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phospholipase a2, group iv a, deficiency of Gene SetFrom OMIM Gene-Disease Associations genes associated with the phospholipase a2, group iv a, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset. |
Phospholipase A2, group XII secretory Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase A2, group XII secretory protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Group IIA secretory phospholipase A2 levels in individuals with elevated hsCRP Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Group IIA secretory phospholipase A2 levels in individuals with elevated hsCRP phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Phospholipase A2 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Phospholipase A2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom 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 SetFrom 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. |
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 SetFrom 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. |
Molybdenum cofactor deficiency, complementation group C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Molybdenum cofactor deficiency, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Molybdenum cofactor deficiency, complementation group B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Molybdenum cofactor deficiency, complementation group B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Molybdenum cofactor deficiency, complementation group A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Molybdenum cofactor deficiency, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mhc class ii deficiency, complementation group b Gene SetFrom OMIM Gene-Disease Associations genes associated with the mhc class ii deficiency, complementation group b phenotype from the curated OMIM Gene-Disease Associations dataset. |
phospholipase c signaling pathway Gene SetFrom Biocarta Pathways proteins participating in the phospholipase c signaling pathway pathway from the Biocarta Pathways dataset. |
phospholipase c delta in phospholipid associated cell signaling Gene SetFrom Biocarta Pathways proteins participating in the phospholipase c delta in phospholipid associated cell signaling pathway from the Biocarta Pathways dataset. |
phospholipase c-epsilon pathway Gene SetFrom Biocarta Pathways proteins participating in the phospholipase c-epsilon pathway pathway from the Biocarta Pathways dataset. |
phospholipase Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term phospholipase in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
phospholipase c-inhibiting g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-inhibiting g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation of phospholipase c activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation of phospholipase c activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase c-activating g-protein coupled glutamate receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating g-protein coupled glutamate receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cytosolic calcium ion concentration involved in phospholipase c-activating g-protein coupled signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cytosolic calcium ion concentration involved in phospholipase c-activating g-protein coupled signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase c-activating dopamine receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating dopamine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of phospholipase a2 activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of phospholipase a2 activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of phospholipase c activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of phospholipase c activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase c-activating adrenergic receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating adrenergic receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase d-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase d-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of phospholipase c-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of phospholipase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of phospholipase c-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of phospholipase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation of phospholipase d activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation of phospholipase d activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase c-activating angiotensin-activated signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating angiotensin-activated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of phospholipase a2 activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of phospholipase a2 activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of phospholipase c activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of phospholipase c activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase c-activating g-protein coupled acetylcholine receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating g-protein coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of phospholipase c activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of phospholipase c activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase c-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of phospholipase c-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of phospholipase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of phospholipase a2 activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of phospholipase a2 activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation of phospholipase a2 activity by calcium-mediated signaling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation of phospholipase a2 activity by calcium-mediated signaling biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase c-activating serotonin receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipase c-activating serotonin receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation of phospholipase a2 activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation of phospholipase a2 activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipase activator activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase activator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase inhibitor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase inhibitor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
calcium-dependent phospholipase a2 activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the calcium-dependent phospholipase a2 activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
calcium-independent phospholipase a2 activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the calcium-independent phospholipase a2 activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase a2 inhibitor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase a2 inhibitor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphatidylinositol phospholipase c activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphatidylinositol phospholipase c activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase a2 activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase a2 activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
n-acylphosphatidylethanolamine-specific phospholipase d activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the n-acylphosphatidylethanolamine-specific phospholipase d activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
calcium-dependent phospholipase c activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the calcium-dependent phospholipase c activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
glycosylphosphatidylinositol phospholipase d activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the glycosylphosphatidylinositol phospholipase d activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase d inhibitor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase d inhibitor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase a2 activator activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase a2 activator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase c activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase c activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phospholipase d activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phospholipase d activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Lipoprotein-associated phospholipase A2 activity change in response to statin therapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to statin therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Lipoprotein-associated phospholipase A2 activity and mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Glycoprotein phospholipase D Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycoprotein phospholipase D protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase D/Transphosphatidylase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase D/Transphosphatidylase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inactive phospholipase C-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inactive phospholipase C-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inactive phospholipase C-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inactive phospholipase C-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase B-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase B-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Patatin/Phospholipase A2-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Patatin/Phospholipase A2-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase/carboxylesterase/thioesterase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase/carboxylesterase/thioesterase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase C, phosphatidylinositol-specific , X domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase C, phosphatidylinositol-specific , X domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase C, phosphatidylinositol-specific, Y domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase C, phosphatidylinositol-specific, Y domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase C, phosphoinositol-specific, EF-hand-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase C, phosphoinositol-specific, EF-hand-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase A2 inhibitor Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase A2 inhibitor protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phosphoinositide phospholipase C family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phosphoinositide phospholipase C family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase A2 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase A2 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase A2, active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase A2, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase D1/D2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase D1/D2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase C/D Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase C/D protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
N-acyl-phosphatidylethanolamine-hydrolysing phospholipase D Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the N-acyl-phosphatidylethanolamine-hydrolysing phospholipase D protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase A2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase A2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase D family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase D family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase D, phosphatidylserine synthase type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase D, phosphatidylserine synthase type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phospholipase D-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phospholipase D-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
phospholipase Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term phospholipase in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
EGFR interacts with phospholipase C-gamma Gene Setproteins participating in the EGFR interacts with phospholipase C-gamma pathway from the Reactome Pathways dataset. |
Phospholipase C-mediated cascade Gene Setproteins participating in the Phospholipase C-mediated cascade pathway from the Reactome Pathways dataset. |
positive regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of phospholipase C activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of phospholipase C activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
activation of phospholipase C activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the activation of phospholipase C activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of phospholipase C activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of phospholipase C activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of phospholipase C activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of phospholipase C activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G protein-coupled signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G protein-coupled signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
activation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the activation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-inhibiting G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-inhibiting G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-activating adrenergic receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating adrenergic receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
activation of phospholipase D activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the activation of phospholipase D activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-activating dopamine receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating dopamine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-activating serotonin receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating serotonin receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-activating angiotensin-activated signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating angiotensin-activated signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipase C-activating G protein-coupled glutamate receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipase C-activating G protein-coupled glutamate receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
phosphatidylinositol phospholipase C activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphatidylinositol phospholipase C activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase D activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase D activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase A2 activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase A2 activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
