Secondary Antibody Deficiency

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Results for "Secondary Antibody Deficiency": 1001 gene sets

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Secondary Antibody Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Antibody Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set From 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.
specific antibody deficiency Gene Set From HPO Gene-Disease Associations genes associated with the specific antibody deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
specific anti-polysaccharide antibody deficiency Gene Set From HPO Gene-Disease Associations genes associated with the specific anti-polysaccharide antibody deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autoinflammation, antibody deficiency, and immune dysregulation syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the autoinflammation, antibody deficiency, and immune dysregulation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Anti-Polysaccharide Antibody Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anti-Polysaccharide Antibody Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Antibody Deficiency Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Antibody Deficiency Due To Defect In Cd19 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Antibody Deficiency Due To Defect In Cd19 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Plcg2-Associated Antibody Deficiency And Immune Dysregulation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Plcg2-Associated Antibody Deficiency And Immune Dysregulation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Specific Anti-Polysaccharide Antibody Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Specific Anti-Polysaccharide Antibody Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Specific Pneumococcal Antibody Deficiency Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Specific Pneumococcal Antibody Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation 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 Set From GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
secondary growth hormone deficiency Gene Set From HPO Gene-Disease Associations genes associated with the secondary growth hormone deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Secondary Growth Hormone Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Growth Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Immune Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Immune Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis from the curated CTD Gene-Disease Associations dataset.
humanized SMART Anti-IL-12 Antibody Gene Set From DrugBank Drug Targets interacting proteins for the humanized SMART Anti-IL-12 Antibody drug from the curated DrugBank Drug Targets dataset.
anti-neutrophil cytoplasmic antibody-associated vasculitis; Gene Set From GAD Gene-Disease Associations genes associated with the disease anti-neutrophil cytoplasmic antibody-associated vasculitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antineutrophil cytoplasmic antibody; (anca)-associated vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease antineutrophil cytoplasmic antibody; (anca)-associated vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
measles antibody level Gene Set From GAD Gene-Disease Associations genes associated with the disease measles antibody level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
liver cancer risk in hcv antibody-positive Gene Set From GAD Gene-Disease Associations genes associated with the disease liver cancer risk in hcv antibody-positive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anti-cyclic citrullianted peptide antibody Gene Set From GAD Gene-Disease Associations genes associated with the disease anti-cyclic citrullianted peptide antibody in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anti neutrophil cytoplasmic antibody; (anca)-associated vasculitis Gene Set From GAD Gene-Disease Associations genes associated with the disease anti neutrophil cytoplasmic antibody; (anca)-associated vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antibody response to pertussis vaccination Gene Set From GAD Gene-Disease Associations genes associated with the disease antibody response to pertussis vaccination in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antibody Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term antibody in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Antibody status in Tripanosoma cruzi seropositivity Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Antibody status in Tripanosoma cruzi seropositivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Thyroid peroxidase antibody positivity Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Thyroid peroxidase antibody positivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Cytomegalovirus antibody response Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Cytomegalovirus antibody response phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Anti-cyclic Citrullinated Peptide Antibody Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Anti-cyclic Citrullinated Peptide Antibody phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Thyroid peroxidase antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Thyroid peroxidase antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Antineutrophil cytoplasmic antibody-associated vasculitis Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Antineutrophil cytoplasmic antibody-associated vasculitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
platelet antibody positive Gene Set From HPO Gene-Disease Associations genes associated with the platelet antibody positive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
smooth muscle antibody positivity Gene Set From HPO Gene-Disease Associations genes associated with the smooth muscle antibody positivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
autoimmune antibody positivity Gene Set From HPO Gene-Disease Associations genes associated with the autoimmune antibody positivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
antineutrophil antibody positivity Gene Set From HPO Gene-Disease Associations genes associated with the antineutrophil antibody positivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
antinuclear antibody positivity Gene Set From HPO Gene-Disease Associations genes associated with the antinuclear antibody positivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent specific antibody response Gene Set From HPO Gene-Disease Associations genes associated with the absent specific antibody response phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
antiphospholipid antibody positivity Gene Set From HPO Gene-Disease Associations genes associated with the antiphospholipid antibody positivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased anti-nuclear antigen antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased anti-nuclear antigen antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased anti-single stranded dna antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased anti-single stranded dna antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased anti-double stranded dna antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased anti-double stranded dna antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased anti-nuclear antigen antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased anti-nuclear antigen antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased anti-chromatin antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased anti-chromatin antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased anti-erythrocyte antigen antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased anti-erythrocyte antigen antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased anti-double stranded dna antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased anti-double stranded dna antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased anti-histone antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased anti-histone antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
antibody-specificity Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term antibody-specificity in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Classical antibody-mediated complement activation Gene Set From Reactome Pathways 2014 proteins participating in the Classical antibody-mediated complement activation pathway from the Reactome Pathways dataset.
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anti-Neutrophil Cytoplasmic Antibody Positive Vasculitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anti-Neutrophil Cytoplasmic Antibody Positive Vasculitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anti-Pit-1 Antibody Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anti-Pit-1 Antibody Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absent Specific Antibody Response Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Specific Antibody Response in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Thyroid Peroxidase Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Thyroid Peroxidase Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Antiphospholipid Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Antiphospholipid Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Antibody Level In Blood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Antibody Level In Blood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thyroglobulin Antibody Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thyroglobulin Antibody Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Antibody Level In Blood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Antibody Level In Blood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Cyclic Citrullinated Peptide Antibody Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Cyclic Citrullinated Peptide Antibody in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Cyclic Citrullinated Peptide Antibody Level Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Cyclic Citrullinated Peptide Antibody Level in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Antineutrophil Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Antineutrophil Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Platelet Antibody Positive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Platelet Antibody Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autoimmune Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autoimmune Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Nuclear Antibody Measurement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Nuclear Antibody Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Liver Cytosolic Antigen Type 1 Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Liver Cytosolic Antigen Type 1 Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Insulin Receptor Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Insulin Receptor Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Glutamic Acid Decarboxylase Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Glutamic Acid Decarboxylase Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Maternal Anticardiolipin Antibody Positive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal Anticardiolipin Antibody Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anti-Multiple Nuclear Dots Antibody Positivity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anti-Multiple Nuclear Dots Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
increased anti-double stranded DNA antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased anti-double stranded DNA antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased anti-single stranded DNA antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased anti-single stranded DNA antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased anti-nuclear antigen antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased anti-nuclear antigen antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased anti-histone antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased anti-histone antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased anti-erythrocyte antigen antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased anti-erythrocyte antigen antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased anti-chromatin antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased anti-chromatin antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased anti-nuclear antigen antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased anti-nuclear antigen antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased anti-double stranded DNA antibody level Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased anti-double stranded DNA antibody level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased anti-nuclear antigen antibody level Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the increased anti-nuclear antigen antibody level phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Antibody-secreting cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody-secreting cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Antibody Secreting B cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody Secreting B cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Antibody-secreting cell_Bone marrow_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody-secreting cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Antibody-secreting cell_Bone marrow_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody-secreting cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Antibody-secreting cell_Lymph_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody-secreting cell_Lymph_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Antibody-secreting cell_Nasal polyp_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody-secreting cell_Nasal polyp_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Antibody-secreting cell_Salivary gland_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody-secreting cell_Salivary gland_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Antibody-secreting cell_Undefined_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Antibody-secreting cell_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Classical antibody-mediated complement activation Gene Set From Reactome Pathways 2024 proteins participating in the Classical antibody-mediated complement activation pathway from the Reactome Pathways 2024 dataset.
antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of antibody-dependent cellular cytotoxicity Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of antibody-dependent cellular cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
Anti-SEMA4D Monoclonal Antibody VX15/2 Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Anti-SEMA4D Monoclonal Antibody VX15/2 phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Immune response to measles vaccine (measles-specific neutralising antibody titre) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immune response to measles vaccine (measles-specific neutralising antibody titre) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vasculitis associated with antineutrophil cytoplasmic antibody reactive to myeloperoxidase Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vasculitis associated with antineutrophil cytoplasmic antibody reactive to myeloperoxidase phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Antineutrophil cytoplasmic antibody-associated vasculitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Antineutrophil cytoplasmic antibody-associated vasculitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Meningococcal C functional antibody titers post childhood immunization Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meningococcal C functional antibody titers post childhood immunization phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Antinuclear antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Antinuclear antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thyroid peroxidase antibody positivity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thyroid peroxidase antibody positivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Thyroid peroxidase antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thyroid peroxidase antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cytomegalovirus antibody response Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cytomegalovirus antibody response phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Antibody level in response to infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Antibody level in response to infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Antibody status in Tripanosoma cruzi seropositivity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Antibody status in Tripanosoma cruzi seropositivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Helicobacter pylori OMP antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Helicobacter pylori OMP antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cytomegalovirus pp28 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cytomegalovirus pp28 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Polyomavirus 2 JC VP1 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Polyomavirus 2 JC VP1 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Merkel cell polyomavirus VP1 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Merkel cell polyomavirus VP1 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epstein-Barr virus ZEBRA antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epstein-Barr virus ZEBRA antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Toxoplasma gondii sag1 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Toxoplasma gondii sag1 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
BK polyomavirus VP1 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the BK polyomavirus VP1 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Helicobacter pylori UREA antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Helicobacter pylori UREA antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chlamydia trachomatis PorB antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chlamydia trachomatis PorB antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Herpes simplex virus 2 mgG-1 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Herpes simplex virus 2 mgG-1 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epstein-Barr virus EA-D antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epstein-Barr virus EA-D antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epstein-Barr virus EBNA-1 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epstein-Barr virus EBNA-1 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epstein-Barr virus VCA p18 antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epstein-Barr virus VCA p18 antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Varicella zoster virus glycoproteins E and I antibody levels Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Varicella zoster virus glycoproteins E and I antibody levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anti-cyclic Citrullinated Peptide Antibody Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anti-cyclic Citrullinated Peptide Antibody phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anti-adalimumab antibody production in response to treatment in Crohn's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anti-adalimumab antibody production in response to treatment in Crohn's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
ANTI-ANGIOPOIETIN MONOCLONAL ANTIBODY AMG 780 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-ANGIOPOIETIN MONOCLONAL ANTIBODY AMG 780 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-PD-L1 MONOCLONAL ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-PD-L1 MONOCLONAL ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-LAG-3/PD-L1 BISPECIFIC ANTIBODY FS118 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-LAG-3/PD-L1 BISPECIFIC ANTIBODY FS118 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-PD-L1 MONOCLONAL ANTIBODY FAZ053 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-PD-L1 MONOCLONAL ANTIBODY FAZ053 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-PD-L1 MONOCLONAL ANTIBODY MDX-1105 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-PD-L1 MONOCLONAL ANTIBODY MDX-1105 drug from theDGIdb Drug Targets 2026 dataset.
BISPECIFIC ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the BISPECIFIC ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD3 MONOCLONAL ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD3 MONOCLONAL ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-GPA33/CD3 MONOCLONAL ANTIBODY MGD007 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-GPA33/CD3 MONOCLONAL ANTIBODY MGD007 drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY SGN-14 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY SGN-14 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD40 MONOCLONAL ANTIBODY CHI LOB 7/4 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD40 MONOCLONAL ANTIBODY CHI LOB 7/4 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD40/ANTI-MESOTHELIN BISPECIFIC ANTIBODY ABBV-428 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD40/ANTI-MESOTHELIN BISPECIFIC ANTIBODY ABBV-428 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD47 MONOCLONAL ANTIBODY CC-90002 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD47 MONOCLONAL ANTIBODY CC-90002 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD27L ANTIBODY-DRUG CONJUGATE AMG 172 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD27L ANTIBODY-DRUG CONJUGATE AMG 172 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD70 ANTIBODY-DDRUG CONJUGATE MDX-1203 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD70 ANTIBODY-DDRUG CONJUGATE MDX-1203 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CEA/ANTI-HSG BISPECIFIC MONOCLONAL ANTIBODY TF2 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CEA/ANTI-HSG BISPECIFIC MONOCLONAL ANTIBODY TF2 drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY 3H1 ANTI-IDIOTYPE VACCINE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY 3H1 ANTI-IDIOTYPE VACCINE drug from theDGIdb Drug Targets 2026 dataset.
YTTRIUM Y 90 ANTI-CEA MONOCLONAL ANTIBODY CT84.66 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the YTTRIUM Y 90 ANTI-CEA MONOCLONAL ANTIBODY CT84.66 drug from theDGIdb Drug Targets 2026 dataset.
HUMAN MONOCLONAL ANTIBODY B11-HCG BETA FUSION PROTEIN CDX-1307 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the HUMAN MONOCLONAL ANTIBODY B11-HCG BETA FUSION PROTEIN CDX-1307 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-C-FMS MONOCLONAL ANTIBODY AMG 820 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-C-FMS MONOCLONAL ANTIBODY AMG 820 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CTLA-4 MONOCLONAL ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CTLA-4 MONOCLONAL ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-EGFR MONOCLONAL ANTIBODY EMD 55900 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-EGFR MONOCLONAL ANTIBODY EMD 55900 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-EGFR MONOCLONAL ANTIBODY GT-MAB 5.2-GEX Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-EGFR MONOCLONAL ANTIBODY GT-MAB 5.2-GEX drug from theDGIdb Drug Targets 2026 dataset.
ANTI-EGFR MONOCLONAL ANTIBODY SYN004 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-EGFR MONOCLONAL ANTIBODY SYN004 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-EGFR/HER2/HER3 MONOCLONAL ANTIBODY MIXTURE SYM013 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-EGFR/HER2/HER3 MONOCLONAL ANTIBODY MIXTURE SYM013 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-EGFRVIII ANTIBODY DRUG CONJUGATE AMG 595 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-EGFRVIII ANTIBODY DRUG CONJUGATE AMG 595 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-ERBB3 MONOCLONAL ANTIBODY AV-203 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-ERBB3 MONOCLONAL ANTIBODY AV-203 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-MET MONOCLONAL ANTIBODY MIXTURE SYM015 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-MET MONOCLONAL ANTIBODY MIXTURE SYM015 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-MET/EGFR MONOCLONAL ANTIBODY LY3164530 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-MET/EGFR MONOCLONAL ANTIBODY LY3164530 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-PD1 MONOCLONAL ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-PD1 MONOCLONAL ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-ENPP3/MMAF ANTIBODY-DRUG CONJUGATE AGS-16M8F Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-ENPP3/MMAF ANTIBODY-DRUG CONJUGATE AGS-16M8F drug from theDGIdb Drug Targets 2026 dataset.
ANTI-HER2 ANTIBODY-DRUG CONJUGATE MEDI4276 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-HER2 ANTIBODY-DRUG CONJUGATE MEDI4276 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-ERBB3 MONOCLONAL ANTIBODY CDX-3379 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-ERBB3 MONOCLONAL ANTIBODY CDX-3379 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-ERBB3 MONOCLONAL ANTIBODY REGN1400 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-ERBB3 MONOCLONAL ANTIBODY REGN1400 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-HER3 MONOCLONAL ANTIBODY GSK2849330 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-HER3 MONOCLONAL ANTIBODY GSK2849330 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-TF MONOCLONAL ANTIBODY ALT-836 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-TF MONOCLONAL ANTIBODY ALT-836 drug from theDGIdb Drug Targets 2026 dataset.
