; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
urinary infection Gene Set From GAD Gene-Disease Associations genes associated with the disease urinary infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection Gene Set From GAD Gene-Disease Associations genes associated with the disease infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; infection; neoplasms; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; infection; neoplasms; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydia pneumoniae infection Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydia pneumoniae infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diarrhea; hematologic diseases; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease diarrhea; hematologic diseases; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hpv infection and cervical disease Gene Set From GAD Gene-Disease Associations genes associated with the disease hpv infection and cervical disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis c infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis c infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoviral infection and decreased lung function Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoviral infection and decreased lung function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatitis b virus infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatitis b virus infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
human t lymphotropic virus type i infection Gene Set From GAD Gene-Disease Associations genes associated with the disease human t lymphotropic virus type i infection 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.
chronic hepatitis c virus infection. Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic hepatitis c virus infection. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
helicobacter pylori caga subtype infection Gene Set From GAD Gene-Disease Associations genes associated with the disease helicobacter pylori caga subtype infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endotoxemia; inflammation; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease endotoxemia; inflammation; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; infection of amniotic sac and membranes; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
burns; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease burns; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection; multiple myeloma Gene Set From GAD Gene-Disease Associations genes associated with the disease infection; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv infection Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
critical illness; sepsis; systemic infection; systemic inflam response synd; systemic inflammatory response syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease critical illness; sepsis; systemic infection; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-1 infection Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-1 infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
otitis media; pneumococcal infection Gene Set From GAD Gene-Disease Associations genes associated with the disease otitis media; pneumococcal infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cicatrization; escherichia coli infections; pyelonephritis; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux Gene Set From GAD Gene-Disease Associations genes associated with the disease cicatrization; escherichia coli infections; pyelonephritis; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; hypersensitivity; infection; nasal polyps; rhinitis; sinusitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cicatrization; kidney diseases; recurrence; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux Gene Set From GAD Gene-Disease Associations genes associated with the disease cicatrization; kidney diseases; recurrence; urinary tract infection; urinary tract infections; vesico-ureteral reflux; vesicoureteral reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bacterial infections; urinary tract infection; urinary tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bacterial infections; urinary tract infection; urinary tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sars infection Gene Set From GAD Gene-Disease Associations genes associated with the disease sars infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gram-negative infection Gene Set From GAD Gene-Disease Associations genes associated with the disease gram-negative infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic fibrosis; p. aeruginosa infection Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; p. aeruginosa infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leishmania chagasi infection Gene Set From GAD Gene-Disease Associations genes associated with the disease leishmania chagasi infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
communicable diseases; critical illness; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease communicable diseases; critical illness; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; infection of amniotic sac and membranes; leukomalacia, periventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
puerperal disorders; sepsis; streptococcal infections; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease puerperal disorders; sepsis; streptococcal infections; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple organ failure; multiple trauma; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple organ failure; multiple trauma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth Gene Set From GAD Gene-Disease Associations genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic hepatitis c infection Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic hepatitis c infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
common variable immunodeficiency; hemochromatosis; igg deficiency; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease common variable immunodeficiency; hemochromatosis; igg deficiency; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
communicable diseases; disease susceptibility; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease communicable diseases; disease susceptibility; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infection Gene Set From GAD High Level Gene-Disease Associations genes associated with the disease infection in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset.
infection Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term infection in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Infection by Yersinia enterocolitica_macrophage_GSE2973 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Infection by Yersinia enterocolitica_macrophage_GSE2973 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Rotavirus infection of children_Peripheral blood mononuclear cell_GSE2729 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Rotavirus infection of children_Peripheral blood mononuclear cell_GSE2729 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Escherichia coli infection of the central nervous system_CNS - Brain (MMHCC)_GSE3253 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
HCMV_24Hour-Infection+PP2_21084488_GSE24238 Gene Set From GEO Signatures of Differentially Expressed Genes for Viral Infections genes differentially expressed following the HCMV_24Hour-Infection+PP2_21084488_GSE24238 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.
CVB3_9Hour-Infection+U0126_None_GSE697 Gene Set From GEO Signatures of Differentially Expressed Genes for Viral Infections genes differentially expressed following the CVB3_9Hour-Infection+U0126_None_GSE697 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.
Chronic hepatitis C infection Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic hepatitis C infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Schizophrenia (cytomegalovirus infection interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Schizophrenia (cytomegalovirus infection interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Staphylococcus aureus infection Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Staphylococcus aureus infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Carotid atherosclerosis in HIV infection Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Carotid atherosclerosis in HIV infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Chronic hepatitis B infection Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic hepatitis B infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
helicobacter pylori infection Gene Set From GWASdb SNP-Phenotype Associations genes associated with the helicobacter pylori infection phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cns infection Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cns infection phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent infection of the gastrointestinal tract Gene Set From GWASdb SNP-Phenotype Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