calcium-dependent phospholipase A2 activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the calcium-dependent phospholipase A2 activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase activator activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase activator activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
calcium-independent phospholipase A2 activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the calcium-independent phospholipase A2 activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase inhibitor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase inhibitor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase A2 inhibitor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase A2 inhibitor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase A1 activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase A1 activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase C activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase C activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
calcium-dependent phospholipase C activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the calcium-dependent phospholipase C activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phospholipase D inhibitor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phospholipase D inhibitor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
glycosylphosphatidylinositol phospholipase D activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the glycosylphosphatidylinositol phospholipase D activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
N-acylphosphatidylethanolamine-specific phospholipase D activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the N-acylphosphatidylethanolamine-specific phospholipase D activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
decreased phospholipase A2 level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased phospholipase A2 level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
EGFR interacts with phospholipase C-gamma Gene Setproteins participating in the EGFR interacts with phospholipase C-gamma pathway from the Reactome Pathways 2024 dataset. |
Erythropoietin activates Phospholipase C gamma (PLCG) Gene Setproteins participating in the Erythropoietin activates Phospholipase C gamma (PLCG) pathway from the Reactome Pathways 2024 dataset. |
Phospholipase C-mediated cascade: FGFR1 Gene Setproteins participating in the Phospholipase C-mediated cascade: FGFR1 pathway from the Reactome Pathways 2024 dataset. |
Phospholipase C-mediated cascade; FGFR2 Gene Setproteins participating in the Phospholipase C-mediated cascade; FGFR2 pathway from the Reactome Pathways 2024 dataset. |
Phospholipase C-mediated cascade; FGFR3 Gene Setproteins participating in the Phospholipase C-mediated cascade; FGFR3 pathway from the Reactome Pathways 2024 dataset. |
Phospholipase C-mediated cascade; FGFR4 Gene Setproteins participating in the Phospholipase C-mediated cascade; FGFR4 pathway from the Reactome Pathways 2024 dataset. |
phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of phospholipase C/protein kinase C signal transduction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of phospholipase C/protein kinase C signal transduction biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-inhibiting G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-inhibiting G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
activation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the activation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-activating angiotensin-activated signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating angiotensin-activated signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase D-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase D-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of phospholipase C/protein kinase C signal transduction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of phospholipase C/protein kinase C signal transduction biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-activating adrenergic receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating adrenergic receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
activation of phospholipase D activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the activation of phospholipase D activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-activating dopamine receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating dopamine receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-activating serotonin receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating serotonin receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-activating G protein-coupled glutamate receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating G protein-coupled glutamate receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C/protein kinase C signal transduction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C/protein kinase C signal transduction biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of phospholipase A2 activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of phospholipase A2 activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipase C-activating endothelin receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipase C-activating endothelin receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of phospholipase activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of phospholipase activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of phospholipase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of phospholipase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
phosphatidylinositol phospholipase C activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphatidylinositol phospholipase C activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase D activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase D activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase A2 activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase A2 activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
calcium-dependent phospholipase A2 activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the calcium-dependent phospholipase A2 activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase activator activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase activator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
calcium-independent phospholipase A2 activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the calcium-independent phospholipase A2 activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase C activator activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase C activator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase inhibitor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase inhibitor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase A2 inhibitor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase A2 inhibitor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase A1 activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase A1 activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase C activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase C activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase D activator activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase D activator activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
calcium-dependent phospholipase C activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the calcium-dependent phospholipase C activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phospholipase D inhibitor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phospholipase D inhibitor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
glycosylphosphatidylinositol phospholipase D activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the glycosylphosphatidylinositol phospholipase D activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
N-acylphosphatidylethanolamine-specific phospholipase D activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the N-acylphosphatidylethanolamine-specific phospholipase D activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Lipoprotein-associated phospholipase A2 activity and mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein-associated phospholipase A2 activity change in response to statin therapy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to statin therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein-associated phospholipase A2 activity change in response to darapladib treatment in cardiovascular disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to darapladib treatment in cardiovascular disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipoprotein phospholipase A2 activity in cardiovascular disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipoprotein phospholipase A2 activity in cardiovascular disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Phospholipase D signaling pathway Gene SetFrom KEGG Pathways 2026 proteins participating in the Phospholipase D signaling pathway pathway from the KEGG Pathways 2026 dataset. |
Neuraminidase deficiency with beta-galactosidase deficiency Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene SetFrom 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. |
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 Setproteins 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 Setproteins 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 Setproteins 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 Setproteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset. |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene SetFrom 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. |
gigantocellular group, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in gigantocellular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central medullary reticular group, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
rostral group of intralaminar nuclei, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in rostral group of intralaminar nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
medial group of nuclei, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in medial group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
anterior group of nuclei, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
caudal group of intralaminar nuclei, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
rostral group of intralaminar nuclei, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in rostral group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral medullary reticular group, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral medullary reticular group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
caudal group of intralaminar nuclei, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal group of intralaminar nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral group of nuclei, left, ventral division Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral group of nuclei, left, ventral division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
gigantocellular group, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in gigantocellular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral group of nuclei, right, ventral division Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral group of nuclei, right, ventral division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
cortico-medial group, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in cortico-medial group, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral medullary reticular group, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
cortico-medial group, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in cortico-medial group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
anterior group of nuclei, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in anterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral group of nuclei, left, dorsal division Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral group of nuclei, left, dorsal division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior group of nuclei, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior group of nuclei, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
lateral group of nuclei, right, dorsal division Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral group of nuclei, right, dorsal division relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
medial group of nuclei, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in medial group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
central medullary reticular group, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in central medullary reticular group, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
anterior digastric muscle trigeminal motor cell group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in anterior digastric muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Geniculate group, ventral thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Geniculate group, ventral thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Medial group of the dorsal thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Medial group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
A4 noradrenergic cell group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in A4 noradrenergic cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Anterior group of the dorsal thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
temporal muscle trigeminal motor cell group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in temporal muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Geniculate group, dorsal thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Geniculate group, dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Lateral group of the dorsal thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Ventral group of the dorsal thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventral group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Dopaminergic A13 group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Dopaminergic A13 group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
r5 part of A5 noradrenergic cell group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r5 part of A5 noradrenergic cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
pterigoid muscle trigeminal motor cell group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in pterigoid muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
temporotympanic muscle trigeminal motor cell group Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in temporotympanic muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Midline group of the dorsal thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Midline group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
