{resistance to malaria due to g6pd deficiency}

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Results for "{resistance to malaria due to g6pd deficiency}": 1001 gene sets

Name
{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 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.
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.
anemia; malaria, cerebral; malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, malaria related; malaria, cerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, malaria related; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, cerebral; malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, cerebral; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; malaria, vivax Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; malaria, vivax 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.
malaria, cerebral; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria; malaria, cerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria; malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria; malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
{malaria, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, severe, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, severe, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
[malaria, resistance to] Gene Set From OMIM Gene-Disease Associations genes associated with the [malaria, resistance to] phenotype from the curated OMIM Gene-Disease Associations dataset.
g6pd deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease g6pd deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
sickle cell anemia; g6pd deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease sickle cell anemia; g6pd deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
G6PD deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.
Tetracycline resistance protein, TetA/multidrug resistance protein MdtG Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Tetracycline resistance protein, TetA/multidrug resistance protein MdtG protein domain from the InterPro Predicted Protein Domain Annotations dataset.
alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucosephosphate dehydrogenase deficiency; malaria, vivax Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; malaria, vivax in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucosephosphate dehydrogenase deficiency; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucosephosphate dehydrogenase deficiency; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease glucosephosphate dehydrogenase deficiency; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease 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.
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 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 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.
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.
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.
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 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.
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.
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.
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.
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
g6pd Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term g6pd in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
G6PD Gene Set From NURSA Protein-Protein Interactions interacting proteins for G6PD from the NURSA Protein-Protein Interactions dataset.
G6PD Gene Set From Pathway Commons Protein-Protein Interactions interacting proteins for G6PD from the Pathway Commons Protein-Protein Interactions dataset.
G6Pd Tomah Phenotype Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype G6Pd Tomah Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
G6PD Gene Set From LINCS L1000 CMAP CRISPR Knockout Consensus Signatures genes differentially expressed following the G6PD gene perturbation from the LINCS L1000 CMAP CRISPR Knockout Consensus Signatures dataset.
G6PD AS Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD AS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD CHAT Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD CHAT phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD MAHI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD MAHI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD SASS Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD SASS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD MEDITERRAN Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD MEDITERRAN phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD CAGLI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD CAGLI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD deficient hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD deficient hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD PORT Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD PORT phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD NASHVI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD NASHVI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD ANAH Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD ANAH phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD SANTIAGO DE C Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD SANTIAGO DE C phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD SEATTLE-L Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD SEATTLE-L phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD MOD Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD MOD phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD IOWA C Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD IOWA C phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD I Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD I phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD SPRINGFI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD SPRINGFI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD WALTER R Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD WALTER R phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD BEVERLY HI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD BEVERLY HI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD TO Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD TO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD RIVERS Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD RIVERS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD ANDA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD ANDA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD AGRIGE Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD AGRIGE phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD G Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD G phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD TAIWAN-HA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD TAIWAN-HA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD CAN Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD CAN phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD PUERTO LI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD PUERTO LI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD MAL Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD MAL phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD GASTO Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD GASTO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD MINNES Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD MINNES phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD MAR Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD MAR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD IERAPE Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD IERAPE phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD VIANGC Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD VIANGC phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD JA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD JA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD LOMA LI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD LOMA LI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD COIM Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD COIM phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD TAIWAN-HAKKA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD TAIWAN-HAKKA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD GUADALAJ Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD GUADALAJ phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD KERALA-KAL Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD KERALA-KAL phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD KER Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD KER phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD KAL Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD KAL phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD AU Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD AU phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD GA Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD GA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD QUING Y Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD QUING Y phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD ORI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD ORI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD NANK Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD NANK phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD NEAPO Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD NEAPO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD AVE Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD AVE phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD NAM Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD NAM phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD NILG Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD NILG phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD COSE Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the G6PD COSE phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