BISPECIFIC ANTIBODY MDX447 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the BISPECIFIC ANTIBODY MDX447 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-FLT3/CD3 BISPECIFIC ANTIBODY CLN-049 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-FLT3/CD3 BISPECIFIC ANTIBODY CLN-049 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-GLYPICAN 3/CD3 BISPECIFIC ANTIBODY ERY974 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-GLYPICAN 3/CD3 BISPECIFIC ANTIBODY ERY974 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-TIM-3 MONOCLONAL ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-TIM-3 MONOCLONAL ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-TIM3 MONOCLONAL ANTIBODY LY3321367 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-TIM3 MONOCLONAL ANTIBODY LY3321367 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-HBEGF MONOCLONAL ANTIBODY U3-1565 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-HBEGF MONOCLONAL ANTIBODY U3-1565 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-HGF MONOCLONAL ANTIBODY TAK-701 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-HGF MONOCLONAL ANTIBODY TAK-701 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-IGF-1R RECOMBINANT MONOCLONAL ANTIBODY BIIB022 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-IGF-1R RECOMBINANT MONOCLONAL ANTIBODY BIIB022 drug from theDGIdb Drug Targets 2026 dataset.
HUMANIZED SMART ANTI-IL-12 ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the HUMANIZED SMART ANTI-IL-12 ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-IL17A MONOCLONAL ANTIBODY CJM112 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-IL17A MONOCLONAL ANTIBODY CJM112 drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY R24 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY R24 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD123/CD3 BISPECIFIC ANTIBODY JNJ-63709178 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD123/CD3 BISPECIFIC ANTIBODY JNJ-63709178 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-ILT7 ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-ILT7 ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-C-MET MONOCLONAL ANTIBODY SAIT301 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-C-MET MONOCLONAL ANTIBODY SAIT301 drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY 11D10 ANTI-IDIOTYPE VACCINE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY 11D10 ANTI-IDIOTYPE VACCINE drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY 1F5 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY 1F5 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-PD-1 MONOCLONAL ANTIBODY MEDI0680 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-PD-1 MONOCLONAL ANTIBODY MEDI0680 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-MUC16/MMAE ANTIBODY-DRUG CONJUGATE DMUC4064A Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-MUC16/MMAE ANTIBODY-DRUG CONJUGATE DMUC4064A drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY L6 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY L6 drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY ICR62 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY ICR62 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-PD-1 MONOCLONAL ANTIBODY SYM021 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-PD-1 MONOCLONAL ANTIBODY SYM021 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-EGFR MONOCLONAL ANTIBODY Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-EGFR MONOCLONAL ANTIBODY drug from theDGIdb Drug Targets 2026 dataset.
ANTI-PSCA MONOCLONAL ANTIBODY AGS-1C4D4 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-PSCA MONOCLONAL ANTIBODY AGS-1C4D4 drug from theDGIdb Drug Targets 2026 dataset.
MONOCLONAL ANTIBODY 11D10 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the MONOCLONAL ANTIBODY 11D10 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-TIGIT MONOCLONAL ANTIBODY ASP8374 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-TIGIT MONOCLONAL ANTIBODY ASP8374 drug from theDGIdb Drug Targets 2026 dataset.
IODINE I 131 MONOCLONAL ANTIBODY 81C6 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the IODINE I 131 MONOCLONAL ANTIBODY 81C6 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-GITR MONOCLONAL ANTIBODY MK-4166 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-GITR MONOCLONAL ANTIBODY MK-4166 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-HUMAN GITR MONOCLONAL ANTIBODY TRX518 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-HUMAN GITR MONOCLONAL ANTIBODY TRX518 drug from theDGIdb Drug Targets 2026 dataset.
AGONISTIC ANTI-OX40 MONOCLONAL ANTIBODY INCAGN01949 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the AGONISTIC ANTI-OX40 MONOCLONAL ANTIBODY INCAGN01949 drug from theDGIdb Drug Targets 2026 dataset.
ANTI-CD30 MONOCLONAL ANTIBODY MDX-1401 Gene Set From DGIdb Drug Targets 2026 interacting proteins for the ANTI-CD30 MONOCLONAL ANTIBODY MDX-1401 drug from theDGIdb Drug Targets 2026 dataset.
Neuraminidase deficiency with beta-galactosidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choline deficiency; dna damage; folic acid deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
protein c deficiency; protein s deficiency; venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset.
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset.
Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Set From Reactome Pathways 2014 proteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset.
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Set From Reactome Pathways 2024 proteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset.
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Secondary motor area Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
caudal secondary prosencephalon Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in caudal secondary prosencephalon relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 2/3 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 1 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 5 Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
rostral secondary prosencephalon Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in rostral secondary prosencephalon relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 6a Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary motor area, layer 6b Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Secondary motor area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
secondary prosencephalon Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in secondary prosencephalon relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Secondary hypothyroidism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Secondary hypothyroidism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
secondary lysosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the secondary lysosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
secondary lysosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the secondary lysosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
secondary cell wall cellulose synthase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the secondary cell wall cellulose synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
secondary cell wall Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the secondary cell wall cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Hyperparathyroidism, Secondary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyperparathyroidism, Secondary from the curated CTD Gene-Disease Associations dataset.
Parkinson Disease, Secondary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease, Secondary from the curated CTD Gene-Disease Associations dataset.
secondary syphilis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease secondary syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
secondary parkinson disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease secondary parkinson disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
malignant secondary hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
secondary hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
secondary hyperparathyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease secondary hyperparathyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
secondary hypertrophic osteoarthropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease secondary hypertrophic osteoarthropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hyperparathyroidism, secondary Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperparathyroidism, secondary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
secondary and fmf amyloidosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease secondary and fmf amyloidosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperparathyroidism, secondary; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperparathyroidism, secondary; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; hyperparathyroidism, secondary; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hyperparathyroidism, secondary; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
premature ovarian failure; primary amenorrhea; secondary amenorrhea Gene Set From GAD Gene-Disease Associations genes associated with the disease premature ovarian failure; primary amenorrhea; secondary amenorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
secondary Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term secondary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
development of secondary sexual characteristics Gene Set From GO Biological Process Annotations 2015 genes participating in the development of secondary sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset.
development of secondary male sexual characteristics Gene Set From GO Biological Process Annotations 2015 genes participating in the development of secondary male sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of secondary metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of secondary metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
viral capsid secondary envelopment Gene Set From GO Biological Process Annotations 2015 genes participating in the viral capsid secondary envelopment biological process from the curated GO Biological Process Annotations 2015 dataset.
rna secondary structure unwinding Gene Set From GO Biological Process Annotations 2015 genes participating in the rna secondary structure unwinding biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
alveolar secondary septum development Gene Set From GO Biological Process Annotations 2015 genes participating in the alveolar secondary septum development biological process from the curated GO Biological Process Annotations 2015 dataset.
development of secondary female sexual characteristics Gene Set From GO Biological Process Annotations 2015 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
secondary metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the secondary metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
secondary alcohol metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.
notch signaling pathway involved in regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the notch signaling pathway involved in regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
secondary heart field specification Gene Set From GO Biological Process Annotations 2015 genes participating in the secondary heart field specification biological process from the curated GO Biological Process Annotations 2015 dataset.
secondary lysosome Gene Set From GO Cellular Component Annotations 2015 proteins localized to the secondary lysosome cellular component from the curated GO Cellular Component Annotations 2015 dataset.
secondary active monocarboxylate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the secondary active monocarboxylate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
proton-dependent peptide secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the proton-dependent peptide secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
sulfur-containing amino acid secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the sulfur-containing amino acid secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
dna secondary structure binding Gene Set From GO Molecular Function Annotations 2015 genes performing the dna secondary structure binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
proton-dependent oligopeptide secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the proton-dependent oligopeptide secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
secondary active sulfate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the secondary active sulfate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
cystine secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the cystine secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
secondary active organic cation transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the secondary active organic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
neutral l-amino acid secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the neutral l-amino acid secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
secondary active oligopeptide transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the secondary active oligopeptide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
pyruvate secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2015 genes performing the pyruvate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
secondary amenorrhea Gene Set From GWASdb SNP-Phenotype Associations genes associated with the secondary amenorrhea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of secondary sexual hair Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