recurrent infection of the gastrointestinal tract Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
respiratory tract infection Gene Set From HPO Gene-Disease Associations genes associated with the respiratory tract infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acute respiratory tract infection Gene Set From HPO Gene-Disease Associations genes associated with the acute respiratory tract infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stress/infection-induced lactic acidosis Gene Set From HPO Gene-Disease Associations genes associated with the stress/infection-induced lactic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cns infection Gene Set From HPO Gene-Disease Associations genes associated with the cns infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Wound Infection Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Wound Infection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Infection Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Infection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cross Infection Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cross Infection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Surgical Wound Infection Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Surgical Wound Infection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Modulator of retrovirus infection Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Modulator of retrovirus infection protein domain from the InterPro Predicted Protein Domain Annotations dataset.
pathogenic escherichia coli infection ehec Gene Set From KEGG Pathways proteins participating in the pathogenic escherichia coli infection ehec pathway from the KEGG Pathways dataset.
pathogenic escherichia coli infection epec Gene Set From KEGG Pathways proteins participating in the pathogenic escherichia coli infection epec pathway from the KEGG Pathways dataset.
cholera infection Gene Set From KEGG Pathways proteins participating in the cholera infection pathway from the KEGG Pathways dataset.
epithelial cell signaling in helicobacter pylori infection Gene Set From KEGG Pathways proteins participating in the epithelial cell signaling in helicobacter pylori infection pathway from the KEGG Pathways dataset.
decreased susceptibility to viral infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bacterial infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
altered susceptibility to parasitic infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
altered susceptibility to bacterial infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to parasitic infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bacterial infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
altered susceptibility to viral infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to viral infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased tumor incidence following infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased tumor incidence following infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to bacterial infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to fungal infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to viral infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to prion infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to parasitic infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to parasitic infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to bacterial infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
altered susceptibility to fungal infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to viral infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to fungal infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to parasitic infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
altered susceptibility to infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
altered susceptibility to infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
altered susceptibility to prion infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the altered susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal response to infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal response to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to prion infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
sars infection, protection against Gene Set From OMIM Gene-Disease Associations genes associated with the sars infection, protection against phenotype from the curated OMIM Gene-Disease Associations dataset.
{encephalopathy, acute, infection-induced, 4, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {encephalopathy, acute, infection-induced, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{hiv1 infection, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hiv1 infection, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{tuberculosis infection, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {tuberculosis infection, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
{pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} Gene Set From OMIM Gene-Disease Associations genes associated with the {pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis} phenotype from the curated OMIM Gene-Disease Associations dataset.
hyper-ige recurrent infection syndrome, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
{hepatitis c virus infection, response to therapy of} Gene Set From OMIM Gene-Disease Associations genes associated with the {hepatitis c virus infection, response to therapy of} phenotype from the curated OMIM Gene-Disease Associations dataset.
{hiv infection, susceptibility/resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hiv infection, susceptibility/resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{hiv infection, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hiv infection, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{schistosoma mansoni infection, susceptibility/resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {schistosoma mansoni infection, susceptibility/resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{gastric cancer risk after h. pylori infection} Gene Set From OMIM Gene-Disease Associations genes associated with the {gastric cancer risk after h. pylori infection} phenotype from the curated OMIM Gene-Disease Associations dataset.
{h. pylori infection, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {h. pylori infection, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, intensity of infection} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, intensity of infection} phenotype from the curated OMIM Gene-Disease Associations dataset.
immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
hyper-ige recurrent infection syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
{norwalk virus infection, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {norwalk virus infection, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{viral infection, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {viral infection, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set From OMIM Gene-Disease Associations genes associated with the alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated OMIM Gene-Disease Associations dataset.
{hepatitis b virus infection, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hepatitis b virus infection, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{rapid progression to aids from hiv1 infection} Gene Set From OMIM Gene-Disease Associations genes associated with the {rapid progression to aids from hiv1 infection} phenotype from the curated OMIM Gene-Disease Associations dataset.
infection Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term infection in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Influenza Infection Gene Set From Reactome Pathways 2014 proteins participating in the Influenza Infection pathway from the Reactome Pathways dataset.
HIV Infection Gene Set From Reactome Pathways 2014 proteins participating in the HIV Infection pathway from the Reactome Pathways dataset.
APOBEC3G mediated resistance to HIV-1 infection Gene Set From Reactome Pathways 2014 proteins participating in the APOBEC3G mediated resistance to HIV-1 infection pathway from the Reactome Pathways dataset.