G6PD Gene Set From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the G6PD gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.
activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; factor v deficiency; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
{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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
?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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Malaria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Malaria from the curated CTD Gene-Disease Associations dataset.
Malaria, Falciparum Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Malaria, Falciparum from the curated CTD Gene-Disease Associations dataset.
Malaria Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Malaria in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
malaria Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease malaria in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
plasmodium ovale malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease plasmodium ovale malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
plasmodium malariae malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease plasmodium malariae malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mixed malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mixed malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
plasmodium vivax malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease plasmodium vivax malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
plasmodium falciparum malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease plasmodium falciparum malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anemia; malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, plasmodium falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, plasmodium falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pre-term delivery infant mortality and malaria morbidity Gene Set From GAD Gene-Disease Associations genes associated with the disease pre-term delivery infant mortality and malaria morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, systemic; malaria; systemic lupus erythematosus Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, systemic; malaria; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; pregnancy complications, parasitic Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; parasitemia; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; parasitemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, vivax Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, vivax 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.
crohn's disease; asthma; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn's disease; asthma; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; malaria; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; malaria; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heterozygous haemoglobin s; malaria; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease heterozygous haemoglobin s; malaria; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; elliptocytosis, hereditary; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; elliptocytosis, hereditary; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
severe malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease severe malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; placenta diseases; pregnancy complications, parasitic Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased nitric oxide production and protection from malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease increased nitric oxide production and protection from malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha-thalassemia; anemia; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malarial anemia and cerebral malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease malarial anemia and cerebral malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
placental malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease placental malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type i; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type i; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebral malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebral malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria; schistosomiasis Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria; schistosomiasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bacteremia; malaria; tuberculosis Gene Set From GAD Gene-Disease Associations genes associated with the disease bacteremia; malaria; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastric ulcer, hiv, malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease gastric ulcer, hiv, malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ovalocytosis and malaria susceptibility Gene Set From GAD Gene-Disease Associations genes associated with the disease ovalocytosis and malaria susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glycogen storage disease type i; hemolysis; malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease glycogen storage disease type i; hemolysis; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria; parasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria; parasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; multiple sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria, cerebral Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria, cerebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
plasmodium falciparum malaria Gene Set From GAD Gene-Disease Associations genes associated with the disease plasmodium falciparum malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria; hypoglycemia; hyperparasitemia Gene Set From GAD Gene-Disease Associations genes associated with the disease malaria; hypoglycemia; hyperparasitemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
malaria Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term malaria in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Malaria Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Malaria phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
malaria Gene Set From GWASdb SNP-Disease Associations genes associated with the disease malaria in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Malaria, Cerebral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Malaria, Cerebral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Malaria Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Malaria phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Malaria, Vivax Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Malaria, Vivax phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Malaria, Falciparum Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Malaria, Falciparum phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
{malaria, cerebral, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, cerebral, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, mild, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, mild, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, vivax, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, vivax, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, cerebral, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, cerebral, reduced risk of} 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.
{malaria, protection against} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, protection against} phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, severe, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, severe, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Malaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complicated Malaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complicated Malaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Clinical Malaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Clinical Malaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Malaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Malaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malaria, Susceptibility To (Finding) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malaria, Susceptibility To (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malaria Relapse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malaria Relapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ovale Malaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ovale Malaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Malaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Malaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malaria, Cerebral, Susceptibility To (Finding) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malaria, Cerebral, Susceptibility To (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Malaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Malaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malaria Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Malaria in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Plasmodium falciparum malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Plasmodium falciparum malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Plasmodium vivax malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Plasmodium vivax malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mixed malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mixed malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Plasmodium malariae malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Plasmodium malariae malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Plasmodium ovale malaria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Plasmodium ovale malaria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Malaria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Malaria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe malaria Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe malaria phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe malaria (adjusted for sickle cell variant rs334) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe malaria (adjusted for sickle cell variant rs334) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Malaria Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Malaria phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrence of malaria infection (mild or asymptomatic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrence of malaria infection (mild or asymptomatic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrence of mild malaria attacks Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrence of mild malaria attacks phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Malaria Gene Set From KEGG Pathways 2026 proteins participating in the Malaria pathway from the KEGG Pathways 2026 dataset.
Neuraminidase deficiency with beta-galactosidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choline deficiency; dna damage; folic acid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
protein c deficiency; protein s deficiency; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.
Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Set From Reactome Pathways 2024 proteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset.
stathmin and breast cancer resistance to antimicrotubule agents Gene Set From Biocarta Pathways proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.
multi-drug resistance factors Gene Set From Biocarta Pathways proteins participating in the multi-drug resistance factors pathway from the Biocarta Pathways dataset.
reversal of insulin resistance by leptin Gene Set From Biocarta Pathways proteins participating in the reversal of insulin resistance by leptin pathway from the Biocarta Pathways dataset.
hiv-1 defeats host-mediated resistance by cem15 Gene Set From Biocarta Pathways proteins participating in the hiv-1 defeats host-mediated resistance by cem15 pathway from the Biocarta Pathways dataset.
Insulin resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Androgen resistance syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Androgen resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyrotropin-releasing hormone resistance, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyrotropin-releasing hormone resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-like growth factor 1 resistance to Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-like growth factor 1 resistance to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acrodysostosis 2, with or without hormone resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acrodysostosis 2, with or without hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ACTH resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ACTH resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Colchicine resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Colchicine resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid resistance, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Estrogen resistance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Estrogen resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, selective pituitary Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, selective pituitary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Insulin-Like Growth Factor I, Resistance To Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insulin-Like Growth Factor I, Resistance To from the curated CTD Gene-Disease Associations dataset.
Hypertension, Diastolic, Resistance to Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Diastolic, Resistance to from the curated CTD Gene-Disease Associations dataset.
Activated Protein C Resistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance Syndrome from the curated CTD Gene-Disease Associations dataset.
Coumarin Resistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coumarin Resistance from the curated CTD Gene-Disease Associations dataset.
Insulin Resistance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insulin Resistance from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Selective Pituitary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Selective Pituitary from the curated CTD Gene-Disease Associations dataset.
Insulin Resistance Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Insulin Resistance in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
thyroid hormone resistance syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thyroid hormone resistance syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; postphlebitic syndrome; varicose ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; postphlebitic syndrome; varicose ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
platelet reactivity and clopidogrel resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease platelet reactivity and clopidogrel resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; hypertension; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; obesity; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
exercise-mediated changes of insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease exercise-mediated changes of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; postoperative complications; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
features of the insulin resistance syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease features of the insulin resistance syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass diabetes, type 2 glucose insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass diabetes, type 2 glucose insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
reduced muscle mrna levels and insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease reduced muscle mrna levels and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; insulin resistance; overweight Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; growth disorders; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; growth disorders; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperlipidemia, familial combined; insulin resistance; mixed hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyslipidemias; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease dyslipidemias; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; free fatty acid Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; free fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes complications; diabetes mellitus; inflammation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes complications; diabetes mellitus; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; arterial occlusive diseases; graft occlusion, vascular Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; arterial occlusive diseases; graft occlusion, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased risk of insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased risk of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; thrombophilia; thrombosis; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thrombophilia; thrombosis; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperglycemia; insulin resistance; sepsis Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperglycemia; insulin resistance; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; glucose intolerance; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; glucose intolerance; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; diabetes mellitus, type 2; hyperglycemia; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus, type 2; hyperglycemia; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resistance to thyroid hormone Gene Set From GAD Gene-Disease Associations genes associated with the disease resistance to thyroid hormone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; obesity; weight gain Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resistance to liver graft rejection to steroid therapy Gene Set From GAD Gene-Disease Associations genes associated with the disease resistance to liver graft rejection to steroid therapy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; obesity, abdominal Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; obesity, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; inflammation; insulin resistance; metabolic syndrome x; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; eye diseases; hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aspirin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease aspirin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; insulin resistance; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophy, left ventricular; insulin resistance; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophy, left ventricular; insulin resistance; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; thromboembolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; insulin resistance; postoperative complications Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; insulin resistance; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hypertension; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; retinal vein occlusion; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal vein occlusion; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; hellp syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; hellp syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; hepatitis c, chronic; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; hepatitis c, chronic; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