rostral ventral respiratory cell group Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in rostral ventral respiratory cell group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
central nuclear group Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in central nuclear group relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Fanconi anemia, complementation group O Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group O phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Blood group, john milton hagen system Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Blood group, john milton hagen system phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BLOOD GROUP--WALDNER TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BLOOD GROUP--WALDNER TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Xeroderma pigmentosum, group C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Xeroderma pigmentosum, group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cromer blood group system Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cromer blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group Q Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group M Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group M phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group N Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group N phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group E Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group F Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group F phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group G Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group G phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Radin blood group Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Radin blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Blood group, junior system Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Blood group, junior system phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Xeroderma pigmentosum, complementation group b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Xeroderma pigmentosum, complementation group b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Blood group, gerbich system Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Blood group, gerbich system phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adult i Blood Group with or without Congenital Cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BLOOD GROUP--OK Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BLOOD GROUP--OK phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antigen in Scianna blood group system Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antigen in Scianna blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Langereis blood group Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Langereis blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BLOOD GROUP--FROESE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BLOOD GROUP--FROESE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BLOOD GROUP--LUTHERAN INHIBITOR Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BLOOD GROUP--LUTHERAN INHIBITOR phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Blood group, dombrock system Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Blood group, dombrock system phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Xeroderma pigmentosum, group D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Xeroderma pigmentosum, group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Xeroderma pigmentosum, group E Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Xeroderma pigmentosum, group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bare lymphocyte syndrome type 2, complementation group E Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bare lymphocyte syndrome type 2, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bare lymphocyte syndrome type 2, complementation group A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bare lymphocyte syndrome type 2, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fanconi anemia, complementation group D2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fanconi anemia, complementation group D2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BLOOD GROUP--WRIGHT ANTIGEN Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BLOOD GROUP--WRIGHT ANTIGEN phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
FANCONI ANEMIA, COMPLEMENTATION GROUP C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP C from the curated CTD Gene-Disease Associations dataset. |
FANCONI ANEMIA, COMPLEMENTATION GROUP E Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP E from the curated CTD Gene-Disease Associations dataset. |
FANCONI ANEMIA, COMPLEMENTATION GROUP F Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP F from the curated CTD Gene-Disease Associations dataset. |
Fanconi Anemia, Complementation Group J Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group J from the curated CTD Gene-Disease Associations dataset. |
Fanconi Anemia, Complementation Group B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group B from the curated CTD Gene-Disease Associations dataset. |
Fanconi Anemia, Complementation Group N Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group N from the curated CTD Gene-Disease Associations dataset. |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP D2 from the curated CTD Gene-Disease Associations dataset. |
Xeroderma Pigmentosum, Complementation Group C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group C from the curated CTD Gene-Disease Associations dataset. |
Xeroderma Pigmentosum, Complementation Group B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group B from the curated CTD Gene-Disease Associations dataset. |
Xeroderma Pigmentosum, Complementation Group E Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group E from the curated CTD Gene-Disease Associations dataset. |
Xeroderma Pigmentosum, Complementation Group D Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group D from the curated CTD Gene-Disease Associations dataset. |
Xeroderma Pigmentosum, Complementation Group G Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group G from the curated CTD Gene-Disease Associations dataset. |
Xeroderma Pigmentosum, Complementation Group F Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Xeroderma Pigmentosum, Complementation Group F from the curated CTD Gene-Disease Associations dataset. |
Fanconi Anemia, Complementation Group I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group I from the curated CTD Gene-Disease Associations dataset. |
FANCONI ANEMIA, COMPLEMENTATION GROUP O Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease FANCONI ANEMIA, COMPLEMENTATION GROUP O from the curated CTD Gene-Disease Associations dataset. |
Fanconi Anemia, Complementation Group D1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fanconi Anemia, Complementation Group D1 from the curated CTD Gene-Disease Associations dataset. |
blood group incompatibility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease blood group incompatibility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Monoisopropyl Ester Phosphonic Acid Group Gene Setinteracting proteins for the Monoisopropyl Ester Phosphonic Acid Group drug from the curated DrugBank Drug Targets dataset. |
Diisopropylphosphono Group Gene Setinteracting proteins for the Diisopropylphosphono Group drug from the curated DrugBank Drug Targets dataset. |
4-Methylpiperazin-1-Yl Carbonyl Group Gene Setinteracting proteins for the 4-Methylpiperazin-1-Yl Carbonyl Group drug from the curated DrugBank Drug Targets dataset. |
(1S)-MENTHYL HEXYL PHOSPHONATE GROUP Gene Setinteracting proteins for the (1S)-MENTHYL HEXYL PHOSPHONATE GROUP drug from the curated DrugBank Drug Targets dataset. |
Methylphosphonic Acid Ester Group Gene Setinteracting proteins for the Methylphosphonic Acid Ester Group drug from the curated DrugBank Drug Targets dataset. |
(1R)-MENTHYL HEXYL PHOSPHONATE GROUP Gene Setinteracting proteins for the (1R)-MENTHYL HEXYL PHOSPHONATE GROUP drug from the curated DrugBank Drug Targets dataset. |
Pyruvoyl Group Gene Setinteracting proteins for the Pyruvoyl Group drug from the curated DrugBank Drug Targets dataset. |
Diethylphosphono Group Gene Setinteracting proteins for the Diethylphosphono Group drug from the curated DrugBank Drug Targets dataset. |
2-Bromoacetyl Group Gene Setinteracting proteins for the 2-Bromoacetyl Group drug from the curated DrugBank Drug Targets dataset. |
blood group incompatibility; rh isoimmunization Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood group incompatibility; rh isoimmunization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; blood group incompatibility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; blood group incompatibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
i/d ace gene polymorphism and abo blood group system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease i/d ace gene polymorphism and abo blood group system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
group Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term group in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
quaternary ammonium group transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the quaternary ammonium group transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
prosthetic group metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the prosthetic group metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphotransferase activity, phosphate group as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphotransferase activity, phosphate group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
quaternary ammonium group transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the quaternary ammonium group transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
steroid dehydrogenase activity, acting on the ch-oh group of donors, nad or nadp as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the steroid dehydrogenase activity, acting on the ch-oh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh2 group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-ch group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-ch group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
prosthetic group binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the prosthetic group binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on a heme group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on a heme group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
quaternary ammonium group binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the quaternary ammonium group binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphotransferase activity, nitrogenous group as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphotransferase activity, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on ch-oh group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on ch-oh group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
group ii metabotropic glutamate receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the group ii metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on a sulfur group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on a sulfur group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
steroid dehydrogenase activity, acting on the ch-ch group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the steroid dehydrogenase activity, acting on the ch-ch group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
group iii metabotropic glutamate receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the group iii metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphotransferase activity, carboxyl group as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphotransferase activity, carboxyl group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-nh group of donors Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-nh group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2015 genes performing the oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
group E 1682-2106 [PMID:16118363] Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the group E 1682-2106 [PMID:16118363] ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
blood group antigen abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Psychotherapy, Group Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Psychotherapy, Group phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Blood Group Incompatibility Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Group Incompatibility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
G-protein alpha subunit, group I Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G-protein alpha subunit, group I protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G-protein alpha subunit, group S Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G-protein alpha subunit, group S protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G-protein alpha subunit, group Q Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G-protein alpha subunit, group Q protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group I, CYP1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group I, CYP1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group I, CYP2D-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group I, CYP2D-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pre-SET zinc-binding sub-group Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pre-SET zinc-binding sub-group protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group I, CYP2J-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group I, CYP2J-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fanconi anaemia group C protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fanconi anaemia group C protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group box domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group box domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group II Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group II protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group IV Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group IV protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Xeroderma pigmentosum group D protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Xeroderma pigmentosum group D protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G-protein alpha subunit, group 12 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G-protein alpha subunit, group 12 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fanconi anemia group I protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fanconi anemia group I protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Blood group Rhesus C/E/D polypeptide Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Blood group Rhesus C/E/D polypeptide protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group I, CYP2B-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group I, CYP2B-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fanconi Anaemia group E protein, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fanconi Anaemia group E protein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group, HMG-I/HMG-Y Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group, HMG-I/HMG-Y protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group I Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group I protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alanine racemase/group IV decarboxylase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alanine racemase/group IV decarboxylase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group nucleosome-binding domain-containing family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group nucleosome-binding domain-containing family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group I, CYP2A-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group I, CYP2A-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kell blood group glycoprotein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kell blood group glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Fanconi anaemia group A protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Fanconi anaemia group A protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bacterial Ig-like, group 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bacterial Ig-like, group 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome P450, E-class, group I, CYP2E-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome P450, E-class, group I, CYP2E-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