Influenza A virus infection(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Influenza A virus infection(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Pathogenic Escherichia coli infection(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Pathogenic Escherichia coli infection(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Clostridium Difficile Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Clostridium Difficile Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Helicobacter Pylori (H. Pylori) Infection In Conditions Classified Elsewhere And Of Unspecified Site Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Helicobacter Pylori (H. Pylori) Infection In Conditions Classified Elsewhere And Of Unspecified Site in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Respiratory Syncytial Virus (Rsv) Infection In Conditions Classified Elsewhere And Of Unspecified Site Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Respiratory Syncytial Virus (Rsv) Infection In Conditions Classified Elsewhere And Of Unspecified Site in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhinovirus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhinovirus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Helicobacter Pylori Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Helicobacter Pylori in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brucella Melitensis Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brucella Melitensis Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Infection Nos Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Infection Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudomonas Aeruginosa Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudomonas Aeruginosa Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mrsa - Methicillin Resistant Staphylococcus Aureus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mrsa - Methicillin Resistant Staphylococcus Aureus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chlamydia Trachomatis Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chlamydia Trachomatis Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Febrile Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Febrile Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Epstein Barr Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Epstein Barr Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Ascaris Lumbricoides Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Ascaris Lumbricoides in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Trichuris Trichiura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Trichuris Trichiura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Organ Surgical Site Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Organ Surgical Site Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection In Children Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Staphylococcus Aureus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Staphylococcus Aureus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Herpes Simplex Type 1 Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Herpes Simplex Type 1 Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Plasmodium Vivax Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Plasmodium Vivax Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Babesia Bovis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Babesia Bovis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Infection With Hiv Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Infection With Hiv in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Human Herpesvirus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Human Herpesvirus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Human Papilloma Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Human Papilloma Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Xmrv Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Xmrv Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Active Ebv Infection Of T-And Nk-Cell Type, Systemic Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Active Ebv Infection Of T-And Nk-Cell Type, Systemic Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Cryptococcus Neoformans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Cryptococcus Neoformans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Lower Respiratory Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Lower Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pleural Effusion Associated With Pulmonary Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pleural Effusion Associated With Pulmonary Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prosthetic Joint Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prosthetic Joint Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Upper Respiratory Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Upper Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Hiv Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Hiv Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Zika Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zika Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neonatal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neonatal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrauterine Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrauterine Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Respiratory Tract Infection Viral Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Respiratory Tract Infection Viral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asymptomatic Human Immunodeficiency Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asymptomatic Human Immunodeficiency Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pediatric Human Immunodeficiency Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pediatric Human Immunodeficiency Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Perinatal Hiv Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Perinatal Hiv Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Hiv Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Hiv Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Group B Streptococcal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Group B Streptococcal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mink Parvovirus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mink Parvovirus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bluetongue Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bluetongue Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Leishmania Braziliensis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Leishmania Braziliensis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mucosal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mucosal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Bacterial Skin And Skin Structure Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Bacterial Skin And Skin Structure Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Of Bone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Invasive Bacterial Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Invasive Bacterial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hantavirus Infection In Conditions Classified Elsewhere And Of Unspecified Site Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hantavirus Infection In Conditions Classified Elsewhere And Of Unspecified Site in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Respiratory Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Candida Albicans Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Candida Albicans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Trypanosoma Brucei Brucei Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Trypanosoma Brucei Brucei in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Human Herpesvirus 8 Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Human Herpesvirus 8 Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bcg Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bcg Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gastrointestinal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gastrointestinal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Jc Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Jc Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reproductive Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reproductive Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Direct Contact Transmission Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Direct Contact Transmission Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vaccinia Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vaccinia Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Larvae Of Trichinella Spiralis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Larvae Of Trichinella Spiralis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sindbis Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sindbis Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatic Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Coxiella Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Coxiella in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sendai Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sendai Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disseminated Infection Caused By Neisseria Gonorrhoeae Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Infection Caused By Neisseria Gonorrhoeae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neisseria Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neisseria Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Systemic Bacterial Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Systemic Bacterial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Human Metapneumovirus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Human