treatment resistance to typical neuroleptics Gene Set From GAD Gene-Disease Associations genes associated with the disease treatment resistance to typical neuroleptics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; insulin resistance; liver diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; insulin resistance; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; obesity; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels Gene Set From GAD Gene-Disease Associations genes associated with the disease blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; central nervous system vascular malformations Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; central nervous system vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; hypertension; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, habitual; activated protein c resistance; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colonic neoplasms; insulin resistance; rectal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease colonic neoplasms; insulin resistance; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; insulin resistance; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; insulin resistance; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; hyperhomocysteinemia; intracranial thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; hyperhomocysteinemia; intracranial thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, habitual; activated protein c resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stroke; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease stroke; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; insulin resistance; metabolic syndrome x; obesity 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.
diabetes mellitus, type 2; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body fat; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body fat; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; cardiovascular diseases; polycythemia vera; recurrence; thrombocythemia, hemorrhagic; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; kidney diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
beta-cell function; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease beta-cell function; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary disease; coronary heart disease; inflammation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperinsulinism; insulin resistance; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperinsulinism; insulin resistance; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
coronary artery disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease coronary artery disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, habitual; activated protein c resistance; infertility, female; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; infertility, female; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; fatty acid Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thyroid hormone resistance syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease thyroid hormone resistance syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased fatty acid binding increased fat oxidation and insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease increased fatty acid binding increased fat oxidation and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; myocardial infarction Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; prediabetic state Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; prediabetic state in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; hypertriglyceridemia; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; hypertriglyceridemia; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart failure; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease heart failure; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute coronary syndrome; aspirin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; aspirin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; diabetes mellitus; hyperinsulinism; insulin resistance; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; diabetes mellitus; hyperinsulinism; insulin resistance; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; hyperinsulinism; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; obesity; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; acute disease; disseminated intravascular coagulation; poisoning Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; acute disease; disseminated intravascular coagulation; poisoning in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin-resistance syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin-resistance syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; inflammation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperglycemia; insulin resistance; myocardial infarction; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperglycemia; insulin resistance; myocardial infarction; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; hyperhomocysteinemia; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; hyperhomocysteinemia; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acanthosis nigricans; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease acanthosis nigricans; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; diabetes, gestational; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; diabetes, gestational; insulin resistance 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.
hypercholesterolemia; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; overweight; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; insulin resistance; weight loss Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; obesity; overweight Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; insulin resistance; metabolic syndrome x; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyslipidemias; fatty liver; hypertension; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease dyslipidemias; fatty liver; hypertension; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance in obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance in obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesterol, ldl; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intrauterine growth; obesity; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease intrauterine growth; obesity; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; insulin resistance; liver cirrhosis Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thrombosis and resistance to activated protein c Gene Set From GAD Gene-Disease Associations genes associated with the disease thrombosis and resistance to activated protein c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; venous thromboembolism; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; venous thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; insulin resistance; kidney diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyslipidemia and insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease dyslipidemia and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; hypertension; hypotension; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; hypertension; hypotension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resistance in vitro to low-dose aspirin Gene Set From GAD Gene-Disease Associations genes associated with the disease resistance in vitro to low-dose aspirin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperglycemia; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin sensitivity; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin sensitivity; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