low gonadotropins (secondary hypogonadism) Gene Set From HPO Gene-Disease Associations genes associated with the low gonadotropins (secondary hypogonadism) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
facial palsy secondary to cranial hyperostosis Gene Set From HPO Gene-Disease Associations genes associated with the facial palsy secondary to cranial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
failure to thrive secondary to recurrent infections Gene Set From HPO Gene-Disease Associations genes associated with the failure to thrive secondary to recurrent infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absence of secondary sex characteristics Gene Set From HPO Gene-Disease Associations genes associated with the absence of secondary sex characteristics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
secondary hyperparathyroidism Gene Set From HPO Gene-Disease Associations genes associated with the secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft secondary palate Gene Set From HPO Gene-Disease Associations genes associated with the cleft secondary palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad secondary alveolar ridge Gene Set From HPO Gene-Disease Associations genes associated with the broad secondary alveolar ridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subperiosteal erosions due to secondary hyperparathyroidism Gene Set From HPO Gene-Disease Associations genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
secondary amenorrhea Gene Set From HPO Gene-Disease Associations genes associated with the secondary amenorrhea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hyperparathyroidism, Secondary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperparathyroidism, Secondary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Parkinson Disease, Secondary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Parkinson Disease, Secondary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Headache Disorders, Secondary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Headache Disorders, Secondary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
decreased secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spleen secondary b follicle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen secondary b follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lymph node secondary follicle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node secondary follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary palate development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
disorganized secondary lens fibers Gene Set From MPO Gene-Phenotype Associations gene mutations causing the disorganized secondary lens fibers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
secondary sex reversal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the secondary sex reversal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary muscle spindle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary muscle spindle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial loss of secondary muscle spindle Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary ovarian follicle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary ovarian follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of secondary bone resorption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of secondary bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cleft secondary palate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cleft secondary palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary polar body morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary polar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary sex determination Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set From OMIM Gene-Disease Associations genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.
{?amyloidosis, secondary, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {?amyloidosis, secondary, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
secondary spermatocyte Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue secondary spermatocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
secondary root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue secondary root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
secondary oocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue secondary oocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
secondary spermatocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue secondary spermatocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Secondary Malignant Neoplasm Of Lymph Node Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Lymph Node in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Bone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Lung Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Lung in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Acute Myeloid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Bone Marrow Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Colon And/Or Rectum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Colon And/Or Rectum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Parkinson Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Parkinson Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Biliary Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Biliary Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Hypothyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Pulmonary Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Pulmonary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Polycythemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Polycythemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary SjÃ¶gren'S Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary SjÃ¶gren'S Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Focal Segmental Glomerulosclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Focal Segmental Glomerulosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Peritoneum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Peritoneum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Acquired Sideroblastic Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Acquired Sideroblastic Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Haemophagocytic Lymphohistiocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Haemophagocytic Lymphohistiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypocortisolism Secondary To Another Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypocortisolism Secondary To Another Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Adrenal Insufficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Adrenal Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Omentum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Omentum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Physiologic Amenorrhea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Physiologic Amenorrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Hemochromatosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hemochromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Trigeminal Neuralgia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Trigeminal Neuralgia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Adrenal Gland Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Adrenal Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Vertebral Column Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Vertebral Column in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Female Breast Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Female Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Microcephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dilated Cardiomyopathy Secondary To Metabolic Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dilated Cardiomyopathy Secondary To Metabolic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Open Angle Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Open Angle Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentin, Secondary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentin, Secondary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Peripheral Chondrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Peripheral Chondrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Angle-Closure Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Angle-Closure Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Osteoporosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Pulmonary Arterial Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Pulmonary Arterial Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Axilla Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Axilla in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Peritonitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Secondary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Small Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Small Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scleroderma-Like Secondary Cutaneous Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scleroderma-Like Secondary Cutaneous Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Myelodysplastic Syndromes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Myelodysplastic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Prostate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Rectum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Rectum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Hyperaldosteronism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hyperaldosteronism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Raynaud'S Phenomenon Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Raynaud'S Phenomenon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Treatment Related Secondary Malignancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Treatment Related Secondary Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Mediastinum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Mediastinum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Roseola Rash Of Secondary Syphilis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Roseola Rash Of Secondary Syphilis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Bacterial Pneumonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Bacterial Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intracranial Hypotension, Secondary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intracranial Hypotension, Secondary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Pulmonary Alveolar Proteinosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Pulmonary Alveolar Proteinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Caries Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Caries in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteomalacia Secondary To Drug Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteomalacia Secondary To Drug in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dilated Cardiomyopathy Secondary To Viral Myocarditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dilated Cardiomyopathy Secondary To Viral Myocarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Pleura Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Pleura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Antiphospholipid Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Antiphospholipid Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Chondrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Chondrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Secondary Sexual Hair Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Secondary Sexual Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Angle-Closure Glaucoma - Synechial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Angle-Closure Glaucoma - Synechial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Esotropia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Esotropia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Hypertriglyceridemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hypertriglyceridemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Hypercholesterolemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hypercholesterolemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microspherophakia And/Or Megalocornea, With Ectopia Lentis And With Or Without Secondary Glaucoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Heart Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Heart in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Sclerosing Cholangitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Sclerosing Cholangitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Male Infertility Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Male Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Hypoparathyroidism Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Hypoparathyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Lymph Nodes Of Neck Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Lymph Nodes Of Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Spleen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Spleen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Insomnia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Secondary Insomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Secondary Amenorrhea Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Secondary Amenorrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Secondary Sex Characteristics Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Secondary Sex Characteristics in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Failure To Thrive Secondary To Recurrent Infections Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Failure To Thrive Secondary To Recurrent Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Secondary Caesarian Section Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Secondary Caesarian Section in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Secondary Anemia Nos Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Secondary Anemia Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Secondary Alveolar Ridge Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Secondary Alveolar Ridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal Eeg Discharges With Secondary Generalization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal Eeg Discharges With Secondary Generalization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Secondary Hyperlipidemia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Secondary Hyperlipidemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Facial Palsy Secondary To Cranial Hyperostosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Palsy Secondary To Cranial Hyperostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Secondary Carcinoma Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Secondary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