High mobility group box domain 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group box domain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
fanconi anemia, complementation group p Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group p phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group q Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group q phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group i Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group i phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group j Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group j phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group l Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group l phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group m Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group m phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group n Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group n phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group o Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group o phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group a Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group b Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group b phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group c Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group e Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group f Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group f phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group g Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group g phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, swann] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, swann] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, rodgers] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, rodgers] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, colton] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, colton] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, knops system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, knops system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[junior blood group system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [junior blood group system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, raph] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, raph] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group gil] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group gil] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, dombrock] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, dombrock] phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group g/cockayne syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group g/cockayne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, waldner] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, waldner] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, scianna system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, scianna system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, mn] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, mn] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, xg system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, xg system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group d1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group d1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
fanconi anemia, complementation group d2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the fanconi anemia, complementation group d2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, lutheran system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, lutheran system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group b Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group b phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group c Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group c phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group a Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group a phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group f Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group f phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group g Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group g phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group d Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group d phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, abo system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, abo system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, ok] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, ok] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, auberger system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, auberger system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
bare lymphocyte syndrome, type ii, complementation group c Gene SetFrom OMIM Gene-Disease Associations genes associated with the bare lymphocyte syndrome, type ii, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset. |
bare lymphocyte syndrome, type ii, complementation group a Gene SetFrom OMIM Gene-Disease Associations genes associated with the bare lymphocyte syndrome, type ii, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset. |
bare lymphocyte syndrome, type ii, complementation group d Gene SetFrom OMIM Gene-Disease Associations genes associated with the bare lymphocyte syndrome, type ii, complementation group d phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, indian system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, indian system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, p1pk system, p phenotype] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, p1pk system, p phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, froese] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, froese] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, landsteiner-wiener] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, landsteiner-wiener] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, rhesus] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, rhesus] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, globoside system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, globoside system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, lutheran null] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, lutheran null] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, kell] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, kell] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, radin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, radin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, kidd] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, kidd] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, yt system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, yt system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, p1pk system, p(k) phenotype] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, p1pk system, p(k) phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset. |
trichothiodystrophy, complementation group a Gene SetFrom OMIM Gene-Disease Associations genes associated with the trichothiodystrophy, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset. |
blood group--lutheran inhibitor Gene SetFrom OMIM Gene-Disease Associations genes associated with the blood group--lutheran inhibitor phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, vel system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, vel system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, ss] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, ss] phenotype from the curated OMIM Gene-Disease Associations dataset. |
xeroderma pigmentosum, group e, ddb-negative subtype Gene SetFrom OMIM Gene-Disease Associations genes associated with the xeroderma pigmentosum, group e, ddb-negative subtype phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, stoltzfus system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, stoltzfus system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, lewis] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, lewis] phenotype from the curated OMIM Gene-Disease Associations dataset. |
bare lymphocyte syndrome, type ii, complementation group e Gene SetFrom OMIM Gene-Disease Associations genes associated with the bare lymphocyte syndrome, type ii, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, diego] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, diego] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, ii] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, ii] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, langereis system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, langereis system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, gerbich] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, gerbich] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, wright] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, wright] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group cromer] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group cromer] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, john-milton-hagen system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, john-milton-hagen system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, p1pk system, p(2) phenotype] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, p1pk system, p(2) phenotype] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[blood group, duffy system] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood group, duffy system] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Metabotropic glutamate receptor group I pathway Gene SetFrom PANTHER Pathways proteins participating in the Metabotropic glutamate receptor group I pathway pathway from the PANTHER Pathways dataset. |
Metabotropic glutamate receptor group III pathway Gene SetFrom PANTHER Pathways proteins participating in the Metabotropic glutamate receptor group III pathway pathway from the PANTHER Pathways dataset. |
Metabotropic glutamate receptor group II pathway Gene SetFrom PANTHER Pathways proteins participating in the Metabotropic glutamate receptor group II pathway pathway from the PANTHER Pathways dataset. |
phosphotransferases-alcohol-group-acceptor Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term phosphotransferases-alcohol-group-acceptor in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Human immunodeficiency virus type 1 group M subtype B (isolate MN) Gene SetFrom Virus MINT Protein-Virus Interactions interacting proteins for the virus Human immunodeficiency virus type 1 group M subtype B (isolate MN) from the Virus MINT Protein-Virus Interactions dataset. |
Blood Group Incompatibility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Blood Group Incompatibility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Typhus Group Rickettsial Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Typhus Group Rickettsial Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Group B Streptococcal Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Group B Streptococcal Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Group B Streptococcal Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Group B Streptococcal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gil Blood Group Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gil Blood Group in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spotted Fever Group Rickettsiosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spotted Fever Group Rickettsiosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Group A Streptococcal Infections Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Group A Streptococcal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Group 3 Pulmonary Hypertension Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Group 3 Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Blood Group Deletion Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Blood Group Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult I Blood Group Phenotype Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult I Blood Group Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bent Bone Dysplasia Group Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bent Bone Dysplasia Group in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Invasive Group A Beta-Hemolytic Streptococcal Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Invasive Group A Beta-Hemolytic Streptococcal Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Blood Group Antigen Abnormality Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blood Group Antigen Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Duffy Blood Group System, Fy(A-B-) Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duffy Blood Group System, Fy(A-B-) Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Duffy Blood Group System, Fy(Bwk) Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duffy Blood Group System, Fy(Bwk) Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Blood Group--Lutheran Null Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blood Group--Lutheran Null in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cromer Blood Group System, Dr(A-) Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cromer Blood Group System, Dr(A-) Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radin Blood Group Antigen Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radin Blood Group Antigen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Scianna Blood Group System, Sc:-1,-2 Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scianna Blood Group System, Sc:-1,-2 Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Gerbich Blood Group System, Gerbich Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gerbich Blood Group System, Gerbich Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Blood Group--Froese Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blood Group--Froese in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Blood Group--Waldner Type Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blood Group--Waldner Type in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Blood Group--Wright Antigen Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blood Group--Wright Antigen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Swann Blood Group Antigen Phenotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Swann Blood Group Antigen Phenotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