endometrial neoplasms; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease endometrial neoplasms; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatty liver; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; hyperlipidemias; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; hyperlipidemias; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; huntington disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; huntington disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; fatty liver; hepatitis c, chronic; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; fatty liver; hepatitis c, chronic; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, gestational; gestational diabetes mellitus ; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, gestational; gestational diabetes mellitus ; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; thromboembolism; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyslipidemias; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease dyslipidemias; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; overweight; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; overweight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure Gene Set From GAD Gene-Disease Associations genes associated with the disease cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance and intra-abdominal fat thickness Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance and intra-abdominal fat thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; hemochromatosis; iron overload; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; hemochromatosis; iron overload; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; insulin resistance; lipodystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; lipodystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; hypertriglyceridemia; insulin resistance; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hypertriglyceridemia; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
respiratory airway resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease respiratory airway resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; precursor cell lymphoblastic leukemia-lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; obesity, morbid Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; obesity, morbid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resistance Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term resistance in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2015 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset.
extracellular matrix structural constituent conferring compression resistance Gene Set From GO Molecular Function Annotations 2015 genes performing the extracellular matrix structural constituent conferring compression resistance molecular function from the curated GO Molecular Function Annotations 2015 dataset.
Insulin resistance/response Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Insulin resistance/response phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Homeostasis model assessment of insulin resistance (interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Homeostasis model assessment of insulin resistance (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
insulin resistance Gene Set From GWASdb SNP-Phenotype Associations genes associated with the insulin resistance phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
insulin resistance Gene Set From HPO Gene-Disease Associations genes associated with the insulin resistance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased pulmonary vascular resistance Gene Set From HPO Gene-Disease Associations genes associated with the increased pulmonary vascular resistance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased red cell osmotic resistance Gene Set From HPO Gene-Disease Associations genes associated with the increased red cell osmotic resistance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
resistance to activated protein c Gene Set From HPO Gene-Disease Associations genes associated with the resistance to activated protein c phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Activated Protein C Resistance Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Activated Protein C Resistance phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Thyroid Hormone Resistance Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Thyroid Hormone Resistance Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Insulin Resistance Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Insulin Resistance phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
glutamate dependent acid resistance Gene Set From HumanCyc Pathways proteins participating in the glutamate dependent acid resistance pathway from the HumanCyc Pathways dataset.
Multidrug resistance protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Arsenite-resistance protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Arsenite-resistance protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glyoxalase/fosfomycin resistance/dioxygenase domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glyoxalase/fosfomycin resistance/dioxygenase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
UV radiation resistance protein/autophagy-related protein 14 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the UV radiation resistance protein/autophagy-related protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Breast cancer anti-estrogen resistance protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Breast cancer anti-estrogen resistance protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Breast cancer anti-estrogen resistance protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Breast cancer anti-estrogen resistance protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance-associated protein 9 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance-associated protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance-associated protein 7 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance-associated protein 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance-associated protein 6 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance-associated protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance-associated protein 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance-associated protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance-associated protein 4 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance-associated protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance-associated protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Glyoxalase/Bleomycin resistance protein/Dihydroxybiphenyl dioxygenase Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Glyoxalase/Bleomycin resistance protein/Dihydroxybiphenyl dioxygenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multi drug resistance-associated protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multi drug resistance-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Bile acid:sodium symporter/arsenical resistance protein Acr3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Bile acid:sodium symporter/arsenical resistance protein Acr3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Multidrug resistance protein 1 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Multidrug resistance protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Resistance to inhibitors of cholinesterase protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Resistance to inhibitors of cholinesterase protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal pulmonary vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pulmonary vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased renal vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased renal vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal systemic vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal systemic vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
insulin resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the insulin resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal renal vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal renal vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased systemic vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased systemic vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pulmonary vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased systemic vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased systemic vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
glucocorticoid resistance Gene Set From OMIM Gene-Disease Associations genes associated with the glucocorticoid resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
thyroid hormone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the thyroid hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
{hiv-1, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hiv-1, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{atopy, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {atopy, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, resistance to Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, resistance to phenotype from the curated OMIM Gene-Disease Associations dataset.
[obesity, resistance to] Gene Set From OMIM Gene-Disease Associations genes associated with the [obesity, resistance to] phenotype from the curated OMIM Gene-Disease Associations dataset.
estrogen resistance Gene Set From OMIM Gene-Disease Associations genes associated with the estrogen resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
insulin resistance, severe, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the insulin resistance, severe, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
?progesterone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the ?progesterone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
{creutzfeldt-jakob disease, variant, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {creutzfeldt-jakob disease, variant, resistance 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.