Metapneumovirus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reoviral Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reoviral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Enteropathogenic Escherichia Coli Gastrointestinal Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Enteropathogenic Escherichia Coli Gastrointestinal Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Systemic Viral Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Systemic Viral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Strongyloides Stercoralis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Strongyloides Stercoralis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Salivary Gland Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Salivary Gland Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alphaviral Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alphaviral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chlamydia Trachomatis Infection Of Genital Structure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chlamydia Trachomatis Infection Of Genital Structure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Acute Respiratory Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Acute Respiratory Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bacteroides Fragilis Infection In Conditions Classified Elsewhere And Of Unspecified Site Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bacteroides Fragilis Infection In Conditions Classified Elsewhere And Of Unspecified Site in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Campylobacter Jejuni Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Campylobacter Jejuni Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodontal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Susceptibility To Viral And Mycobacterial Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Susceptibility To Viral And Mycobacterial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Rubella Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Rubella Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcutaneous Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcutaneous Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Viral Hepatitis E Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Viral Hepatitis E Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Campylobacter Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Campylobacter Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Verotoxigenic Escherichia Coli Gastrointestinal Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Verotoxigenic Escherichia Coli Gastrointestinal Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aeromonas Hydrophila Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aeromonas Hydrophila Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Upper Respiratory Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Upper Respiratory Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bronchopulmonary Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bronchopulmonary Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vancomycin Intermediate Staphylococcus Aureus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vancomycin Intermediate Staphylococcus Aureus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chlamydia Psittaci Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chlamydia Psittaci Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Aspergillus Fumigatus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Aspergillus Fumigatus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Haemophilus Influenzae Type B Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Haemophilus Influenzae Type B Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Taenia Saginata Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Taenia Saginata Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Merkel Cell Polyomavirus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Merkel Cell Polyomavirus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Musculoskeletal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Musculoskeletal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Necrotizing Soft Tissue Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Soft Tissue Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Shunt Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Shunt Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cryptococcus Gattii Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cryptococcus Gattii Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fracture Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fracture Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Male Accessory Gland Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Male Accessory Gland Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Giardia Duodenalis Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Giardia Duodenalis Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Herpetosoma Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Herpetosoma Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Toxocara Canis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Toxocara Canis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Febrile Infection Related Epilepsy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Febrile Infection Related Epilepsy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Enterovirus 71 Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Enterovirus 71 Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mumps Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mumps Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Klebsiella Pneumoniae Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Klebsiella Pneumoniae Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cytomegalovirus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cytomegalovirus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complicated Urinary Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complicated Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Opisthorchis Felineus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Opisthorchis Felineus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Opisthorchis Viverrini Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Opisthorchis Viverrini Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Polymorphus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Polymorphus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Pyogenic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Pyogenic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Keratitis Caused By Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Keratitis Caused By Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Viral Infection-Induced Rhabdomyolysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Viral Infection-Induced Rhabdomyolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coxiella Burnetii Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coxiella Burnetii Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Loa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Loa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nipah Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nipah Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Postnatal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Postnatal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Syphilis Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Syphilis Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oncovirus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oncovirus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Wuchereria Bancrofti Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Wuchereria Bancrofti in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Trichinella Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Trichinella in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Herpes Simplex Infection Of Eye Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Infection Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Burn Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Burn Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Molluscum Contagiosum Skin Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Molluscum Contagiosum Skin Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection As A Complication Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection As A Complication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Enterotoxigenic Escherichia Coli Gastrointestinal Tract Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Enterotoxigenic Escherichia Coli Gastrointestinal Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Erysipelothrix Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Erysipelothrix Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bk Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bk Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Lassa Virus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Lassa