RNA secondary structure unwinding Gene Set From GO Biological Process Annotations 2023 genes participating in the RNA secondary structure unwinding biological process from the curated GO Biological Process Annotations 2023 dataset.
secondary palate development Gene Set From GO Biological Process Annotations 2023 genes participating in the secondary palate development biological process from the curated GO Biological Process Annotations 2023 dataset.
secondary heart field specification Gene Set From GO Biological Process Annotations 2023 genes participating in the secondary heart field specification biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
secondary piRNA processing Gene Set From GO Biological Process Annotations 2023 genes participating in the secondary piRNA processing biological process from the curated GO Biological Process Annotations 2023 dataset.
development of secondary female sexual characteristics Gene Set From GO Biological Process Annotations 2023 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2023 dataset.
secondary alcohol metabolic process Gene Set From GO Biological Process Annotations 2023 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
secondary alcohol biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the secondary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.
secondary lysosome Gene Set From GO Cellular Component Annotations 2023 proteins localized to the secondary lysosome cellular component from the curated GO Cellular Component Annotations 2023 dataset.
pyruvate secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the pyruvate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
citrate secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the citrate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
secondary active sulfate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the secondary active sulfate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
proton-dependent oligopeptide secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the proton-dependent oligopeptide secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
DNA secondary structure binding Gene Set From GO Molecular Function Annotations 2023 genes performing the DNA secondary structure binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
secondary active organic cation transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the secondary active organic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
secondary active monocarboxylate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the secondary active monocarboxylate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
sulfur-containing amino acid secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the sulfur-containing amino acid secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
tricarboxylate secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the tricarboxylate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
secondary active oligopeptide transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the secondary active oligopeptide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
cystine secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2023 genes performing the cystine secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal secondary sex determination Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary sex determination phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
secondary sex reversal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the secondary sex reversal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cleft secondary palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft secondary palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal secondary palate development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary palate development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal lymph node secondary follicle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymph node secondary follicle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spleen secondary B follicle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spleen secondary B follicle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
disorganized secondary lens fibers Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized secondary lens fibers phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased secondary ovarian follicle number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased secondary ovarian follicle number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
partial loss of secondary muscle spindle Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased secondary ovarian follicle number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased secondary ovarian follicle number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent secondary ovarian follicles Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent secondary ovarian follicles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal primary and secondary palatal fusion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal primary and secondary palatal fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal secondary ovarian follicle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary ovarian follicle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal secondary polar body morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary polar body morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal secondary palate morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal secondary palate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
secondary palate development Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary palate development biological process from the curated GO Biological Process Annotations 2025 dataset.
secondary heart field specification Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary heart field specification biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of secondary heart field cardioblast proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of secondary heart field cardioblast proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
secondary piRNA processing Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary piRNA processing biological process from the curated GO Biological Process Annotations 2025 dataset.
development of secondary female sexual characteristics Gene Set From GO Biological Process Annotations 2025 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2025 dataset.
secondary alcohol metabolic process Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
secondary alcohol biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of secondary metabolite biosynthetic process Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of secondary metabolite biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.
secondary lysosome Gene Set From GO Cellular Component Annotations 2025 proteins localized to the secondary lysosome cellular component from the curated GO Cellular Component Annotations 2025 dataset.
pyruvate secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the pyruvate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
citrate secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the citrate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
secondary active sulfate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the secondary active sulfate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
proton-dependent oligopeptide secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the proton-dependent oligopeptide secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
DNA secondary structure binding Gene Set From GO Molecular Function Annotations 2025 genes performing the DNA secondary structure binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
secondary active organic cation transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the secondary active organic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
secondary active monocarboxylate transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the secondary active monocarboxylate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
tricarboxylate secondary active transmembrane transporter activity Gene Set From GO Molecular Function Annotations 2025 genes performing the tricarboxylate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Secondary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary hyperparathyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary hyperparathyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary hypertrophic osteoarthropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary hypertrophic osteoarthropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary syphilis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary Parkinson disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary Parkinson disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary corneal edema Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary corneal edema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary hyperparathyroidism of renal origin Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary hyperparathyroidism of renal origin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Malignant secondary hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Benign secondary hypertension Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign secondary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-renal secondary hyperparathyroidism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-renal secondary hyperparathyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary oocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Secondary oocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Secondary spermatocyte Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Secondary spermatocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Secondary enamel knot Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Secondary enamel knot in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Secondary root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Secondary root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Secondary lysosome Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Secondary lysosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Secondary lysosome Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Secondary lysosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Secondary cell wall Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Secondary cell wall cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Secondary cell wall cellulose synthase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Secondary cell wall cellulose synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Secondary plasmodesma Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Secondary plasmodesma cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Endplate acetylcholinesterase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sepiapterin reductase deficiency Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Birbeck granule deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid deficiency 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid deficiency 4 Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Properdin deficiency, X-linked Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral folate deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral folate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Phosphoserine aminotransferase deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnitine acylcarnitine translocase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