thyrotropin-releasing hormone resistance, generalized Gene Set From OMIM Gene-Disease Associations genes associated with the thyrotropin-releasing hormone resistance, generalized phenotype from the curated OMIM Gene-Disease Associations dataset.
acrodysostosis 1, with or without hormone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the acrodysostosis 1, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
dna topoisomerase ii, resistance to inhibition of, by amsacrine Gene Set From OMIM Gene-Disease Associations genes associated with the dna topoisomerase ii, resistance to inhibition of, by amsacrine phenotype from the curated OMIM Gene-Disease Associations dataset.
warfarin resistance Gene Set From OMIM Gene-Disease Associations genes associated with the warfarin resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
coumarin resistance Gene Set From OMIM Gene-Disease Associations genes associated with the coumarin resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
{hiv1, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hiv1, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{systemic lupus erythematosus, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {systemic lupus erythematosus, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{aids, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {aids, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{colchicine resistance} Gene Set From OMIM Gene-Disease Associations genes associated with the {colchicine resistance} phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypertension, insulin resistance-related, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypertension, insulin resistance-related, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
insulin-like growth factor i, resistance to Gene Set From OMIM Gene-Disease Associations genes associated with the insulin-like growth factor i, resistance to phenotype from the curated OMIM Gene-Disease Associations dataset.
{insulin resistance, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {insulin resistance, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple myeloma, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple myeloma, resistance to} 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.
thyroid hormone resistance, selective pituitary Gene Set From OMIM Gene-Disease Associations genes associated with the thyroid hormone resistance, selective pituitary phenotype from the curated OMIM Gene-Disease Associations dataset.
{coronary artery disease, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {coronary artery disease, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{hypertension, diastolic, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hypertension, diastolic, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{lung cancer, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {lung cancer, 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.
thyroid hormone resistance, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the thyroid hormone resistance, autosomal recessive 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.
{hepatitis c virus, resistance to} Gene Set From OMIM Gene-Disease Associations genes associated with the {hepatitis c virus, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.
somatostatin analog, resistance to Gene Set From OMIM Gene-Disease Associations genes associated with the somatostatin analog, resistance to phenotype from the curated OMIM Gene-Disease Associations dataset.
acrodysostosis 2, with or without hormone resistance Gene Set From OMIM Gene-Disease Associations genes associated with the acrodysostosis 2, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.
luteinizing hormone resistance, female Gene Set From OMIM Gene-Disease Associations genes associated with the luteinizing hormone resistance, female phenotype from the curated OMIM Gene-Disease Associations dataset.
resistance Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term resistance in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations 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.
Resistance To Insulin-Like Growth Factor I Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Resistance To Insulin-Like Growth Factor I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Insulin Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Insulin Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Activated Protein C Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Activated Protein C Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Insulin Resistance In Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Insulin Resistance In Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progesterone Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progesterone Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Thyroid Hormone Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Thyroid Hormone Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Estrogen Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Estrogen Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Androgen Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Androgen Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperkalemic Mineralocorticoid Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperkalemic Mineralocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromate Resistance (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromate Resistance (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Hormone Resistance Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Resistance Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Upper Airway Resistance Sleep Apnea Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Upper Airway Resistance Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Hormone Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Recessive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glucagon Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glucagon Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Luteinizing Hormone Resistance, Female Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Luteinizing Hormone Resistance, Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Cortisol Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Cortisol Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Glucocorticoid Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Glucocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Resistance To Thyroid Hormone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Resistance To Thyroid Hormone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyrotropin-Releasing Hormone Resistance, Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyrotropin-Releasing Hormone Resistance, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Colchicine Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Colchicine Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Coumarin Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Coumarin Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Drug Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Drug Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Insulin Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Insulin Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hiv-1, Resistance To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hiv-1, Resistance To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Drug Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Drug Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Pulmonary Vascular Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Pulmonary Vascular Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Glucocorticoid Resistance, Cellular Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glucocorticoid Resistance, Cellular in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Total Respiratory System Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Total Respiratory System Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Red Cell Osmotic Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Cell Osmotic Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thyroid Stimulating Hormone Resistance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thyroid Stimulating Hormone Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2023 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset.
insulin resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the insulin resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal pulmonary vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pulmonary vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal systemic vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal systemic vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased pulmonary vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pulmonary vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased renal vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased renal vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased systemic vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased systemic vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased airway resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased airway resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased systemic vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased systemic vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased airway resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased airway resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal renal vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal renal vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased pulmonary vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pulmonary vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal airway resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal airway resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased renal vascular resistance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased renal vascular resistance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased airway resistance Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased airway resistance phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