quaternary ammonium group transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the quaternary ammonium group transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
quaternary ammonium group transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the quaternary ammonium group transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
group III metabotropic glutamate receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the group III metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
group II metabotropic glutamate receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the group II metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phosphotransferase activity, phosphate group as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphotransferase activity, phosphate group as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phosphotransferase activity, nitrogenous group as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphotransferase activity, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
phosphotransferase activity, carboxyl group as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the phosphotransferase activity, carboxyl group as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
steroid dehydrogenase activity, acting on the CH-CH group of donors Gene SetFrom GO Molecular Function Annotations 2023 genes performing the steroid dehydrogenase activity, acting on the CH-CH group of donors molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor Gene SetFrom GO Molecular Function Annotations 2023 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
Group 2 innate lymphoid cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Group 2 innate lymphoid cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Group 1 innate lymphoid cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Group 1 innate lymphoid cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Group 3 innate lymphoid cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Group 3 innate lymphoid cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Group 2 innate lymphoid cell_Lymph node_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Group 2 innate lymphoid cell_Lymph node_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Group 2 innate lymphoid cell_Pancreas_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Group 2 innate lymphoid cell_Pancreas_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Serotonin HTR1 group and FOS pathway Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Serotonin HTR1 group and FOS pathway pathway from the WikiPathways Pathways 2024 dataset. |
ABO blood group biosynthesis Gene Setproteins participating in the ABO blood group biosynthesis pathway from the Reactome Pathways 2024 dataset. |
Blood group systems biosynthesis Gene Setproteins participating in the Blood group systems biosynthesis pathway from the Reactome Pathways 2024 dataset. |
Lewis blood group biosynthesis Gene Setproteins participating in the Lewis blood group biosynthesis pathway from the Reactome Pathways 2024 dataset. |
Rhesus blood group biosynthesis Gene Setproteins participating in the Rhesus blood group biosynthesis pathway from the Reactome Pathways 2024 dataset. |
quaternary ammonium group transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the quaternary ammonium group transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
quaternary ammonium group transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the quaternary ammonium group transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phosphotransferase activity, alcohol group as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphotransferase activity, alcohol group as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
group III metabotropic glutamate receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the group III metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
group II metabotropic glutamate receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the group II metabotropic glutamate receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phosphotransferase activity, phosphate group as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphotransferase activity, phosphate group as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phosphotransferase activity, nitrogenous group as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphotransferase activity, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
phosphotransferase activity, carboxyl group as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the phosphotransferase activity, carboxyl group as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
steroid dehydrogenase activity, acting on the CH-CH group of donors Gene SetFrom GO Molecular Function Annotations 2025 genes performing the steroid dehydrogenase activity, acting on the CH-CH group of donors molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor Gene SetFrom GO Molecular Function Annotations 2025 genes performing the oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Xeroderma pigmentosum group A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Xeroderma pigmentosum group A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Xeroderma pigmentosum group G Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Xeroderma pigmentosum group G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Blood group incompatibility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Blood group incompatibility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group I Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group I in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Xeroderma pigmentosum group D Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Xeroderma pigmentosum group D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Xeroderma pigmentosum group F Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Xeroderma pigmentosum group F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Xeroderma pigmentosum group C Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Xeroderma pigmentosum group C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Xeroderma pigmentosum group B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Xeroderma pigmentosum group B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group D1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group D1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Xeroderma pigmentosum group E Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Xeroderma pigmentosum group E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group E Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group U Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group U in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group F Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group C Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group J Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group J in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group N Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group N in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group D2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group D2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior fossa group B ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior fossa group B ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior fossa group A ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior fossa group A ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group L Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group L in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group T Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group T in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group Q Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group Q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group G Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group V Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group V in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Fanconi anemia complementation group O Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fanconi anemia complementation group O in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
AUBERGER BLOOD GROUP POLYMORPHISM Au Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the AUBERGER BLOOD GROUP POLYMORPHISM Au phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
BLOOD GROUP--LUTHERAN SYS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the BLOOD GROUP--LUTHERAN SYS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Fanconi anemia complementation group Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Fanconi anemia complementation group phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Xeroderma pigmentosum group Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Xeroderma pigmentosum group phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
BLOOD GROUP--LUTHERAN INHIBI Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the BLOOD GROUP--LUTHERAN INHIBI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
DUFFY BLOOD GROUP SYS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the DUFFY BLOOD GROUP SYS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
DIEGO BLOOD GROUP ANTI Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the DIEGO BLOOD GROUP ANTI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
DUFFY BLOOD GROUP SYSTEM, FY(bwk) PHENOTYPE Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the DUFFY BLOOD GROUP SYSTEM, FY(bwk) PHENOTYPE phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Blood group Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Blood group phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Langereis blood group Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Langereis blood group phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
KNOPS BLOOD GROUP SYS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the KNOPS BLOOD GROUP SYS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cromer blood group system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cromer blood group system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ER BLOOD GROUP SYS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ER BLOOD GROUP SYS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
RAPH BLOOD GROUP SYS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the RAPH BLOOD GROUP SYS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
BLOOD GROUP--DIEGO SYS Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the BLOOD GROUP--DIEGO SYS phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
John Milton Hagen blood group system Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the John Milton Hagen blood group system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ABO blood group (O vs non-O) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the ABO blood group (O vs non-O) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
ABO blood group (A vs O) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the ABO blood group (A vs O) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
ABO blood group (B vs O) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the ABO blood group (B vs O) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
ABO blood group (AB vs O) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the ABO blood group (AB vs O) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
ABO blood group (A vs non-A) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the ABO blood group (A vs non-A) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
ABO blood group (B vs non-B) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the ABO blood group (B vs non-B) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
ABO blood group (AB vs non-AB) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the ABO blood group (AB vs non-AB) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Regular attendance at a religious group Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Regular attendance at a religious group phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
MENINGOCOCCAL GROUP B VACCINE Gene Setinteracting proteins for the MENINGOCOCCAL GROUP B VACCINE drug from theDGIdb Drug Targets 2026 dataset. |
GROUP E 1682-2106 [PMID:16118363] Gene Setinteracting proteins for the GROUP E 1682-2106 [PMID:16118363] drug from theDGIdb Drug Targets 2026 dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bifunctional peroxisomal enzyme deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bifunctional peroxisomal enzyme deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked ichthyosis with steryl-sulfatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked ichthyosis with steryl-sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Phosphoglycerate dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phosphoglycerate dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Galactosylceramide beta-galactosidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Galactosylceramide beta-galactosidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Isolated 17,20-lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Isolated 17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Endplate acetylcholinesterase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Endplate acetylcholinesterase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sepiapterin reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sepiapterin reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Methionine adenosyltransferase deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Methionine adenosyltransferase deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carbonic anhydrase va deficiency, hyperammonemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of ribose-5-phosphate isomerase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of ribose-5-phosphate isomerase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kininogen deficiency, total Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kininogen deficiency, total phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