HNSHA due to aldolase A deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-activating factor acetylhydrolase deficiency Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Lipase deficiency combined phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
5-Oxoprolinase deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid deficiency with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proopiomelanocortin deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proopiomelanocortin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Intrinsic factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
21-hydroxylase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Molybdenum cofactor deficiency, complementation group C Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Molybdenum cofactor deficiency, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Biotinidase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adenine phosphoribosyltransferase deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamate formiminotransferase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Ganglioside sialidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
C1q deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the C1q deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interferon gamma receptor deficiency Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the N-acetylaspartate deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adenylosuccinate lyase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adenylosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Triosephosphate isomerase deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aromatase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome due to mitochondrial complex I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple sulfatase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of galactokinase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ACTH deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ACTH deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PROPERDIN DEFICIENCY, TYPE III Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Antithrombin III deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inosine triphosphatase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sarcosine dehydrogenase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Arginase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hepatic lipase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hepatic lipase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor X deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Vitamin k-dependent clotting factors, combined deficiency of, 1 Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of iodide peroxidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glycosylphosphatidylinositol deficiency Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Caspase-8 deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Phosphoglycerate kinase 1 deficiency Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Cytochrome-c oxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Enterokinase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Myeloperoxidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial phosphate carrier deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the IRAK4 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukocyte adhesion deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Muscle AMP deaminase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dihydropyrimidinase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dihydropyrimidinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dimethylglycine dehydrogenase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Isovaleryl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cd59 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cd59 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ornithine aminotransferase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-like growth factor I deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined 4 Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pyruvate carboxylase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pyruvate carboxylase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gluthathione synthetase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gluthathione synthetase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fumarase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fumarase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of transaldolase Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the MASP2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Argininosuccinate lyase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Argininosuccinate lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Prekallikrein deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prekallikrein deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chitotriosidase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Mineralocorticoid deficiency, isolated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement 1s deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complement 1s deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dihydropteridine reductase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Myd88 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cd8 deficiency, familial Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acid-labile subunit deficiency Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complement factor B deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Beta-hydroxyisobutyryl-CoA deacylase deficiency Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Proline dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Factor H deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Factor H deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glutamine deficiency, congenital Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Ornithine carbamoyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sucrase-isomaltase deficiency Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Fucosyltransferase 6 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Asparagine synthetase deficiency Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pituitary hormone deficiency, combined, 5 Gene Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Protein S deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Combined deficiency of sialidase AND beta galactosidase Gene Set From 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 Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Prolidase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Deficiency of beta-ureidopropionase Gene Set From 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 Set From ClinVar Gene-Phenotype Associations genes associated with the Deficiency of guanidinoacetate methyltransferase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MYD88 Deficiency Gene Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Platelet Glycoprotein IV Deficiency Gene Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prekallikrein Deficiency from the curated CTD Gene-Disease Associations dataset.
Methylenetetrahydrofolate reductase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Glucocorticoid Deficiency 3 Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease IgA Deficiency from the curated CTD Gene-Disease Associations dataset.
Lipase deficiency combined Gene Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.
DNA Repair-Deficiency Disorders Gene Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.
Enterokinase Deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.
Beta ketothiolase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta ketothiolase deficiency from the curated CTD Gene-Disease Associations dataset.
Transaldolase Deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset.
Vitamin B 12 Deficiency Gene Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset.
Familial HDL deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease VLCAD deficiency from the curated CTD Gene-Disease Associations dataset.
18-Hydroxylase deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of Gene Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.
3-Hydroxyacyl-CoA Dehydrogenase Deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoglycerate Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset.
Vitamin D Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin D Deficiency from the curated CTD Gene-Disease Associations dataset.
Factor V Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor V Deficiency from the curated CTD Gene-Disease Associations dataset.
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.
Pyruvate Dehydrogenase Complex Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase Complex Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Ataxia with vitamin E deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ataxia with vitamin E deficiency from the curated CTD Gene-Disease Associations dataset.
Aromatic amino acid decarboxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aromatic amino acid decarboxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Factor X Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor X Deficiency from the curated CTD Gene-Disease Associations dataset.
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset.
Holocarboxylase Synthetase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Holocarboxylase Synthetase Deficiency from the curated CTD Gene-Disease Associations dataset.
N-acetyl glutamate synthetase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease N-acetyl glutamate synthetase deficiency from the curated CTD Gene-Disease Associations dataset.
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1 from the curated CTD Gene-Disease Associations dataset.
Dimethylglycine Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dimethylglycine Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Pituitary Hormone Deficiency, Combined, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pituitary Hormone Deficiency, Combined, 1 from the curated CTD Gene-Disease Associations dataset.
Pituitary Hormone Deficiency, Combined, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pituitary Hormone Deficiency, Combined, 2 from the curated CTD Gene-Disease Associations dataset.
Trehalase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trehalase Deficiency from the curated CTD Gene-Disease Associations dataset.
Guanidinoacetate methyltransferase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Guanidinoacetate methyltransferase deficiency from the curated CTD Gene-Disease Associations dataset.
Aminoacylase 1 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aminoacylase 1 deficiency from the curated CTD Gene-Disease Associations dataset.
Antithrombin III Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Antithrombin III Deficiency from the curated CTD Gene-Disease Associations dataset.
Phosphoenolpyruvate carboxykinase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoenolpyruvate carboxykinase deficiency from the curated CTD Gene-Disease Associations dataset.
17-Hydroxysteroid Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 17-Hydroxysteroid Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Heparin Cofactor II Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Heparin Cofactor II Deficiency from the curated CTD Gene-Disease Associations dataset.
Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency from the curated CTD Gene-Disease Associations dataset.
D-BIFUNCTIONAL PROTEIN DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease D-BIFUNCTIONAL PROTEIN DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset.
Arginine:Glycine Amidinotransferase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arginine:Glycine Amidinotransferase Deficiency from the curated CTD Gene-Disease Associations dataset.
Biotinidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Biotinidase Deficiency from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT C1r/C1s DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Methionine Adenosyltransferase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methionine Adenosyltransferase Deficiency from the curated CTD Gene-Disease Associations dataset.
Phosphoenolpyruvate carboxykinase 2 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Phosphoenolpyruvate carboxykinase 2 deficiency from the curated CTD Gene-Disease Associations dataset.
Glycine N-Methyltransferase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycine N-Methyltransferase Deficiency from the curated CTD Gene-Disease Associations dataset.
Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.
Magnesium Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Magnesium Deficiency from the curated CTD Gene-Disease Associations dataset.