decreased airway resistance Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased airway resistance phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
lncRNA mediated mechanisms of therapeutic resistance Gene Set From WikiPathways Pathways 2024 proteins participating in the lncRNA mediated mechanisms of therapeutic resistance pathway from the WikiPathways Pathways 2024 dataset.
EGFR tyrosine kinase inhibitor resistance Gene Set From WikiPathways Pathways 2024 proteins participating in the EGFR tyrosine kinase inhibitor resistance pathway from the WikiPathways Pathways 2024 dataset.
Roles of ceramides in development of insulin resistance Gene Set From WikiPathways Pathways 2024 proteins participating in the Roles of ceramides in development of insulin resistance pathway from the WikiPathways Pathways 2024 dataset.
APOBEC3G mediated resistance to HIV-1 infection Gene Set From Reactome Pathways 2024 proteins participating in the APOBEC3G mediated resistance to HIV-1 infection pathway from the Reactome Pathways 2024 dataset.
Drug resistance in ERBB2 KD mutants Gene Set From Reactome Pathways 2024 proteins participating in the Drug resistance in ERBB2 KD mutants pathway from the Reactome Pathways 2024 dataset.
Drug resistance in ERBB2 TMD/JMD mutants Gene Set From Reactome Pathways 2024 proteins participating in the Drug resistance in ERBB2 TMD/JMD mutants pathway from the Reactome Pathways 2024 dataset.
Drug resistance of ALK mutants Gene Set From Reactome Pathways 2024 proteins participating in the Drug resistance of ALK mutants pathway from the Reactome Pathways 2024 dataset.
Drug resistance of FLT3 mutants Gene Set From Reactome Pathways 2024 proteins participating in the Drug resistance of FLT3 mutants pathway from the Reactome Pathways 2024 dataset.
Drug resistance of KIT mutants Gene Set From Reactome Pathways 2024 proteins participating in the Drug resistance of KIT mutants pathway from the Reactome Pathways 2024 dataset.
Drug resistance of PDGFR mutants Gene Set From Reactome Pathways 2024 proteins participating in the Drug resistance of PDGFR mutants pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to AEE788 Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to AEE788 pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to afatinib Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to afatinib pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to lapatinib Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to lapatinib pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to neratinib Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to neratinib pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to osimertinib Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to osimertinib pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to sapitinib Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to sapitinib pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to tesevatinib Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to tesevatinib pathway from the Reactome Pathways 2024 dataset.
Resistance of ERBB2 KD mutants to trastuzumab Gene Set From Reactome Pathways 2024 proteins participating in the Resistance of ERBB2 KD mutants to trastuzumab pathway from the Reactome Pathways 2024 dataset.
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene Set From GO Biological Process Annotations 2025 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset.
Warfarin resistance Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Warfarin resistance from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Warfarin resistance Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Warfarin resistance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Thyroid hormone resistance syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Thyroid hormone resistance syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Selective pituitary thyroid hormone resistance Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Selective pituitary thyroid hormone resistance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
EDS1 disease-resistance complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the EDS1 disease-resistance complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Androgen resistance syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Androgen resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thyroid hormone resistance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroid hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Thyroid hormone resistance syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Thyroid hormone resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Selective pituitary resistance to thyroid hormone Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Selective pituitary resistance to thyroid hormone phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Luteinizing hormone resistance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Luteinizing hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Insulin resistance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Insulin resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glucocorticoid resistance Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Resistance to thyroid hormone Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Resistance to thyroid hormone phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Estrogen resistance syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Estrogen resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Homeostasis model assessment of insulin resistance Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Corneal resistance factor Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corneal resistance factor phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Resistance to antihypertensive treatment in hypertension Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Resistance to antihypertensive treatment in hypertension 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 (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.
Insulin resistance/response Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Insulin resistance/response phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Homeostasis model assessment of insulin resistance (dietary factor interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance (dietary factor interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Homeostasis model assessment of insulin resistance in less-fat diet Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance in less-fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Homeostasis model assessment of insulin resistance x saturated fatty acids interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance x saturated fatty acids interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Antidepressant treatment resistance (> 2 drugs prescribed) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Antidepressant treatment resistance (> 2 drugs prescribed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Antidepressant treatment resistance (number of drugs prescribed) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Antidepressant treatment resistance (number of drugs prescribed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to resistance training (vastus lateralis fiber area change) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to resistance training (vastus lateralis fiber area change) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Insulin resistance Gene Set From KEGG Pathways 2026 proteins participating in the Insulin resistance pathway from the KEGG Pathways 2026 dataset.
MULTIDRUG RESISTANCE MODULATOR Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MULTIDRUG RESISTANCE MODULATOR drug from theDGIdb Drug Targets 2026 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.
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.
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-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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
{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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
{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.
{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.
?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.
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.
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.
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.
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.
{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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.