6-pyruvoyl-tetrahydropterin synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 6-pyruvoyl-tetrahydropterin synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
N-terminal acetyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the N-terminal acetyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 7 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Creatine deficiency, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Creatine deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Birbeck granule deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Birbeck granule deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucocorticoid deficiency 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucocorticoid deficiency 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
SCID due to ADA deficiency, delayed onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Properdin deficiency, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Properdin deficiency, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PROPERDIN DEFICIENCY, TYPE II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PROPERDIN DEFICIENCY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement factor d deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement factor d deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to protein S deficiency, autosomal recessive Gene SetFrom 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. |
Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Methylmalonyl-CoA epimerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Methylmalonyl-CoA epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 8 deficiency type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 8 deficiency type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Testosterone 17-beta-dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Testosterone 17-beta-dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acyl-CoA dehydrogenase family, member 9, deficiency of Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acyl-CoA dehydrogenase family, member 9, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of 2-methylbutyryl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of 2-methylbutyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of isobutyryl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of isobutyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene SetFrom 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. |
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral folate deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebral folate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Phosphoserine aminotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phosphoserine aminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency due to ADA deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carnitine acylcarnitine translocase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carnitine acylcarnitine translocase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Partial hypoxanthine-guanine phosphoribosyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Succinyl-CoA acetoacetate transferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Succinyl-CoA acetoacetate transferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carnitine palmitoyltransferase I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Platelet-activating factor acetylhydrolase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Platelet-activating factor acetylhydrolase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary C1 esterase inhibitor deficiency - dysfunctional factor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipase deficiency combined Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lipase deficiency combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
5-Oxoprolinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 5-Oxoprolinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucocorticoid deficiency with achalasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proopiomelanocortin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proopiomelanocortin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrinsic factor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrinsic factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
21-hydroxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 21-hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutaryl-CoA oxidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutaryl-CoA oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corticosterone methyloxidase type 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corticosterone methyloxidase type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thiopurine methyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thiopurine methyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
METHYLCOBALAMIN DEFICIENCY, cblG TYPE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the METHYLCOBALAMIN DEFICIENCY, cblG TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carnitine palmitoyltransferase II deficiency, infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carnitine palmitoyltransferase II deficiency, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lactate dehydrogenase b deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lactate dehydrogenase b deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 18 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 16 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of 3-hydroxyacyl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of 3-hydroxyacyl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Plasminogen deficiency, type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Plasminogen deficiency, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Biotinidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Biotinidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant isolated somatotropin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant isolated somatotropin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypohidrotic ectodermal dysplasia with immune deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypohidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of phosphoserine phosphatase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of phosphoserine phosphatase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Isolated growth hormone deficiency type 1B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Isolated growth hormone deficiency type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of butyryl-CoA dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of butyryl-CoA dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anhidrotic ectodermal dysplasia with immune deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anhidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3 Methylcrotonyl-CoA carboxylase 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3 Methylcrotonyl-CoA carboxylase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of hyaluronoglucosaminidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of hyaluronoglucosaminidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sulfite oxidase deficiency, isolated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sulfite oxidase deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Plasminogen activator inhibitor type 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Plasminogen activator inhibitor type 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase phosphatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase phosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 22 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 20 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 21 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monoamine oxidase A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monoamine oxidase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor V deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor V deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene SetFrom 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. |
Adenine phosphoribosyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenine phosphoribosyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene SetFrom 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. |
Glutamate formiminotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutamate formiminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypoglycemia with deficiency of glycogen synthetase in the liver Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypoglycemia with deficiency of glycogen synthetase in the liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LEUKOCYTE ADHESION DEFICIENCY, TYPE III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LEUKOCYTE ADHESION DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Follicle-stimulating hormone deficiency, isolated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Follicle-stimulating hormone deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ganglioside sialidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ganglioside sialidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
C1q deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the C1q deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interferon gamma receptor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interferon gamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Platelet glycoprotein IV deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Platelet glycoprotein IV deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
N-acetylaspartate deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the N-acetylaspartate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adenylosuccinate lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenylosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Triosephosphate isomerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Triosephosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, atypical, due to saposin C deficiency Gene SetFrom 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 SetFrom 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. |
Aromatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aromatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor II deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex III deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor xiii, a subunit, deficiency of Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor xiii, a subunit, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex III deficiency, nuclear type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency, nuclear type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex III deficiency, nuclear type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex III deficiency, nuclear type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-methylcrotonyl CoA carboxylase 2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-methylcrotonyl CoA carboxylase 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia due to hexokinase deficiency Gene SetFrom 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 SetFrom 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. |
Multiple sulfatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corticosteroid-binding globulin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corticosteroid-binding globulin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined oxidative phosphorylation deficiency 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined oxidative phosphorylation deficiency 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corticosterone methyloxidase type 2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corticosterone methyloxidase type 2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 9 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 9 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Holocarboxylase synthetase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Holocarboxylase synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
2,4-Dienoyl-CoA reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 2,4-Dienoyl-CoA reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of glycerate kinase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of glycerate kinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ataxia with vitamin E deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ataxia with vitamin E deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of galactokinase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of galactokinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
ACTH deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the ACTH deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
PROPERDIN DEFICIENCY, TYPE III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the PROPERDIN DEFICIENCY, TYPE III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Carboxylesterase 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carboxylesterase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Purine-nucleoside phosphorylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Purine-nucleoside phosphorylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neonatal intrahepatic cholestasis caused by citrin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neonatal intrahepatic cholestasis caused by citrin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 6 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 6 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Antithrombin III deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Antithrombin III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inosine triphosphatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inosine triphosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth hormone deficiency with pituitary anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth hormone deficiency with pituitary anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase lipoic acid synthetase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase lipoic acid synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ulna and fibula absence of with severe limb deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocysteinemia due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of pyrroline-5-carboxylate reductase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of pyrroline-5-carboxylate reductase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency due to ficolin 3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sarcosine dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sarcosine dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor v and factor viii, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Branched-chain ketoacid dehydrogenase kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Branched-chain ketoacid dehydrogenase kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