2-Methylbutyryl-CoA Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 2-Methylbutyryl-CoA Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Glycosylphosphatidylinositol deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glycosylphosphatidylinositol deficiency from the curated CTD Gene-Disease Associations dataset.
Factor Xiii, A Subunit, Deficiency Of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor Xiii, A Subunit, Deficiency Of from the curated CTD Gene-Disease Associations dataset.
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.
Leukocyte adhesion deficiency type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte adhesion deficiency type 1 from the curated CTD Gene-Disease Associations dataset.
Isobutyryl-CoA dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Isobutyryl-CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
Dihydropyrimidine Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dihydropyrimidine Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Corticosteroid-Binding Globulin Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Corticosteroid-Binding Globulin Deficiency from the curated CTD Gene-Disease Associations dataset.
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.
ACTH Deficiency, Isolated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ACTH Deficiency, Isolated from the curated CTD Gene-Disease Associations dataset.
Factor XIII, B Subunit, Deficiency Of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor XIII, B Subunit, Deficiency Of from the curated CTD Gene-Disease Associations dataset.
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.
GLUT1 DEFICIENCY SYNDROME 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease GLUT1 DEFICIENCY SYNDROME 2 from the curated CTD Gene-Disease Associations dataset.
Iron-Refractory Iron Deficiency Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Iron-Refractory Iron Deficiency Anemia from the curated CTD Gene-Disease Associations dataset.
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset.
Specific Granule Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Specific Granule Deficiency from the curated CTD Gene-Disease Associations dataset.
Insulin-Like Growth Factor I Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Insulin-Like Growth Factor I Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement component 5 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement component 5 deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Component 7 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 7 Deficiency from the curated CTD Gene-Disease Associations dataset.
Lactate dehydrogenase deficiency type A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lactate dehydrogenase deficiency type A from the curated CTD Gene-Disease Associations dataset.
Pyruvate Dehydrogenase E3-Binding Protein Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase E3-Binding Protein Deficiency from the curated CTD Gene-Disease Associations dataset.
Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.
Cortisone reductase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cortisone reductase deficiency from the curated CTD Gene-Disease Associations dataset.
Peroxisomal ACYL-COA oxidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peroxisomal ACYL-COA oxidase deficiency from the curated CTD Gene-Disease Associations dataset.
NADH cytochrome B5 reductase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NADH cytochrome B5 reductase deficiency from the curated CTD Gene-Disease Associations dataset.
3b-Hydroxysteroid Dehydrogenase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3b-Hydroxysteroid Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.
Thiamine Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thiamine Deficiency from the curated CTD Gene-Disease Associations dataset.
Mitochondrial Complex II Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mitochondrial Complex II Deficiency from the curated CTD Gene-Disease Associations dataset.
Sucrase-isomaltase deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sucrase-isomaltase deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
Systemic carnitine deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Systemic carnitine deficiency from the curated CTD Gene-Disease Associations dataset.
Gamma-cystathionase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gamma-cystathionase deficiency from the curated CTD Gene-Disease Associations dataset.
Pituitary Hormone Deficiency, Combined, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pituitary Hormone Deficiency, Combined, 4 from the curated CTD Gene-Disease Associations dataset.
Combined Saposin Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Saposin Deficiency from the curated CTD Gene-Disease Associations dataset.
Radial Ray Deficiency, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Radial Ray Deficiency, X-Linked from the curated CTD Gene-Disease Associations dataset.
Beta-Ureidopropionase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta-Ureidopropionase Deficiency from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 5 from the curated CTD Gene-Disease Associations dataset.
Combined Oxidative Phosphorylation Deficiency 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Combined Oxidative Phosphorylation Deficiency 4 from the curated CTD Gene-Disease Associations dataset.
Protein C Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Protein C Deficiency from the curated CTD Gene-Disease Associations dataset.
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
succinic semialdehyde dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease succinic semialdehyde dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
Carboxypeptidase N Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carboxypeptidase N Deficiency from the curated CTD Gene-Disease Associations dataset.
Purine Nucleoside Phosphorylase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Purine Nucleoside Phosphorylase Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Component 4, Partial Deficiency Of Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 4, Partial Deficiency Of from the curated CTD Gene-Disease Associations dataset.
Familial Glucocorticoid Deficiency 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial Glucocorticoid Deficiency 1 from the curated CTD Gene-Disease Associations dataset.
Endplate Acetylcholinesterase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Endplate Acetylcholinesterase Deficiency from the curated CTD Gene-Disease Associations dataset.
Factor XIII Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor XIII Deficiency from the curated CTD Gene-Disease Associations dataset.
NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.
Fructose-1,6-Diphosphatase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fructose-1,6-Diphosphatase Deficiency from the curated CTD Gene-Disease Associations dataset.
MASP2 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MASP2 Deficiency from the curated CTD Gene-Disease Associations dataset.
2,4-Dienoyl-CoA Reductase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 2,4-Dienoyl-CoA Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.
Alpha-ketoglutarate dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alpha-ketoglutarate dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Factor H Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Factor H Deficiency from the curated CTD Gene-Disease Associations dataset.
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset.
COMPLEMENT COMPONENT 2 DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease COMPLEMENT COMPONENT 2 DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
TRANSCOBALAMIN II DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease TRANSCOBALAMIN II DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Prolidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Prolidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Leukocyte-Adhesion Deficiency Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukocyte-Adhesion Deficiency Syndrome from the curated CTD Gene-Disease Associations dataset.
Dihydropyrimidinase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dihydropyrimidinase Deficiency from the curated CTD Gene-Disease Associations dataset.
Deficiency Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deficiency Diseases from the curated CTD Gene-Disease Associations dataset.
BISPHOSPHOGLYCERATE MUTASE DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BISPHOSPHOGLYCERATE MUTASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
Vitamin E Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Vitamin E Deficiency from the curated CTD Gene-Disease Associations dataset.
PROTHROMBIN DEFICIENCY, CONGENITAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROTHROMBIN DEFICIENCY, CONGENITAL from the curated CTD Gene-Disease Associations dataset.
Carnitine Palmitoyltransferase II Deficiency, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Infantile from the curated CTD Gene-Disease Associations dataset.
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency from the curated CTD Gene-Disease Associations dataset.
CD59 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CD59 Deficiency from the curated CTD Gene-Disease Associations dataset.
Myeloperoxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myeloperoxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Methylmalonyl-CoA Epimerase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonyl-CoA Epimerase Deficiency from the curated CTD Gene-Disease Associations dataset.
Mevalonate Kinase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mevalonate Kinase Deficiency from the curated CTD Gene-Disease Associations dataset.
Complement Factor I Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Factor I Deficiency from the curated CTD Gene-Disease Associations dataset.
Beta-Hydroxyisobutyryl CoA Deacylase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Beta-Hydroxyisobutyryl CoA Deacylase Deficiency from the curated CTD Gene-Disease Associations dataset.
Cytochrome-c Oxidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cytochrome-c Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Hyaluronidase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyaluronidase Deficiency from the curated CTD Gene-Disease Associations dataset.
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
3-methylcrotonyl CoA carboxylase 1 deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 3-methylcrotonyl CoA carboxylase 1 deficiency from the curated CTD Gene-Disease Associations dataset.
Multiple Sulfatase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Lysosomal beta-mannosidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lysosomal beta-mannosidase deficiency from the curated CTD Gene-Disease Associations dataset.
Medium chain acyl CoA dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Medium chain acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
Familial apoceruloplasmin deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial apoceruloplasmin deficiency from the curated CTD Gene-Disease Associations dataset.
Metachromatic Leukodystrophy due to Saposin B Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset.
Glutamine deficiency, congenital Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutamine deficiency, congenital from the curated CTD Gene-Disease Associations dataset.
Sulfite oxidase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sulfite oxidase deficiency from the curated CTD Gene-Disease Associations dataset.
Pyruvate Kinase Deficiency of Red Cells Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Kinase Deficiency of Red Cells from the curated CTD Gene-Disease Associations dataset.
Factor VII Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor VII Deficiency from the curated CTD Gene-Disease Associations dataset.
MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.
IRAK4 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease IRAK4 Deficiency from the curated CTD Gene-Disease Associations dataset.
Butyrylcholinesterase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Butyrylcholinesterase deficiency from the curated CTD Gene-Disease Associations dataset.
Short chain Acyl CoA dehydrogenase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.
Gamma aminobutyric acid transaminase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gamma aminobutyric acid transaminase deficiency from the curated CTD Gene-Disease Associations dataset.
Pyruvate Carboxylase Deficiency Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Carboxylase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.
Complement Component 6 Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Complement Component 6 Deficiency from the curated CTD Gene-Disease Associations dataset.
Glutamate formiminotransferase deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Glutamate formiminotransferase deficiency from the curated CTD Gene-Disease Associations dataset.
Factor XII Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Factor XII Deficiency from the curated CTD Gene-Disease Associations dataset.