Harmonizome 3.0

{resistance to malaria due to g6pd deficiency} Gene Set

hemolytic anemia due to g6pd deficiency Gene Set

Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency Gene Set

anemia; malaria, cerebral; malaria, falciparum; parasitemia Gene Set

alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set

anemia, malaria related; malaria, cerebral Gene Set

malaria, cerebral; malaria, falciparum; parasitemia Gene Set

malaria, falciparum; malaria, vivax Gene Set

myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set

malaria, cerebral; malaria, falciparum Gene Set

malaria; malaria, cerebral Gene Set

anemia; malaria; malaria, falciparum; parasitemia Gene Set

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

{malaria, resistance to} Gene Set

{malaria, severe, resistance to} Gene Set

[malaria, resistance to] Gene Set

g6pd deficiency Gene Set

sickle cell anemia; g6pd deficiency Gene Set

G6PD deficiency Gene Set

activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set

Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene Set

Tetracycline resistance protein, TetA/multidrug resistance protein MdtG Gene Set

alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

glucosephosphate dehydrogenase deficiency; malaria, vivax Gene Set

glucosephosphate dehydrogenase deficiency; malaria, falciparum Gene Set

anemia, iron-deficiency; malaria Gene Set

glucosephosphate dehydrogenase deficiency; malaria Gene Set

Thrombophilia due to activated protein C resistance Gene Set

Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set

Thrombophilia due to Activated Protein C Resistance Gene Set

thrombophilia due to activated protein c resistance Gene Set

Thyrotoxicosis Due To Pituitary Thyroid Hormone Resistance Gene Set

Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance Gene Set

Thrombophilia due to activated protein C resistance Gene Set

Thrombophilia due to activated protein C resistance Gene Set

Growth delay due to insulin-like growth factor I resistance Gene Set

Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta Gene Set

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

factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene Set

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

g6pd Gene Set

G6PD Gene Set

G6PD Gene Set

G6Pd Tomah Phenotype Gene Set

G6PD Gene Set

G6PD AS Gene Set

G6PD CHAT Gene Set

G6PD MAHI Gene Set

G6PD SASS Gene Set

G6PD MEDITERRAN Gene Set

G6PD CAGLI Gene Set

G6PD deficient hemolytic anemia Gene Set

G6PD PORT Gene Set

G6PD NASHVI Gene Set

G6PD ANAH Gene Set

G6PD SANTIAGO DE C Gene Set

G6PD SEATTLE-L Gene Set

G6PD MOD Gene Set

G6PD IOWA C Gene Set

G6PD I Gene Set

G6PD SPRINGFI Gene Set

G6PD WALTER R Gene Set

G6PD BEVERLY HI Gene Set

G6PD TO Gene Set

G6PD RIVERS Gene Set

G6PD ANDA Gene Set

G6PD AGRIGE Gene Set

G6PD G Gene Set

G6PD TAIWAN-HA Gene Set

G6PD CAN Gene Set

G6PD PUERTO LI Gene Set

G6PD MAL Gene Set

G6PD GASTO Gene Set

G6PD MINNES Gene Set

G6PD MAR Gene Set

G6PD IERAPE Gene Set

G6PD VIANGC Gene Set

G6PD JA Gene Set