L-ferritin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the L-ferritin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arginase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arginase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hepatic lipase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hepatic lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor X deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E3-binding protein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E3-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor IX deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha-fetoprotein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha-fetoprotein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermethioninemia due to adenosine kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vitamin k-dependent clotting factors, combined deficiency of, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of iodide peroxidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of iodide peroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycosylphosphatidylinositol deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycosylphosphatidylinositol deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Vitamin k-dependent clotting factors, combined deficiency of, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Vitamin k-dependent clotting factors, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukocyte adhesion deficiency type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukocyte adhesion deficiency type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital lactase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Caspase-8 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Caspase-8 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene SetFrom 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. |
Phosphoglycerate kinase 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phosphoglycerate kinase 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anaphylotoxin inactivator deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anaphylotoxin inactivator deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cytochrome-c oxidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cytochrome-c oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Enterokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Enterokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Erythrocyte amp deaminase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Erythrocyte amp deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor VII deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor VII deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant CD11C+/CD1C+ dendritic cell deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Apolipoprotein a-i deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Apolipoprotein a-i deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glut1 deficiency syndrome 1, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glut1 deficiency syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gamma-aminobutyric acid transaminase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gamma-aminobutyric acid transaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myeloperoxidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myeloperoxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial phosphate carrier deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial phosphate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor XI deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Porphobilinogen synthase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Porphobilinogen synthase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Very long chain acyl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Very long chain acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
IRAK4 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the IRAK4 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leukocyte adhesion deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leukocyte adhesion deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cortisone reductase deficiency 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cortisone reductase deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arginine:glycine amidinotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arginine:glycine amidinotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Methionine adenosyltransferase deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Methionine adenosyltransferase deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle AMP deaminase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscle AMP deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dihydropyrimidinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dihydropyrimidinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dimethylglycine dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dimethylglycine dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of hydroxymethylglutaryl-CoA lyase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of hydroxymethylglutaryl-CoA lyase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Monocyte and dendritic cell deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E1-alpha deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E1-alpha deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Isovaleryl-CoA dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Isovaleryl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cd59 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd59 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ornithine aminotransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ornithine aminotransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sphingolipid activator protein 1 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sphingolipid activator protein 1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of ferroxidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of ferroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of steroid 11-beta-monooxygenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of steroid 11-beta-monooxygenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lysosomal acid lipase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lysosomal acid lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dopamine beta hydroxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dopamine beta hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Butyrylcholinesterase deficiency, fluoride-resistant, japanese type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Butyrylcholinesterase deficiency, fluoride-resistant, japanese type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
UDPglucose-4-epimerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the UDPglucose-4-epimerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocystinuria due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of alpha-mannosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of alpha-mannosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene SetFrom 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. |
Insulin-like growth factor I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Insulin-like growth factor I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex II deficiency Gene SetFrom 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. |
Pituitary hormone deficiency, combined 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene SetFrom 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. |
Pyruvate carboxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate carboxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gluthathione synthetase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gluthathione synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fumarase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fumarase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of transaldolase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of transaldolase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial pyruvate carrier deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial pyruvate carrier deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pyruvate dehydrogenase E1-beta deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pyruvate dehydrogenase E1-beta deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MASP2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the MASP2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Argininosuccinate lyase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Argininosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prekallikrein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prekallikrein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chitotriosidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chitotriosidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Anti-plasmin deficiency, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prothrombin deficiency, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial trifunctional protein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial trifunctional protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
GTP cyclohydrolase I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the GTP cyclohydrolase I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of malonyl-CoA decarboxylase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of malonyl-CoA decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
3 beta-Hydroxysteroid dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 3 beta-Hydroxysteroid dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Succinate-semialdehyde dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Succinate-semialdehyde dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked agammaglobulinemia with growth hormone deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked agammaglobulinemia with growth hormone deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Okt4 epitope deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Okt4 epitope deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of acetyl-CoA acetyltransferase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of acetyl-CoA acetyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mitochondrial complex II deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mineralocorticoid deficiency, isolated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement 1s deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement 1s deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dihydropteridine reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dihydropteridine reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mannose-binding protein deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mannose-binding protein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glucose transporter type 1 deficiency syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myd88 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myd88 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cd8 deficiency, familial Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cd8 deficiency, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene SetFrom 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. |
Acid-labile subunit deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fructose-biphosphatase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fructose-biphosphatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia due to dihydrofolate reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement factor B deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement factor B deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, severe, due to leptin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Beta-hydroxyisobutyryl-CoA deacylase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Beta-hydroxyisobutyryl-CoA deacylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Proline dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Proline dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor H deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor H deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutamine deficiency, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of aromatic-L-amino-acid decarboxylase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of aromatic-L-amino-acid decarboxylase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycine N-methyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycine N-methyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ornithine carbamoyltransferase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ornithine carbamoyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sucrase-isomaltase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sucrase-isomaltase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cholesterol monooxygenase (side-chain cleaving) deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cholesterol monooxygenase (side-chain cleaving) deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fucosyltransferase 6 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fucosyltransferase 6 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Asparagine synthetase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Asparagine synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adenylate kinase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pituitary hormone deficiency, combined, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pituitary hormone deficiency, combined, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of butyrylcholine esterase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of butyrylcholine esterase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene SetFrom 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. |
Protein S deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Protein S deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of glycerol kinase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of glycerol kinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of xanthine oxidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of xanthine oxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Urocanate hydratase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Urocanate hydratase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