Virus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Schistosoma Hematobium Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Schistosoma Hematobium Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Haemonchus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Haemonchus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurological Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neurological Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Leishmania Infantum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Leishmania Infantum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Induced Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Induced Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Trypanosoma Evansi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Trypanosoma Evansi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gastric Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gastric Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disseminated Bacillus Calmette-Guerin Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Bacillus Calmette-Guerin Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Entamoeba Histolytica Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Entamoeba Histolytica Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oral Herpes Simplex Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oral Herpes Simplex Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Enterovirus D68 Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Enterovirus D68 Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oral Candida Albicans Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oral Candida Albicans Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Superficial Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Superficial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Breakthrough Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Breakthrough Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Of Amniotic Cavity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Of Amniotic Cavity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pleural Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pleural Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Burkholderia Cenocepacia Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Burkholderia Cenocepacia Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Francisella Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Francisella in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Root Canal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Root Canal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection By Aspergillus Flavus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection By Aspergillus Flavus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Beta Haemolytic Streptococcal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Beta Haemolytic Streptococcal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vibrio Vulnificus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vibrio Vulnificus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disseminated Viral Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Viral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cytomegalovirus Infection Reactivation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cytomegalovirus Infection Reactivation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prostatic Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prostatic Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Granulomatous Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Granulomatous Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Blister With Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Blister With Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Uncomplicated Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Uncomplicated Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tooth Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tooth Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complicated Intra-Abdominal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complicated Intra-Abdominal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Burkholderia Cepacia Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Burkholderia Cepacia Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Burkholderia Multivorans Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Burkholderia Multivorans Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Disseminated Cryptosporidium Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Disseminated Cryptosporidium Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Human T-Lymphotropic Virus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Human T-Lymphotropic Virus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection In Solid Organ Transplant Recipients Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection In Solid Organ Transplant Recipients in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acanthamoeba Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acanthamoeba Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intestinal Nematode Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Nematode Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stress/Infection-Induced Lactic Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stress/Infection-Induced Lactic Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
B Virus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease B Virus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sporothrix Schenckii Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sporothrix Schenckii Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Catheter Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Catheter Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Kidney Infection Acute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Kidney Infection Acute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Staphylococcus Epidermidis Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Staphylococcus Epidermidis Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vascular Graft Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vascular Graft Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Testicular Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Testicular Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Streptococcal Infection Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Streptococcal Infection Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infection Caused By Malassezia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infection Caused By Malassezia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Enterococcal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Enterococcal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Helicobacter Pylori Infection, Susceptibility To Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Helicobacter Pylori Infection, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alpha/Beta T-Cell Lymphopenia With Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alpha/Beta T-Cell Lymphopenia With Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Klebsiella Oxytoca Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Klebsiella Oxytoca Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhodococcus Equi Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhodococcus Equi Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complicated Skin And Skin Structure Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complicated Skin And Skin Structure Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hepatic Cyst Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatic Cyst Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hip Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hip Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oral Fungal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oral Fungal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intraocular Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intraocular Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Yeast Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Yeast Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bacillus Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bacillus Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Splenic Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Splenic Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aeromonas Caviae Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aeromonas Caviae Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Bacterial Infection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bacterial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Viral Infection Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Viral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Infection Of The Gastrointestinal Tract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infection Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Harmonizome 3.0