Harmonizome 3.0

Secondary Antibody Deficiency Gene Set

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

specific antibody deficiency Gene Set

specific anti-polysaccharide antibody deficiency Gene Set

autoinflammation, antibody deficiency, and immune dysregulation syndrome Gene Set

Anti-Polysaccharide Antibody Deficiency Gene Set

Antibody Deficiency Syndrome Gene Set

Antibody Deficiency Due To Defect In Cd19 Gene Set

Plcg2-Associated Antibody Deficiency And Immune Dysregulation Gene Set

Specific Anti-Polysaccharide Antibody Deficiency Gene Set

Specific Pneumococcal Antibody Deficiency Gene Set

Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Gene Set

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

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

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

secondary growth hormone deficiency Gene Set

Secondary Growth Hormone Deficiency Gene Set

Secondary Immune Deficiency Gene Set

Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Gene Set

humanized SMART Anti-IL-12 Antibody Gene Set

anti-neutrophil cytoplasmic antibody-associated vasculitis; Gene Set

antineutrophil cytoplasmic antibody; (anca)-associated vasculitis Gene Set

measles antibody level Gene Set

liver cancer risk in hcv antibody-positive Gene Set

anti-cyclic citrullianted peptide antibody Gene Set

anti neutrophil cytoplasmic antibody; (anca)-associated vasculitis Gene Set

antibody response to pertussis vaccination Gene Set

antibody Gene Set

Antibody status in Tripanosoma cruzi seropositivity Gene Set

Thyroid peroxidase antibody positivity Gene Set

Cytomegalovirus antibody response Gene Set

Anti-cyclic Citrullinated Peptide Antibody Gene Set

Thyroid peroxidase antibody levels Gene Set

Antineutrophil cytoplasmic antibody-associated vasculitis Gene Set

platelet antibody positive Gene Set

smooth muscle antibody positivity Gene Set

autoimmune antibody positivity Gene Set

antineutrophil antibody positivity Gene Set

antinuclear antibody positivity Gene Set

absent specific antibody response Gene Set

antiphospholipid antibody positivity Gene Set

increased anti-nuclear antigen antibody level Gene Set

increased anti-single stranded dna antibody level Gene Set

increased anti-double stranded dna antibody level Gene Set

decreased anti-nuclear antigen antibody level Gene Set

increased anti-chromatin antibody level Gene Set

increased anti-erythrocyte antigen antibody level Gene Set

decreased anti-double stranded dna antibody level Gene Set

increased anti-histone antibody level Gene Set

antibody-specificity Gene Set

Classical antibody-mediated complement activation Gene Set

Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Gene Set

Anti-Neutrophil Cytoplasmic Antibody Positive Vasculitis Gene Set

Anti-Pit-1 Antibody Syndrome Gene Set

Absent Specific Antibody Response Gene Set

Anti-Thyroid Peroxidase Antibody Positivity Gene Set

Antiphospholipid Antibody Positivity Gene Set

Decreased Antibody Level In Blood Gene Set

Thyroglobulin Antibody Measurement Gene Set

Increased Antibody Level In Blood Gene Set

Anti-Cyclic Citrullinated Peptide Antibody Gene Set

Anti-Cyclic Citrullinated Peptide Antibody Level Gene Set

Antineutrophil Antibody Positivity Gene Set

Platelet Antibody Positive Gene Set

Autoimmune Antibody Positivity Gene Set

Anti-Nuclear Antibody Measurement Gene Set

Anti-Liver Cytosolic Antigen Type 1 Antibody Positivity Gene Set

Insulin Receptor Antibody Positivity Gene Set

Anti-Glutamic Acid Decarboxylase Antibody Positivity Gene Set

Maternal Anticardiolipin Antibody Positive Gene Set

Anti-Multiple Nuclear Dots Antibody Positivity Gene Set

antibody-dependent cellular cytotoxicity Gene Set

positive regulation of antibody-dependent cellular cytotoxicity Gene Set

negative regulation of antibody-dependent cellular cytotoxicity Gene Set

regulation of antibody-dependent cellular cytotoxicity Gene Set

increased anti-double stranded DNA antibody level Gene Set

increased anti-single stranded DNA antibody level Gene Set

increased anti-nuclear antigen antibody level Gene Set

increased anti-histone antibody level Gene Set