4-Hydroxyphenylpyruvate dioxygenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the 4-Hydroxyphenylpyruvate dioxygenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Combined deficiency of factor V and factor VIII, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Factor xiii, b subunit, deficiency of Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Factor xiii, b subunit, deficiency of phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Growth deficiency and mental retardation with facial dysmorphism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene SetFrom 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. |
Combined deficiency of sialidase AND beta galactosidase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of (R)-20-hydroxysteroid dehydrogenase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of (R)-20-hydroxysteroid dehydrogenase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prolidase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prolidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of beta-ureidopropionase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of beta-ureidopropionase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deficiency of guanidinoacetate methyltransferase Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deficiency of guanidinoacetate methyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
MYD88 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYD88 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal from the curated CTD Gene-Disease Associations dataset. |
Anemia, Iron-Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Anemia, Iron-Deficiency from the curated CTD Gene-Disease Associations dataset. |
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene SetFrom 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. |
Platelet Glycoprotein IV Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Glycoprotein IV Deficiency from the curated CTD Gene-Disease Associations dataset. |
Mitochondrial Phosphate Carrier Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Phosphate Carrier Deficiency from the curated CTD Gene-Disease Associations dataset. |
Leukocyte Adhesion Deficiency, Type III Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte Adhesion Deficiency, Type III from the curated CTD Gene-Disease Associations dataset. |
Prekallikrein Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prekallikrein Deficiency from the curated CTD Gene-Disease Associations dataset. |
Methylenetetrahydrofolate reductase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylenetetrahydrofolate reductase deficiency from the curated CTD Gene-Disease Associations dataset. |
6-pyruvoyl-tetrahydropterin synthase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 6-pyruvoyl-tetrahydropterin synthase deficiency from the curated CTD Gene-Disease Associations dataset. |
Factor XI Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Factor XI Deficiency from the curated CTD Gene-Disease Associations dataset. |
Carnitine palmitoyl transferase 1A deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine palmitoyl transferase 1A deficiency from the curated CTD Gene-Disease Associations dataset. |
Preaxial deficiency, postaxial polydactyly and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset. |
THYROTROPIN-RELEASING HORMONE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THYROTROPIN-RELEASING HORMONE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
Carbamoyl-Phosphate Synthase I Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carbamoyl-Phosphate Synthase I Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Tyrosine Kinase 2 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tyrosine Kinase 2 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Properdin deficiency, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Properdin deficiency, X-linked from the curated CTD Gene-Disease Associations dataset. |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease COENZYME Q10 DEFICIENCY, PRIMARY, 1 from the curated CTD Gene-Disease Associations dataset. |
Glutathione synthetase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glutathione synthetase deficiency from the curated CTD Gene-Disease Associations dataset. |
Glucocorticoid Deficiency 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glucocorticoid Deficiency 2 from the curated CTD Gene-Disease Associations dataset. |
Aniridia cerebellar ataxia mental deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aniridia cerebellar ataxia mental deficiency from the curated CTD Gene-Disease Associations dataset. |
Combined Oxidative Phosphorylation Deficiency 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 3 from the curated CTD Gene-Disease Associations dataset. |
Proopiomelanocortin Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Proopiomelanocortin Deficiency from the curated CTD Gene-Disease Associations dataset. |
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene SetFrom 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 SetFrom 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. |
Glucocorticoid Deficiency 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glucocorticoid Deficiency 3 from the curated CTD Gene-Disease Associations dataset. |
Intrinsic Factor Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intrinsic Factor Deficiency from the curated CTD Gene-Disease Associations dataset. |
Adenosine monophosphate deaminase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adenosine monophosphate deaminase deficiency from the curated CTD Gene-Disease Associations dataset. |
alpha 1-Antitrypsin Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease alpha 1-Antitrypsin Deficiency from the curated CTD Gene-Disease Associations dataset. |
Combined Oxidative Phosphorylation Deficiency 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 2 from the curated CTD Gene-Disease Associations dataset. |
Plasminogen Deficiency, Type I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Plasminogen Deficiency, Type I from the curated CTD Gene-Disease Associations dataset. |
IgA Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease IgA Deficiency from the curated CTD Gene-Disease Associations dataset. |
Lipase deficiency combined Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipase deficiency combined from the curated CTD Gene-Disease Associations dataset. |
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene SetFrom 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. |
DNA Repair-Deficiency Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease DNA Repair-Deficiency Disorders from the curated CTD Gene-Disease Associations dataset. |
Congenital thrombotic disease, due to Protein C deficiency Gene SetFrom 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. |
Enterokinase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Enterokinase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Carnitine Palmitoyltransferase II Deficiency, Late-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Late-Onset from the curated CTD Gene-Disease Associations dataset. |
Lactase Deficiency, Congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lactase Deficiency, Congenital from the curated CTD Gene-Disease Associations dataset. |
Lecithin Acyltransferase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lecithin Acyltransferase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Interleukin 2 Receptor, Alpha, Deficiency of Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Interleukin 2 Receptor, Alpha, Deficiency of from the curated CTD Gene-Disease Associations dataset. |
ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset. |
Beta ketothiolase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Beta ketothiolase deficiency from the curated CTD Gene-Disease Associations dataset. |
Transaldolase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Transaldolase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Anti-plasmin deficiency, congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset. |
Succinyl-CoA:3-oxoacid CoA transferase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Succinyl-CoA:3-oxoacid CoA transferase deficiency from the curated CTD Gene-Disease Associations dataset. |
CD8 Deficiency, Familial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CD8 Deficiency, Familial from the curated CTD Gene-Disease Associations dataset. |
Neuraminidase 1 deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase 1 deficiency from the curated CTD Gene-Disease Associations dataset. |
Folic Acid Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Folic Acid Deficiency from the curated CTD Gene-Disease Associations dataset. |
Lysosomal acid lipase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lysosomal acid lipase deficiency from the curated CTD Gene-Disease Associations dataset. |
Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene SetFrom 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. |
Vitamin B 12 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin B 12 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Isolated Growth Hormone Deficiency, Type II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type II from the curated CTD Gene-Disease Associations dataset. |
Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene SetFrom 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. |
Familial HDL deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Familial HDL deficiency from the curated CTD Gene-Disease Associations dataset. |
Carnitine-Acylcarnitine Translocase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine-Acylcarnitine Translocase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Methylcobalamin Deficiency, CblG Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylcobalamin Deficiency, CblG Type from the curated CTD Gene-Disease Associations dataset. |
Flaujeac factor deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Flaujeac factor deficiency from the curated CTD Gene-Disease Associations dataset. |
Ribose 5-Phosphate Isomerase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ribose 5-Phosphate Isomerase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Pyruvate dehydrogenase phosphatase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate dehydrogenase phosphatase deficiency from the curated CTD Gene-Disease Associations dataset. |
VLCAD deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VLCAD deficiency from the curated CTD Gene-Disease Associations dataset. |
18-Hydroxylase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 18-Hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset. |
Creatine deficiency, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Creatine deficiency, X-linked from the curated CTD Gene-Disease Associations dataset. |
Mitochondrial Complex III Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Complex III Deficiency from the curated CTD Gene-Disease Associations dataset. |
PROPROTEIN CONVERTASE 1/3 DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROPROTEIN CONVERTASE 1/3 DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
dopamine beta hydroxylase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease dopamine beta hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset. |
Ehlers-Danlos syndrome caused by tenascin-X deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ehlers-Danlos syndrome caused by tenascin-X deficiency from the curated CTD Gene-Disease Associations dataset. |
Growth mental deficiency syndrome of Myhre Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Growth mental deficiency syndrome of Myhre from the curated CTD Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset. |
Ornithine Carbamoyltransferase Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ornithine Carbamoyltransferase Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Protein Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Protein Deficiency from the curated CTD Gene-Disease Associations dataset. |
Factor 8 deficiency, acquired Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Factor 8 deficiency, acquired from the curated CTD Gene-Disease Associations dataset. |
3-methylcrotonyl CoA carboxylase 2 deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 3-methylcrotonyl CoA carboxylase 2 deficiency from the curated CTD Gene-Disease Associations dataset. |
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I from the curated CTD Gene-Disease Associations dataset. |
Adenylosuccinate lyase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adenylosuccinate lyase deficiency from the curated CTD Gene-Disease Associations dataset. |
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene SetFrom 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. |
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of from the curated CTD Gene-Disease Associations dataset. |
Thiopurine S methyltranferase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thiopurine S methyltranferase deficiency from the curated CTD Gene-Disease Associations dataset. |
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene SetFrom 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. |
3-Hydroxyacyl-CoA Dehydrogenase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 3-Hydroxyacyl-CoA Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset. |
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Isolated Growth Hormone Deficiency, Type IB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Isolated Growth Hormone Deficiency, Type IB from the curated CTD Gene-Disease Associations dataset. |
Vitamin A Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin A Deficiency from the curated CTD Gene-Disease Associations dataset. |
Molybdenum cofactor deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Molybdenum cofactor deficiency from the curated CTD Gene-Disease Associations dataset. |
Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset. |
Phosphoglycerate Kinase 1 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoglycerate Kinase 1 Deficiency from the curated CTD Gene-Disease Associations dataset. |
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II from the curated CTD Gene-Disease Associations dataset. |
Severe combined immunodeficiency due to adenosine deaminase deficiency Gene SetFrom 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. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset. |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7 from the curated CTD Gene-Disease Associations dataset. |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 from the curated CTD Gene-Disease Associations dataset. |
Plasminogen Activator Inhibitor-1 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Plasminogen Activator Inhibitor-1 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Pyruvate Dehydrogenase E2 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase E2 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Phosphoglycerate Dehydrogenase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoglycerate Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset. |