SM2 Gene

MTBS1 Gene

MTBSX Gene

OPHLC Gene

PSHK2 Gene

MTBS3 Gene

MTBS2 Gene

PFBI Gene

Infection Due To Mycobacterium Kansasii Gene Set

Disseminated Mycobacterium Kansasii Infection Gene Set

lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical Gene Set

lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections Gene Set

lung diseases; mycobacterium avium-intracellulare infection Gene Set

mycobacterium avium-intracellulare infection; respiratory tract infections Gene Set

aids-related opportunistic infections; cytomegalovirus retinitis; encephalomyelitis; hiv infections; hypersensitivity; mycobacterium avium-intracellulare infection; [x]human immunodeficiency virus disease Gene Set

Mycobacterium avium-intracellulare Infection Gene Set

{mycobacterium tuberculosis, susceptibility to infection by} Gene Set

Latent infection of Homo sapiens with Mycobacterium tuberculosis Gene Set

Mycobacterium Infection Gene Set

Pulmonary Mycobacterium Avium Complex Infection Gene Set

Disseminated Mycobacterium Avium Complex Infection Gene Set

Mycobacterium Tuberculosis, Susceptibility To Infection By Gene Set

Infection with Mycobacterium tuberculosis Gene Set

THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set

HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene Set

chronic hepatitis due to cryptospridium infection Gene Set

{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene Set

Chronic Hepatitis Due To Cryptosporidium Infection Gene Set

Infection Due To Brucella Suis Gene Set

Infection Due To Vancomycin Resistant Staphylococcus Aureus Gene Set

Infection Due To Clostridium Chauvoei Gene Set

infection; multiple myeloma; sepsis; systemic infection Gene Set

h. pylori infection; helicobacter pylori infection Gene Set

hiv infection; hepatitis c infection Gene Set

cross infection; pneumonia, ventilator-associated; sepsis; systemic infection Gene Set

Mycobacterium Infections Gene Set

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO Gene Set

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 3 Gene Set

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, X-LINKED Gene Set

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 2 Gene Set

MYCOBACTERIUM TUBERCULOSIS, SUSCEPTIBILITY TO, 1 Gene Set

Mycobacterium Infections, Nontuberculous Gene Set

mycobacterium avium complex disease Gene Set

cryptosporidiosis; mycobacterium avium complex; pneumocystis carinii pneumonia; toxoplasmosis Gene Set

pulmonary disease, mycobacterium malmoense Gene Set

lymphadenitis; mycobacterium infections; periodontitis Gene Set

lung diseases; mycobacterium infections, atypical Gene Set

alpha 1-antitrypsin deficiency; cystic fibrosis; mycobacterium infections Gene Set

mycobacterium infections, atypical; skin ulcer Gene Set

mycobacterium Gene Set

recurrent mycobacterium avium complex infections Gene Set

recurrent mycobacterium avium complex infections Gene Set

Mycobacterium Infections Gene Set

Mycobacterium Infections, Atypical Gene Set

{mycobacterium tuberculosis, susceptibility to, 2} Gene Set

{mycobacterium tuberculosis, protection against} Gene Set

{mycobacterium tuberculosis, susceptibility to, 3} Gene Set

{mycobacterium tuberculosis, susceptibility to} Gene Set

Mycobacterium Tuberculosis, Susceptibility To (Finding) Gene Set

Mycobacterium Tuberculosis Meningitis Gene Set

Mycobacterium; Ulcerans (Disease) Gene Set

Recurrent Mycobacterium Avium Complex Infections Gene Set

Mycobacterium avium complex disease Gene Set

Mycobacterium tuberculosis Gene Set

Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (continuous) Gene Set

Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (dichotomous) Gene Set

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

SCID due to ADA deficiency, delayed onset Gene Set

Thrombophilia due to protein S deficiency, autosomal recessive Gene Set

Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene Set

Severe combined immunodeficiency due to ADA deficiency Gene Set

Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene Set

HNSHA due to aldolase A deficiency Gene Set

Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene Set

Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set

Gaucher disease, atypical, due to saposin C deficiency Gene Set

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

Megaloblastic anemia due to inborn errors of metabolism Gene Set

Hemolytic anemia due to hexokinase deficiency Gene Set